通过测量药物占有比来确定HIV感染者依从性欠佳的危险因素:一项横断面研究。

IF 1.2 4区 医学 Q4 HEALTH POLICY & SERVICES
Julieth Carolina Castillo-Cañón, Diana Consuelo Acero Torres, Ángela Viviana Pérez Gómez
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引用次数: 0

摘要

在防治艾滋病毒/艾滋病方面取得的最重大进展是开发了抗逆转录病毒疗法。然而,确保高度的治疗依从性对于防止耐药性和疾病进展是必要的。我们进行了一项横断面研究,通过计算药物占有比(MPR)来评估抗逆转录病毒治疗的依从性,并确定在哥伦比亚16个城市的一家医疗机构接受治疗的hiv阳性患者队列中依从性欠佳的危险因素。对12145名患者的记录进行分析,并以最佳依从性(MPR > = 95%)与次优依从性(MPR < 95%)为参考,建立多元逻辑回归模型。29%的使用者发现抗逆转录病毒治疗依从性不理想。居住地、hiv定义疾病的存在、慢性肾脏疾病(CKD)、合并感染(如丙型肝炎、结核病和性传播感染)、治疗时间超过5年以及未抑制的病毒载量被确定为不依从性的危险因素。这突出表明需要确定针对这些弱势群体的干预措施,以尽量减少不遵守规定的可能性,并干预以这些患者的医疗需求为重点的护理模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of risk factors for suboptimal adherence in people living with HIV through measurement of medication possession ratio: a cross-sectional study.

The most significant progress in addressing the HIV/AIDS epidemic has been the development of antiretroviral therapy (ART). However, ensuring a high degree of treatment adherence is necessary to prevent resistance and disease progression. We conducted a cross-sectional study to evaluate adherence to ART through the calculation of the medication possession ratio (MPR) and to identify risk factors for suboptimal adherence in a cohort of HIV-positive patients receiving care at a Colombian healthcare institution across 16 cities. Records of 12,145 users were analyzed, and a multivariate logistic regression model was performed, considering optimal adherence (MPR > =  95%) versus suboptimal adherence (MPR < 95%) as the reference. Suboptimal adherence to ART was identified in 29% of users. Residence region, presence of HIV-defining illnesses, chronic kidney disease (CKD), co-infections such as hepatitis C, tuberculosis, and sexually transmitted infections, treatment duration of more than 5 years, and non-suppressed viral load were identified as risk factors for non-adherence. This underscores the need to identify interventions for those vulnerable groups to minimize the likelihood of non-adherence and to intervene in care models focused on the medical needs of these patients.

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CiteScore
3.50
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