Hughto Jaclyn M W, Varma Hiren, Yee Kim, Babbs Gray, Hughes Landon D, Pletta David R, Meyers David J, Shireman Theresa I
Departments of Behavioral and Social Sciences and Epidemiology, Brown University School of Public Health, Providence, RI, United States.
Center for Health Promotion and Health Equity, Brown University School of Public Health, Providence, RI, United States.
medRxiv. 2024 Mar 20:2024.03.19.24304525. doi: 10.1101/2024.03.19.24304525.
In the US, transgender and gender-diverse (TGD) individuals, particularly trans feminine individuals, experience a disproportionately high burden of HIV relative to their cisgender counterparts. While engagement in the HIV Care Continuum (e.g., HIV care visits, antiretroviral (ART) prescribed, ART adherence) is essential to reduce viral load, HIV transmission, and related morbidity, the extent to which TGD people engage in one or more steps of the HIV Care Continuum at similar levels as cisgender people is understudied on a national level and by gendered subgroups.
We used Medicare Fee-for-Service claims data from 2009 to 2017 to identify TGD (trans feminine and non-binary (TFN), trans masculine and non-binary (TMN), unclassified gender) and cisgender (male, female) beneficiaries with HIV. Using a retrospective cross-sectional design, we explored within- and between-gender group differences in the predicted probability (PP) of engaging in one or more steps of the HIV Care Continuum. TGD individuals had a higher predicted probability of every HIV Care Continuum outcome compared to cisgender individuals [HIV Care Visits: TGD PP=0.22, 95% Confidence Intervals (CI)=0.22-0.24; cisgender PP=0.21, 95% CI=0.21-0.22); Sexually Transmitted Infection (STI) Screening (TGD PP=0.12, 95% CI=0.11-0.12; cisgender PP=0.09, 95% CI=0.09-0.10); ART Prescribed (TGD PP=0.61, 95% CI=0.59-0.63; cisgender PP=0.52, 95% CI=0.52-0.54); and ART Persistence or adherence (90% persistence: TGD PP=0.27, 95% CI=0.25-0.28; 95% persistence: TGD PP=0.13, 95% CI=0.12-0.14; 90% persistence: cisgender PP=0.23, 95% CI=0.22-0.23; 95% persistence: cisgender PP=0.11, 95% CI=0.11-0.12)]. Notably, TFN individuals had the highest probability of every outcome (HIV Care Visits PP =0.25, 95% CI=0.24-0.27; STI Screening PP =0.22, 95% CI=0.21-0.24; ART Prescribed PP=0.71, 95% CI=0.69-0.74; 90% ART Persistence PP=0.30, 95% CI=0.28-0.32; 95% ART Persistence PP=0.15, 95% CI=0.14-0.16) and TMN people or cisgender females had the lowest probability of every outcome (HIV Care Visits: TMN PP =0.18, 95% CI=0.14-0.22; STI Screening: Cisgender Female PP =0.11, 95% CI=0.11-0.12; ART Receipt: Cisgender Female PP=0.40, 95% CI=0.39-0.42; 90% ART Persistence: TMN PP=0.15, 95% CI=0.11-0.20; 95% ART Persistence: TMN PP=0.07, 95% CI=0.04-0.10). The main limitation of this research is that TGD and cisgender beneficiaries were included based on their observed care, whereas individuals who did not access relevant care through Fee-for-Service Medicare at any point during the study period were not included. Thus, our findings may not be generalizable to all TGD and cisgender individuals with HIV, including those with Medicare Advantage or other types of insurance.
Although TGD beneficiaries living with HIV had superior engagement in the HIV Care Continuum than cisgender individuals, findings highlight notable disparities in engagement for TMN individuals and cisgender females, and engagement was still low for all Medicare beneficiaries, independent of gender. Interventions are needed to reduce barriers to HIV care engagement for all Medicare beneficiaries to improve treatment outcomes and reduce HIV-related morbidity and mortality in the US.
在美国,跨性别和性别多样化(TGD)个体,尤其是跨性别女性个体,相对于其顺性别同龄人,感染艾滋病毒的负担 disproportionately 高。虽然参与艾滋病毒护理连续体(例如,艾滋病毒护理就诊、开抗逆转录病毒药物(ART)、坚持服用ART)对于降低病毒载量、艾滋病毒传播及相关发病率至关重要,但在国家层面以及按性别亚组研究时,TGD人群与顺性别者以相似水平参与艾滋病毒护理连续体一个或多个步骤的程度仍未得到充分研究。
我们使用了2009年至2017年医疗保险按服务收费的理赔数据,以识别感染艾滋病毒的TGD(跨性别女性和非二元性别(TFN)、跨性别男性和非二元性别(TMN)、未分类性别)和顺性别(男性、女性)受益人。采用回顾性横断面设计,我们探讨了在参与艾滋病毒护理连续体一个或多个步骤的预测概率(PP)方面的性别组内和组间差异。与顺性别个体相比,TGD个体在艾滋病毒护理连续体的每个结果上的预测概率更高[艾滋病毒护理就诊:TGD的PP = 0.22,95%置信区间(CI)= 0.22 - 0.24;顺性别者的PP = 0.21,95% CI = 0.21 - 0.22);性传播感染(STI)筛查(TGD的PP = 0.12,95% CI = 0.11 - 0.12;顺性别者的PP = 0.09,95% CI = 0.09 - 0.10);开抗逆转录病毒药物(TGD的PP = 0.61,95% CI = 0.59 - 0.63;顺性别者的PP = 0.52,95% CI = 0.52 - 0.54);以及抗逆转录病毒药物坚持服用或依从性(90%坚持服用:TGD的PP = 0.27,95% CI = 0.25 - 0.28;95%坚持服用:TGD的PP = 0.13,95% CI = 0.12 - 0.14;90%坚持服用:顺性别者的PP = 0.23,95% CI = 0.22 - 0.23;95%坚持服用:顺性别者的PP = 0.11,95% CI = 0.11 - 0.12)]。值得注意的是,TFN个体在每个结果上的概率最高(艾滋病毒护理就诊PP = 0.25,95% CI = 0.24 - 0.27;性传播感染筛查PP = 0.22,95% CI = 0.21 - 0.24;开抗逆转录病毒药物PP = 0.71,95% CI = 0.69 - 0.74;90%抗逆转录病毒药物坚持服用PP = 0.30,95% CI = 0.28 - 0.32;95%抗逆转录病毒药物坚持服用PP = 0.15,95% CI = 0.14 - 0.16),而TMN个体或顺性别女性在每个结果上的概率最低(艾滋病毒护理就诊:TMN的PP = 0.18,95% CI = 0.14 - 0.22;性传播感染筛查:顺性别女性的PP = 0.11,95% CI = 0.11 - 0.12;接受抗逆转录病毒药物治疗:顺性别女性的PP = 0.40,95% CI = 0.39 - 0.42;90%抗逆转录病毒药物坚持服用:TMN的PP = 0.15,95% CI = 0.11 - 0.20;95%抗逆转录病毒药物坚持服用:TMN的PP = 0.07,95% CI = 0.04 - 0.10)。本研究的主要局限性在于,TGD和顺性别受益人是根据他们接受的护理情况纳入的,而在研究期间任何时候未通过按服务收费的医疗保险获得相关护理的个体未被纳入。因此,我们的研究结果可能不适用于所有感染艾滋病毒的TGD和顺性别个体,包括那些拥有医疗保险优势计划或其他类型保险的个体。
尽管感染艾滋病毒的TGD受益人在艾滋病毒护理连续体方面的参与度高于顺性别个体,但研究结果突出了TMN个体和顺性别女性在参与度方面的显著差异,并且所有医疗保险受益人的参与度仍然较低,与性别无关。需要采取干预措施,减少所有医疗保险受益人的艾滋病毒护理参与障碍,以改善治疗结果并降低美国与艾滋病毒相关的发病率和死亡率。