Barker G J, Call S K, Gamis A S
Children's Mercy Hospital, University of Missouri-Kansas City, School of Dentistry 64108, USA.
J Pediatr Hematol Oncol. 1995 May;17(2):151-5. doi: 10.1097/00043426-199505000-00009.
alpha-Hemolytic streptococcal (AHS) sepsis is increasing in oncology patients receiving myelosuppressive chemotherapy. In response to a high rate of AHS sepsis in this population at our institution, an oral care protocol was instituted, including vancomycin 0.5% in flavored methylcellulose (vanc paste) applied orally t.i.d. at the oncologists' discretion.
A retrospective cohort study of 239 neutropenic episodes among 42 children receiving myelosuppressive chemotherapy between 1988 and 1991 compared the incidence of septicemia based on the prophylactic use of vanc paste.
A total of 236 consecutive neutropenic episodes were evaluable, 121 with vanc paste and 115 without. AHS sepsis occurred in one child using vanc paste and in six children not using vanc paste (p = 0.06). Excluding staph-only positive blood cultures, which would not be reduced with a topical oral antibiotic drug, there were 6 and 13 positive blood cultures in the vanc-paste and nonvanc-paste patients, respectively (p = 0.09). There was no increase in incidence of gram-negative bacteremia among vanc-paste recipients. Vancomycin resistance was not encountered.
This analysis suggests that vanc paste effectively reduces AHS sepsis, does not increase gram-negative bacteremia, and is not associated with vancomycin resistance. A multicentered, placebo-controlled, double-blind study is currently planned.
在接受骨髓抑制化疗的肿瘤患者中,α溶血性链球菌(AHS)败血症的发生率正在上升。针对我院该人群中AHS败血症的高发生率,制定了一项口腔护理方案,包括根据肿瘤学家的判断,每日三次口服含0.5%万古霉素的调味甲基纤维素(万古霉素糊剂)。
对1988年至1991年间接受骨髓抑制化疗的42名儿童中的239次中性粒细胞减少发作进行回顾性队列研究,比较基于万古霉素糊剂预防性使用的败血症发生率。
总共236次连续的中性粒细胞减少发作可进行评估,121次使用万古霉素糊剂,115次未使用。使用万古霉素糊剂的一名儿童和未使用万古霉素糊剂的六名儿童发生了AHS败血症(p = 0.06)。排除仅葡萄球菌阳性的血培养结果(局部口服抗生素药物不会降低其发生率),使用万古霉素糊剂的患者和未使用万古霉素糊剂的患者分别有6次和13次血培养阳性(p = 0.09)。接受万古霉素糊剂治疗的患者中革兰氏阴性菌血症的发生率没有增加。未发现万古霉素耐药情况。
该分析表明,万古霉素糊剂可有效降低AHS败血症的发生率,不会增加革兰氏阴性菌血症,且与万古霉素耐药无关。目前正在计划进行一项多中心、安慰剂对照、双盲研究。