The DOI matches its Crossref record; 43 of the 45 references it cites were found in a registry or an index; none of the 23 sources its claims cite is checked for support yet.
Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate
Open accessAbstract
Objective To use aromatase inhibition for induction of ovulation in women in whom clomiphene citrate (CC) treatment was unsuccessful. Design Prospective trial in infertility patients treated with CC. Setting Two tertiary-referral infertility clinics associated with the Division of Reproductive Sciences, University of Toronto. Patient(s) Twelve patients with anovulatory polycystic ovary syndrome (PCOS) and 10 patients with ovulatory infertility, all of whom had previously received CC with an inadequate outcome (no ovulation and/or endometrial thickness of Intervention(s) The aromatase inhibitor letrozole was given orally in a dose of 2.5 mg on days 3-7 after menses. Main outcome measure(s) Occurrence of ovulation, endometrial thickness, and pregnancy rates. Result(s) With CC treatment in patients with PCOS, ovulation occurred in 8 of 18 cycles (44.4%), and all ovulatory cycles for the women included in this study had endometrial thickness of Conclusion(s) Oral administration of the aromatase inhibitor letrozole is effective for ovulation induction in anovulatory infertility and for increased follicle recruitment in ovulatory infertility. Letrozole appears to avoid the unfavorable effects on the endometrium frequently seen with antiestrogen use for ovulation induction.
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A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In ovulatory patients, the serum E 2 level was 719 pmol/L in letrozole treatment cycles versus 3,003 pmol/L in CC treatment cycles.”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > RESULTS
plainn = 10- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
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A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In the 10 patients with ovulatory infertility, letrozole treatment resulted in a mean number of 2.3 mature follicles and mean endometrial thickness of 0.8 cm.”
- Also stated in: § RESULTS · plain
“The mean number of follicles measuring Ͼ1.5 cm on the day of hCG administration was 2.3 (range, 1-4).”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > Abstract Objective: To use aromatase inhibition for induction of ovulation in women in whom clomiphene citrate (CC) treatment was unsuccessful.Design: Prospective trial in infertility patients treated with CC.Setting: Two tertiary-referral infertility clinics associated with the Division of Reproductive Sciences, University of Toronto.Patient(s): Twelve patients with anovulatory polycystic ovary syndrome (PCOS) and 10 patients with ovulatory infertility, all of whom had previously received CC with an inadequate outcome (no ovulation and/or endometrial thickness of Յ0.5 cm).Intervention(s): The aromatase inhibitor letrozole was given orally in a dose of 2.5 mg on days 3-7 after menses.Main Outcome Measure(s): Occurrence of ovulation, endometrial thickness, and pregnancy rates.Result(s): With CC treatment in patients with PCOS, ovulation occurred in 8 of 18 cycles (44.4%), and all ovulatory cycles for the women included in this study had endometrial thickness of Յ0.5 cm.In 10 ovulatory patients, 15 CC cycles resulted in a mean number of 2.5 mature follicles, but all cycles had endometrial thickness of Յ0.5 cm on the day of hCG administration.With letrozole treatment in the same patients with PCOS, ovulation occurred in 9 of 12 cycles (75%) and pregnancy was achieved in 3 patients (25%).In the 10 patients with ovulatory infertility, letrozole treatment resulted in a mean number of 2.3 mature follicles and mean endometrial thickness of 0.8 cm.Pregnancy was achieved in 1 patient (10%).Conclusion(s): Oral administration of the aromatase inhibitor letrozole is effective for ovulation induction in anovulatory infertility and for increased follicle recruitment in ovulatory infertility.Letrozole appears to avoid the unfavorable effects on the endometrium frequently seen with antiestrogen use for ovulation induction.(Fertil Steril 2001;75:305-9.©2001 by American Society for Reproductive Medicine.) In women with World Health Organization type II anovulatory infertility, the treatment of first choice for the induction of ovulation is an antiestrogen, most commonly clomiphene citrate (CC) (1,2).However, 20%-25% of women are resistant to CC and do not ovulate.In addition, clinical data have revealed a discrepancy between ovulation and conception rates during CC treatment and a higher than expected incidence of miscarriage in conception cycles (3)(4)(5)(6).These observations have been attributed to the antiestrogenic mechanism of action of CC, which involves long-lasting estrogen receptor (ER) depletion.It also appears that CC accumulates in the body because of its long half-life (7).As a result, CC may have a negative effect on the quality and quantity of cervical mucus (8), on endometrial development (9), and on other as yet undetermined fertility factors (10,11). After failure of CC, gonadotropin preparations such as hMG or pure FSH have been used as a second-line treatment for ovulation induction.In women with polycystic ovary syndrome (PCOS), because of the high sensitivity of the ovaries to gonadotropin stimulation, treatment with hMG or pure FSH is difficult to control and characteristically induces several ovulatory follicles, leading to the risk of multiple pregnancies and ovarian hyperstimulation syndrome (OHSS) (12).Therefore, a simple oral treatment that could be used without risk of hyperstimulation and with minimal monitoring would be the preferred therapy.
plaindirectn = 10- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Also stated in: § RESULTS · plain
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“On the day of hCG administration in patients with PCOS, the mean serum E 2 concentration was 962 pmol/L in letrozole treatment cycles, versus 1,638 pmol/L in CC treatment cycles.”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > RESULTS
plainn = 10- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In the 10 patients with ovulatory infertility, letrozole treatment resulted in a mean number of 2.3 mature follicles and mean endometrial thickness of 0.8 cm.”
- Also stated in: § RESULTS · plain
“Mean endometrial thicknesses on the day of hCG administration in patients with PCOS and ovulatory patients was 0.81 and 0.89 cm with letrozole, compared with 0.62 and 0.52 cm in CC treatment cycles, respectively.”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > Abstract Objective: To use aromatase inhibition for induction of ovulation in women in whom clomiphene citrate (CC) treatment was unsuccessful.Design: Prospective trial in infertility patients treated with CC.Setting: Two tertiary-referral infertility clinics associated with the Division of Reproductive Sciences, University of Toronto.Patient(s): Twelve patients with anovulatory polycystic ovary syndrome (PCOS) and 10 patients with ovulatory infertility, all of whom had previously received CC with an inadequate outcome (no ovulation and/or endometrial thickness of Յ0.5 cm).Intervention(s): The aromatase inhibitor letrozole was given orally in a dose of 2.5 mg on days 3-7 after menses.Main Outcome Measure(s): Occurrence of ovulation, endometrial thickness, and pregnancy rates.Result(s): With CC treatment in patients with PCOS, ovulation occurred in 8 of 18 cycles (44.4%), and all ovulatory cycles for the women included in this study had endometrial thickness of Յ0.5 cm.In 10 ovulatory patients, 15 CC cycles resulted in a mean number of 2.5 mature follicles, but all cycles had endometrial thickness of Յ0.5 cm on the day of hCG administration.With letrozole treatment in the same patients with PCOS, ovulation occurred in 9 of 12 cycles (75%) and pregnancy was achieved in 3 patients (25%).In the 10 patients with ovulatory infertility, letrozole treatment resulted in a mean number of 2.3 mature follicles and mean endometrial thickness of 0.8 cm.Pregnancy was achieved in 1 patient (10%).Conclusion(s): Oral administration of the aromatase inhibitor letrozole is effective for ovulation induction in anovulatory infertility and for increased follicle recruitment in ovulatory infertility.Letrozole appears to avoid the unfavorable effects on the endometrium frequently seen with antiestrogen use for ovulation induction.(Fertil Steril 2001;75:305-9.©2001 by American Society for Reproductive Medicine.) In women with World Health Organization type II anovulatory infertility, the treatment of first choice for the induction of ovulation is an antiestrogen, most commonly clomiphene citrate (CC) (1,2).However, 20%-25% of women are resistant to CC and do not ovulate.In addition, clinical data have revealed a discrepancy between ovulation and conception rates during CC treatment and a higher than expected incidence of miscarriage in conception cycles (3)(4)(5)(6).These observations have been attributed to the antiestrogenic mechanism of action of CC, which involves long-lasting estrogen receptor (ER) depletion.It also appears that CC accumulates in the body because of its long half-life (7).As a result, CC may have a negative effect on the quality and quantity of cervical mucus (8), on endometrial development (9), and on other as yet undetermined fertility factors (10,11). After failure of CC, gonadotropin preparations such as hMG or pure FSH have been used as a second-line treatment for ovulation induction.In women with polycystic ovary syndrome (PCOS), because of the high sensitivity of the ovaries to gonadotropin stimulation, treatment with hMG or pure FSH is difficult to control and characteristically induces several ovulatory follicles, leading to the risk of multiple pregnancies and ovarian hyperstimulation syndrome (OHSS) (12).Therefore, a simple oral treatment that could be used without risk of hyperstimulation and with minimal monitoring would be the preferred therapy.
plaindirectn = 10- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Also stated in: § RESULTS · plain
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“No pregnancy was achieved in any of the ovulatory cycles.”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > RESULTS
plainn = 12- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“With letrozole treatment in the same patients with PCOS, ovulation occurred in 9 of 12 cycles (75%) and pregnancy was achieved in 3 patients (25%).”
- Also stated in: § RESULTS · plain
“Pregnancy was achieved in 3 cycles (25%), 2 of which were singleton clinical pregnancies and 1 of which was a chemical pregnancy.”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > Abstract Objective: To use aromatase inhibition for induction of ovulation in women in whom clomiphene citrate (CC) treatment was unsuccessful.Design: Prospective trial in infertility patients treated with CC.Setting: Two tertiary-referral infertility clinics associated with the Division of Reproductive Sciences, University of Toronto.Patient(s): Twelve patients with anovulatory polycystic ovary syndrome (PCOS) and 10 patients with ovulatory infertility, all of whom had previously received CC with an inadequate outcome (no ovulation and/or endometrial thickness of Յ0.5 cm).Intervention(s): The aromatase inhibitor letrozole was given orally in a dose of 2.5 mg on days 3-7 after menses.Main Outcome Measure(s): Occurrence of ovulation, endometrial thickness, and pregnancy rates.Result(s): With CC treatment in patients with PCOS, ovulation occurred in 8 of 18 cycles (44.4%), and all ovulatory cycles for the women included in this study had endometrial thickness of Յ0.5 cm.In 10 ovulatory patients, 15 CC cycles resulted in a mean number of 2.5 mature follicles, but all cycles had endometrial thickness of Յ0.5 cm on the day of hCG administration.With letrozole treatment in the same patients with PCOS, ovulation occurred in 9 of 12 cycles (75%) and pregnancy was achieved in 3 patients (25%).In the 10 patients with ovulatory infertility, letrozole treatment resulted in a mean number of 2.3 mature follicles and mean endometrial thickness of 0.8 cm.Pregnancy was achieved in 1 patient (10%).Conclusion(s): Oral administration of the aromatase inhibitor letrozole is effective for ovulation induction in anovulatory infertility and for increased follicle recruitment in ovulatory infertility.Letrozole appears to avoid the unfavorable effects on the endometrium frequently seen with antiestrogen use for ovulation induction.(Fertil Steril 2001;75:305-9.©2001 by American Society for Reproductive Medicine.) In women with World Health Organization type II anovulatory infertility, the treatment of first choice for the induction of ovulation is an antiestrogen, most commonly clomiphene citrate (CC) (1,2).However, 20%-25% of women are resistant to CC and do not ovulate.In addition, clinical data have revealed a discrepancy between ovulation and conception rates during CC treatment and a higher than expected incidence of miscarriage in conception cycles (3)(4)(5)(6).These observations have been attributed to the antiestrogenic mechanism of action of CC, which involves long-lasting estrogen receptor (ER) depletion.It also appears that CC accumulates in the body because of its long half-life (7).As a result, CC may have a negative effect on the quality and quantity of cervical mucus (8), on endometrial development (9), and on other as yet undetermined fertility factors (10,11). After failure of CC, gonadotropin preparations such as hMG or pure FSH have been used as a second-line treatment for ovulation induction.In women with polycystic ovary syndrome (PCOS), because of the high sensitivity of the ovaries to gonadotropin stimulation, treatment with hMG or pure FSH is difficult to control and characteristically induces several ovulatory follicles, leading to the risk of multiple pregnancies and ovarian hyperstimulation syndrome (OHSS) (12).Therefore, a simple oral treatment that could be used without risk of hyperstimulation and with minimal monitoring would be the preferred therapy.
plaindirectn = 3- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Also stated in: § RESULTS · plain
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Mean endometrial thicknesses on the day of hCG administration in patients with PCOS and ovulatory patients was 0.81 and 0.89 cm with letrozole, compared with 0.62 and 0.52 cm in CC treatment cycles, respectively.”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > RESULTS
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Pregnancy was achieved in 1 patient (10%).”
- Also stated in: § RESULTS · plain
“A singleton clinical pregnancy (10%) resulted from timed intrauterine insemination in one couple with unexplained infertility who developed 2 follicles of Ͼ1.5 cm.”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > Abstract Objective: To use aromatase inhibition for induction of ovulation in women in whom clomiphene citrate (CC) treatment was unsuccessful.Design: Prospective trial in infertility patients treated with CC.Setting: Two tertiary-referral infertility clinics associated with the Division of Reproductive Sciences, University of Toronto.Patient(s): Twelve patients with anovulatory polycystic ovary syndrome (PCOS) and 10 patients with ovulatory infertility, all of whom had previously received CC with an inadequate outcome (no ovulation and/or endometrial thickness of Յ0.5 cm).Intervention(s): The aromatase inhibitor letrozole was given orally in a dose of 2.5 mg on days 3-7 after menses.Main Outcome Measure(s): Occurrence of ovulation, endometrial thickness, and pregnancy rates.Result(s): With CC treatment in patients with PCOS, ovulation occurred in 8 of 18 cycles (44.4%), and all ovulatory cycles for the women included in this study had endometrial thickness of Յ0.5 cm.In 10 ovulatory patients, 15 CC cycles resulted in a mean number of 2.5 mature follicles, but all cycles had endometrial thickness of Յ0.5 cm on the day of hCG administration.With letrozole treatment in the same patients with PCOS, ovulation occurred in 9 of 12 cycles (75%) and pregnancy was achieved in 3 patients (25%).In the 10 patients with ovulatory infertility, letrozole treatment resulted in a mean number of 2.3 mature follicles and mean endometrial thickness of 0.8 cm.Pregnancy was achieved in 1 patient (10%).Conclusion(s): Oral administration of the aromatase inhibitor letrozole is effective for ovulation induction in anovulatory infertility and for increased follicle recruitment in ovulatory infertility.Letrozole appears to avoid the unfavorable effects on the endometrium frequently seen with antiestrogen use for ovulation induction.(Fertil Steril 2001;75:305-9.©2001 by American Society for Reproductive Medicine.) In women with World Health Organization type II anovulatory infertility, the treatment of first choice for the induction of ovulation is an antiestrogen, most commonly clomiphene citrate (CC) (1,2).However, 20%-25% of women are resistant to CC and do not ovulate.In addition, clinical data have revealed a discrepancy between ovulation and conception rates during CC treatment and a higher than expected incidence of miscarriage in conception cycles (3)(4)(5)(6).These observations have been attributed to the antiestrogenic mechanism of action of CC, which involves long-lasting estrogen receptor (ER) depletion.It also appears that CC accumulates in the body because of its long half-life (7).As a result, CC may have a negative effect on the quality and quantity of cervical mucus (8), on endometrial development (9), and on other as yet undetermined fertility factors (10,11). After failure of CC, gonadotropin preparations such as hMG or pure FSH have been used as a second-line treatment for ovulation induction.In women with polycystic ovary syndrome (PCOS), because of the high sensitivity of the ovaries to gonadotropin stimulation, treatment with hMG or pure FSH is difficult to control and characteristically induces several ovulatory follicles, leading to the risk of multiple pregnancies and ovarian hyperstimulation syndrome (OHSS) (12).Therefore, a simple oral treatment that could be used without risk of hyperstimulation and with minimal monitoring would be the preferred therapy.
plaindirectSingle case- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Also stated in: § RESULTS · plain
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In 10 ovulatory patients, 15 CC cycles resulted in a mean number of 2.5 mature follicles, but all cycles had endometrial thickness of Յ0.5 cm on the day of hCG administration.”
- Also stated in: § RESULTS · plain
“The mean number of follicles measuring Ͼ1.5 cm on the day of hCG administration was 2.5 follicles (range, 1-5).”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > Abstract Objective: To use aromatase inhibition for induction of ovulation in women in whom clomiphene citrate (CC) treatment was unsuccessful.Design: Prospective trial in infertility patients treated with CC.Setting: Two tertiary-referral infertility clinics associated with the Division of Reproductive Sciences, University of Toronto.Patient(s): Twelve patients with anovulatory polycystic ovary syndrome (PCOS) and 10 patients with ovulatory infertility, all of whom had previously received CC with an inadequate outcome (no ovulation and/or endometrial thickness of Յ0.5 cm).Intervention(s): The aromatase inhibitor letrozole was given orally in a dose of 2.5 mg on days 3-7 after menses.Main Outcome Measure(s): Occurrence of ovulation, endometrial thickness, and pregnancy rates.Result(s): With CC treatment in patients with PCOS, ovulation occurred in 8 of 18 cycles (44.4%), and all ovulatory cycles for the women included in this study had endometrial thickness of Յ0.5 cm.In 10 ovulatory patients, 15 CC cycles resulted in a mean number of 2.5 mature follicles, but all cycles had endometrial thickness of Յ0.5 cm on the day of hCG administration.With letrozole treatment in the same patients with PCOS, ovulation occurred in 9 of 12 cycles (75%) and pregnancy was achieved in 3 patients (25%).In the 10 patients with ovulatory infertility, letrozole treatment resulted in a mean number of 2.3 mature follicles and mean endometrial thickness of 0.8 cm.Pregnancy was achieved in 1 patient (10%).Conclusion(s): Oral administration of the aromatase inhibitor letrozole is effective for ovulation induction in anovulatory infertility and for increased follicle recruitment in ovulatory infertility.Letrozole appears to avoid the unfavorable effects on the endometrium frequently seen with antiestrogen use for ovulation induction.(Fertil Steril 2001;75:305-9.©2001 by American Society for Reproductive Medicine.) In women with World Health Organization type II anovulatory infertility, the treatment of first choice for the induction of ovulation is an antiestrogen, most commonly clomiphene citrate (CC) (1,2).However, 20%-25% of women are resistant to CC and do not ovulate.In addition, clinical data have revealed a discrepancy between ovulation and conception rates during CC treatment and a higher than expected incidence of miscarriage in conception cycles (3)(4)(5)(6).These observations have been attributed to the antiestrogenic mechanism of action of CC, which involves long-lasting estrogen receptor (ER) depletion.It also appears that CC accumulates in the body because of its long half-life (7).As a result, CC may have a negative effect on the quality and quantity of cervical mucus (8), on endometrial development (9), and on other as yet undetermined fertility factors (10,11). After failure of CC, gonadotropin preparations such as hMG or pure FSH have been used as a second-line treatment for ovulation induction.In women with polycystic ovary syndrome (PCOS), because of the high sensitivity of the ovaries to gonadotropin stimulation, treatment with hMG or pure FSH is difficult to control and characteristically induces several ovulatory follicles, leading to the risk of multiple pregnancies and ovarian hyperstimulation syndrome (OHSS) (12).Therefore, a simple oral treatment that could be used without risk of hyperstimulation and with minimal monitoring would be the preferred therapy.
plaindirectn = 10- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Also stated in: § RESULTS · plain
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Ovulation occurred in 8 cycles (44.4%) with an endometrial thickness of Յ0.5 cm.”
- Also stated in: § Abstract Objective: To use aromatase inhibition for induction of ovulation in women in whom clomiphene citrate (CC) treatment was unsuccessful.Design: Prospective trial in infertility patients treated with CC.Setting: Two tertiary-referral infertility clinics associated with the Division of Reproductive Sciences, University of Toronto.Patient(s): Twelve patients with anovulatory polycystic ovary syndrome (PCOS) and 10 patients with ovulatory infertility, all of whom had previously received CC with an inadequate outcome (no ovulation and/or endometrial thickness of Յ0.5 cm).Intervention(s): The aromatase inhibitor letrozole was given orally in a dose of 2.5 mg on days 3-7 after menses.Main Outcome Measure(s): Occurrence of ovulation, endometrial thickness, and pregnancy rates.Result(s): With CC treatment in patients with PCOS, ovulation occurred in 8 of 18 cycles (44.4%), and all ovulatory cycles for the women included in this study had endometrial thickness of Յ0.5 cm.In 10 ovulatory patients, 15 CC cycles resulted in a mean number of 2.5 mature follicles, but all cycles had endometrial thickness of Յ0.5 cm on the day of hCG administration.With letrozole treatment in the same patients with PCOS, ovulation occurred in 9 of 12 cycles (75%) and pregnancy was achieved in 3 patients (25%).In the 10 patients with ovulatory infertility, letrozole treatment resulted in a mean number of 2.3 mature follicles and mean endometrial thickness of 0.8 cm.Pregnancy was achieved in 1 patient (10%).Conclusion(s): Oral administration of the aromatase inhibitor letrozole is effective for ovulation induction in anovulatory infertility and for increased follicle recruitment in ovulatory infertility.Letrozole appears to avoid the unfavorable effects on the endometrium frequently seen with antiestrogen use for ovulation induction.(Fertil Steril 2001;75:305-9.©2001 by American Society for Reproductive Medicine.) In women with World Health Organization type II anovulatory infertility, the treatment of first choice for the induction of ovulation is an antiestrogen, most commonly clomiphene citrate (CC) (1,2).However, 20%-25% of women are resistant to CC and do not ovulate.In addition, clinical data have revealed a discrepancy between ovulation and conception rates during CC treatment and a higher than expected incidence of miscarriage in conception cycles (3)(4)(5)(6).These observations have been attributed to the antiestrogenic mechanism of action of CC, which involves long-lasting estrogen receptor (ER) depletion.It also appears that CC accumulates in the body because of its long half-life (7).As a result, CC may have a negative effect on the quality and quantity of cervical mucus (8), on endometrial development (9), and on other as yet undetermined fertility factors (10,11). After failure of CC, gonadotropin preparations such as hMG or pure FSH have been used as a second-line treatment for ovulation induction.In women with polycystic ovary syndrome (PCOS), because of the high sensitivity of the ovaries to gonadotropin stimulation, treatment with hMG or pure FSH is difficult to control and characteristically induces several ovulatory follicles, leading to the risk of multiple pregnancies and ovarian hyperstimulation syndrome (OHSS) (12).Therefore, a simple oral treatment that could be used without risk of hyperstimulation and with minimal monitoring would be the preferred therapy. · plain
“With CC treatment in patients with PCOS, ovulation occurred in 8 of 18 cycles (44.4%), and all ovulatory cycles for the women included in this study had endometrial thickness of Յ0.5 cm.”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > RESULTS
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Also stated in: § Abstract Objective: To use aromatase inhibition for induction of ovulation in women in whom clomiphene citrate (CC) treatment was unsuccessful.Design: Prospective trial in infertility patients treated with CC.Setting: Two tertiary-referral infertility clinics associated with the Division of Reproductive Sciences, University of Toronto.Patient(s): Twelve patients with anovulatory polycystic ovary syndrome (PCOS) and 10 patients with ovulatory infertility, all of whom had previously received CC with an inadequate outcome (no ovulation and/or endometrial thickness of Յ0.5 cm).Intervention(s): The aromatase inhibitor letrozole was given orally in a dose of 2.5 mg on days 3-7 after menses.Main Outcome Measure(s): Occurrence of ovulation, endometrial thickness, and pregnancy rates.Result(s): With CC treatment in patients with PCOS, ovulation occurred in 8 of 18 cycles (44.4%), and all ovulatory cycles for the women included in this study had endometrial thickness of Յ0.5 cm.In 10 ovulatory patients, 15 CC cycles resulted in a mean number of 2.5 mature follicles, but all cycles had endometrial thickness of Յ0.5 cm on the day of hCG administration.With letrozole treatment in the same patients with PCOS, ovulation occurred in 9 of 12 cycles (75%) and pregnancy was achieved in 3 patients (25%).In the 10 patients with ovulatory infertility, letrozole treatment resulted in a mean number of 2.3 mature follicles and mean endometrial thickness of 0.8 cm.Pregnancy was achieved in 1 patient (10%).Conclusion(s): Oral administration of the aromatase inhibitor letrozole is effective for ovulation induction in anovulatory infertility and for increased follicle recruitment in ovulatory infertility.Letrozole appears to avoid the unfavorable effects on the endometrium frequently seen with antiestrogen use for ovulation induction.(Fertil Steril 2001;75:305-9.©2001 by American Society for Reproductive Medicine.) In women with World Health Organization type II anovulatory infertility, the treatment of first choice for the induction of ovulation is an antiestrogen, most commonly clomiphene citrate (CC) (1,2).However, 20%-25% of women are resistant to CC and do not ovulate.In addition, clinical data have revealed a discrepancy between ovulation and conception rates during CC treatment and a higher than expected incidence of miscarriage in conception cycles (3)(4)(5)(6).These observations have been attributed to the antiestrogenic mechanism of action of CC, which involves long-lasting estrogen receptor (ER) depletion.It also appears that CC accumulates in the body because of its long half-life (7).As a result, CC may have a negative effect on the quality and quantity of cervical mucus (8), on endometrial development (9), and on other as yet undetermined fertility factors (10,11). After failure of CC, gonadotropin preparations such as hMG or pure FSH have been used as a second-line treatment for ovulation induction.In women with polycystic ovary syndrome (PCOS), because of the high sensitivity of the ovaries to gonadotropin stimulation, treatment with hMG or pure FSH is difficult to control and characteristically induces several ovulatory follicles, leading to the risk of multiple pregnancies and ovarian hyperstimulation syndrome (OHSS) (12).Therefore, a simple oral treatment that could be used without risk of hyperstimulation and with minimal monitoring would be the preferred therapy. · plain
- It may state two separate claims as one. 10
- The quote only partly states this claim. 1
- Probably not a substantial claim. 8
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“At the time of writing, the three clinical pregnancies had resulted in a normal live birth and two ongoing singleton pregnancies.”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > RESULTS
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
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It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“However, the endometrial thickness was Յ0.5 cm in all cycles, and no pregnancy was achieved.”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > RESULTS
plainn = 10- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
The quote only partly states this claim.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Compared with CC, letrozole produced a significantly thicker endometrium on the day of hCG administration despite the significantly lower E 2 levels in both patients with PCOS and the ovulatory patients.”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > FERTILITY & STERILITY
plaindirect- Asserted: passes — The authors put it forward as true.
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A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Aromatase inhibitors have potential as alternatives to, or even replacements for, CC as a first-line treatment for ovulation induction in anovulatory infertility and for augmentation of ovulation in ovulatory infertility patients.”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > FERTILITY & STERILITY
hedgedconditionaln = 10- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“Recent data support a stimulatory role for androgens in early follicular growth in primates, in contrast to the inhibitory effect observed in rodents (21).”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > FERTILITY & STERILITY
What the sources say
- Not checked — no full text of the sourcecites [21] Weil, 1998, Androgen receptor gene expression in the primate ovary, J Clin Endocrinol Metab source
plaindirect- Asserted: passes — The authors put it forward as true.
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- Load-bearing: passes — The paper’s conclusions depend on it.
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It may state two separate claims as one.
In the paper
“In women with polycystic ovary syndrome (PCOS), because of the high sensitivity of the ovaries to gonadotropin stimulation, treatment with hMG or pure FSH is difficult to control and characteristically induces several ovulatory follicles, leading to the risk of multiple pregnancies and ovarian hyperstimulation syndrome (OHSS) (12).”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > Abstract Objective: To use aromatase inhibition for induction of ovulation in women in whom clomiphene citrate (CC) treatment was unsuccessful.Design: Prospective trial in infertility patients treated with CC.Setting: Two tertiary-referral infertility clinics associated with the Division of Reproductive Sciences, University of Toronto.Patient(s): Twelve patients with anovulatory polycystic ovary syndrome (PCOS) and 10 patients with ovulatory infertility, all of whom had previously received CC with an inadequate outcome (no ovulation and/or endometrial thickness of Յ0.5 cm).Intervention(s): The aromatase inhibitor letrozole was given orally in a dose of 2.5 mg on days 3-7 after menses.Main Outcome Measure(s): Occurrence of ovulation, endometrial thickness, and pregnancy rates.Result(s): With CC treatment in patients with PCOS, ovulation occurred in 8 of 18 cycles (44.4%), and all ovulatory cycles for the women included in this study had endometrial thickness of Յ0.5 cm.In 10 ovulatory patients, 15 CC cycles resulted in a mean number of 2.5 mature follicles, but all cycles had endometrial thickness of Յ0.5 cm on the day of hCG administration.With letrozole treatment in the same patients with PCOS, ovulation occurred in 9 of 12 cycles (75%) and pregnancy was achieved in 3 patients (25%).In the 10 patients with ovulatory infertility, letrozole treatment resulted in a mean number of 2.3 mature follicles and mean endometrial thickness of 0.8 cm.Pregnancy was achieved in 1 patient (10%).Conclusion(s): Oral administration of the aromatase inhibitor letrozole is effective for ovulation induction in anovulatory infertility and for increased follicle recruitment in ovulatory infertility.Letrozole appears to avoid the unfavorable effects on the endometrium frequently seen with antiestrogen use for ovulation induction.(Fertil Steril 2001;75:305-9.©2001 by American Society for Reproductive Medicine.) In women with World Health Organization type II anovulatory infertility, the treatment of first choice for the induction of ovulation is an antiestrogen, most commonly clomiphene citrate (CC) (1,2).However, 20%-25% of women are resistant to CC and do not ovulate.In addition, clinical data have revealed a discrepancy between ovulation and conception rates during CC treatment and a higher than expected incidence of miscarriage in conception cycles (3)(4)(5)(6).These observations have been attributed to the antiestrogenic mechanism of action of CC, which involves long-lasting estrogen receptor (ER) depletion.It also appears that CC accumulates in the body because of its long half-life (7).As a result, CC may have a negative effect on the quality and quantity of cervical mucus (8), on endometrial development (9), and on other as yet undetermined fertility factors (10,11). After failure of CC, gonadotropin preparations such as hMG or pure FSH have been used as a second-line treatment for ovulation induction.In women with polycystic ovary syndrome (PCOS), because of the high sensitivity of the ovaries to gonadotropin stimulation, treatment with hMG or pure FSH is difficult to control and characteristically induces several ovulatory follicles, leading to the risk of multiple pregnancies and ovarian hyperstimulation syndrome (OHSS) (12).Therefore, a simple oral treatment that could be used without risk of hyperstimulation and with minimal monitoring would be the preferred therapy.
What the sources say
- Not checked — no full text of the sourcecites [12] Kettel, 1993, Hypothalamic-pituitary-ovarian response to clomiphene citrate in women with polycystic ovary syndrome, Fertil Steril source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“These aromatase inhibitors have a relatively short half-life compared with CC and therefore would be eliminated from the body rapidly (14,15).”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > Abstract Objective: To use aromatase inhibition for induction of ovulation in women in whom clomiphene citrate (CC) treatment was unsuccessful.Design: Prospective trial in infertility patients treated with CC.Setting: Two tertiary-referral infertility clinics associated with the Division of Reproductive Sciences, University of Toronto.Patient(s): Twelve patients with anovulatory polycystic ovary syndrome (PCOS) and 10 patients with ovulatory infertility, all of whom had previously received CC with an inadequate outcome (no ovulation and/or endometrial thickness of Յ0.5 cm).Intervention(s): The aromatase inhibitor letrozole was given orally in a dose of 2.5 mg on days 3-7 after menses.Main Outcome Measure(s): Occurrence of ovulation, endometrial thickness, and pregnancy rates.Result(s): With CC treatment in patients with PCOS, ovulation occurred in 8 of 18 cycles (44.4%), and all ovulatory cycles for the women included in this study had endometrial thickness of Յ0.5 cm.In 10 ovulatory patients, 15 CC cycles resulted in a mean number of 2.5 mature follicles, but all cycles had endometrial thickness of Յ0.5 cm on the day of hCG administration.With letrozole treatment in the same patients with PCOS, ovulation occurred in 9 of 12 cycles (75%) and pregnancy was achieved in 3 patients (25%).In the 10 patients with ovulatory infertility, letrozole treatment resulted in a mean number of 2.3 mature follicles and mean endometrial thickness of 0.8 cm.Pregnancy was achieved in 1 patient (10%).Conclusion(s): Oral administration of the aromatase inhibitor letrozole is effective for ovulation induction in anovulatory infertility and for increased follicle recruitment in ovulatory infertility.Letrozole appears to avoid the unfavorable effects on the endometrium frequently seen with antiestrogen use for ovulation induction.(Fertil Steril 2001;75:305-9.©2001 by American Society for Reproductive Medicine.) In women with World Health Organization type II anovulatory infertility, the treatment of first choice for the induction of ovulation is an antiestrogen, most commonly clomiphene citrate (CC) (1,2).However, 20%-25% of women are resistant to CC and do not ovulate.In addition, clinical data have revealed a discrepancy between ovulation and conception rates during CC treatment and a higher than expected incidence of miscarriage in conception cycles (3)(4)(5)(6).These observations have been attributed to the antiestrogenic mechanism of action of CC, which involves long-lasting estrogen receptor (ER) depletion.It also appears that CC accumulates in the body because of its long half-life (7).As a result, CC may have a negative effect on the quality and quantity of cervical mucus (8), on endometrial development (9), and on other as yet undetermined fertility factors (10,11). After failure of CC, gonadotropin preparations such as hMG or pure FSH have been used as a second-line treatment for ovulation induction.In women with polycystic ovary syndrome (PCOS), because of the high sensitivity of the ovaries to gonadotropin stimulation, treatment with hMG or pure FSH is difficult to control and characteristically induces several ovulatory follicles, leading to the risk of multiple pregnancies and ovarian hyperstimulation syndrome (OHSS) (12).Therefore, a simple oral treatment that could be used without risk of hyperstimulation and with minimal monitoring would be the preferred therapy.
What the sources say
- Not checked — no full text of the sourcecites [14] Lipton, 1995, Letrozole (CGS 20267), Cancer source
- Not checked — no full text of the sourcecites [15] Iveson, 1993, Phase I study of the oral nonsteroidal aromatase inhibitor CGS 20267 in postmenopausal patients with advanced breast cancer, Cancer Res source
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
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It may state two separate claims as one.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“Continuous administration of letrozole up to 5 mg/d produced marked suppression of E 2 , estrone, and estrone sulfate, with very few side effects (14,15).”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > FERTILITY & STERILITY
What the sources say
- Not checked — no full text of the sourcecites [14] Lipton, 1995, Letrozole (CGS 20267), Cancer source
- Not checked — no full text of the sourcecites [15] Iveson, 1993, Phase I study of the oral nonsteroidal aromatase inhibitor CGS 20267 in postmenopausal patients with advanced breast cancer, Cancer Res source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“In addition, androgen accumulation in the follicle may stimulate insulin-like growth factor, along with other endocrine and paracrine factors, which may synergize with FSH to promote folliculogenesis (25)(26)(27).”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > FERTILITY & STERILITY
What the sources say
- Not matchedcites (25)(26)(27)
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
- Not matched
In the paper
“The absolute systemic bioavailability of letrozole after oral administration was 100% compared with the same dose given IV (19).”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > FERTILITY & STERILITY
What the sources say
- Not checked — no full text of the sourcecites [19] Sioufi, 1997, Absolute bioavailability of letrozole in healthy post-menopausal women, Biopharm Drug Dispos source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Testosterone was found to augment follicular FSH receptor expression in primates, which suggests that androgens promote follicular growth and estrogen biosynthesis indirectly by amplifying FSH effects (22)(23)(24).”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > FERTILITY & STERILITY
What the sources say
- Not matchedcites (22)(23)(24)
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
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It may state two separate claims as one.
- Not matched
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“Some investigators have proposed combined CC and low-dose glucocorticoid therapy for the treatment of CCresistant anovulation (28 -31).”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > FERTILITY & STERILITY
What the sources say
- Not checked — no full text of the sourcecites [28] Lobo, 1982, Clomiphene and dexamethasone in women unresponsive to clomiphene alone, Obstet Gynecol
- Not checked — no full text of the sourcecites [29] Singh, 1992, Clomiphene-dexamethasone treatment of clomiphene resistant women with and without the polycystic ovary syndrome, J Reprod Med
- Not checked — no full text of the sourcecites [30] Daly, 1984, A randomized study of dexamethasone in ovulation induction with clomiphene citrate, Fertil Steril source
- Not checked — no full text of the sourcecites [31] Diamant, 1980, Induction of ovulation by combined clomiphene citrate and dexamethasone treatment in clomiphene citrate nonresponders, Eur J Obstet Gynecol Reprod Biol source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“In addition, clinical data have revealed a discrepancy between ovulation and conception rates during CC treatment and a higher than expected incidence of miscarriage in conception cycles (3)(4)(5)(6).”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > Abstract Objective: To use aromatase inhibition for induction of ovulation in women in whom clomiphene citrate (CC) treatment was unsuccessful.Design: Prospective trial in infertility patients treated with CC.Setting: Two tertiary-referral infertility clinics associated with the Division of Reproductive Sciences, University of Toronto.Patient(s): Twelve patients with anovulatory polycystic ovary syndrome (PCOS) and 10 patients with ovulatory infertility, all of whom had previously received CC with an inadequate outcome (no ovulation and/or endometrial thickness of Յ0.5 cm).Intervention(s): The aromatase inhibitor letrozole was given orally in a dose of 2.5 mg on days 3-7 after menses.Main Outcome Measure(s): Occurrence of ovulation, endometrial thickness, and pregnancy rates.Result(s): With CC treatment in patients with PCOS, ovulation occurred in 8 of 18 cycles (44.4%), and all ovulatory cycles for the women included in this study had endometrial thickness of Յ0.5 cm.In 10 ovulatory patients, 15 CC cycles resulted in a mean number of 2.5 mature follicles, but all cycles had endometrial thickness of Յ0.5 cm on the day of hCG administration.With letrozole treatment in the same patients with PCOS, ovulation occurred in 9 of 12 cycles (75%) and pregnancy was achieved in 3 patients (25%).In the 10 patients with ovulatory infertility, letrozole treatment resulted in a mean number of 2.3 mature follicles and mean endometrial thickness of 0.8 cm.Pregnancy was achieved in 1 patient (10%).Conclusion(s): Oral administration of the aromatase inhibitor letrozole is effective for ovulation induction in anovulatory infertility and for increased follicle recruitment in ovulatory infertility.Letrozole appears to avoid the unfavorable effects on the endometrium frequently seen with antiestrogen use for ovulation induction.(Fertil Steril 2001;75:305-9.©2001 by American Society for Reproductive Medicine.) In women with World Health Organization type II anovulatory infertility, the treatment of first choice for the induction of ovulation is an antiestrogen, most commonly clomiphene citrate (CC) (1,2).However, 20%-25% of women are resistant to CC and do not ovulate.In addition, clinical data have revealed a discrepancy between ovulation and conception rates during CC treatment and a higher than expected incidence of miscarriage in conception cycles (3)(4)(5)(6).These observations have been attributed to the antiestrogenic mechanism of action of CC, which involves long-lasting estrogen receptor (ER) depletion.It also appears that CC accumulates in the body because of its long half-life (7).As a result, CC may have a negative effect on the quality and quantity of cervical mucus (8), on endometrial development (9), and on other as yet undetermined fertility factors (10,11). After failure of CC, gonadotropin preparations such as hMG or pure FSH have been used as a second-line treatment for ovulation induction.In women with polycystic ovary syndrome (PCOS), because of the high sensitivity of the ovaries to gonadotropin stimulation, treatment with hMG or pure FSH is difficult to control and characteristically induces several ovulatory follicles, leading to the risk of multiple pregnancies and ovarian hyperstimulation syndrome (OHSS) (12).Therefore, a simple oral treatment that could be used without risk of hyperstimulation and with minimal monitoring would be the preferred therapy.
What the sources say
- Not matchedcites (3)(4)(5)(6)
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Not matched
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In summary, the results of this preliminary study suggest that the aromatase inhibitor letrozole is an orally effective, inexpensive method for stimulating follicular development.”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > FERTILITY & STERILITY
hedgeddirectn = 10- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“The subsequent increase in gonadotropin secretion could stimulate ovarian follicle development, as reported previously in the Bonnet monkey (20).”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > FERTILITY & STERILITY
What the sources say
- Not checked — no full text of the sourcecites [20] Shetty, 1997, Effect of estrogen deprivation on the reproductive physiology of male and female primates, J Steroid Biochem Mol Biol source
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“A 2-month washout period before the letrozole cycles was used to eliminate any posttreatment effect of CC.”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > MATERIALS AND METHODS
plaindirectn = 22- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
In the paper
“Endometrial thickness was assessed as we have described previously (9) and as performed routinely in our clinic for the last 10 years.”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > MATERIALS AND METHODS
What the sources say
- Not checked — no full text of the sourcecites [9] Gonen, 1990, Sonographic determination of an adverse effect of clomiphene citrate on endometrial growth, Hum Reprod source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Other investigators have described the use of extended duration and higher doses of CC (32)(33)(34)(35).”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > FERTILITY & STERILITY
What the sources say
- Not matchedcites (32)(33)(34)(35)
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Not matched
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“Identical criteria were used for administration of hCG in both the CC-and letrozole-treated cycles.”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > MATERIALS AND METHODS
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
The paper relies on this without support.
20%-25% of women are resistant to CC and do not ovulate.
“However, 20%-25% of women are resistant to CC and do not ovulate.”
The paper relies on this without support.
Letrozole is a specific, reversible, nonsteroidal aromatase inhibitor that suppresses estrogen biosynthesis.
“Letrozole (4,4Ј-[1H-1, 2, 4-triazol-1-ylmethylene]-bis-benzonitrile) is a specific, reversible, nonsteroidal aromatase inhibitor that suppresses estrogen biosynthesis.”
The paper relies on this without support.
The disposition of letrozole in healthy postmenopausal women is characterized by steady-state plasma concentrations in 4-8 hours and a half-life of approximately 45 hours.
“The disposition of letrozole in healthy postmenopausal women is characterized by steady-state plasma concentrations in 4 -8 hours and a half-life of approximately 45 hours.”
The paper relies on this without support.
CC is the most commonly prescribed medication for ovulation induction.
“CC is the most commonly prescribed medication for ovulation induction.”
The paper relies on this without support.
Women with ovulatory disorders who are resistant to standard doses of CC generally become candidates for gonadotropin therapy.
“Women with ovulatory disorders who are resistant to standard doses of CC generally become candidates for gonadotropin therapy.”
The paper relies on this without support.
Severe OHSS and the high risk of multiple pregnancy are major disadvantages of gonadotropin treatment, especially in young women with PCOS.
“However, severe OHSS and the high risk of multiple pregnancy are major disadvantages of gonadotropin treatment, especially in young women with PCOS.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“In a small study (50), 12 PCOS patients with inadequate response to CC were treated with letrozole.Of 12 patients, 9 (75%) ovulated, and 3 conceived; the mean endometrial thickness was 8.1 mm (6.2 mm with CC).”
From A new era in ovulation induction (2006) · cites this paper as [50]
In the citing paper
“Aromatase inhibitors were proposed as ovulation-inducing agents in 2001. 236”
From Assessment and management of polycystic ovary syndrome: Summary of an evidence-based guideline (2011) · cites this paper as [236]
In the citing paper
“Ovulation induction with letrozole is associated with an ovulation rate of 70%-84% and a pregnancy rate of 20%-27% per cycle.”
From A new era in ovulation induction (2006) · cites this paper as [50]
In the citing paper
“Recently, it was suggested that letrozole, a specific reversible, nonsteroidal aromatase inhibitor that suppresses estrogen biosynthesis (16), can successfully replace clomiphene citrate in superovulation treatment of patients with unexplained infertility or polycystic ovarian disease and in poor responders (17,18).”
From Effects of letrozole on superovulation with gonadotropins in women undergoing intrauterine insemination (2003) · cites this paper as [17]
In the citing paper
“Two doses regimens have been tested (2.5 mg and 5 mg) with similar response (8,9).”
From A randomized trial of letrozole versus clomiphene citrate in women undergoing superovulation (2004) · cites this paper as [8]
In the citing paper
“Mitwally and Casper (8) used letrozole (2.5 mg daily for 5 days) in 12 women with inadequate response to CC. Ovulation occurred in 9 of 12 cycles and 3 patients conceived.”
From A randomized trial of letrozole versus clomiphene citrate in women undergoing superovulation (2004) · cites this paper as [8]
In the citing paper
“The ideal dose of letrozole for superovulation or ovulation induction is still unknown.”
From A randomized trial of letrozole versus clomiphene citrate in women undergoing superovulation (2004) · cites this paper as [8]
In the citing paper
“Compared with CC, letrozole is associated with a thicker endometrium (8).”
From A randomized trial of letrozole versus clomiphene citrate in women undergoing superovulation (2004) · cites this paper as [8]
In the citing paper
“In a selected population of women with a thin endometrium (mean, 5 mm) after clomiphene treatment, letrozole treatment in the early follicular phase resulted in a significant increase in midcycle endometrial thickness (mean, 9 mm) (21).”
From A randomized double-blind comparison of the effects of clomiphene citrate and the aromatase inhibitor letrozole on ovulatory function in normal women (2002) · cites this paper as [21]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Rated major: it would touch a result — a value a result rests on, reported and recomputed p-values on opposite sides of the significance level, two passages that conflict with no sign which is right, or a cited work retracted before this paper was published.
In the paper
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > RESULTS
“Ovulation occurred in 8 cycles (44.4%) with an endometrial thickness of Յ0.5 cm.”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > DISCUSSION
“Endometrial thickness (cm) on day of hCG 0.81 Ϯ 0.14 0.62 Ϯ 0.25 Ͻ.01 0.7-1.1 0.3-1.20.8 0.6”
Rated minor: it would not touch a result — a value no result rests on, a p-value that stays on the same side of the significance level, or a conflict that is clerical, resolved elsewhere in the paper, or outside its own findings.
In the paper
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > RESULTS
“However, the endometrial thickness was Յ0.5 cm in all cycles, and no pregnancy was achieved.”
§ Use of an aromatase inhibitor for induction of ovulation in patients with an inadequate response to clomiphene citrate > FERTILITY & STERILITY
“Endometrial thickness (cm) on day of hCG 0.89 Ϯ 0.12 0.5 Ϯ 0.1 Ͻ.001 0.7-1.1 0.3-0.6 0.9 0.5”
Citations
Cites
Franks, S. (1995) · New England Journal of Medicine · doi:10.1056/nejm199509283331307 · Cited by 2,463
Franks, S. (1997) · Archives of Disease in Childhood · doi:10.1136/adc.77.1.89 · Cited by 802
Androgens stimulate early stages of follicular growth in the primate ovary
Vendola, K. A., Zhou, J., Adesanya, O. O., Weil, S. J., & Bondy, C. A. (1998) · Journal of Clinical Investigation · doi:10.1172/jci2081 · Cited by 712
Androgen and follicle stimulating hormone interactions in primate ovarian follicle development
Weil, S., Vendola, K., Zhou, J., & Bondy, C. A. (1999) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.84.8.5929 · Cited by 592
Insulin-Like Growth Factors and Ovarian Follicular Development*
Giudice, L. C. (1992) · Endocrine Reviews · doi:10.1210/edrv-13-4-641 · Cited by 521
Weil, S. J., Vendola, K., Zhou, J., Adesanya, O. O., Wang, J., Okafor, J., & Bondy, C. A. (1998) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.83.7.4917 · Cited by 359
Vendola, K., Zhou, J., Wang, J., Famuyiwa, O. A., Bievre, M., & Bondy, C. A. (1999) · Biology of Reproduction · doi:10.1095/biolreprod61.2.353 · Cited by 324
Effect of estrogen deprivation on the reproductive physiology of male and female primates
Shetty, G., Krishnamurthy, H., Krishnamurthy, H. N., Bhatnagar, A. S., & Moudgal, R. N. (1997) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/s0960-0760(97)80008-8 · Cited by 306
Dunaif, A., Heindel, J. J., & Chang, R. (2002) · CRC Press eBooks · doi:10.3109/9780203910948 · Cited by 283
Gysler, M., March, C. M., Mishell, D. R., & Bailey, E. J. (1982) · Fertility and Sterility · doi:10.1016/s0015-0282(16)46033-4 · Cited by 270
Research works printed but not linked: 1
- Shoham Z, Weissman A. Polycystic ovarian disease: obesity and insulin resistance. In: Kempers RD, Cohen J, Haney AF, Younger JB, eds. Fertility and reproductive medicine. Amsterdam, New York, Oxford, Shannon, Singapore, Tokyo: Elsevier, 1998:263–72.
Cited by
Sorted by citations
Items 601–700 of 799
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Vishwakarma, M. B., Vakharia, S. D., Borade, V. R., Nagare, P. S., & Jaiswal, S. A. (2017) · Otorhinolaryngology Clinics - An International Journal · doi:10.5005/jp-journals-10003-1263 · Cited by 1
Hamilton, M. (2012) · Wiley-Blackwell eBooks · doi:10.1002/9781119979449.ch45 · Cited by 2
Tulandi, T., & Weibel, H. S. (2017) · Springer eBooks · doi:10.1007/978-3-319-52210-4_16 · Cited by 2
Manish, P. (2022) · Open Access Journal of Gynecology · doi:10.23880/oajg-16000230 · Cited by 1
Hasnat, F., Ferdousi, M. A., Hasan, M. M., et al. (2023) · International Journal of Reproduction Contraception Obstetrics and Gynecology · doi:10.18203/2320-1770.ijrcog20233618 · Cited by 1
Hormonal Therapy of the Infertile Woman
Kol, S. (2003) · Humana Press eBooks · doi:10.1007/978-1-59259-375-0_27 · Cited by 1
The endometrial factor in human embryo implantation
Boomsma, C. M. (2009) · Utrecht University Repository (Utrecht University) · Cited by 1
Role of Estrogens in Ovarian Dysfunction and Fertility. Options for New Therapies with SERMs
Fauser, B. C. J. M., & Laven, J. S. E. (2004) · Springer eBooks · doi:10.1007/978-3-662-05386-7_11 · Cited by 1
Aromatase inhibitors forfemaleinfertility treatment
Atay, V., Yaralı́, H., Bozdağ, G., Özışık, G., Akin, D., & Muhçu, M. (2007) · Expert Opinion on Therapeutic Patents · doi:10.1517/13543776.17.2.137 · Cited by 1
“A singleton clinical pregnancy resulted from timed intrauterine insemination (IUI) in one infertile couple who developed two follicles > 15 mm [15].”
Background„Off-label-Anwendung“ von Aromatasehemmern
Bohlmann, M. K., Hornemann, A., Weichert, J., Stichtenoth, G., Ortmann, J., Diedrich, K., & Lüdders, D. (2008) · Gynäkologische Endokrinologie · doi:10.1007/s10304-008-0265-6 · Cited by 1
Hadžiomerović, D., Kreienberg, R., & Weiss, J. M. (2007) · Der Gynäkologe · doi:10.1007/s00129-007-2013-8 · Cited by 1
Medical management of polycystic ovarian syndrome and its sequelae
Kodaman, P. H., & Dulęba, A. J. (2006) · CRC Press eBooks · doi:10.3109/9781420042726-14 · Cited by 1
Nazemian, Z. (2011) · TSpace (University of Toronto) · Cited by 1
Panda, S. R., Sharmila, V., Kalidoss, V. K., et al. (2021) · doi:10.22541/au.162462630.08012172/v1 · Cited by 1
Infertility and reproductive endocrinology
Bieber, E. J., Sanfilippo, J. S., Horowitz, I., & Shafi, M. I. (2015) · Cambridge University Press eBooks · doi:10.1017/cbo9781139628938.058 · Cited by 1
Yapura, M. J. (2013) · HARVEST (University of Saskatchewan) · Cited by 1
Use of Ultrasound to Predict and Optimize Outcomes of Ovulation Induction
Syrop, C. H., & Voorhis, B. J. V. (2003) · Iowa Research Online (The University of Iowa) · doi:10.1016/s1047-9422(03)00009-9
Physiologic Basis of Ovulation Induction
Casper, R. F. (2011) · doi:10.1002/9781444393958.ch11
Self-citationMild forms of ovarian stimulation
Aboulghar, M. A., & Rizk, B. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511762390.004
Panorama actual de los inhibidores de la aromatasa en la inducción de la ovulación
Pachón-Rincón, J. D. J., & Posada-Villa, N. (2007) · Revista Colombiana de Obstetricia y Ginecología · doi:10.18597/rcog.476
“Se ha planteado que los IA pueden tener un rol estimulante en el crecimiento folicular temprano mediante el aumento de los receptores de FSH a nivel ovárico y por tanto amplificarían la acción de esta hormona.(7,8)”
BackgroundReproductive Endocrinology Diseases: Hormone Replacement and Therapy for Peri/Menopause
Ρούπα, Ζ., Wozniak, G., Tsipras, K., & Sotiropoulou, P. (2011) · InTech eBooks · doi:10.5772/20618
Aspects of Mono- and Multiple Dominant Follicle Development in the Human Ovary
Hohmann, F. P. (2005) · RePub (Erasmus University Rotterdam)
Possible additional therapeutic uses of aromatase inhibitors
Furr, B. J. A. (2008) · Birkhäuser Basel eBooks · doi:10.1007/978-3-7643-8693-1_9
“A mean of 2.3 mature follicles were produced without any impact on endometrial thickness; pregnancy ensued in one patient [ 21 ].”
BackgroundInfluentialZuk�nftige Wege der ovariellen Stimulation
Griesinger, G., Schultze-Mosgau, A., Felberbaum, R. E., & Diedrich, K. (2003) · Gynäkologische Endokrinologie · doi:10.1007/s10304-003-0037-2
Reply of the Authors: Letrozole monotherapy in the treatment of uterine myomas
Parsanezhad, M. E. (2010) · Fertility and Sterility · doi:10.1016/j.fertnstert.2010.01.071
‘Teeth in a Day’—An Innovative, Cost-Effective Technique for Immediate Loading of Implants
Sethi, S., Jambhekar, S. S., Kheur, M. G., & Kheur, S. M. (2012) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1066
Aromatasehemmer in der Therapie der Endometriose
Juhasz-Böss, I., Treeck, O., Malik, E., & Ortmann, O. (2006) · Gynäkologische Endokrinologie · doi:10.1007/s10304-006-0156-7
“AH steigern das Follikelwachstum und können zu einer Ovarstimulation und Zystenbildung führen [21].”
BackgroundPharmacological profile of MEN 11066, a novel potent and selective aromatase inhibitor
Muratori, M., Lippi, A., Mancina, R., Iafrate, E., Cirillo, R., Lopez, G., Bigioni, M., Maggi, M., Criscuoli, M., & Maggi, C. A. (2003) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/s0960-0760(03)00073-6
“A novel clinical application for aromatase inhibitors is emerging[10,11].”
BackgroundInfluentialRecommandations pour le diagnostic et le suivi du syndrome des ovaires polykystiques
Théron-Gérard, L., Cédrin‐Durnerin, I., & Hugues, J. (2008) · EMC - Gynécologie · doi:10.1016/s0246-1064(08)44358-x
Potential use of aromatase inhibitors in gynecology
Lukic, J., & Tulandi, T. (2006) · Expert Review of Obstetrics & Gynecology · doi:10.1586/17474108.1.1.41
Recomendaciones para el diagnóstico y el seguimiento del síndrome de ovarios poliquísticos
Théron-Gérard, L., Cédrin‐Durnerin, I., & Hugues, J. (2008) · EMC - Ginecología-Obstetricia · doi:10.1016/s1283-081x(08)70803-8
Polycystic Ovary Syndrome and IVF
Gürgan, T., & Demi̇rol, A. (2008) · Cambridge University Press eBooks · doi:10.1017/cbo9780511547287.044
The future for aromatase inhibitors is bright
Vladimirov, I. K. (2002) · Fertility and Sterility · doi:10.1016/s0015-0282(02)04223-1
Fertility preservation in young breast cancer patients: addressing individual patient needs
Rodriguez‐Wallberg, K. A., & Oktay, K. (2013) · Breast Cancer Management · doi:10.2217/bmt.12.68
Optimization of Ovarian Stimulation to Improve Success Rate in ‘ART’
Sinha, S. (2012) · Apollo Medicine · doi:10.1016/j.apme.2012.07.008
Implantable Devices: A Review of Current Treatment Modalities
Jaggi, N., Bhutani, R., & Mehan, P. (2012) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1061
Mild strategies for IVF: from theory to practice
Verberg, M. F. G. (2007) · Utrecht University Repository (Utrecht University)
Use of aromatase inhibitors in gynecology
Elnahhas, I. M., & Mitwally, M. F. (2010) · Expert Review of Obstetrics & Gynecology · doi:10.1586/eog.10.10
Self-citationOrief, Y. I., El-Agwany, A. S., Darwish, E. A. E., Abdelrahman, A. H., & Ghazal, S. (2014) · Middle East Fertility Society Journal · doi:10.1016/j.mefs.2014.05.009
Balakrishnan, D., & Aparna, I. N. (2012) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1059
Tissue Stability following Soft-tissue Augmentation and Zirconia Prosthesis: A 6 Years Follow-up
Mahesh, L., Dhir, S., & Afrashtehfar, K. I. (2012) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1071
Implant Supported Overdenture: An Ameliorating Alternative for Edentulism
Govindwar, P. G., Dange, S. P., Khalikar, S. A., & Khalikar, A. (2013) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1092
Suresh, S. N., & Bhojaraju, N. (2011) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1034
Implant Supported Overdenture: An Ameliorating Alternative for Edentulism
Govindwar, P. G. (2012) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10021-1092
Aromatase Inhibitors: New Drug of Choice for Induction of Ovulation
Siddiqui, M., Mahmud, N., Begum, M., & Chowdhury, T. (1970) · Journal of Bangladesh College of Physicians and Surgeons · doi:10.3329/jbcps.v28i1.4642
Aromatase Inhibitors in Infertility Treatment: Risks and Benefits
Daya, S. (2006) · Women s Health · doi:10.2217/17455057.2.4.501
“Good rates of ovulation and pregnancy were observed in two small studies [10,11], but the rates in a larger study were less encouraging [12].”
BackgroundResultMini Dental Implants as a Simple Treatment Alternative for Edentulous Mandibular Cases
Jacob, P. C., Rai, N., & Patil, D. P. (2011) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1042
Estimulación ovárica en reproducción asistida
Velando, L. E. E. (2014) · Revista Peruana de Ginecología y Obstetricia · doi:10.31403/rpgo.v58i71
“Los IA dan el mensaje de falta de estrógenos, con lo que aumentan los andrógenos intrafoliculares y, a su vez, la expresión de los receptores para FSH; esta retroalimentación favorece la producción de gonadotropinas, pero sin tener los efectos adversos antiestrogénicos del CC(8).”
BackgroundAromatase Inhibitors for Assisted Reproduction
Mitwally, M. F., & Casper, R. F. (2008) · Cambridge University Press eBooks · doi:10.1017/cbo9780511547287.027
Self-citationThe future for aromatase inhibitors is bright: Reply of the authors
Mitwally, M. F., & Casper, R. F. (2002) · Fertility and Sterility · doi:10.1016/s0015-0282(02)04224-3
Self-citationClinicoradiographic Evaluation and Feasibility of Dental Implant in Infected Dentoalveolar Socket
Batra, R. S., Rao, J. D., Vijaylaxmy, L. N. U., & Kukreja, A. (2011) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1039
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Sagittal Distraction of Edentulous Maxillary Skeletal Base Prior to Implant Therapy
Kumar, V. V., & Malik, N. (2011) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1033
Nakamoto, T., Hosokawa, R., Murashima, Y., Masaki, C., Makino, M., & Kojo, T. (2011) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1028
Dhanalakshmi, G., Palaniswamy, S., & Pasupathy, P. (2012)
Effective Regimens for Ovulation Induction in Polycystic Ovary Syndrome
Tapanainen, J. S., & Morin-Papunen, L. C. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-108-6_19
“In CC-resistant women with PCOS, letrozole at doses of 2.5–5 mg daily on days 3–7 of the cycle has been found to induce ovulation in 75% of cases and to result in a PR of 25% ( 87 ,88).”
BackgroundInfluentialForouzanfard, F., Pezhmanmanesh, M., Mahdian, M., & Abas, M. S. G. (2010) · KAUMS Journal
Brito, C. (2011) · Americanae (AECID Library)
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Kuang, Y., Hong, Q., & Chen, Q. (2015) · Springer eBooks · doi:10.1007/978-81-322-1118-1_8
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Bhutani, R., & Mehan, P. (2012) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1062
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Chandnani, K., & Jawalkar, K. (2013) · Journal of Evolution of Medical and Dental Sciences · doi:10.14260/jemds/541
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Durrani, F. (2013) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1101
Jain, A. R. (2013) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1104
Transfer of Esthetic Gingival Contour for Anterior Implant Prosthetics
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Wülfing, P., & Kiesel, L. (2005) · Der Gynäkologe · doi:10.1007/s00129-005-1668-2
Timing of Implant Placement in Anterior Zone: A Clinical Perspective
Tunkiwala, B., & Tunkiwala, A. (2011) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1056
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Gupta, H., Singh, A. V., Tandon, K., & Paul, R. (2013) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1099
Khalikar, A., Vaidya, S. P., & Govindwar, P. G. (2012) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1084
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Abbass, S., Ahmed, D. E., & Shabbir, I. (2016) · The Professional Medical Journal · doi:10.17957/tpmj/16.3052
Prashanth, N. T., Shobha, E. S., Kumar, R. D., & Verma, H. (2013) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1102
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Mahesh, L., & Dhir, S. (2013) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1105
Natural Crown as Immediate Implant Provisional Prosthesis
(2014) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1112
Sundar, M. K., & Lakhanpal, S. (2014) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1125
Singh, S., Singh, S., & Ashraf, C. M. (2015) · Springer eBooks · doi:10.1007/978-81-322-1686-5_5
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Rathod, D. M., Dange, S., Khalikar, A., & Khalikar, S. (2015) · International Journal of Clinical Implant Dentistry · doi:10.5005/jp-journals-10004-1027
eStIMulacIón O váRIca en RePROduccIón aSIStIda
Escudero, E. (2012)
Ovarian Stimulation in Cancer Patient
Verma, S. (2015) · Springer eBooks · doi:10.1007/978-81-322-1686-5_34
Alvarez, S. (2007) · Gynécologie Obstétrique & Fertilité · doi:10.1016/j.gyobfe.2007.07.014
Aromatase Inhibitors in the Treatment of Unexplained Female Infertility
Sekhon, L. H., Rekawek, P., & Grunfeld, L. (2015) · Springer eBooks · doi:10.1007/978-1-4939-2140-9_26
Controlled Ovarian Stimulation Protocols in Cancer Patients
Çakmak, H., & Rosen, M. P. (2016) · Springer eBooks · doi:10.1007/978-4-431-55963-4_2
Rai, S. A., Jeevan, C., & Jeevan, V. (2015) · International Journal of Clinical Implant Dentistry · doi:10.5005/jp-journals-10004-1044
Ovulation induction for anovulatory patients
van Santbrink, E. J. P., & Fauser, B. C. J. M. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511762390.005
Implant-supported Overdenture using Resilient Reliner
Gupta, H., Singh, A. V., Priyadarshi, S., & Yusuf, S. M. (2015) · International Journal of Clinical Implant Dentistry · doi:10.5005/jp-journals-10004-1045
Novel treatments for polycystic ovary syndrome, including in vitro maturation
Buckett, W. M., & Tan, S. L. (2001) · Cambridge University Press eBooks · doi:10.1017/cbo9780511545191.014
Clinical relevance of endometrial assessment
Seungdamrong, A., & McGovern, P. G. (2008) · CRC Press eBooks · doi:10.3109/9780203091500-49
Petráková, K., Krásenská, M., Valík, D., et al. (2016) · Klinicka onkologie · doi:10.14735/amko20163s50
Letrozole in ovulation induction (a review)
Kirienko, K. V., Lvova, A. G., & Апрышко, В. П. (2016) · Russian Journal of Human Reproduction · doi:10.17116/repro201622651-57
Reversal of Subgingival pH by Ascorbic Acid: A Weapon against Periopathogens
Dani, N., Joshi, C., Bhatt, V. H., Khanna, D., & Khedkar, S. (2014) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1124
An Introduction to the Longest Fixtures: Zygomatic Implants
Vikram, J., Anand, D., Sharma, R., & Hasti, A. (2016) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1155
Feline Dental Implants: New Paradigm Shift in Maxillary Cuspid Extraction Treatment Planning
Kurtzman, G. M., Mele, R. E., & Caiafa, A. (2016) · International Journal of Oral Implantology and Clinical Research · doi:10.5005/jp-journals-10012-1156
MaNEjo dEl SíNdroME dE ovario P oliqUíStiCo EN la MUjEr iNfértil
Revisión, T. D. (2008)
Effects of letrozole on patients with symptomatic leiomyoma in the reproductive age women
Prakash, R., Pandey, S., & Chawla, I. (2017) · International Journal of Reproduction Contraception Obstetrics and Gynecology · doi:10.18203/2320-1770.ijrcog20171970
Quand le clomiphène ne sera plus offert…
Tulandi, T., & Casper, R. F. (2017) · Journal of Obstetrics and Gynaecology Canada · doi:10.1016/j.jogc.2017.06.024
Self-citation
Metadata
- Authors
- Mitwally, M. F. M., & Casper, R. F.
- Affiliations
- Mount Sinai Hospital (CA)
- University of Toronto (CA)
- Corresponding author
- Casper, Robert F
- ORCID
- Casper, Robert F
- Venue
- Fertility and Sterility
- Publisher
- Elsevier BV
- Published
- 2001-02
- Volume
- 75
- Issue
- 2
- Pages
- 305-309
- ISSN
- 0015-0282 (ISSN-L)
- OpenAlex
- W2165232862
- Cited by
- 800
- References
- 45
- Citations by year
- 2026: 7 · 2025: 10 · 2024: 13 · 2023: 20 · 2022: 28 · 2021: 26 · 2020: 23 · 2019: 22 · 2018: 25 · 2017: 56 · 2016: 24 · 2015: 69 · 2014: 49 · 2013: 52 · 2012: 63
- FWCI
- 14.93
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Fertility and Sterility (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Reproductive Medicine › Ovarian function and disorders
- Health Sciences › Medicine › Reproductive Medicine › Reproductive Biology and Fertility
- Health Sciences › Medicine › Reproductive Medicine › Reproductive Health and Technologies
- Keywords
- letrozole, aromatase inhibitors, ovulation induction, polycystic ovary syndrome, ovulatory infertility, anovulatory infertility, endometrial thickness, pregnancy rate, follicle recruitment
- MeSH terms
- Letrozole, Anovulation, Endometrium, Enzyme Inhibitors, Estradiol, Female, Chorionic Gonadotropin, Humans, Infertility, Female, Luteinizing Hormone, Nitriles, Ovulation Induction, Polycystic Ovary Syndrome, Pregnancy, Prospective Studies, Triazoles, Aromatase Inhibitors
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