Department of Management Science and Information Systems, Spears School of Business, Oklahoma State University, Tulsa, Oklahoma, United States of America.
Department of Health Policy and Management, Yale School of Public Health, New Haven, Connecticut, United States of America.
PLoS Med. 2024 Jul 8;21(7):e1004424. doi: 10.1371/journal.pmed.1004424. eCollection 2024 Jul.
Since common diagnostic tests for gonorrhea do not provide information about susceptibility to antibiotics, treatment of gonorrhea remains empiric. Antibiotics used for empiric therapy are usually changed once resistance prevalence exceeds a certain threshold (e.g., 5%). A low switch threshold is intended to increase the probability that an infection is successfully treated with the first-line antibiotic, but it could also increase the pace at which recommendations are switched to newer antibiotics. Little is known about the impact of changing the switch threshold on the incidence of gonorrhea, the rate of treatment failure, and the overall cost and quality-adjusted life-years (QALYs) associated with gonorrhea.
We developed a transmission model of gonococcal infection with multiple resistant strains to project gonorrhea-associated costs and loss in QALYs under different switch thresholds among men who have sex with men (MSM) in the United States. We accounted for the costs and disutilities associated with symptoms, diagnosis, treatment, and sequelae, and combined costs and QALYs in a measure of net health benefit (NHB). Our results suggest that under a scenario where 3 antibiotics are available over the next 50 years (2 suitable for the first-line therapy of gonorrhea and 1 suitable only for the retreatment of resistant infections), changing the switch threshold between 1% and 10% does not meaningfully impact the annual number of gonorrhea cases, total costs, or total QALY losses associated with gonorrhea. However, if a new antibiotic is to become available in the future, choosing a lower switch threshold could improve the population NHB. If in addition, drug-susceptibility testing (DST) is available to inform retreatment regimens after unsuccessful first-line therapy, setting the switch threshold at 1% to 2% is expected to maximize the population NHB. A limitation of our study is that our analysis only focuses on the MSM population and does not consider the influence of interventions such as vaccine and common use of rapid drugs susceptibility tests to inform first-line therapy.
Changing the switch threshold for first-line antibiotics may not substantially change the health and financial outcomes associated with gonorrhea. However, the switch threshold could be reduced when newer antibiotics are expected to become available soon or when in addition to future novel antibiotics, DST is also available to inform retreatment regimens.
由于常见的淋病诊断测试不能提供抗生素敏感性的信息,淋病的治疗仍然是经验性的。用于经验性治疗的抗生素通常在耐药率超过一定阈值(例如 5%)时才会更换。较低的转换阈值旨在提高首次使用一线抗生素成功治疗感染的概率,但也可能增加推荐使用更新抗生素的速度。关于改变转换阈值对淋病发病率、治疗失败率以及与淋病相关的总成本和质量调整生命年(QALY)的影响知之甚少。
我们开发了一种淋病感染传播模型,该模型有多种耐药菌株,用于预测美国男男性行为者(MSM)中不同转换阈值下与淋病相关的成本和 QALY 损失。我们考虑了与症状、诊断、治疗和后遗症相关的成本和不良影响,并将成本和 QALY 合并为一个衡量净健康收益(NHB)的指标。我们的结果表明,在未来 50 年内有 3 种抗生素可用的情况下(2 种适合淋病的一线治疗,1 种仅适合耐药感染的再治疗),将转换阈值在 1%到 10%之间变化并不会对淋病病例的年发生数、总成本或与淋病相关的总 QALY 损失产生重大影响。然而,如果未来有新的抗生素可用,选择较低的转换阈值可能会提高人群的 NHB。如果另外,药敏试验(DST)可用于指导首次治疗失败后的再治疗方案,那么将转换阈值设定为 1%到 2%预计将使人群的 NHB 最大化。我们研究的一个局限性是,我们的分析仅关注 MSM 人群,并未考虑疫苗等干预措施的影响,也未考虑常规使用快速药物敏感性检测来指导一线治疗的影响。
改变一线抗生素的转换阈值可能不会显著改变与淋病相关的健康和财务结果。然而,当新的抗生素有望很快上市时,或者当除了未来的新型抗生素外,DST 也可用于指导再治疗方案时,可以降低转换阈值。