TY - JOUR
T1 - mucormycosis
T2 - The international ID-IRI study
AU - Sahin, Meyha
AU - Yilmaz, Mesut
AU - Mert, Ali
AU - Naghili, Behrouz
AU - Ravanbakhsh, Fatemeh
AU - Varshochi, Mojtaba
AU - Darazam, Ilad Alavi
AU - Ebrahimi, Mohammad Javad
AU - Moafi, Maral
AU - Tehrani, Hamed Azhdari
AU - Mahboob, Amjad
AU - Rashid, Naveed
AU - Khan, Ejaz Ahmed
AU - Hakamifard, Atousa
AU - Eser-Karlidag, Gülden
AU - Babamahmoodi, Abdolreza
AU - El-Kholy, Amani
AU - Mosawi, Sayed Hussain
AU - Albayrak, Ayşe
AU - Al Ramahi, Jamal Wadi
AU - Addepalli, Syam Kumar
AU - Balin, Şafak Özer
AU - Khan, Asfandiyar
AU - Pandya, Nirav
AU - Gurbuz, Esra
AU - Sincan, Gülden
AU - Azami, Hadia
AU - Dumlu, Rıdvan
AU - Khedr, Reham
AU - Ripon, Rezaul Karim
AU - Alkan, Sevil
AU - Kose, Şükran
AU - Ceylan, Bahadır
AU - Erdem, Hakan
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/7/1
Y1 - 2024/7/1
N2 - The emergence of COVID-19, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), triggered a global pandemic. Concurrently, reports of mucormycosis cases surged, particularly during the second wave in India. This study aims to investigate mortality factors in COVID-19-associated mucormycosis (CAM) cases, exploring clinical, demographic, and therapeutic variables across mostly Asian and partly African countries. A retrospective, cross-sectional analysis of CAM patients from 22 medical centers across eight countries was conducted, focusing on the first 3 months post-COVID-19 diagnosis. Data collected through the ID-IRI included demographics, comorbidities, treatments, and outcomes. A total of 162 CAM patients were included. The mean age was 54.29 ± 13.04 years, with 54% male. Diabetes mellitus (85%) was prevalent, and 91% had rhino-orbital-cerebral mucormycosis. Surgical debridement was performed in 84% of the cases. Mortality was 39%, with advanced age (hazard ratio [HR] = 1.06, [P < .001]), rituximab use (HR = 21.2, P = .05), and diabetic ketoacidosis (HR = 3.58, P = .009) identified as risk factors. The mortality risk increases by approximately 5.6% for each additional year of age. Surgical debridement based on organ involvement correlated with higher survival (HR = 8.81, P < .001). The utilization of rituximab and diabetic ketoacidosis, along with advancing age, has been associated with an increased risk of mortality in CAM patients. A combination of antifungal treatment and surgical intervention has demonstrated a substantial improvement in survival outcomes.
AB - The emergence of COVID-19, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), triggered a global pandemic. Concurrently, reports of mucormycosis cases surged, particularly during the second wave in India. This study aims to investigate mortality factors in COVID-19-associated mucormycosis (CAM) cases, exploring clinical, demographic, and therapeutic variables across mostly Asian and partly African countries. A retrospective, cross-sectional analysis of CAM patients from 22 medical centers across eight countries was conducted, focusing on the first 3 months post-COVID-19 diagnosis. Data collected through the ID-IRI included demographics, comorbidities, treatments, and outcomes. A total of 162 CAM patients were included. The mean age was 54.29 ± 13.04 years, with 54% male. Diabetes mellitus (85%) was prevalent, and 91% had rhino-orbital-cerebral mucormycosis. Surgical debridement was performed in 84% of the cases. Mortality was 39%, with advanced age (hazard ratio [HR] = 1.06, [P < .001]), rituximab use (HR = 21.2, P = .05), and diabetic ketoacidosis (HR = 3.58, P = .009) identified as risk factors. The mortality risk increases by approximately 5.6% for each additional year of age. Surgical debridement based on organ involvement correlated with higher survival (HR = 8.81, P < .001). The utilization of rituximab and diabetic ketoacidosis, along with advancing age, has been associated with an increased risk of mortality in CAM patients. A combination of antifungal treatment and surgical intervention has demonstrated a substantial improvement in survival outcomes.
KW - COVID-19
KW - COVID-19-associated mucormycosis
KW - immunosuppression
KW - mortality
UR - https://www.scopus.com/pages/publications/85199223686
U2 - 10.1093/mmy/myae064
DO - 10.1093/mmy/myae064
M3 - Article
C2 - 38914466
AN - SCOPUS:85199223686
SN - 1369-3786
VL - 62
JO - Medical Mycology
JF - Medical Mycology
IS - 7
M1 - myae064
ER -