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. 2024 Jun 27;62(6):myad130. doi: 10.1093/mmy/myad130

Table 2.

Mortality associated with invasive fungal disease due to Mucorales.

Author Year Study design Study design Study period Country Level of care Population description (%) Number of patients Mortality type (n/N (%))
Bonifaz et al.23 2014 Retrospective cohort study Multi-center January 1985–December 2012 Mexico Tertiary Children with mucormycosis
ROC (77.27%), primary cutaneous, pulmonary
22 Death: 16/22 (72.7%)
Bonifaz et al.32 2021 Retrospective cohort study Single-center January 1985–December 2019 Mexico Tertiary Pediatric patients with mucormycosis
ROC (75.9%), primary cutaneous (8.41%), pulmonary (7.47%)
214 Overall: 46/111 (41.4%)
Bonifaz et al.35 2021 Retrospective cohort study Single-center January 1985–December 2019 Mexico Tertiary Adults and children
Primary cutaneous* (n = 18), secondary# cutaneous (n = 97)
115 Mortality:
Primary cutaneous:
9/18 (50%)
Secondary: 42/97 (43.3%)
Chakrabarti et al.24 2019 Prospective cohort study Multi-center April 2016–September 2017 India Tertiary Adult patients in ICU ROC (n = 29), pulmonary (n = 17) 398 Overall 42-day: 64.8%
Overall 84-day: 65.8%
Chowdhary et al.29 2014 Antifungal susceptibility study Multi-center 2004–2013 India Tertiary Pulmonary (n = 39), ROC (n = 15), cutaneous/subcutaneous (n = 13), disseminated (n = 4) 71 28/54 (51.8%)
Dolatabadi et al.33 2018 Retrospective cohort study Multi-center 2008–2014 Iran Provincial Adults and children sinuses (86%) 208 Mortality: 11/41 (26.8%)
Kontoyiannis et al.14 2016 Retrospective cohort study Multi-center Janary 2005–June 2014 USA Teaching and non-teaching hospital Patients with mucormycosis-related hospitalization.
USA hospital-based database covering more than 560 participating hospitals and 104 million patients
555 Discharge death rate: 130/555 (23%)
Lee et al.22 2020 Retrospective cohort study Single-center January 2011–August 2018 South Korea Tertiary Adult patients with hematological diseases 27 6-week mortality: 6/26 (23.1%)
12-week mortality: 7/26 (26.9%)
Legrand et al.20 2016 Retrospective/period A: October 2013–January 2015
Prospective/period B: January 2015–February 2016
Multi-center October 2013– February 2016 France Tertiary Adult burns patients with invasive wound mucormycosis: >20% total body surface area 77 Period A: 4/5 (80%)
Period B: 1/3 (33.3%)
Manesh et al.21 2019 Retrospective cohort study Single-center September 2005–September 2015 India Tertiary Patients with culture proven mucormycosis
Paranasal sinuses (73.9%), MSK (15.2%)
184 Overall mortality: 57/184 (30.97%)
Mortality in patients with hematological conditions:16/28 (57.14%)
Marty et al.36 2016 Single-arm open-label trial with matched case-control analysis Multi-center April 2008–June 2013 USA, Germany, France, Russia, Belgium, India, Israel, Czech Republic, Brazil, Thailand, Lebanon, and Switzerland Tertiary Adult patients with mucormycosis
Pulmonary only (27%), pulmonary and other organs (32%), non-pulmonary disease (41%)
37 in the single-arm open-label trial33 amphotericin B-treated matched controls Isavuconazole
Day-42 crude all-cause mortality primary treatment: 7/21 (33%)
Day-42 crude all-cause mortality refractory group: 5/11 (45%)
Day-42 crude all-cause mortality intolerant to other antifungal agents: 2/5 (40%)
Day-84 crude all-cause mortality primary treatment: 9/21 (43%)
Day-84 crude all-cause mortality refractory group: 5/11 (45%)
Day-84 crude all-cause mortality intolerant to other antifungal agents: 2/5 (40%)
Weighted all-cause mortality: 33% (13.2–53.5%)
 
Amphotericin B
Day-42 crude all-cause mortality primary treatment: 13/33 (39%)
Weighted all-cause mortality: 41% (20.2%–62.3%)
Millon et al.34 2016 Retrospective cohort study Multi-center January 2012–December 2014 France Tertiary Adult patients
Pulmonary (n = 17), disseminated (n = 14), ROC (n = 8), cutaneous (n = 4), GIT (n = 1)
44 Mortality Day 28: 27/44 (61%)
Mortality Day 84: 32/44 (72%)
Pana et al.31 2016 Retrospective review of prospectively collected cases Multi-center 2005–2014 15 countries (54 in European and 9 in non-European countries) Not stated Pediatric patients
Disseminated (38.1%), pulmonary (19%), skin and soft tissue (19%), paranasal sinuses/sino-orbital (15.8%), ROC (7.5%)
63 Crude mortality, overall: 21 (33.3%)
Patel et al.26 2020 Prospective cohort study Multi-center January 1, 2016–September 30, 2017 India Tertiary Adults with proven mucormycosis
ROC (67.7%), pulmonary (13.3%), cutaneous (1.0.5%), other (8.5%)
485 90-day mortality: 242/465 (52.0%)
Prakash et al.6 2019 Prospective cohort study Multi-center January 2013–December 2015 India Tertiary Children and adults with mucormycosis
ROC (63.9%), pulmonary (12.9%), cutaneous (9.5%), GIT (6.4%), renal (5.4%), other (1.8%)
388 Overall: 129/276 (46.7%)
Salmanton-Garcia et al.25 2020 Retrospective review of prospectively collected cases Multi-center 1997–2019 Multiple: mostly from India (n = 30, 16.1%), the United States (n = 24, 12.9%), Spain (n = 21, 11.3%), and Germany (n = 19, 10.2%) Not stated Adults and children with mucormycosis
Disseminated (18.2%), eye (9.1%)
22 Day 42: 7/22 (31.8%)
Overall: 11/22 (50%)
Attributable: 8/11 (72.7%)
Van den Nest et al.15 2021 Retrospective cohort study Single-center January 2009–August 2017 Austria Tertiary Children and adults with invasive or localized filamentous fungi
Pulmonary (n = 11), disseminated (n = 4), heart (n = 2), CNS (n = 1)
18 30-day mortality: 9/11 (81.8%; 95% CI 55.8%–97.2%)
90-day mortality: 10/11 (90.9%; 95% CI 66.7%–99.5%)

n/N, number that died/number included in study; ROC, rhino-orbital-cerebral; ICU, intensive care unit; USA, United States of America; MSK, musculoskeletal system; GIT, gastrointestinal tract; CI, confidence interval; CNS, central nervous system.

^Infection sites tabulated if identified for mucormycosis in the study

*Primary cutaneous: face (44.4%), leg (33.3%); forearm (11.1%), simultaneous thorax and leg (5.5%), and ear and neck (5.5%).

#

Secondary cutaneous: face (65.9%), nose and palate (20.6%), gum and palate (11.4%), ear and neck (1.03%), disseminated (1.03%), and organs affected as part of disseminated disease: soft tissue and wounds (n = 4), stomach (n = 1).