Time to Gender-Affirming Hormone Therapy Among US Military-Affiliated Adolescents and Young Adults.

IF 24.7 1区 医学 Q1 PEDIATRICS
Evan R Locke, Krista B Highland, Jennifer A Thornton, Kevin W Sunderland, Wendy Funk, Veronika Pav, Rick Brydum, Noelle S Larson, Natasha A Schvey, Christina M Roberts, David A Klein
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引用次数: 0

Abstract

Importance: Use of exogenous sex steroid hormones, when indicated, may improve outcomes in adolescents and young adults with gender incongruence. Little is known about factors associated with the time from diagnosis of gender dysphoria to initiation of gender-affirming hormone therapy. Identification of inequities in time to treatment may have clinical, policy, and research implications.

Objective: To evaluate factors associated with time to initiation of gender-affirming hormone therapy after a diagnosis of gender dysphoria in adolescents and young adults receiving care within the US Military Health System.

Design, setting, and participants: This retrospective cohort study used TRICARE Prime billing and pharmacy data contained in the Military Health System Data Repository. Patients aged 14 to 22 years, excluding service members and their spouses, who received a diagnosis of gender dysphoria between September 1, 2016, and December 31, 2021, were included. The data were analyzed between August 30 and October 12, 2023.

Exposures: Included patient characteristics were race and ethnicity, age group, first sex assigned in the medical record, and TRICARE Prime sponsor military rank and service at the time of diagnosis. Health care and contextual characteristics included the year of diagnosis and the primary system in which the patient received health care.

Main outcomes and measures: The primary outcome was the time between initial diagnosis of gender dysphoria to the first prescription for gender-affirming hormone medication within a 2-year period. A Poisson generalized additive model was used to evaluate this primary outcome. Adjusted probability estimates were calculated per specified reference categories.

Results: Of the 3066 patients included (median [IQR] age, 17 [15-19] years; 2259 with first assigned gender marker of female [74%]), an unadjusted survival model accounting for censoring indicated that 37% (95% CI, 35%-39%) initiated therapy by 2 years. Age-adjusted curves indicated that the proportion initiating therapy by 2 years increased by age category (aged 14-16 years, 25%; aged 17-18 years, 39%; aged 19-22 years, 55%). Incidence rate ratios (IRRs) and 2-year adjusted probabilities indicated that longer times to hormone initiation were experienced by adolescents aged 14 to 16 years (IRR, 0.36; 95% CI, 0.30-0.44) and 17 to 18 years (IRR, 0.66; 95% CI, 0.54-0.79) compared with young adults aged 19 to 22 years and Black compared with White adolescents (IRR, 0.73; 95% CI, 0.54-0.99). Senior officer compared with junior enlisted insurance sponsor rank (IRR, 1.93; 95% CI, 1.04-3.55) and civilian compared with military health care setting (IRR, 1.21; 95% CI, 1.02-1.43) was associated with shorter time to hormone initiation.

Conclusions and relevance: In this cohort study, most adolescents and young adults with a diagnosis of gender dysphoria receiving health care through the US military did not initiate exogenous sex steroid hormone therapy within 2 years of diagnosis. Inequities in time to treatment indicate the need to identify and reduce barriers to care.

美军青少年和年轻成年人接受性别确认激素治疗的时间。
重要性:如果有必要,使用外源性性甾体激素可以改善患有性别不协调的青少年和年轻成年人的治疗效果。人们对从确诊性别障碍到开始接受性别确认激素治疗的时间相关因素知之甚少。发现治疗时间上的不平等可能会对临床、政策和研究产生影响:目的:评估在美国军事医疗系统内接受治疗的青少年和年轻成年人在确诊性别障碍后开始接受性别确认激素治疗的时间相关因素:这项回顾性队列研究使用了军事医疗系统数据存储库(Military Health System Data Repository)中的 TRICARE Prime 账单和药房数据。研究对象包括在 2016 年 9 月 1 日至 2021 年 12 月 31 日期间确诊为性别障碍的 14 至 22 岁患者(不包括现役军人及其配偶)。数据分析时间为 2023 年 8 月 30 日至 10 月 12 日:纳入的患者特征包括种族和民族、年龄组、病历中分配的第一性别以及诊断时的 TRICARE Prime 赞助军衔和服役情况。医疗保健和环境特征包括诊断年份和患者接受医疗保健的主要系统:主要结果和测量指标:主要结果是在两年时间内,从最初诊断出性别障碍到首次开具确认性别的激素药物处方的时间。采用泊松广义相加模型对这一主要结果进行评估。根据指定的参考类别计算调整后的概率估计值:在纳入的 3066 名患者中(中位数[IQR]年龄为 17 [15-19]岁;2259 名首次分配的性别标记为女性[74%]),考虑到人口普查的未调整生存模型显示,37%(95% CI,35%-39%)的患者在 2 年内开始接受治疗。年龄调整曲线显示,2 年前开始治疗的比例随年龄的增加而增加(14-16 岁,25%;17-18 岁,39%;19-22 岁,55%)。发病率比(IRR)和 2 年调整概率表明,与 19-22 岁的年轻人相比,14-16 岁(IRR,0.36;95% CI,0.30-0.44)和 17-18 岁(IRR,0.66;95% CI,0.54-0.79)的青少年开始使用激素的时间更长;与白人青少年相比,黑人青少年开始使用激素的时间更长(IRR,0.73;95% CI,0.54-0.99)。高级军官与低级士兵相比(IRR,1.93;95% CI,1.04-3.55),平民与军队医疗环境相比(IRR,1.21;95% CI,1.02-1.43),与较短的激素启动时间有关:在这项队列研究中,大多数被诊断出患有性别障碍的青少年和年轻人在接受美国军方的医疗服务时,并没有在确诊后两年内开始接受外源性性类固醇激素治疗。治疗时间上的不平等表明,有必要识别并减少治疗障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JAMA Pediatrics
JAMA Pediatrics PEDIATRICS-
CiteScore
31.60
自引率
1.90%
发文量
357
期刊介绍: JAMA Pediatrics, the oldest continuously published pediatric journal in the US since 1911, is an international peer-reviewed publication and a part of the JAMA Network. Published weekly online and in 12 issues annually, it garners over 8.4 million article views and downloads yearly. All research articles become freely accessible online after 12 months without any author fees, and through the WHO's HINARI program, the online version is accessible to institutions in developing countries. With a focus on advancing the health of infants, children, and adolescents, JAMA Pediatrics serves as a platform for discussing crucial issues and policies in child and adolescent health care. Leveraging the latest technology, it ensures timely access to information for its readers worldwide.
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