Cited by 153Pituitary Gland Disorders and TreatmentsMeningioma and schwannoma managementHead and Neck Surgical Oncology

Outcome of Cushing's disease following transsphenoidal surgery in a single center over 20 years

Hassan-Smith, Zaki K., Sherlock, Mark, Reulen, Raoul C., Arlt, Wiebke, Ayuk, John, Toogood, Andrew A., Cooper, Mark S., Johnson, Alan P. +1 more·2012·The Journal of Clinical Endocrinology & Metabolism

Abstract

CONTEXT: Historically, Cushing's disease (CD) was associated with a 5-yr survival of just 50%. Although advances in CD management have seen mortality rates improve, outcome from transsphenoidal surgery (TSS), the current first-line treatment, varies significantly between centers. OBJECTIVES: The aim of the study was to define outcome including mortality in a cohort of CD patients treated with TSS over 20 yr. DESIGN: We conducted a retrospective cohort study of 80 patients who underwent TSS to treat CD between 1988 and 2009. In 72 cases, data on clinical features and outcomes were collected from medical records. In eight patients, records were unavailable, but in all cases mortality data were obtained from National Health Service (NHS) registries and recorded as standardized mortality ratio. SETTING: The study was conducted in a United Kingdom tertiary referral center. PATIENTS OR OTHER PARTICIPANTS: Adult patients confirmed to have CD participated in the study. INTERVENTIONS: All patients underwent TSS. MAIN OUTCOME MEASURE: Patients were subdivided into groups based on disease response after initial treatment. Mortality according to subgroup was also assessed. RESULTS: Median follow-up for clinical data was 4.6 yr. Three outcome groups were identified: cure, 72% (52 of 72); persistent disease, 17% (12 of 72); and disease recurrence, 11% (eight of 72). Median time to recurrence after initial remission was 2.1 yr (interquartile range, 1.3-3.1 yr). Mean follow-up for mortality was 10.9 yr. Thirteen of 80 patients had died: five of 52 in the cure group, two of eight in the disease recurrence group, two of 12 with persistent disease, and four of eight of those followed up by NHS registry search only. Overall, the standardized mortality ratio was 3.17 [95% confidence interval (CI), 1.70-5.43], whereas in the cure group it was 2.47 (95% CI, 0.80-5.77), and it was 4.12 (95% CI, 1.12-10.54) for disease recurrence/persistent disease groups. CONCLUSIONS: We report long-term cure rates in excess of 70%. Mortality is increased in CD and may be higher in patients with persistent/recurrent disease compared to patients cured after initial treatment.

Integrity signals

Registry

Crossref · 10.1210/jc.2011-2957

Cites

42 of 42 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

  • Patients with CS who achieve remission following curative treatment remain at a slightly increased risk of morbidity and mortality compared to patients without CS.

    “Patients with CS who achieve remission following curative treatment remain at a slightly increased risk of morbidity and mortality compared to patients without CS (27, 28, 113-116).”

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Authors
Hassan-Smith, Z. K., Sherlock, M., Reulen, R. C., Arlt, W., Ayuk, J., Toogood, A. A., Cooper, M. S., Johnson, A. P., & Stewart, P. M.
Affiliations
  • University of Birmingham (GB)
  • National Health Service (GB)
Corresponding author
Stewart, Paul M.
Venue
The Journal of Clinical Endocrinology & Metabolism
Published
2012-04
Volume
97
Issue
4
Pages
1194-1201
ISSN
  • 0021-972X (ISSN-L)
  • 1945-7197
OpenAlex
W2000020742
Cited by
153
References
42
Citations by year
2026: 4 · 2025: 3 · 2024: 10 · 2023: 4 · 2022: 9 · 2021: 11 · 2020: 8 · 2019: 14 · 2018: 15 · 2017: 6 · 2016: 15 · 2015: 21 · 2014: 11 · 2013: 16 · 2012: 5
FWCI
13.58
Type
journal article
Language
en
Open access
closed
Locations
  • The Journal of Clinical Endocrinology & Metabolism (publishedVersion)
  • PubMed (publishedVersion)
  • University of Birmingham Research Portal (University of Birmingham) (submittedVersion)
  • Lenus, The Irish Health Repository (Dr Steevens Hospital Library) (submittedVersion)
Funders
National Institute for Health and Care Research (NF-SI-0508-10356)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Pituitary Gland Disorders and Treatments
  • Health Sciences › Medicine › Epidemiology › Meningioma and schwannoma management
  • Health Sciences › Medicine › Surgery › Head and Neck Surgical Oncology
Keywords
Cushing's disease, transsphenoidal surgery, long-term outcomes, mortality, standardized mortality ratio, recurrence, persistent disease, cure rate, pituitary adenoma, follow-up duration, single-center experience
MeSH terms
Adult, England, Female, Follow-Up Studies, Hospitals, University, Humans, Hypertension, Male, Medical Records, Microsurgery, Middle Aged, Nasal Cavity, Obesity, Pituitary Gland, Postoperative Complications, Recurrence, Registries, Remission Induction, Retrospective Studies, Cohort Studies, Pituitary ACTH Hypersecretion, Natural Orifice Endoscopic Surgery

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.

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.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review