Walmsley S, Levinton C, Brunton J, Muradali D, Rappaport D, Bast M, Spence D, Salit I
Department of Medicine, Toronto Hospital, Ontario, Canada.
J Acquir Immune Defic Syndr Hum Retrovirol. 1995 Apr 1;8(4):348-57.
A multicenter placebo-controlled trial of early short-term high-dose methylprednisolone enrolled 78 patients with moderate to severe Pneumocystis carinii pneumonia (PCP) complicating HIV infection. The mean pressure of oxygen (PO2) at study entry was 55 mm Hg for the 71 patients who had blood gases monitored while breathing room air. Patients were randomized to receive methylprednisolone (40 mg) or placebo parenterally twice daily for 10 days, and the first dose of study medication was given within 24 h of the first dose of antimicrobial therapy for PCP. The primary end point included death, need for mechanical ventilation for > 6 days, or a partial PO2 < 70 mm Hg while breathing room air 10 days after initiation of treatment. There was no statistically significant difference in the primary end point between patients randomized to corticosteroid (CS) or placebo (PL) (p = 0.522; 95% CI = -0.30, 0.16). The incidence of superinfections during therapy or of other HIV-associated infections or malignancies in the 6 months following treatment for PCP was not significantly different between the two groups. More patients randomized to placebo had to discontinue treatment with trimethoprim-sulfamethoxazole because of hypersensitivity than those randomized to corticosteroids (p = 0.039). We conclude that addition of corticosteroids does not significantly affect the outcome of PCP in patients with HIV and a PO2 < 70 mm Hg on room air at presentation but lowers the incidence of hypersensitivity reactions to trimethoprim-sulfamethoxazole.
一项关于早期短期大剂量甲基泼尼松龙的多中心安慰剂对照试验纳入了78例合并人类免疫缺陷病毒(HIV)感染的中度至重度卡氏肺孢子虫肺炎(PCP)患者。在71例于呼吸室内空气时接受血气监测的患者中,研究入组时的平均氧分压(PO2)为55 mmHg。患者被随机分为两组,分别接受甲基泼尼松龙(40 mg)或安慰剂,每日两次静脉注射,共10天,且研究药物的首剂在PCP抗菌治疗首剂后的24小时内给予。主要终点包括死亡、机械通气超过6天、或在治疗开始10天后呼吸室内空气时部分压力氧(PO2)< 70 mmHg。随机接受皮质类固醇(CS)或安慰剂(PL)治疗的患者在主要终点上无统计学显著差异(p = 0.522;95%置信区间 = -0.30,0.16)。两组在PCP治疗期间的二重感染发生率或PCP治疗后6个月内其他HIV相关感染或恶性肿瘤的发生率无显著差异。与随机接受皮质类固醇治疗的患者相比,随机接受安慰剂治疗的患者因超敏反应而不得不停用甲氧苄啶 - 磺胺甲恶唑治疗的人数更多(p = 0.039)。我们得出结论,对于就诊时呼吸室内空气且PO2 < 70 mmHg的HIV患者,加用皮质类固醇对PCP的预后无显著影响,但可降低对甲氧苄啶 - 磺胺甲恶唑超敏反应的发生率。