Combined Internal Medicine and Pediatrics Section, Division of General Internal Medicine, Department of Internal Medicine, Ohio State University College of Medicine, Columbus, Ohio.
Applied Clinical Research Center, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Hosp Pediatr. 2024 Aug 1;14(8):e341-e348. doi: 10.1542/hpeds.2023-007132.
This study seeks to identify demographic and clinical factors prompting clinician prescribing of nirmatrelvir/ritonavir to pediatric patients for management of coronavirus disease 2019 (COVID-19) infection.
Patients aged 12 to 17 years with a COVID-19 infection and nirmatrelvir/ritonavir prescription during an outpatient clinical encounter within a PEDSnet-affiliated institution between January 2022 and August 2023 were identified using electronic health record data. A multivariate logistic regression analysis was used to estimate odds of nirmatrelvir/ritonavir prescription after adjusting for various factors.
A total of 20 959 patients aged 12 to 17 years were diagnosed with a COVID-19 infection on the basis of an electronic health record-documented positive polymerase chain reaction or antigen test or diagnosis during an outpatient clinical visit. Of these patients, 408 received a nirmatrelvir/ritonavir prescription within 5 days of diagnosis. Higher odds of nirmatrelvir/ritonavir treatment were associated with having chronic or complex chronic disease (chronic: odds ratio [OR] 2.50 [95% confidence interval (CI) 1.83-3.38]; complex chronic: OR 2.21 [95% CI 1.58-3.08]). Among patients with chronic disease, each additional body system conferred 1.18 times higher odds of treatment (95% CI 1.10-1.26). Compared with non-Hispanic white patients, Hispanic patients (OR 0.61 [95% CI 0.44-0.83]) had lower odds of treatment.
Children with chronic conditions are more likely than those without to receive nirmatrelvir/ritonavir prescriptions. However, nirmatrelvir/ritonavir prescribing to children with chronic conditions remains infrequent. Pediatric data concerning nirmatrelvir/ritonavir safety and effectiveness in preventing severe disease and hospitalization are critical optimizing clinical decision-making and use among children.
本研究旨在确定促使临床医生为管理 2019 冠状病毒病(COVID-19)感染而向儿科患者开具奈玛特韦/利托那韦的人口统计学和临床因素。
通过电子病历数据,确定 2022 年 1 月至 2023 年 8 月期间,在 PEDSnet 附属机构内门诊就诊时,年龄在 12 至 17 岁的 COVID-19 感染且开具奈玛特韦/利托那韦处方的患者。使用多变量逻辑回归分析,在调整了各种因素后,估计奈玛特韦/利托那韦处方的可能性。
共有 20959 名年龄在 12 至 17 岁的患者在电子病历记录的阳性聚合酶链反应或抗原检测或门诊就诊期间的诊断中被诊断为 COVID-19 感染。在这些患者中,有 408 名在诊断后 5 天内开具了奈玛特韦/利托那韦处方。更高的奈玛特韦/利托那韦治疗可能性与患有慢性或复杂慢性病有关(慢性:比值比[OR] 2.50 [95%置信区间[CI] 1.83-3.38];复杂慢性:OR 2.21 [95% CI 1.58-3.08])。在患有慢性疾病的患者中,每个额外的身体系统增加 1.18 倍的治疗可能性(95% CI 1.10-1.26)。与非西班牙裔白人患者相比,西班牙裔患者(OR 0.61 [95% CI 0.44-0.83])的治疗可能性较低。
患有慢性病的儿童比没有慢性病的儿童更有可能接受奈玛特韦/利托那韦处方。然而,向患有慢性病的儿童开具奈玛特韦/利托那韦处方仍然很少见。关于奈玛特韦/利托那韦在预防严重疾病和住院方面的安全性和有效性的儿科数据对于优化儿童临床决策和使用至关重要。