Cited by 100Health Literacy and Information AccessibilityPatient-Provider Communication in HealthcareElectronic Health Records Systems

A mixed methods systematic review of the effects of patient online self-diagnosing in the ‘smart-phone society’ on the healthcare professional-patient relationship and medical authority

Open access
Farnood, Annabel, Johnston, Bridget, Mair, Frances S.·2020·BMC Medical Informatics and Decision Making

Published version of a preprint

Abstract

Background: As technology continues to advance, the internet is becoming increasingly popular. Self-diagnosis and health information seeking online is growing more common and it will be important to understand the influence this may have on the patient-healthcare professional relationship. Methods: A mixed-method systematic review of quantitative, qualitative and mixed method studies concerning the public and healthcare professionals’ perceptions of online self-diagnosis and health information seeking and how this can impact the patient-healthcare professional relationship. We searched MEDLINE, EMBASE, CINAHL, ACM & SCOPUS between 2007 and 2018. Relevant data were extracted, and a thematic analysis was conducted and conceptualised using the Normalisation Process Theory framework. Results: Of 6107 records identified, 25 articles met the review eligibility criteria which included 16 qualitative, 8 quantitative and 1 mixed method study. The findings indicated that patients found the internet as a complementary information source alongside healthcare professionals. Health care professionals were perceived to be the most reliable and valued information source. People feel responsible for their own health and find the internet to be a source that provides information rapidly with accessibility at their convenience. Most healthcare professionals agreed on the importance of collaboration with patients and the need to develop a partnership and shared decision-making process but struggled to find time in the consultation to do so efficiently. Some healthcare professionals felt that the internet was advantageous for patients looking after their own health, while others felt it was due to a lack of trust in their expertise. Patients tended to present information to the healthcare professional to support the therapeutic relationship rather than to challenge it and to become more involved in the decision-making process of their healthcare. Conclusion: The results of this review suggests that patients value healthcare professionals as a source of medical advice more than the internet. While health professionals’ views were mixed our findings indicate that online health information seeking can potentially improve the patient-healthcare professional relationship as patients reported they usually conducted an online search to form a partnership with the healthcare professional as opposed to trying to prove them wrong.

AI snapshot

Written from the paper’s full text.

TL;DR

This mixed-methods systematic review of 25 studies found that patients generally value healthcare professionals over the internet for medical advice, while using online information as a complementary resource. It suggests online self-diagnosis can potentially improve the patient–healthcare professional relationship when patients share information to partner with clinicians, though healthcare professionals’ views are mixed and time constraints persist.

Key findings

  • The review included 25 articles: 16 qualitative, 8 quantitative, and 1 mixed method study. Patients viewed the internet as a complementary information source alongside healthcare professionals, and healthcare professionals were perceived as the most reliable and valued information source.
  • Trust in clinicians remained high: one survey found 57.5% of participants gave their physicians a perfect trust score but still used the internet after visits; another found 81% of respondents never showed their internet information to their doctors, while 77.9% were interested in their healthcare professional referring them to appropriate online health websites.
  • Healthcare professionals’ views were mixed: most nurses had positive attitudes (72.7%) toward internet-informed patients, and nurses previously exposed to such patients adopted more positive attitudes; some professionals saw online information as beneficial, while others interpreted it as a lack of trust in their expertise.
  • Patients tended to present online information to support the therapeutic relationship rather than challenge it; 82.2% of participants in one study were satisfied or extremely satisfied with their healthcare professional’s reactions to their online support group participation, while 16.2% experienced negative reactions.

Methods

  • Mixed-method systematic review following PRISMA, registered on PROSPERO (CRD42018084230); searched MEDLINE, EMBASE, CINAHL, ACM, and SCOPUS for English-language studies published 2007–April 2018.
  • Inclusion criteria covered adults aged 18 and over, physical health conditions, and primary care or normal settings; cancer, maternal health, and mental health were excluded.
  • Data were extracted, quality assessed with the Mixed Methods Appraisal Tool (MMAT), and synthesised using thematic analysis mapped onto Normalisation Process Theory constructs.

Limitations

  • Stated in the paper: the search criterion was broad because there is no consistently used terminology for the patient–healthcare professional relationship; only English-language articles were searched; conference proceedings, theses, and abstracts were excluded, so related studies may have been missed; all articles meeting inclusion criteria were kept even if methodologically weak.
  • Evident from the text: most included studies focused on the patient perspective, with fewer exploring healthcare professionals’ perspectives; only 2/25 studies included nurses’ perceptions, with most focusing on doctors; the majority examined researching health information rather than self-diagnosis; many studies were generalised across all health conditions, only one focused solely on multiple sclerosis, and only two focused on online health forums; overall study quality was moderate, and samples more frequently included middle-aged females and those of ‘white’ ethnicity.

Model-written summary. Check it against the paper before relying on it.

Integrity signals

Registry

Crossref · 10.1186/s12911-020-01243-6

Cites

47 of 47 references verified0 citation errors · 0 not checkable

Statistics

Nothing to recompute.

Claims the paper makes

0 of 150 cited sources checked · 0 supported · 0 flagged

  • Findingcitation

    Patients find the internet useful for finding out more information about their health conditions or the medications prescribed by their HCP.

    “Patients find the internet useful for finding out more information about their health conditions or the medications prescribed by their HCP [46].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [46] Lee K, Hoti K, Hughes JD, Emmerton L. Dr Google and the consumer: a qualitative study exploring the navigational needs and online health information-seeking behaviors of consumers with chronic health conditions. J Med Internet Res. 2014;16(12):e262–e. source

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  • Findingreasoning

    Overall, the included studies were of moderate quality.

    “Overall, the studies were of moderate quality.”
    Quote in the paperNot a substantial claim
  • Findingcitation

    Patients reported that the internet was often the first source they accessed for health information.

    “Patients reported that the internet was often the first source they accessed for health information [37].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [37] Fiksdal AS, Kumbamu A, Jadhav AS, Cocos C, Nelsen LA, Pathak J, et al. Evaluating the process of online health information searching: a qualitative approach to exploring consumer perspectives. J Med Internet Res. 2014;16(10):e224–e. source

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  • Findingcitation

    Twelve qualitative studies and one mixed methods study reported on patient perspectives on using the internet to seek health information.

    “Twelve qualitative studies [30, 31, 34, 37–39, 45–47, 49–51] and one mixed methods study [36], reported on this theme.”
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  • Findingnone given

    Fewer studies had samples that accurately represented the target population.

    “Fewer studies had samples that accurately represented the target population.”
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    Findingown data

    6109 titles were screened and 708 passed to abstract screening.

    “6109 titles were screened and 708 passed to abstract screening.”
    Quote in the paperNot a substantial claim
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    Findingcitation

    Accessibility and speed were key identified benefits of online self-diagnosing.

    “Accessibility and speed were key identified benefits of online self-diagnosing.”
    Quote in the paperNot a substantial claim
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    Findingown data

    The included studies were from the United Kingdom (5), United States (6), Canada (2), Austria (1), Israel (4), Australia (2), Switzerland (3), Portugal (1) and China (1).

    “Five studies had taken place in the United Kingdom [27–31], six from the United States [32–37], two from Canada [38, 39], one from Austria [40], four from Israel [41–44], two from Australia [45, 46], three from Switzerland [47–49], one from Portugal [50] and one from China [51].”
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    Findingcitation

    The internet allows 24-h access, whereas obtaining an appointment with a HCP can be difficult.

    “The internet allows 24-h access, whereas obtaining an appointment with a HCP can be difficult [30, 31, 34].”
    Quote in the paperNot a substantial claim0 of 3 sources checked
    • cites [30] Donnelly LS, Shaw RL, van den Akker OB. eHealth as a challenge to ‘expert’ power: a focus group study of internet use for health information and management. J R Soc Med. 2008;101(10):501–6. source

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    • cites [31] Stevenson FA, Kerr C, Murray E, Nazareth I. Information from the internet and the doctor-patient relationship: the patient perspective – a qualitative study. J BMC Family Pract. 2007;8(1):47. source

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    • cites [34] Macias W, McMillan S. The return of the house call: The role of internet-based interactivity in bringing health information home to older adults. Health Commun. 2008;23(1):34–44. source

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    Findingnone given

    Fewer studies explored the HCP's perspectives compared to the patient's perspectives.

    “Fewer studies explored the HCP’s perspectives compared to the patient’s perspectives.”
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    Findingnone given

    The internet allowed patients and the public to expand their knowledge and gain a deeper understanding of health information without involving their HCP.

    “It allowed patients and the public to expand their knowledge and gain a deeper understanding of health information without involving their HCP.”
    Quote in the paperNot a substantial claim
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    Findingcitation

    People in countries where patients pay for their healthcare reported online self-diagnosis to be money saving and time efficient.

    “For example, people in countries where patients pay for their healthcare reported online self-diagnosis to be money saving and time efficient; they could access health information with ease for free as opposed to waiting for a healthcare appointment and then having to pay a fee [37].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [37] Fiksdal AS, Kumbamu A, Jadhav AS, Cocos C, Nelsen LA, Pathak J, et al. Evaluating the process of online health information searching: a qualitative approach to exploring consumer perspectives. J Med Internet Res. 2014;16(10):e224–e. source

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    Findingown data

    Database searches retrieved 7026 papers in total, which reduced to 6109 after deduplication.

    “Database searches retrieved 7026 papers in total which reduced to 6109 after deduplication.”
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    Findingown data

    The four main themes are: 1) patient perspectives on using the internet to seek health information; 2) healthcare professionals' perspectives on and reactions to internet-informed patients; 3) sharing online health information with healthcare professionals; 4) impact of online medical searches and diagnosis on patient-healthcare professional relationships.

    “The four main themes are: 1) patient perspectives on using the internet to seek health information; 2) healthcare professionals’ perspectives on and reactions to internet-informed patients; 3) sharing online health information with healthcare professionals; 4) impact of online medical searches and diagnosis on patient-healthcare professional relationships”
    Quote in the paperSubstantial claim
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    Findingcitation

    Patients found the internet convenient and that it allowed them to become more self-aware and to share their experiences within online health forums.

    “Patients found the internet convenient and that it allowed them to become more self-aware and to share their experiences within online health forums [33].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [33] Rupert DJ, Moultrie RR, Read JG, Amoozegar JB, Bornkessel AS, O’Donoghue AC, et al. Perceived healthcare provider reactions to patient and caregiver use of online health communities. J Patient Educ Couns. 2014;96(3):320–6. source

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    Findingcitation

    The internet was seen as beneficial to revisit the information as many times as required for free.

    “It was also seen as beneficial to revisit the information as many times as required for free [33].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [33] Rupert DJ, Moultrie RR, Read JG, Amoozegar JB, Bornkessel AS, O’Donoghue AC, et al. Perceived healthcare provider reactions to patient and caregiver use of online health communities. J Patient Educ Couns. 2014;96(3):320–6. source

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    Findingnone given

    All 25 included studies presented clear research questions and collected data to address the questions.

    “All 25 studies presented clear research questions and collected data to address the questions.”
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    Findingown data

    708 abstracts were screened and 289 were assessed for full text screening.

    “708 abstracts were screened and 289 were assessed for full text screening.”
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    Findingnone given

    Most quantitative studies used appropriate statistical analysis and appropriate measurements.

    “Most quantitative studies used appropriate statistical analysis to answer the research questions and used appropriate measurements.”
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    Findingown data

    Four major themes and several subthemes were identified from the synthesis of the literature.

    “Four major themes and several subthemes were identified from the synthesis of the literature.”
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    Findingcitation

    Contradictory information could result in additional questions arising about health and trigger a seemingly endless cycle of information seeking.

    “Contradictory information could result in additional questions arising about health and trigger a seemingly endless cycle of information seeking [38, 39].”
    Quote in the paperNot a substantial claim0 of 2 sources checked
    • cites [38] Townsend A, Leese J, Adam P, McDonald M, Li LC, Kerr S, et al. eHealth, participatory medicine, and ethical care: a focus group study of patients’ and health care providers’ use of health-related internet information. J Med Internet Res. 2015;17(6):e155. source

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    • cites [39] Silver MP. Patient perspectives on online health information and communication with doctors: a qualitative study of patients 50 years old and over. J Medical Internet Res. 2015;17(1):e19. source

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    Findingnone given

    Almost all quantitative studies had pre-tested and piloted surveys before use.

    “Almost all the quantitative studies had pre-tested and piloted surveys before use.”
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    Findingown data

    Most qualitative studies used appropriate data collection methods, reported findings adequately derived from the data, and provided coherence between qualitative data sources, collection, analysis and interpretation.

    “Most of the qualitative studies used appropriate data collection methods to answer the research questions, reported the findings adequately derived from the data and provided coherence between qualitative data sources, collection, analysis and interpretation.”
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    Findingnone given

    Studies more frequently included middle-aged females and those of 'white' ethnicity.

    “Although studies more frequently included middle-aged females and those of ‘white’ ethnicity.”
    Quote in the paperNot a substantial claim
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    Findingcitation

    The internet was thought to be informative, but there was evidence that people had concerns about the quality of information available on the internet, with the belief it could be contradictory at times and should be seen as provisional.

    “Essentially, the internet was thought to be informative, but there was evidence that people had concerns about the quality of the information available on the internet, with the belief it could be contradictory at times and should be seen as provisional [38].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [38] Townsend A, Leese J, Adam P, McDonald M, Li LC, Kerr S, et al. eHealth, participatory medicine, and ethical care: a focus group study of patients’ and health care providers’ use of health-related internet information. J Med Internet Res. 2015;17(6):e155. source

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    Findingown data

    Of the 25 eligible papers, there were 16 qualitative, 8 quantitative and 1 mixed method study.

    “Of the 25 eligible papers, there were 16 qualitative, 8 quantitative and 1 mixed method study.”
    • Also stated in: § Results · plain
      “Of 6107 records identified, 25 articles met the review eligibility criteria which included 16 qualitative, 8 quantitative and 1 mixed method study.”
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    Findingown data

    The final number of papers deemed eligible from the database search was 23.

    “The final number of papers deemed eligible to be included from the database search, was 23.”
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    Findingown data

    Backward and forward chaining discovered another two papers meeting eligibility criteria, making the final number of included papers 25.

    “During this process, another two papers were discovered to meet the eligibility criteria for review, making the final number of included papers in this mixed methods systematic review, 25”
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    Findingown data

    The sample sizes of included studies ranged from 11 to 975.

    “The sample sizes ranged from 11 to 975 with participants including patients either posting online or attending primary care clinics, carers, physicians such as GP’s, nurses and various other HCP’s.”
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    Findingcitation

    The internet was generally seen as a tool for the treatment of non-serious medical issues or for self-diagnosis.

    “The internet was generally seen as a tool for the treatment of non-serious medical issues or for self-diagnosis [40].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [40] Haluza D, Naszay M, Stockinger A, Jungwirth D. Digital natives versus digital immigrants: influence of online health information seeking on the doctor–patient relationship. J Health Commun. 2017;32(11):1342–9. source

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  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Findingcitation

    Some people saw online self-diagnosis as a method to increase their knowledge, making them better prepared and equipped for health consultations.

    “Some people saw online self-diagnosis as a method to increase their knowledge, making them better prepared and equipped for health consultations.”
    Quote in the paperNot a substantial claim
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    Findingcitation

    Some health knowledge acquired online was beyond the expertise of GPs, causing patients to feel the need to perform research themselves to improve their self-care.

    “It was also reported that some health knowledge acquired online, was beyond the expertise of General Practitioners (GPs), causing patients to feel the need to perform research themselves to improve their self-care [31].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [31] Stevenson FA, Kerr C, Murray E, Nazareth I. Information from the internet and the doctor-patient relationship: the patient perspective – a qualitative study. J BMC Family Pract. 2007;8(1):47. source

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    Findingcitation

    Having a better understanding of symptoms and conditions was thought to help patients engage more effectively with HCPs.

    “Having a better understanding of symptoms and conditions was thought to help them to engage more effectively with HCP’s.”
    Quote in the paperNot a substantial claim
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    Findingcitation

    Difficulties included information overload and complex or contradictory information.

    “Difficulties included information overload and complex or contradictory information [47].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [47] Sommerhalder K, Abraham A, Zufferey MC, Barth J, Abel T. Internet information and medical consultations: experiences from patients’ and physicians’ perspectives. Patient Educ Couns. 2009;77(2):266–71. source

      Not checked in the free run.

  • May combine two claims.

    Findingown data

    Patients tended to present information to the healthcare professional to support the therapeutic relationship rather than to challenge it and to become more involved in the decision-making process of their healthcare.

    “Patients tended to present information to the healthcare professional to support the therapeutic relationship rather than to challenge it and to become more involved in the decision-making process of their healthcare.”
    Quote in the paperSubstantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Findingcitation

    Online self-diagnosis was seen as a way to help patients make the most of the short time in consultations so they know what questions to ask.

    “It was also seen as a way to help them to make the most of the short time they have in consultations so they know what questions to ask [30, 38].”
    Quote in the paperNot a substantial claim0 of 2 sources checked
    • cites [30] Donnelly LS, Shaw RL, van den Akker OB. eHealth as a challenge to ‘expert’ power: a focus group study of internet use for health information and management. J R Soc Med. 2008;101(10):501–6. source

      Not checked in the free run.

    • cites [38] Townsend A, Leese J, Adam P, McDonald M, Li LC, Kerr S, et al. eHealth, participatory medicine, and ethical care: a focus group study of patients’ and health care providers’ use of health-related internet information. J Med Internet Res. 2015;17(6):e155. source

      Not checked in the free run.

  • May combine two claims.

    Findingcitation

    This impacts patients' ability to depend on information and causes the public to find the internet less reliable than other sources of information such as HCPs.

    “This impacts patients’ ability to depend on information and causes the public to find the internet less reliable than other sources of information such as HCPs [50].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [50] Mendes Á, Abreu L, Vilar-Correia MR, Borlido-Santos J. “That should be left to doctors, That’s what they are there for!”—exploring the reflexivity and Trust of Young Adults When Seeking Health Information. Health Commun. 2017;32(9):1076–81. source

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    Findingnone given

    People feel responsible for their own health and find the internet to be a source that provides information rapidly with accessibility at their convenience.

    “People feel responsible for their own health and find the internet to be a source that provides information rapidly with accessibility at their convenience.”
    Quote in the paperNot a substantial claim
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    Findingown data

    Most healthcare professionals agreed on the importance of collaboration with patients and the need to develop a partnership and shared decision-making process but struggled to find time in the consultation to do so efficiently.

    “Most healthcare professionals agreed on the importance of collaboration with patients and the need to develop a partnership and shared decision-making process but struggled to find time in the consultation to do so efficiently.”
    Quote in the paperNot a substantial claim
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    Findingcitation

    The internet was seen to work well as a means for self-diagnosis or to find information to help ease patients' minds while awaiting doctors' appointments.

    “The internet was seen to work well as a means for self-diagnosis or to find information to help ease patients’ minds while awaiting doctors’ appointments [30].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [30] Donnelly LS, Shaw RL, van den Akker OB. eHealth as a challenge to ‘expert’ power: a focus group study of internet use for health information and management. J R Soc Med. 2008;101(10):501–6. source

      Not checked in the free run.

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    Findingown data

    Some healthcare professionals felt that the internet was advantageous for patients looking after their own health, while others felt it was due to a lack of trust in their expertise.

    “Some healthcare professionals felt that the internet was advantageous for patients looking after their own health, while others felt it was due to a lack of trust in their expertise.”
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    Findingcitation

    HCPs were viewed as expert guides who could aid navigation through the otherwise overwhelming quantities of health-related internet information.

    “HCP’s were thus viewed as expert guides who could aid navigation through the otherwise overwhelming quantities of health-related internet information [38].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [38] Townsend A, Leese J, Adam P, McDonald M, Li LC, Kerr S, et al. eHealth, participatory medicine, and ethical care: a focus group study of patients’ and health care providers’ use of health-related internet information. J Med Internet Res. 2015;17(6):e155. source

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    Findingcitation

    Several patients did not want to tread on the HCP's toes; they perceived they would be challenging the professional and did not want to question them or make them feel offended or intimidated by attempts to discuss online health information, thus interrupting the diagnostic process.

    “Several patients did not want to tread on the HCP’s toes; such patients perceived they would be challenging the professional and did not want to question them or make them feel offended or intimidated by attempts to discuss online health information, thus interrupting the diagnostic process [27, 32, 47].”
    Quote in the paperNot a substantial claim0 of 3 sources checked
    • cites [27] Bowes P, Stevenson F, Ahluwalia S, Murray E. ‘I need her to be a doctor’: patients’ experiences of presenting health information from the internet in GP consultations. J Gen Pract. 2012;62(604):e732–e8. source

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    • cites [32] Imes RS, Bylund CL, Sabee CM, Routsong TR, Sanford AA. Patients’ reasons for refraining from discussing internet health information with their healthcare providers. J Health Commun. 2008;23(6):538–47. source

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    • cites [47] Sommerhalder K, Abraham A, Zufferey MC, Barth J, Abel T. Internet information and medical consultations: experiences from patients’ and physicians’ perspectives. Patient Educ Couns. 2009;77(2):266–71. source

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    Findingcitation

    HCPs sometimes experience anxiety around internet-informed patients, and some may find information patients bring to consultations slightly outside their area of expertise.

    “HCP’s do sometimes experience anxiety around internet-informed patients, and some may find some of the information patients bring to consultations, slightly outside their area of expertise [38].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [38] Townsend A, Leese J, Adam P, McDonald M, Li LC, Kerr S, et al. eHealth, participatory medicine, and ethical care: a focus group study of patients’ and health care providers’ use of health-related internet information. J Med Internet Res. 2015;17(6):e155. source

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    Findingcitation

    There is a known fear among HCPs of losing control of the consultation with internet-informed patients and of being perceived as incompetent.

    “There is also a known fear of losing control of the consultation with internet-informed patients and the feeling of being perceived as incompetent [28].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [28] Ahluwalia S, Murray E, Stevenson F, Kerr C, Burns J. ‘A heartbeat moment’: qualitative study of GP views of patients bringing health information from the internet to a consultation. Br J Gen Pract. 2010;60(571):88–94. source

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    Findingcitation

    Other reasons for patients not discussing online health information research included feeling embarrassed and not wanting to be seen negatively.

    “Other reasons for patients not discussing online health information research included feeling embarrassed and not wanting to be seen negatively [27, 32, 39]”
    Quote in the paperNot a substantial claim0 of 3 sources checked
    • cites [27] Bowes P, Stevenson F, Ahluwalia S, Murray E. ‘I need her to be a doctor’: patients’ experiences of presenting health information from the internet in GP consultations. J Gen Pract. 2012;62(604):e732–e8. source

      Not checked in the free run.

    • cites [32] Imes RS, Bylund CL, Sabee CM, Routsong TR, Sanford AA. Patients’ reasons for refraining from discussing internet health information with their healthcare providers. J Health Commun. 2008;23(6):538–47. source

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    • cites [39] Silver MP. Patient perspectives on online health information and communication with doctors: a qualitative study of patients 50 years old and over. J Medical Internet Res. 2015;17(1):e19. source

      Not checked in the free run.

  • May combine two claims.

    Findingcitation

    HCPs agreed on the importance of collaboration with and guidance for patients, though they struggled to find the time to do this efficiently.

    “HCP’s agreed on the importance of collaboration with and guidance for patients, though they struggled to find the time to do this efficiently [38].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [38] Townsend A, Leese J, Adam P, McDonald M, Li LC, Kerr S, et al. eHealth, participatory medicine, and ethical care: a focus group study of patients’ and health care providers’ use of health-related internet information. J Med Internet Res. 2015;17(6):e155. source

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    Findingcitation

    Some HCPs believed patients should take responsibility for their own health and be able to make decisions, provided they can base these decisions on high-quality sources of information.

    “They also believed patients should take responsibility for their own health and be able to make decisions, provided that they can base these decisions on high-quality sources of information [48].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [48] Caiata-Zufferey M, Schulz PJ. Physicians’ communicative strategies in interacting with internet-informed patients: results from a qualitative study. Health Commun. 2012;27(8):738–49. source

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    Findingcitation

    Some HCPs felt that patients have a right to stay well-informed and that they are more satisfied this way.

    “Some HCP’s felt that patients have a right to stay well-informed and that they are more satisfied this way.”
    Quote in the paperNot a substantial claim
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    Findingcitation

    Such patients were concerned about HCPs' reactions to their health research online and felt that they might not be listened to or that professionals might become dismissive or uninterested.

    “such patients were concerned about HCP’s reactions to their health research online and felt that they might not be listened to or that the professionals might become dismissive or uninterested [27, 32, 36, 39].”
    Quote in the paperNot a substantial claim0 of 3 sources checked
    • cites [27] Bowes P, Stevenson F, Ahluwalia S, Murray E. ‘I need her to be a doctor’: patients’ experiences of presenting health information from the internet in GP consultations. J Gen Pract. 2012;62(604):e732–e8. source

      Not checked in the free run.

    • cites [32] Imes RS, Bylund CL, Sabee CM, Routsong TR, Sanford AA. Patients’ reasons for refraining from discussing internet health information with their healthcare providers. J Health Commun. 2008;23(6):538–47. source

      Not checked in the free run.

    • cites [36] Hay MC, Strathmann C, Lieber E, Wick K, Giesser B. Why Patients Go Online: Multiple Sclerosis, the Internet, and Physician-Patient Communication. Neurologist. 2008;14(6):374–81. source

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Findingcitation

    Several HCPs believed that the internet poses risks as patients may misinterpret information and this can cause unnecessary medical visits.

    “Several HCP’s also believed that the internet poses risks as patients may misinterpret information and this can also cause unnecessary medical visits [28, 48].”
    Quote in the paperNot a substantial claim0 of 2 sources checked
    • cites [28] Ahluwalia S, Murray E, Stevenson F, Kerr C, Burns J. ‘A heartbeat moment’: qualitative study of GP views of patients bringing health information from the internet to a consultation. Br J Gen Pract. 2010;60(571):88–94. source

      Not checked in the free run.

    • cites [48] Caiata-Zufferey M, Schulz PJ. Physicians’ communicative strategies in interacting with internet-informed patients: results from a qualitative study. Health Commun. 2012;27(8):738–49. source

      Not checked in the free run.

  • Classified as probably not a substantial claim.

    Findingcitation

    It can become difficult for HCPs to do their jobs efficiently as they may need to explain, interpret or suggest a conflicting opinion to information presented from online resources.

    “It can become difficult for HCP’s to do their jobs efficiently as they may need to explain, interpret or suggest a conflicting opinion to the information presented from online resources [48].”
    Quote in the paperSubstantial claim0 of 1 sources checked
    • cites [48] Caiata-Zufferey M, Schulz PJ. Physicians’ communicative strategies in interacting with internet-informed patients: results from a qualitative study. Health Commun. 2012;27(8):738–49. source

      Not checked in the free run.

  • May combine two claims.

    Findingcitation

    Many HCPs agreed that it was important to show support to patients who used the internet for health information, but that such behaviours can bring associated tensions.

    “Many HCP’s agreed that it was important to show support to patients who used the internet for health information, but that such behaviours can bring associated tensions [38].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [38] Townsend A, Leese J, Adam P, McDonald M, Li LC, Kerr S, et al. eHealth, participatory medicine, and ethical care: a focus group study of patients’ and health care providers’ use of health-related internet information. J Med Internet Res. 2015;17(6):e155. source

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Findingcitation

    Internet-informed patients were considered by some HCPs as potentially preventing a physician from being as effective as they could be.

    “Internet-informed patients were also considered by some as potentially preventing a physician from being as effective as they could be.”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Findingcitation

    Patients/public found adopted reactions from HCPs such as open body language and asking open questions, making the environment more comfortable and allowing them to feel more listened to, encouraging.

    “Patients/public found adopted reactions from HCP’s such as open body language and asking open questions, making the environment more comfortable and allowing them to feel more listened to, encouraging [28].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [28] Ahluwalia S, Murray E, Stevenson F, Kerr C, Burns J. ‘A heartbeat moment’: qualitative study of GP views of patients bringing health information from the internet to a consultation. Br J Gen Pract. 2010;60(571):88–94. source

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Findingcitation

    77.9% of respondents were interested in their HCP referring them to appropriate online health websites.

    “although 77.9% were interested in their HCP referring them to appropriate online health websites.”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [41] Russ H, Giveon SM, Granek Catarivas M, Yaphe J. The effect of the internet on the patient-doctor relationship from the patient’s perspective: a survey from primary care. J IMAJ-Israel Med Assoc J. 2011;13(4):220.

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Findingcitation

    Doctors' body language was extremely important and even a simple smile could change the dynamic of the conversation.

    “They found that doctors’ body language was extremely important and that even a simple smile could change the dynamic of the conversation.”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Findingcitation

    Many patients did not use the internet to replace HCPs but rather to gain a deeper understanding of their symptoms or disease and to become more familiar with the appropriate terminology.

    “However, many patients did not use the internet to replace HCP’s but rather to gain a deeper understanding of their symptoms or disease and to become more familiar with the appropriate terminology [36].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [36] Hay MC, Strathmann C, Lieber E, Wick K, Giesser B. Why Patients Go Online: Multiple Sclerosis, the Internet, and Physician-Patient Communication. Neurologist. 2008;14(6):374–81. source

      Not checked in the free run.

  • May combine two claims.

    Findingcitation

    Patients felt more trust in HCPs and hoped for discussion regarding internet health information while seeking doctors' opinions.

    “Patients felt more trust in HCP’s and hoped for discussion regarding internet health information while seeking doctors’ opinions [27].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [27] Bowes P, Stevenson F, Ahluwalia S, Murray E. ‘I need her to be a doctor’: patients’ experiences of presenting health information from the internet in GP consultations. J Gen Pract. 2012;62(604):e732–e8. source

      Not checked in the free run.

  • May combine two claims.

    Findingcitation

    Physicians' new role can be described as acting as a partner to the patient, who is now more involved in both medical decision-making and consultation.

    “Their new role can be described as acting as a partner to the patient, who is now more involved in both medical decision-making and consultation [47].”
    Quote in the paperSubstantial claim0 of 1 sources checked
    • cites [47] Sommerhalder K, Abraham A, Zufferey MC, Barth J, Abel T. Internet information and medical consultations: experiences from patients’ and physicians’ perspectives. Patient Educ Couns. 2009;77(2):266–71. source

      Not checked in the free run.

  • May combine two claims.

    Findingcitation

    Most studies emphasised that, regardless of the popularity of online self-diagnosis, the majority of respondents valued HCPs' opinions more, understood their explanations of diagnoses better, and had more trust in them.

    “Most studies emphasised that, regardless of the popularity of online self-diagnosis, the majority of respondents valued HCP’s opinions more, understood their explanations of diagnoses better, and had more trust in them [30, 50].”
    Quote in the paperSubstantial claim0 of 2 sources checked
    • cites [30] Donnelly LS, Shaw RL, van den Akker OB. eHealth as a challenge to ‘expert’ power: a focus group study of internet use for health information and management. J R Soc Med. 2008;101(10):501–6. source

      Not checked in the free run.

    • cites [50] Mendes Á, Abreu L, Vilar-Correia MR, Borlido-Santos J. “That should be left to doctors, That’s what they are there for!”—exploring the reflexivity and Trust of Young Adults When Seeking Health Information. Health Commun. 2017;32(9):1076–81. source

      Not checked in the free run.

  • May combine two claims.

    Findingcitation

    Some patients felt that sharing health information they found online with their HCPs could show that they had invested time and energy into the consultation; these respondents hoped this would promote them and their problems being taken more seriously.

    “In contrast to these perceptions of negative reactions, some patients felt that sharing health information they found online with their HCP’s could show that they had invested time and energy into the consultation; these respondents hoped this would promote them and their problems being taken more seriously [27, 45].”
    Quote in the paperNot a substantial claim0 of 2 sources checked
    • cites [27] Bowes P, Stevenson F, Ahluwalia S, Murray E. ‘I need her to be a doctor’: patients’ experiences of presenting health information from the internet in GP consultations. J Gen Pract. 2012;62(604):e732–e8. source

      Not checked in the free run.

    • cites [45] Benetoli A, Chen T, Aslani P. How patients’ use of social media impacts their interactions with healthcare professionals. J Patient education counseling. 2018;101(3):439–44. source

      Not checked in the free run.

  • May combine two claims.

    Findingcitation

    Where the HCP's response to health information seeking is negative and disrespectful, this can seriously impact the patient-HCP relationship, and in some cases, this can lead to a patient changing their doctor or practice.

    “However, where the HCP’s response to health information seeking is negative and disrespectful, this can seriously impact the patient-HCP relationship, and in some cases, this can lead to a patient changing their doctor or practice [27].”
    Quote in the paperSubstantial claim0 of 1 sources checked
    • cites [27] Bowes P, Stevenson F, Ahluwalia S, Murray E. ‘I need her to be a doctor’: patients’ experiences of presenting health information from the internet in GP consultations. J Gen Pract. 2012;62(604):e732–e8. source

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Findingcitation

    Positive experiences of patients sharing online health information with their doctors include all occasions when the doctor listens, acknowledges, and offers further discussion about such information.

    “Positive experiences of patients sharing online health information with their doctors include all occasions when the doctor listens, acknowledges, and offers further discussion about such information [33].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [33] Rupert DJ, Moultrie RR, Read JG, Amoozegar JB, Bornkessel AS, O’Donoghue AC, et al. Perceived healthcare provider reactions to patient and caregiver use of online health communities. J Patient Educ Couns. 2014;96(3):320–6. source

      Not checked in the free run.

  • May combine two claims.

    Findingown data

    Patients expected feedback on the validity of their research and recommendations for online health communities, allowing for more engagement in the decision-making process by the patient in conjunction with the HCP.

    “They expected feedback on the validity of their research and recommendations for online health communities, allowing for more engagement in the decision-making process by the patient in conjunction with the HCP.”
    Quote in the paperSubstantial claim
  • May combine two claims.

    Findingown data

    Patients felt they had a better relationship with their HCP when they were able to discuss their online research with them and when their HCP responded positively to this.

    “It was clear from the findings that patients felt they had a better relationship with their HCP when they were able to discuss their online research with them and when their HCP responded positively to this.”
    Quote in the paperSubstantial claim
  • May combine two claims.

    Findingcitation

    Very few studies (2/25) included the nurse's perceptions of patients' online self-diagnosis and online health research, with most focusing on doctors.

    “Very few studies (2/25) included the nurse’s perceptions of patients’ online self-diagnosis and online health research [42, 44]. with most focusing on doctors.”
    Quote in the paperSubstantial claim0 of 2 sources checked
    • cites [42] Barnoy S, Volfin-Pruss D, Ehrenfeld M, Kushnir T. Self-epistemic authority and nurses’ reactions to medical information that is retrieved from Internet sites of different credibility. Nurs Health Sci. 2011;13(3):366–70. source

      Not checked in the free run.

    • cites [44] Barnoy S, Volfin-Pruss D, Ehrenfeld M, Kushnir T. Factors affecting nurses’ attitudes in Israel toward patients who present them with internet medical information. Nurs Outlook. 2008;56(6):314–21. source

      Not checked in the free run.

  • May combine two claims.

    Findingown data

    Some physicians felt that it was good that patients were looking after their own health, whereas others felt they were being challenged with information found online and that their patient had lost trust in them when they turned to the internet for help.

    “Some physicians felt that it was good that patients were looking after their own health, whereas others felt they were being challenged with information found online and that their patient had lost trust in them when they turned to the internet for help.”
    Quote in the paperSubstantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Findingcitation

    Some HCPs thought online health information could cause anxiety among patients - especially when the information was misinterpreted, and this could lead to unnecessary medical visits.

    “Some also thought it could cause anxiety among patients – especially when the information was misinterpreted, and this could lead to unnecessary medical visits [28, 48].”
    Quote in the paperNot a substantial claim0 of 2 sources checked
    • cites [28] Ahluwalia S, Murray E, Stevenson F, Kerr C, Burns J. ‘A heartbeat moment’: qualitative study of GP views of patients bringing health information from the internet to a consultation. Br J Gen Pract. 2010;60(571):88–94. source

      Not checked in the free run.

    • cites [48] Caiata-Zufferey M, Schulz PJ. Physicians’ communicative strategies in interacting with internet-informed patients: results from a qualitative study. Health Commun. 2012;27(8):738–49. source

      Not checked in the free run.

  • May combine two claims.

    Findingcitation

    The internet is not seen as a replacement for visiting a HCP, but as offering a complimentary source of information.

    “The internet is not seen as a replacement for visiting a HCP, but as offering a complimentary source of information [30, 50, 51].”
    Quote in the paperSubstantial claim0 of 3 sources checked
    • cites [30] Donnelly LS, Shaw RL, van den Akker OB. eHealth as a challenge to ‘expert’ power: a focus group study of internet use for health information and management. J R Soc Med. 2008;101(10):501–6. source

      Not checked in the free run.

    • cites [50] Mendes Á, Abreu L, Vilar-Correia MR, Borlido-Santos J. “That should be left to doctors, That’s what they are there for!”—exploring the reflexivity and Trust of Young Adults When Seeking Health Information. Health Commun. 2017;32(9):1076–81. source

      Not checked in the free run.

    • cites [51] Chu JT, Wang MP, Shen C, Viswanath K, Lam TH, Chan SSC. How, When and Why People Seek Health Information Online: Qualitative Study in Hong Kong. Interactive J Med Res. 2017;6(2):e24–e. source

      Not checked in the free run.

  • May combine two claims.

    Findingown data

    Online resources were viewed as valuable sources of emotional support and helpful resources to inform self-management and self-diagnosis of symptoms or conditions.

    “Online resources were also viewed as valuable sources of emotional support and helpful resources to inform self-management and self-diagnosis of symptoms or conditions.”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Findingcitation

    People used information from the internet to become better informed about their health, to prepare for their consultation, to enable them to ask better questions and to help them better understand the information given to them by HCPs, thus helping to make consultations more productive for them.

    “People used information from the internet to become better informed about their health, to prepare for their consultation, to enable them to ask better questions and to help them better understand the information given to them by HCP’s [30, 38] thus helping to make consultations more productive for them.”
    Quote in the paperNot a substantial claim0 of 2 sources checked
    • cites [30] Donnelly LS, Shaw RL, van den Akker OB. eHealth as a challenge to ‘expert’ power: a focus group study of internet use for health information and management. J R Soc Med. 2008;101(10):501–6. source

      Not checked in the free run.

    • cites [38] Townsend A, Leese J, Adam P, McDonald M, Li LC, Kerr S, et al. eHealth, participatory medicine, and ethical care: a focus group study of patients’ and health care providers’ use of health-related internet information. J Med Internet Res. 2015;17(6):e155. source

      Not checked in the free run.

  • May combine two claims.

    Findingcitation

    The public still tend to trust the advice from a HCP over any other information source and trust in HCPs remained high.

    “the public still tend to trust the advice from a HCP over any other information source and trust in HCP’s remained high.”
    Quote in the paperSubstantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Findingcitation

    One study in this review focused solely on multiple sclerosis patients.

    “One study in this review focused solely on multiple sclerosis patients [36].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [36] Hay MC, Strathmann C, Lieber E, Wick K, Giesser B. Why Patients Go Online: Multiple Sclerosis, the Internet, and Physician-Patient Communication. Neurologist. 2008;14(6):374–81. source

      Not checked in the free run.

  • May combine two claims.

    Findingcitation

    HCPs' reactions to people who had obtained health-related information from the internet were mixed; however, they were mostly positive.

    “HCP’s reactions to people who had obtained health-related information from the internet were mixed; however, they were mostly positive.”
    Quote in the paperSubstantial claim
  • May combine two claims.

    Findingcitation

    Patients found HCPs to be the most valued source of health information but found the internet to be a useful complementary tool.

    “Patients found HCP’s to be the most valued source of health information but found the internet to be a useful complementary tool [30, 36, 47, 49, 50].”
    Quote in the paperSubstantial claim0 of 3 sources checked
    • cites [30] Donnelly LS, Shaw RL, van den Akker OB. eHealth as a challenge to ‘expert’ power: a focus group study of internet use for health information and management. J R Soc Med. 2008;101(10):501–6. source

      Not checked in the free run.

    • cites [36] Hay MC, Strathmann C, Lieber E, Wick K, Giesser B. Why Patients Go Online: Multiple Sclerosis, the Internet, and Physician-Patient Communication. Neurologist. 2008;14(6):374–81. source

      Not checked in the free run.

    • cites [47] Sommerhalder K, Abraham A, Zufferey MC, Barth J, Abel T. Internet information and medical consultations: experiences from patients’ and physicians’ perspectives. Patient Educ Couns. 2009;77(2):266–71. source

      Not checked in the free run.

  • May combine two claims.

    Premisecitation

    The rising use of smartphones and rapidly increasing availability of health information on the internet has led to more people using the internet as their first healthcare resource, often before seeking professional advice.

    “The rising use of smartphones [3] and rapidly increasing availability of health information on the internet has led to more people using the internet as their first healthcare resource, often before seeking professional advice [4].”
    Quote in the paperSubstantial claim0 of 2 sources checked
    • cites [3] Carbonell X, Chamarro A, Oberst U, Rodrigo B, Prades M. Problematic use of the internet and smartphones in university students: 2006–2017. J Int J Enviro Research Public Health. 2018;15(3):475. source

      Not checked in the free run.

    • cites [4] Gualtieri LN. The doctor as the second opinion and the internet as the first. CHI'09 Extended Abstracts on Human Factors in Computing Systems: ACM; 2009. source

      Not checked in the free run.

  • Classified as probably not a substantial claim.

    Premisecitation

    The date range 2007 to April 2018 was chosen to align with the launch of the first Apple iPhone in 2007.

    “Therefore, this date range was chosen to bring the results in line with the launch of the first Apple smartphone, ‘Apple iPhone’ in 2007 [15].”
    Quote in the paperSubstantial claim0 of 1 sources checked
    • cites [15] PROSPERO. International prospective register of systematic reviews 2018 [Available from: https://www.crd.york.ac.uk/prospero/.

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductnone given

    All full papers were screened independently by two reviewers (AF, BJ or FM).

    “All full papers were screened independently by two reviewers (AF, BJ or FM).”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductcitation

    The protocol for this review is registered on PROSPERO (CRD42018084230).

    “The protocol is registered on PROSPERO [15], the International Prospective Register of Systematic Reviews (CRD42018084230).”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [15] PROSPERO. International prospective register of systematic reviews 2018 [Available from: https://www.crd.york.ac.uk/prospero/.

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Premisecitation

    The main concern reported by GPs in the 2015 UK survey was that online self-diagnoses would lead to increased appointment-making by the 'worried well'.

    “The main concern reported by GPs in this survey was that online self-diagnoses would lead to increased appointment-making by the ‘worried well’.”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [6] MDDUS. Data explosion leading to more “worried well”. Glasgow; 2015. Available from: http://www.mddus.com/news/news-digest/2015/january/data-explosion-leading-to-more-worried-well/.

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductcitation

    A standardised data extraction form adapted from Johnston et al. was used to collect study characteristics.

    “A standardised data extraction form adapted from Johnston et al. [19] was used to collect study characteristics for papers that met the eligibility criteria”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [19] Johnston B, McGill M, Milligan S, McElroy D, Foster C, Kearney N. Self care and end of life care in advanced cancer: literature review. J Eur J Oncol Nurs. 2009;13(5):386–98. source

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductcitation

    This mixed method systematic review was developed in accordance with PRISMA quality requirements.

    “This mixed method systematic review was developed in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) quality requirements [14].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [14] Moher D, Liberati A, Tetzlaff J, Altman DG, The PG. Preferred reporting items for systematic reviews and meta-analyses: The PRISMA statement. PLoS Med. 2009;6(7):e1000097. source

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Premisecitation

    By 2013, more than one-third of US adults were searching online for medical information for self-diagnosis.

    “A US survey reported that by 2013, more than one-third of US adults were searching online for medical information for self-diagnosis [5].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [5] Castillo M. More than one third of U.S. adults use internet to diagnose medical condition. New York: CBS News; 2013. Available from: https://www.cbsnews.com/news/more-than-one-third-of-us-adults-use-internet-to-diagnose-medical-condition/.

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductnone given

    Title and abstracts were screened by one researcher (AF).

    “Title and abstracts were screened by one researcher (AF).”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Premisecitation

    The patient-HCP relationship has been known to influence health outcomes and can improve the patient experience in the healthcare system.

    “The patient-HCP relationship has been known to influence health outcomes and can improve the patient experience in the healthcare system [12, 13]”
    Quote in the paperSubstantial claim0 of 2 sources checked
    • cites [12] Sabater-Galindo M, Fernandez-Llimos F, Sabater-Hernandez D, Martinez-Martinez F, Benrimoj SI. Healthcare professional-patient relationships: systematic review of theoretical models from a community pharmacy perspective. J Patient Educ Couns. 2016;99(3):339–47. source

      Not checked in the free run.

    • cites [13] Fox S, Chesla C. Living with chronic illness: A phenomenological study of the health effects of the patient–provider relationship. J Am Acad Nurse Pract. 2008;20(3):109–17. source

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Premisecitation

    Concerns have been raised from within the nursing profession that some information accessed by people online may be of poor quality and may represent commercial interests of website owners rather than robust clinical evidence.

    “Concerns have also been raised from within the nursing profession that some of the information being accessed by people may be of poor quality, and instead of being based on robust clinical evidence, merely represents the commercial interests of the website owners [8].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [8] Warner J. Too much information can be dangerous, not empowering. Nurs Times. 2011;107(35):13.

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Premisecitation

    In the same 2015 UK-wide survey, 21% of GPs had experienced people presenting with information they found online.

    “and, 21% have experienced people presenting with the information they have found online [6].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [6] MDDUS. Data explosion leading to more “worried well”. Glasgow; 2015. Available from: http://www.mddus.com/news/news-digest/2015/january/data-explosion-leading-to-more-worried-well/.

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Premisecitation

    It has been suggested that doctors may feel intimidated by online self-diagnosis.

    “It has also been suggested that doctors may feel intimidated by online self-diagnosis [7].”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [7] McArdle H. ‘Doctors “should not be intimidated” by patients self-diagnosing online. Scotland: Herald; 2015.

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Premisecitation

    NPT has been successfully used in other systematic reviews.

    “and has been successfully used in other systematic reviews [25, 26]”
    Quote in the paperNot a substantial claim0 of 2 sources checked
    • cites [25] Mair FS, May C, O'Donnell C, Finch T, Sullivan F, Murray E. Factors that promote or inhibit the implementation of e-health systems: an explanatory systematic review. Bull World Health Organ. 2012;90(5):357–64. source

      Not checked in the free run.

    • cites [26] O’Connor S, Hanlon P, O’Donnell CA, Garcia S, Glanville J, Mair FS. Understanding factors affecting patient and public engagement and recruitment to digital health interventions: a systematic review of qualitative studies. BMC Med Informatics Decision Making. 2016;16(1):120. source

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    Two reviewers (AF, BJ) independently assessed the quality of the eligible studies.

    “Two reviewers (AF, BJ) independently assessed the quality of the eligible studies for reliability purposes.”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductnone given

    Any data that fell outside the NPT framework was noted to ensure there was no 'shoe-horning' of themes into the framework.

    “Any data that fell outside the framework was noted to ensure there was no “shoe-horning” of themes into the framework.”
    Quote in the paperNot a substantial claim
  • Classified as probably not a substantial claim.

    Premisecitation

    NPT is a useful framework to explain and understand how people integrate new interventions into their everyday routines.

    “NPT is a useful framework to explain and understand how people integrate new interventions into their everyday routines [24].”
    Quote in the paperSubstantial claim0 of 1 sources checked
    • cites [24] May CR, Cummings A, Girling M, Bracher M, Mair FS, May CM, et al. Using normalization process theory in feasibility studies and process evaluations of complex healthcare interventions: a systematic review. Implement Sci. 2018;13(1):80. source

      Not checked in the free run.

  • Classified as probably not a substantial claim. May combine two claims.

    Study design and conductcitation

    The mixed methods appraisal tool (MMAT) was chosen because it is designed specifically for mixed method studies and appraises qualitative, quantitative, mixed methods, and other types of empirical studies.

    “The mixed methods appraisal tool (MMAT) [20] was chosen because it is designed specifically for mixed method studies and appraises qualitative, quantitative, mixed methods, and other types of empirical studies [21]”
    Quote in the paperSubstantial claim0 of 2 sources checked
    • cites [20] Pluye P, Gagnon M-P, Griffiths F, Johnson-Lafleur J. A scoring system for appraising mixed methods research, and concomitantly appraising qualitative, quantitative and mixed methods primary studies in mixed studies reviews. J Int J Nurs Studies. 2009;46(4):529–46. source

      Not checked in the free run.

    • cites [21] Hong QN, PLUYE P, FÀBREGUES S, BARTLETT G, BOARDMAN F, CARGO M, et al. Mixed methods appraisal tool (MMAT), version 2018. 2018.

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Study design and conductnone given

    Each item of extracted data was coded independently through thematic analysis by researcher AF, and reviewed by two researchers (BJ, FM).

    “Each item of extracted data was coded independently through thematic analysis by researcher AF, and reviewed by two researchers (BJ, FM).”
    Quote in the paperNot a substantial claim
  • Classified as probably not a substantial claim.

    Study design and conductreasoning

    All articles that met the study inclusion criteria were kept even if they were found to be methodologically weak based on the quality assessment.

    “All articles that met the study inclusion criteria were kept even if they were found to be methodologically weak based on the quality assessment, as they still have the potential to provide new and valuable insights in a field where the literature is relatively sparse.”
    Quote in the paperSubstantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductnone given

    Uncertainty over content and applicability of data was resolved through discussion within the team.

    “If there was any uncertainty over the content and applicability of the data for the review, this was resolved through discussion within the team.”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Interpretationown data

    Findings from this mixed methods systematic review suggest that the internet can serve as a useful resource and can potentially improve the patient-HCP relationship if used in the correct way and high-quality sources are accessed.

    “yet in contrast findings from this mixed methods systematic review has suggested that the internet can serve as a useful resource and can potentially improve the patient-HCP relationship if used in the correct way and high-quality sources are accessed.”
    Quote in the paperSubstantial claim
  • May combine two claims.

    Interpretationcitation

    Allowing patients to communicate health information obtained online with their HCP in the consultation, as well as the HCP showing that they value the patients' research, can positively affect the relationship between the two.

    “Our findings also demonstrate that allowing patients to communicate health information obtained online with their HCP in the consultation, as well as the HCP showing that they value the patients’ research, can positively affect the relationship between the two.”
    Quote in the paperSubstantial claim
  • May combine two claims.

    Interpretationcitation

    When HCPs create an atmosphere that is open, this can encourage patients to discuss the information they have discovered; additionally the patient's perception of invading the role of the HCP or their embarrassment may be reduced, which, overall, can enhance the relationship between the patient and HCP.

    “When HCP’s create an atmosphere that is open, this can encourage patients to discuss the information they have discovered; additionally the patient’s perception of invading the role of the HCP or their embarrassment may be reduced, which, overall, can enhance the relationship between the patient and HCP [28, 38].”
    Quote in the paperSubstantial claim0 of 2 sources checked
    • cites [28] Ahluwalia S, Murray E, Stevenson F, Kerr C, Burns J. ‘A heartbeat moment’: qualitative study of GP views of patients bringing health information from the internet to a consultation. Br J Gen Pract. 2010;60(571):88–94. source

      Not checked in the free run.

    • cites [38] Townsend A, Leese J, Adam P, McDonald M, Li LC, Kerr S, et al. eHealth, participatory medicine, and ethical care: a focus group study of patients’ and health care providers’ use of health-related internet information. J Med Internet Res. 2015;17(6):e155. source

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductnone given

    There is no consistently used terminology to describe the patient-HCP relationship and related aspects.

    “Unlike clinical type studies, where each condition or intervention has one universally used term, there is no consistently used terminology to describe the patient-HCP relationship and the aspects related to it.”
    Quote in the paperNot a substantial claim
  • Classified as probably not a substantial claim.

    Study design and conductnone given

    The review used a systematic and rigorous approach to identify all relevant literature.

    “Strengths of this review includes the systematic and rigorous approach taken to identify all relevant literature.”
    Quote in the paperSubstantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductcitation

    A review protocol was published to PROSPERO to enhance clarity.

    “A review protocol was published to PROSPERO [15] to enhance clarity”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [15] PROSPERO. International prospective register of systematic reviews 2018 [Available from: https://www.crd.york.ac.uk/prospero/.

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductreasoning

    The search criterion used was broad in order to cover all areas studied and associated with patient's self-diagnosis and use of the internet.

    “Firstly, the search criterion that was used for this systematic review was broad in order to cover all areas that have been studied and that were associated with patient’s self-diagnosis and use of the internet.”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Premisecitation

    Previous evidence found that the internet can potentially have a negative impact on the patient-HCP relationship and can cause barriers in the relationship.

    “Although evidence has previously found that the internet can potentially have a negative impact on the patient-HCP relationship and can cause barriers in the relationship [48]”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [48] Caiata-Zufferey M, Schulz PJ. Physicians’ communicative strategies in interacting with internet-informed patients: results from a qualitative study. Health Commun. 2012;27(8):738–49. source

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Study design and conductnone given

    Only English language articles were searched for, which may have reduced the number of potentially relevant studies.

    “Only English language articles were searched for, which may have reduced the number of potentially relevant studies.”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Study design and conductreasoning

    Sources of information such as conference proceedings, theses and abstracts were not included, which means some related studies may have been missed.

    “Secondly, sources of information such as conference proceedings, theses and abstracts were not included, which means some related studies may have been missed.”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductnone given

    The review used a robust thematic analysis with conceptualisation through Normalisation Process Theory to aid understanding.

    “and a robust thematic analysis with conceptualisation through a theoretical lens Normalisation Process Theory, to aid understanding.”
    Quote in the paperNot a substantial claim
103 of 103
  • The paper relies on this without support.

    The included studies, despite methodological weaknesses and moderate quality, can be synthesised to produce valid conclusions about the effects of online self-diagnosis on the patient-HCP relationship.

    “All articles that met the study inclusion criteria were kept even if they were found to be methodologically weak based on the quality assessment, as they still have the potential to provide new and valuable insights in a field where the literature is relatively sparse.”
    “Overall, the studies were of moderate quality.”
  • The paper relies on this without support.

    Patients' reported reasons for conducting online searches (e.g., to form a partnership) reflect the actual effect of online health information seeking on the patient-HCP relationship.

    “While health professionals’ views were mixed our findings indicate that online health information seeking can potentially improve the patient-healthcare professional relationship as patients reported they usually conducted an online search to form a partnership with the healthcare professional as opposed to trying to prove them wrong.”
  • The paper relies on this without support.

    Online self-diagnosis is a growing phenomenon.

    “although online self-diagnosis is a growing phenomenon”
3 of 3

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?

  • Healthcare professionals have mixed views in relation to patients resorting to the internet and mobile apps, with reservations about sources and accuracy, yet highlighting that active patient engagement can support a positive patient-physician interaction.

    “Healthcare professionals have mixed views in relation to patients resorting to the internet [114] and mobile apps [115], with reservations about the sources and accuracy of information, yet highlighting that active patient engagement can support a positive patient-physician interaction [116,117].”

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.

  • Two quantitative studies claimed, but three cited

    Minor

    The citation range [42-44] contains three studies, not two.

  • Five quantitative studies claimed, but four cited

    Minor

    The accompanying citation list names four studies (29, 32, 40 and 41), not five.

  • Seven quantitative studies claimed, but five cited

    Minor

    The citations identify five studies: 32, 35 and 42-44, rather than seven.

  • Inconsistent record count after deduplication

    Minor

    The abstract reports 6107 records identified, while the results report 6109 records after deduplication and say 6109 titles were screened.

4 of 4

Cites

Flagged first, then by citations

2 of the 49 references couldn’t be matched to a known paper.

Research works printed but not linked: 5

  1. McArdle H. ‘Doctors “should not be intimidated” by patients self-diagnosing online. Scotland: Herald; 2015.
  2. Warner J. Too much information can be dangerous, not empowering. Nurs Times. 2011;107(35):13.
  3. Partners E. Distiller SR, Systematic Review and Literature Review Software by Evidence Partners 2018 [Available from: https://www.evidencepartners.com/products/distillersr-systematic-review-software/.
  4. Hong QN, PLUYE P, FÀBREGUES S, BARTLETT G, BOARDMAN F, CARGO M, et al. Mixed methods appraisal tool (MMAT), version 2018. 2018.
  5. Braun V, Clarke V, Hayfield N, Terry G. Thematic analysis. J Handbook of research methods in health social sciences; 2018. p. 1–18.

Cited by

Sorted by citations

Authors
Farnood, A., Johnston, B., & Mair, F. S.
Affiliations
  • University of Glasgow (GB)
  • NHS Greater Glasgow and Clyde (GB)
Corresponding author
Farnood, Annabel
Venue
BMC Medical Informatics and Decision Making
Published
2020-10-06
Volume
20
Issue
1
Pages
253-253
ISSN
1472-6947 (ISSN-L)
OpenAlex
W3092062938
Cited by
100
References
49
Citations by year
2026: 23 · 2025: 21 · 2024: 22 · 2023: 14 · 2022: 9 · 2021: 9 · 2020: 2
FWCI
1.61
Type
journal article
Language
en
Open access
Locations
  • BMC Medical Informatics and Decision Making (publishedVersion, cc-by)
  • Research Square (acceptedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • ENLIGHTEN (Jurnal Bimbingan dan Konseling Islam) (acceptedVersion, cc-by-sa)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Topics
  • Health Sciences › Health Professions › General Health Professions › Health Literacy and Information Accessibility
  • Health Sciences › Health Professions › General Health Professions › Patient-Provider Communication in Healthcare
  • Health Sciences › Health Professions › Health Information Management › Electronic Health Records Systems
Keywords
health information seeking, medical authority, shared decision-making, patient partnership, trust in healthcare providers, Normalisation Process Theory, smartphone use, online health information
MeSH terms
Delivery of Health Care, Health Personnel, Humans, Professional-Patient Relations, Telemedicine, Internet, Diagnostic Self Evaluation

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Claims read by deepseek-v4.1-flash under definition version 3 (extract-v3) on 2026-10-09.

Classified by jev-1.13-20260917 (gold-guideline-v0.2) on 2026-10-09.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

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