Falletta J M, Woods G M, Verter J I, Buchanan G R, Pegelow C H, Iyer R V, Miller S T, Holbrook C T, Kinney T R, Vichinsky E
Division of Pediatric Hematology-Oncology, Duke Comprehensive Sickle Cell Center, Duke University Medical Center, Durham, North Carolina 27710, USA.
J Pediatr. 1995 Nov;127(5):685-90. doi: 10.1016/s0022-3476(95)70154-0.
To evaluate the consequences of discontinuing penicillin prophylaxis at 5 years of age in children with sickle cell anemia who had received prophylactic penicillin for much of their lives.
Randomized, double-blind, placebo-controlled trial.
Eighteen teaching hospitals throughout the United States.
Children with sickle cell anemia (hemoglobin SS or hemoglobin S beta 0-thalassemia) who had received prophylactic penicillin therapy for at least 2 years immediately before their fifth birthday and had received the 23-valent pneumococcal vaccine between 2 and 3 years of age and again at the time of randomization. Of 599 potential candidates, 400 were randomly selected and followed for an average of 3.2 years.
After randomization, patients received the study medication twice daily--either penicillin V potassium, 250 mg, or an identical placebo tablet. Patients were either seen in the clinic or contacted every 3 months thereafter for an interval history and dispensing of the study drug. A physical examination was scheduled every 6 months.
The primary end point was a comparison of the incidence of bacteremia or meningitis caused by Streptococcus pneumoniae in children continuing penicillin prophylaxis versus those receiving the placebo.
Six children had a systemic infection caused by S. pneumoniae, four in the placebo group (2.0%; 95% confidence interval 0.5%, 5.0%) and two in the continued penicillin prophylaxis group (1.0%; 95% confidence interval 0.1%, 3.6%) with a relative risk of 0.5 (95% confidence interval 0.1, 2.7). All invasive isolates were either serotype 6(A or B) or serotype 23F. Four of the isolates were penicillin susceptible, and two (one from each treatment group) were penicillin and multiply antibiotic resistant. Adverse effects of the study drug were reported for three patients (nausea, vomiting, or both), one of whom was in the placebo group.
Children with sickle cell anemia who have not had a prior severe pneumococcal infection or a splenectomy and are receiving comprehensive care may safely stop prophylactic penicillin therapy at 5 years of age. Parents must be aggressively counseled to seek medical attention for all febrile events in children with sickle cell anemia.
评估镰状细胞贫血患儿在5岁时停止青霉素预防性治疗的后果,这些患儿一生中大部分时间都接受了青霉素预防性治疗。
随机、双盲、安慰剂对照试验。
美国18家教学医院。
镰状细胞贫血患儿(血红蛋白SS或血红蛋白Sβ0地中海贫血),在其5岁生日前至少接受了2年的青霉素预防性治疗,并且在2至3岁时以及随机分组时接种了23价肺炎球菌疫苗。在599名潜在候选人中,随机选择了400名并平均随访3.2年。
随机分组后,患者每天服用两次研究药物——250毫克青霉素V钾或相同的安慰剂片剂。患者此后每3个月在诊所就诊或接受联系,以获取间隔期病史并发放研究药物。每6个月安排一次体格检查。
主要终点是继续接受青霉素预防性治疗的儿童与接受安慰剂的儿童中由肺炎链球菌引起的菌血症或脑膜炎发病率的比较。
6名儿童发生了由肺炎链球菌引起的全身感染,安慰剂组4名(2.0%;95%置信区间0.5%,5.0%),继续接受青霉素预防性治疗组2名(1.0%;95%置信区间0.1%,3.6%),相对风险为0.5(95%置信区间0.1,2.7)。所有侵袭性分离株均为6型(A或B)或23F型。其中4株分离株对青霉素敏感,2株(各来自一个治疗组)对青霉素及多种抗生素耐药。有3名患者报告了研究药物的不良反应(恶心、呕吐或两者皆有),其中1名在安慰剂组。
未发生过严重肺炎球菌感染或脾切除术且正在接受综合治疗的镰状细胞贫血患儿,5岁时可安全停用青霉素预防性治疗。必须积极建议家长,镰状细胞贫血患儿出现任何发热事件时都要寻求医疗关注。