Clinicians in the Veterans Health Administration initiate gender-affirming hormone therapy in high concordance with clinical guideline recommendations, particularly for feminizing GAHT.
Key Findings
Results
Veterans receiving feminizing GAHT were demographically distinct from those receiving masculinizing GAHT in age, race/ethnicity, and comorbidity burden.
A higher proportion of veterans receiving feminizing GAHT were aged ≥60 years (23.7% vs. 6.3%) compared to those receiving masculinizing GAHT.
White non-Hispanic veterans comprised 83.5% of those receiving feminizing GAHT vs. 57.6% of those receiving masculinizing GAHT.
Veterans receiving feminizing GAHT had a higher number of comorbidities (≥7: 14.0% vs. 10.6%).
All demographic and comorbidity comparisons had p-values <0.001.
Results
Veterans receiving masculinizing GAHT had higher rates of Black race, PTSD, and military sexual trauma compared to those receiving feminizing GAHT.
Black non-Hispanic veterans represented 21.5% of those receiving masculinizing GAHT vs. 3.5% of those receiving feminizing GAHT.
PTSD was documented in 43.0% of veterans receiving masculinizing GAHT vs. 33.9% of those receiving feminizing GAHT.
Positive military sexual trauma was documented in 33.5% of masculinizing GAHT recipients vs. 16.8% of feminizing GAHT recipients.
All p-values were <0.001.
Results
The vast majority of veterans initiating estrogen as part of feminizing GAHT were guideline concordant due to absence of documented contraindications.
97.0% of veterans who started feminizing GAHT with estrogen were guideline concordant.
Concordance was defined as no documentation of contraindications including venous thromboembolism, breast cancer, stroke, or myocardial infarction.
The sample included 3,547 veterans receiving feminizing GAHT initiated between 2007 and 2018 in VHA.
Results
Nearly all veterans initiating spironolactone as part of feminizing GAHT were guideline concordant.
98.1% of veterans who started spironolactone as part of feminizing GAHT were guideline concordant.
Concordance was defined as no documentation of contraindications including hyperkalemia or acute renal failure.
Results
The majority of veterans initiating masculinizing GAHT were guideline concordant with respect to contraindications.
90.1% of veterans starting masculinizing GAHT were guideline concordant due to no documentation of contraindications such as breast or prostate cancer.
The sample included 1,129 veterans receiving masculinizing GAHT.
Results
Hematocrit was measured in the majority of veterans prior to initiating masculinizing GAHT, and most did not have elevated hematocrit at baseline.
Hematocrit had been measured in 91.8% of veterans before initiating masculinizing GAHT.
96.5% of those measured did not have an elevated hematocrit (>50%) prior to starting masculinizing GAHT.
Results
Documentation of a gender identity disorder diagnosis prior to GAHT initiation was present in the large majority of veterans.
91.2% of veterans initiating both feminizing and masculinizing GAHT had documentation of a gender identity disorder diagnosis prior to GAHT initiation.
This metric applied across the combined sample of 4,676 veterans.
Methods
The study sample consisted of 4,676 veterans with a gender identity disorder diagnosis who initiated GAHT in VHA between 2007 and 2018.
3,547 veterans initiated feminizing GAHT and 1,129 initiated masculinizing GAHT.
Guideline concordance was assessed across six VHA guidelines on feminizing and masculinizing GAHT initiation.
Demographics and health conditions were assessed for both groups.
Jasuja G, Wolfe H, Reisman J, Vimalananda V, Rao S, Blosnich J, et al.. (2024). Clinicians in the Veterans Health Administration initiate gender-affirming hormone therapy in concordance with clinical guideline recommendations.. Frontiers in endocrinology. https://doi.org/10.3389/fendo.2024.1086158