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Clinical Characteristics, Prognosis Factors and Metagenomic Next-Generation Sequencing Diagnosis of Mucormycosis in patients With Hematologic Diseases.
Wang, Jieru; Liu, Li; Li, Jia; Feng, Xiaomeng; Yi, Huiming; Jiang, Erlie; Zheng, Yizhou; Zhang, Fengkui; Zhu, Xiaofan; Mi, Yingchang; Han, Mingzhe; Wang, Jianxiang; Feng, Sizhou.
Afiliación
  • Wang J; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
  • Liu L; Tianjin Institutes of Health Science, Tianjin, China.
  • Li J; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
  • Feng X; Tianjin Institutes of Health Science, Tianjin, China.
  • Yi H; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
  • Jiang E; Tianjin Institutes of Health Science, Tianjin, China.
  • Zheng Y; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
  • Zhang F; Tianjin Institutes of Health Science, Tianjin, China.
  • Zhu X; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
  • Mi Y; Tianjin Institutes of Health Science, Tianjin, China.
  • Han M; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
  • Wang J; Tianjin Institutes of Health Science, Tianjin, China.
  • Feng S; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Mycopathologia ; 189(4): 71, 2024 Aug 01.
Article en En | MEDLINE | ID: mdl-39088077
ABSTRACT

INTRODUCTION:

New diagnostic methods and antifungal strategies may improve prognosis of mucormycosis. We describe the diagnostic value of metagenomic next⁃generation sequencing (mNGS) and identify the prognostic factors of mucormycosis.

METHODS:

We conducted a retrospective study of hematologic patients suffered from mucormycosis and treated with monotherapy [amphotericin B (AmB) or posaconazole] or combination therapy (AmB and posaconazole). The primary outcome was 84-day all-cause mortality after diagnosis.

RESULTS:

Ninety-five patients were included, with "proven" (n = 27), "probable" (n = 16) mucormycosis confirmed by traditional diagnostic methods, and "possible" (n = 52) mucormycosis with positive mNGS results. The mortality rate at 84 days was 44.2%. Possible + mNGS patients and probable patients had similar diagnosis processes, overall survival rates (44.2% vs 50.0%, p = 0.685) and overall response rates to effective drugs (44.0% vs 37.5%, p = 0.647). Furthermore, the median diagnostic time was shorter in possible + mNGS patients than proven and probable patients (14 vs 26 days, p < 0.001). Combination therapy was associated with better survival compared to monotherapy at six weeks after treatment (78.8% vs 53.1%, p = 0.0075). Multivariate analysis showed that combination therapy was the protective factor (HR = 0.338, 95% CI 0.162-0.703, p = 0.004), though diabetes (HR = 3.864, 95% CI 1.897-7.874, p < 0.001) and hypoxemia (HR = 3.536, 95% CI 1.874-6.673, p < 0.001) were risk factors for mortality.

CONCLUSIONS:

Mucormycosis is a life-threatening infection. Early management of diabetes and hypoxemia may improve the prognosis. Exploring effective diagnostic and treatment methods is important, and combination antifungal therapy seems to hold potential benefits.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anfotericina B / Secuenciación de Nucleótidos de Alto Rendimiento / Enfermedades Hematológicas / Mucormicosis / Antifúngicos Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Mycopathologia Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anfotericina B / Secuenciación de Nucleótidos de Alto Rendimiento / Enfermedades Hematológicas / Mucormicosis / Antifúngicos Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Mycopathologia Año: 2024 Tipo del documento: Article País de afiliación: China
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