Consensus on criteria for acromegaly diagnosis and remission
An erratum to this article was published (Pituitary, Feb 2024 ↗)
Methodological details56 acromegaly experts from 16 countries reviewed and discussed current evidence
- 56 acromegaly experts from 16 countries reviewed and discussed current evidence
Recommendations
As issued by the authors
In a patient with typical acromegaly features, IGF-I > 1.3 times the upper limit of normal for age confirms the diagnosis
Random growth hormone (GH) after overnight fasting may be useful for informing prognosis, but is not required for diagnosis
For equivocal results, IGF-I can be repeated using the same validated assay; oral glucose tolerance testing might also be useful
Biochemical remission is the primary assessment of treatment outcome, but biochemical findings should be interpreted within the clinical context of acromegaly
Follow up should consider biochemical evaluation of treatment effectiveness, imaging of residual/recurrent adenoma mass, and clinical signs and symptoms of acromegaly, its complications and comorbidities
Referral to a multidisciplinary pituitary center should be considered for equivocal biochemical, pathology or imaging findings at diagnosis, and for patients insufficiently responsive to standard treatment
Original publication
Composed by AI from the published abstract and checked against it. How Briefs are made →