Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Infectious and Tropical Diseases Unit, Azienda Ospedaliero-Universitaria Careggi, largo Brambilla 3, Firenze (FI), Florence 50134, Italy.
J Travel Med. 2021 Aug 27;28(6). doi: 10.1093/jtm/taab065.
We performed a systematic review of the literature to investigate the efficacy and safety of pentamidine isethionate for the treatment of human tegumentary and visceral leishmaniasis.
A total of 616 papers were evaluated, and 88 studies reporting data on 3108 cases of leishmaniasis (2082 patients with tegumentary leishmaniasis and 1026 with visceral leishmaniasis) were finally included. The majority of available studies were on New World cutaneous leishmaniasis and visceral leishmaniasis caused by Leishmania donovani. At the same time, few data are available for Old World cutaneous leishmaniasis, mucosal leishmaniasis, and visceral leishmaniasis caused by L. infantum. Pooled cure rate for tegumentary leishmaniasis was 78.8% (CI 95%, 76.9-80.6%) and 92.7% (CI 95%, 88.3-97.1%) according to controlled randomized trial and observational studies and case report and case series respectively. Pooled cure rate for visceral leishmaniasis was 84.8% (CI 95%, 82.6-87.1%) and 90.7% (CI 95%, 84.1-97.3%) according to controlled randomized trial and observational studies and case report and case series, respectively. Comparable cure rate was observed in recurrent and refractory cases of visceral leishmaniasis. Concerning the safety profile, among about 2000 treated subjects with some available information, the most relevant side effects were six cases of arrhythmia (including four cases of fatal ventricular fibrillation), 20 cases of irreversible diabetes, 26 cases of muscular aseptic abscess following intramuscular administration.
CONCLUSIONS/RECOMMENDATIONS: Pentamidine isethionate is associated with a similar cure rate of the first-line anti-leishmanial drugs. Severe and irreversible adverse effect appear to be rare. The drug may still have a role in the treatment of any form of human leishmaniasis when the first-line option has failed or in patients who cannot tolerate other drugs also in the setting of travel medicine. In difficult cases, the drug can also be considered as a component of a combination treatment regimen.
我们进行了系统评价,以研究双羟萘酸喷他脒治疗人体皮肤和内脏利什曼病的疗效和安全性。
共评估了 616 篇论文,最终纳入了 88 项研究,这些研究共报告了 3108 例利什曼病(2082 例皮肤利什曼病患者和 1026 例内脏利什曼病患者)的数据。大多数可用的研究都是关于新世界皮肤利什曼病和由利什曼原虫引起的内脏利什曼病。同时,有关旧世界皮肤利什曼病、黏膜利什曼病和由婴儿利什曼原虫引起的内脏利什曼病的数据很少。根据对照随机试验、观察性研究和病例报告及病例系列研究,皮肤利什曼病的总治愈率分别为 78.8%(95%可信区间,76.9%-80.6%)和 92.7%(95%可信区间,88.3%-97.1%)。根据对照随机试验、观察性研究和病例报告及病例系列研究,内脏利什曼病的总治愈率分别为 84.8%(95%可信区间,82.6%-87.1%)和 90.7%(95%可信区间,84.1%-97.3%)。在复发性和难治性内脏利什曼病病例中观察到了可比的治愈率。关于安全性概况,在大约 2000 名接受过治疗且有一些相关信息的患者中,最相关的副作用是 6 例心律失常(包括 4 例致命性室性颤动)、20 例不可逆性糖尿病、26 例肌肉无菌性脓肿,这些都是肌肉注射后的不良反应。
结论/建议:双羟萘酸喷他脒的治愈率与一线抗利什曼病药物相当。严重且不可逆转的不良反应似乎很少见。当一线药物治疗失败或患者不能耐受其他药物时,该药也可用于治疗任何形式的人类利什曼病,并且在旅行医学领域也可考虑将该药作为联合治疗方案的一部分。在困难的情况下,该药也可以作为联合治疗方案的一部分。