Screening and Diagnosis of Type 2 Diabetes in Sickle Cell Disease.
review · Level V
Where this comes from
- Record sourced from PubMed, PMID 39978849.
- Also identified by DOI 10.3122/jabfm.2024.240042R1.
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Abstract
Diagnosing type 2 diabetes mellitus (T2DM) in people with sickle cell disease (SCD) is complicated due to hemoglobin A variance in affected individuals. Accurate screening assessments are needed to prevent excessive morbidity and mortality. Primary care physicians need recommendations for screening and diagnosis in this unique population. To synthesize recommendations regarding medical diagnosis criteria for T2DM in SCD. PubMed, Standards of Medical Care in Diabetes, US Preventative Services Task Force, National Institute of Diabetes and Digestive and Kidney Diseases, searched on December 28, 2022. One reviewer searched each database to select applicable studies pertaining to "sickle cell disease," "type 2 diabetes," "HbA1c," and "fructosamine" from December 28, 2022, to March 15, 2023. A comprehensive literature review was done to extract current data/facts and assess certainty of evidence. This review reviews 5 articles that met inclusion criteria to outline outpatient screening and diagnosis of T2DM in SCD. Based on these findings, we recommend fasting plasma glucose as the standard screening starting at age 35 based on USPSTF guidelines. We do not recommend using HbA1c, fructosamine, or glycated albumin for screening or diagnosis of T2DM in individuals with SCD; the latter entities have limited implications in their use. There are limited studies available for diagnosis of T2DM in SCD. Fasting plasma glucose is the standard screening for T2DM for SCD to ensure early diagnosis and prevent worsening macro and microvascular complications from both comorbid conditions.
Medical subject headings
- Anemia, Sickle Cell
- Diabetes Mellitus, Type 2
- Mass Screening