Division of Clinical Pharmacology, Department of Medicine, Stellenbosch University, Cape Town, South Africa.
Division of Clinical Pharmacology, University of Cape Town, Cape Town, South Africa.
J Trop Pediatr. 2020 Aug 1;66(4):385-394. doi: 10.1093/tropej/fmz077.
Antiretroviral therapeutic drug monitoring (TDM) is not routinely used in the management of human immunodeficiency virus, but may be useful in pediatric patients who are prone to altered pharmacokinetics. Data on the routine use of antiretroviral TDM in pediatrics are sparse especially data from sub-Saharan Africa.
We retrospectively reviewed the antiretroviral TDM indications at Tygerberg Children's Hospital, identified pediatric patients who had antiretroviral TDM requests from January 2012 until June 2017 and reviewed their clinical records.
Fifty-nine patients were identified who presented with 64 clinical problems for which TDM was requested. TDM was requested for lopinavir, efavirenz and nevirapine in 83% (53/64), 14% (9/64) and 3% (2/64) of clinical problems, respectively. Lopinavir was mostly requested in patients when adherence measures did not correlate with the clinical picture, suspected non-adherence, lopinavir-rifampicin interactions and for neonatal safety monitoring. Efavirenz was requested when toxicity was suspected and nevirapine in patients receiving rifampicin. Lopinavir TDM confirmed non-adherence in 25% (4/16) of cases when adherence measures did not correlate with the clinical picture and in 43% (3/7) of cases when non-adherence was suspected by the clinician. Efavirenz TDM confirmed toxicity in 100% (6/6) of patients.
Lopinavir TDM was mostly requested when adherence measures did not correlate with the clinical picture, when rifampicin was co-administered and for perinatal safety monitoring. Lopinavir TDM excluded pharmacokinetic reasons for failure in patients failing treatment when lopinavir dosing was supervised. Efavirenz TDM was requested for suspected toxicity with a 100% positive predictive value.
抗逆转录病毒治疗药物监测(TDM)在人类免疫缺陷病毒的治疗管理中并未常规使用,但对于易发生药代动力学改变的儿科患者可能有用。关于儿科中常规使用抗逆转录病毒 TDM 的数据很少,特别是来自撒哈拉以南非洲的数据。
我们回顾性审查了泰格尔伯格儿童医院的抗逆转录病毒 TDM 适应证,确定了 2012 年 1 月至 2017 年 6 月期间有抗逆转录病毒 TDM 请求的儿科患者,并回顾了他们的临床记录。
确定了 59 名患者,他们因 64 种临床问题接受了 TDM 请求。TDM 请求分别用于洛匹那韦、依非韦伦和奈韦拉平的临床问题占 83%(53/64)、14%(9/64)和 3%(2/64)。当依从性措施与临床表现不相关、怀疑不依从、洛匹那韦-利福平相互作用和新生儿安全性监测时,洛匹那韦主要用于患者;怀疑毒性时请求依非韦伦,接受利福平治疗时请求奈韦拉平。洛匹那韦 TDM 在依从性措施与临床表现不相关时,确认了 25%(4/16)的不依从病例,在临床医生怀疑不依从时,确认了 43%(3/7)的不依从病例。依非韦伦 TDM 确认了 100%(6/6)的患者存在毒性。
当依从性措施与临床表现不相关、同时合用利福平以及进行围产期安全性监测时,主要请求洛匹那韦 TDM;当洛匹那韦剂量得到监督时,洛匹那韦 TDM 排除了治疗失败的药代动力学原因。当怀疑毒性时,请求进行依非韦伦 TDM,其阳性预测值为 100%。