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Prevalence of Nelson's syndrome after bilateral adrenalectomy in patients with cushing's disease: a systematic review and meta-analysis
Department of Internal Medicine and Clinical Nutrition, Institute of Medicine at Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden; The Department of Endocrinology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Department of Internal Medicine and Clinical Nutrition, Institute of Medicine at Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden; The Department of Endocrinology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Department of Environmental and Occupational Health School of Public Health and Community Medicine, University of Gothenburg, Gothenburg, Sweden.
Department of Internal Medicine and Clinical Nutrition, Institute of Medicine at Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden; The Department of Endocrinology, Sahlgrenska University Hospital, Gothenburg, Sweden.
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2021 (English)In: Pituitary, ISSN 1386-341X, E-ISSN 1573-7403, Vol. 24, no 5, p. 797-809Article, review/survey (Refereed) Published
Abstract [en]

PURPOSE: Bilateral adrenalectomy (BA) still plays an important role in the management of Cushing's disease (CD). Nelson's syndrome (NS) is a severe complication of BA, but conflicting data on its prevalence and predicting factors have been reported. The aim of this study was to determine the prevalence of NS, and identify factors associated with its development.

DATA SOURCES: Systematic literature search in four databases.

STUDY SELECTION: Observational studies reporting the prevalence of NS after BA in adult patients with CD.

DATA EXTRACTION: Data extraction and risk of bias assessment were performed by three independent investigators.

DATA SYNTHESIS: 67%, P < 0.01). The time from BA to NS varied from 2 months to 39 years. The prevalence of NS in the most recently published studies, where magnet resonance imaging was used, was 38% (95% CI 27-50%). The prevalence of treatment for NS was 21% (95% CI 18-26%). Relative risk for NS was not significantly affected by prior pituitary radiotherapy [0.9 (95% CI 0.5-1.6)] or pituitary surgery [0.6 (95% CI 0.4-1.0)].

CONCLUSIONS: Every fourth patient with CD treated with BA develops NS, and every fifth patient requires pituitary-specific treatment. The risk of NS may persist for up to four decades after BA. Life-long follow-up is essential for early detection and adequate treatment of NS.

Place, publisher, year, edition, pages
Springer, 2021. Vol. 24, no 5, p. 797-809
Keywords [en]
Bilateral adrenalectomy, Corticotroph adenoma, Cushing’s disease, Nelson’s syndrome
National Category
Rheumatology and Autoimmunity
Identifiers
URN: urn:nbn:se:oru:diva-91952DOI: 10.1007/s11102-021-01158-zISI: 000654097700001PubMedID: 34036460Scopus ID: 2-s2.0-85106532324OAI: oai:DiVA.org:oru-91952DiVA, id: diva2:1557741
Note

Funding Agencies:

University of Gothenburg  

Swedish government  

County councils  

ALF ALFGBG-593301

Gothenburg Society of Medicine 

Available from: 2021-05-27 Created: 2021-05-27 Last updated: 2024-01-02Bibliographically approved

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Wahlberg, Jeanette

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