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Efficacy of caspofungin combined with trimethoprim/sulfamethoxazole as first-line therapy to treat non-HIV patients with severe pneumocystis pneumonia

机译:卡泊芬净联合甲氧苄氨嘧啶/磺胺甲恶唑治疗非HIV重症肺孢子菌肺炎患者的一线治疗

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摘要

Combined treatment with caspofungin and trimethoprim/sulfamethoxazole (TMP/SMZ) as salvage therapy in non-HIV positive patients with severe pneumocystis pneumonia (PCP) yields poor outcomes. It remains unknown whether the use of this combination strategy as a first-line therapy would improve patient outcomes. The present study aimed to assess the efficacy of caspofungin combined with TMP/SMZ as a first-line therapy in non-HIV positive patients with severe PCP. A retrospective cohort study was conducted between March 2016 and February 2017. Patient clinical characteristics and outcomes were compared between two groups receiving first-line and second-line therapy respectively. In addition, similar cases from previous studies were assessed. A total of 14 patients were included in the present study (mean age, 58.79±14.41 years); including 9 patients receiving caspofungin and TMP/SMZ as a first-line therapy and 5 that received it as a second-line therapy. The overall positive response rate was 71.43% (10/14), with 88.89 (8/9) and 40.00% (2/5) in the first-line and second-line therapy groups, respectively (P=0.095). The positive response rates of patients requiring invasive mechanical ventilation differed significantly between the first-line (5/6, 83.33%) and the second-line (0/3, 0%) therapy groups (P=0.048). All-cause hospital mortality was 42.86% (6/14), with mortality rates of 33.33 (3/9) and 60.00% (3/5) in the first-line and second-line therapy groups, respectively (P=0.580). Combined with previously reported cases (n=27), the positive response rate was significantly greater in the first-line therapy group (11/12, 91.67%) than in the second-line therapy group (8/15, 53.33%, P=0.043). No significant differences were in all-cause mortality rates between the two groups (25.00 vs. 46.67%, P=0.424) were identified, despite the fact that all-course mortality in the first-line therapy group was ~50% that of the second-line therapy group. Therefore, the results of the present study indicate that combined caspofungin and TMP/SMZ as first-line therapy may be a promising and effective strategy to treat non-HIV positive patients with severe PCP, particularly for those requiring invasive mechanical ventilation.
机译:卡泊芬净和甲氧苄氨嘧啶/磺胺甲恶唑(TMP / SMZ)的联合治疗在非HIV阳性重症肺孢子菌肺炎(PCP)阳性患者中作为挽救性疗法的结果较差。将这种联合策略作为一线治疗药物是否可以改善患者预后还不清楚。本研究旨在评估卡泊芬净联合TMP / SMZ作为非HIV阳性重症PCP患者的一线治疗的疗效。在2016年3月至2017年2月之间进行了一项回顾性队列研究。比较了分别接受一线和二线治疗的两组患者的临床特征和结局。此外,评估了以前研究中的类似病例。本研究共纳入14例患者(平均年龄58.79±14.41岁)。包括9例接受卡泊芬净和TMP / SMZ作为一线治疗的患者,5例接受了卡泊芬净和二线治疗的患者。一线和二线治疗组的总阳性反应率为71.43%(10/14),分别为88.89(8/9)和40.00%(2/5)(P = 0.095)。一线(5 / 6,83.33%)和二线(0 / 3,0%)治疗组之间需要有创机械通气的患者的阳性反应率差异显着(P = 0.048)。一线治疗组和二线治疗组的全因医院死亡率分别为42.86%(6/14)和33.33(3/9)和60.00%(3/5)(P = 0.580) 。结合先前报道的病例(n = 27),一线治疗组的阳性反应率(11 / 12,91.67%)显着高于二线治疗组(8 / 15,53.33%,P = 0.043)。尽管一线治疗组的全程死亡率约为对照组的50%,但两组之间的全因死亡率没有显着差异(25.00对46.67%,P = 0.424)。二线治疗组。因此,本研究结果表明,卡泊芬净和TMP / SMZ联合作为一线治疗可能是治疗非PC阳性,重度PCP阳性患者的有希望和有效的策略,特别是对于那些需要有创机械通气的患者。

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