Managing penicillin resistant pneumococcal meningitis: an international id-iri study.

IF 3 3区 医学 Q2 INFECTIOUS DISEASES
Hakan Erdem, Elif Dogan, Handan Ankarali, Gorana Dragovac, Derya Seyman, Arzu Tarakci, Enes Dalmanoglu, Ayse Kaya-Kalem, Ayse Batirel, Seniha Senbayrak, Marija Cvetanovska, Sumeyye Kazancioglu, Abdullah Umut Pekok, Bilal Ahmad Rahimi, Mustafa Uguz, Selva Ala-Selek, Atahan Cagatay, Serap Demir-Tekol, Halil Kul, Tuba Kuruoglu, Fatih Temocin, Sevil Alkan, Furkan Baris Arikan, Turan Aslan, Meltem Tasbakan, Serife Altun-Demircan, Tuba Damar-Cakirca, Amani El-Kholy, Hasip Kahraman, Yordan Kalchev, Sholpan Kulzhanova, Anna Líšková, Serkan Oncu, Mehmet Özdemir, Deniz Özer, Nefise Öztoprak Cuvalci, Tugce Simsek-Bozok, Luca Mihaela Catalina, Egidia Miftode, Larisa Miftode, Marianna Murdjeva, Chizaram Onyeaghala, Bahar Busra Sivrikaya, Selcen Ozer-Kokkizil, Aysun Yalci, Oktay Yapici, Joanna Zajkowska, Teresa Fasciana
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引用次数: 0

Abstract

Penicillin-resistant pneumococcal meningitis (PRPM) is a challenging and fatal infection. We conducted a multicentre international retrospective study to evaluate the clinical features, outcomes, predictors of outcomes antimicrobial efficacy and drug susceptibility in patients with PRPM. The study, conducted through the "Infectious Diseases-International Research Initiative" across 33 centers in 11 countries, analyzed PRPM patients treated between 2019 and 2024 using univariate and multivariate analyses. A total of 138 patients were included. Of these, 83 (60.1%) were fully cured, 27 (19.6%) died, and 28 (20.3%) survived with sequelae. Mortality was associated with ICU admission (OR 14.886; p = 0.021), mechanical ventilation (OR 7.205; p = 0.049), and vasopressor use (OR 8.983; p = 0.025). Higher CSF leukocyte count (OR 0.854; p = 0.060) and blood leukocyte count (OR 0.283; p = 0.021) were linked to lower mortality risk. Patients who developed sequelae were more likely to require mechanical ventilation (OR 9.354; p = 0.001), experience recurrent meningitis (OR 5.562; p = 0.081), and have lower platelet counts (OR 0.001; p = 0.050), compared to those who fully recovered. Sequelae patients had higher GCS scores (OR 1.365; p = 0.014), more corticosteroid use (OR 5.301; p = 0.061), and less vasopressor use (OR 0.205; p = 0.019) compared to those who died. The antibiotic susceptibility profiles of the isolates in our PRSP cohort were: Ceftriaxone (75/134, 55.9%), meropenem (26/44, 59%), moxifloxacin (47/48, 97.9%). PRPM is a fatal disease in which mortality and sequelae occurring in two-fifths of cases. Severe illness markers such as ICU admission, mechanical ventilation, and vasopressor use, along with recurrent meningitis are linked to worse outcomes. Thrombocytopenia, low leukocyte counts, and lower GCS scores are indicators of poor prognosis, while corticosteroid therapy appears protective in PRPM. Therapeutic optimization is challenged by rising resistance and pharmacokinetic limitations, though moxifloxacin shows the highest susceptibility; further research is warranted.

管理青霉素耐药肺炎球菌脑膜炎:一项国际id-iri研究。
耐青霉素肺炎球菌脑膜炎(PRPM)是一种具有挑战性和致命性的感染。我们进行了一项多中心的国际回顾性研究,以评估PRPM患者的临床特征、结局、结局预测因素、抗菌效果和药物敏感性。这项研究是通过“传染病-国际研究倡议”在11个国家的33个中心进行的,使用单变量和多变量分析分析了2019年至2024年期间治疗的PRPM患者。共纳入138例患者。其中83例(60.1%)完全治愈,27例(19.6%)死亡,28例(20.3%)有后遗症存活。死亡率与ICU住院(OR 14.886; p = 0.021)、机械通气(OR 7.205; p = 0.049)和血管加压药使用(OR 8.983; p = 0.025)相关。较高的脑脊液白细胞计数(OR 0.854; p = 0.060)和血液白细胞计数(OR 0.283; p = 0.021)与较低的死亡风险相关。与完全康复的患者相比,出现后遗症的患者更有可能需要机械通气(OR 9.354, p = 0.001)、复发性脑膜炎(OR 5.562, p = 0.081)、血小板计数更低(OR 0.001, p = 0.050)。与死亡患者相比,后遗症患者GCS评分较高(OR 1.365; p = 0.014),皮质类固醇使用较多(OR 5.301; p = 0.061),血管加压剂使用较少(OR 0.205; p = 0.019)。PRSP队列中分离株的药敏谱为:头孢曲松(75/134,55.9%)、美罗培南(26/44,59%)、莫西沙星(47/48,97.9%)。PRPM是一种致命疾病,五分之二的病例会出现死亡和后遗症。重症监护病房入院、机械通气和血管加压剂使用等严重疾病标志,以及复发性脑膜炎与更糟糕的结果有关。血小板减少、白细胞计数低和GCS评分较低是预后不良的指标,而皮质类固醇治疗对PRPM具有保护作用。尽管莫西沙星表现出最高的易感性,但不断上升的耐药性和药代动力学限制对优化治疗提出了挑战;进一步的研究是有必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.40
自引率
2.20%
发文量
138
审稿时长
1 months
期刊介绍: EJCMID is an interdisciplinary journal devoted to the publication of communications on infectious diseases of bacterial, viral and parasitic origin.
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