TY - JOUR
T1 - Survival and quality-of-life in mucormycosis
T2 - a multicentric ambispective cohort study
AU - All-India Mucormycosis Consortium
AU - Abdulkader, Rizwan Suliankatchi
AU - Mohan, Malu
AU - Saravanakumar, Divya
AU - Ponnaiah, Manickam
AU - Bhatnagar, Tarun
AU - Devika, S.
AU - Gayathri, K.
AU - Rozario, Amanda G.A.
AU - Moorthy, Aditya
AU - Devaraja, K.
AU - Saravanam, Prasanna Kumar
AU - Panigrahi, Sunil Kumar
AU - Srivastava, Abhinav
AU - Chandra Baishya, Achyut
AU - Garg, Ajai
AU - Mishra, Amit Kumar
AU - Tyagi, Amit
AU - Talukdar, Anjana Jyoti
AU - Kankaria, Ankita
AU - Bhatnagar, Aparna
AU - Karat, Arathi
AU - Kumar, Arul Sundaresh
AU - Chug, Ashi
AU - Vankudre, Ashok
AU - Ramaswamy, Balakrishnan
AU - Parmar, Bhagirathsinh
AU - Bharathi, M. B.
AU - Jadav, Bhargav R.
AU - Unnikrishnan, Bhaskaran
AU - Karuppannasamy, Divya
AU - Medikeri, Gaurav
AU - Ghate, Girija
AU - Shah, Hardik
AU - Saha, Ipsita
AU - Ojah, Jutika
AU - Pujary, Kailesh
AU - Srivastava, Kajal
AU - Shanmugam, Karthikeyan
AU - Krishnasamy, Karthikeyan
AU - Saravu, Kavitha
AU - Sivapuram, Kavya
AU - Joshi, Krupal
AU - Singh, Mahendra
AU - Bairwa, Mukesh
AU - Muthurajesh, Easwaran
AU - Gupta, Nitin
AU - Shenoy, Vijendra
AU - Kumar, Arvind
AU - Madi, Deepak
AU - Kudlu, Kshithi
N1 - Publisher Copyright:
© 2025 European Society of Clinical Microbiology and Infectious Diseases
PY - 2025
Y1 - 2025
N2 - Objectives: We aimed to evaluate long-term survival and identify predictors of mortality among patients hospitalized with mucormycosis. Methods: This prospective, multicentre cohort study included patients hospitalized for mucormycosis across 26 sites in India from March to July 2021. Follow-up data were collected at 1-, 3-, 6-, and 12-month intervals post-discharge through telephonic or in-person interviews with patients or caregivers. Primary outcomes were survival, sequelae, and quality of life, assessed using the EURO-QOL 5D-5L scale. Survival analyses were performed using the shared frailty Cox proportional hazards model for predefined subgroups. Additional sensitivity analyses using inverse probability of censoring weights and marginal structural modelling were conducted to account for loss to follow-up and the time-varying nature of the treatment and confounders. Results: Of the 686 patients, 101 deaths (14.7%) occurred within 1 year, with a median survival time of 230 days. The majority of deaths (64.3%) occurred early, i.e. during hospitalization. Independent predictors of mortality included orbit involvement (hazard ratio [HR]: 2.0, 95% CI: 1.2–3.4), intracranial/cerebral involvement (HR: 2.6, 95% CI: 1.5–4.4), admission to an intensive care unit (HR: 6.4, 95% CI: 3.5–11.6), poor glycaemic control (HR: 2.3, 95% CI: 1.1–4.7), and other comorbidities (HR: 1.6, 95% CI: 1.0–2.5), and those associated with lower mortality were combination antifungal therapy (HR: 0.2, 95% CI: 0.1–0.4) and receipt of surgical treatment (HR: 0.1, 95% CI: 0.07–0.2). Survivors demonstrated improved quality of life, especially those who were gainfully employed. Sensitivity analysis indicated no major impact of loss to follow-up on survival. Discussion: Poor glycaemic control, severe disease, and involvement of the orbit or intracranial/cerebral regions predict higher mortality in mucormycosis. Aggressive therapeutic strategies, including combination of antifungal therapy and surgical interventions, substantially improved survival. The study highlights the importance of integrating psychological rehabilitation and socioeconomic support into management protocols to enhance the quality of life among survivors.
AB - Objectives: We aimed to evaluate long-term survival and identify predictors of mortality among patients hospitalized with mucormycosis. Methods: This prospective, multicentre cohort study included patients hospitalized for mucormycosis across 26 sites in India from March to July 2021. Follow-up data were collected at 1-, 3-, 6-, and 12-month intervals post-discharge through telephonic or in-person interviews with patients or caregivers. Primary outcomes were survival, sequelae, and quality of life, assessed using the EURO-QOL 5D-5L scale. Survival analyses were performed using the shared frailty Cox proportional hazards model for predefined subgroups. Additional sensitivity analyses using inverse probability of censoring weights and marginal structural modelling were conducted to account for loss to follow-up and the time-varying nature of the treatment and confounders. Results: Of the 686 patients, 101 deaths (14.7%) occurred within 1 year, with a median survival time of 230 days. The majority of deaths (64.3%) occurred early, i.e. during hospitalization. Independent predictors of mortality included orbit involvement (hazard ratio [HR]: 2.0, 95% CI: 1.2–3.4), intracranial/cerebral involvement (HR: 2.6, 95% CI: 1.5–4.4), admission to an intensive care unit (HR: 6.4, 95% CI: 3.5–11.6), poor glycaemic control (HR: 2.3, 95% CI: 1.1–4.7), and other comorbidities (HR: 1.6, 95% CI: 1.0–2.5), and those associated with lower mortality were combination antifungal therapy (HR: 0.2, 95% CI: 0.1–0.4) and receipt of surgical treatment (HR: 0.1, 95% CI: 0.07–0.2). Survivors demonstrated improved quality of life, especially those who were gainfully employed. Sensitivity analysis indicated no major impact of loss to follow-up on survival. Discussion: Poor glycaemic control, severe disease, and involvement of the orbit or intracranial/cerebral regions predict higher mortality in mucormycosis. Aggressive therapeutic strategies, including combination of antifungal therapy and surgical interventions, substantially improved survival. The study highlights the importance of integrating psychological rehabilitation and socioeconomic support into management protocols to enhance the quality of life among survivors.
UR - https://www.scopus.com/pages/publications/105009690105
UR - https://www.scopus.com/pages/publications/105009690105#tab=citedBy
U2 - 10.1016/j.cmi.2025.06.001
DO - 10.1016/j.cmi.2025.06.001
M3 - Article
C2 - 40516755
AN - SCOPUS:105009690105
SN - 1198-743X
VL - 31
SP - 1842
EP - 1854
JO - Clinical Microbiology and Infection
JF - Clinical Microbiology and Infection
IS - 11
ER -