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Invasive non-Aspergillus mold infections in transplant recipients, United States, 2001-2006.

Invasive mold infections are a major source of illness and death in transplant recipients. Non-Aspergillus invasive infections are of particular concern because of the following factors: the difficulty in distinguishing them clinically from Aspergillus spp. infections and from each other; their progressive and aggressive course; and the intrinsic resistance of many of these fungi to several antimicrobial agents, including voriconazole. Recent reports have described an increase at some medical centers in non-Aspergillus mold infections, particularly mucormycosis (formerly zygomycosis), often in persons receiving antifungal agents that have activity against Aspergillus spp. (1-4).

Most reports have come from single institutions and might not be broadly representative of general trends. A comprehensive look at the modern epidemiology of these infections, including trends at multiple sites, can increase understanding of their public health implications. The Transplant-Associated Infection Surveillance Network (TRANSNET), a multicenter network of 23 academic tertiary care medical centers in the United States, performed prospective surveillance for invasive fungal infections (IFIs) during 2001-2006 (5-7). We analyzed the uniquely comprehensive TRANSNET cohort for epidemiology, patient demographics, clinical features, and outcomes of infections caused by the most common non-Aspergillus invasive molds detected: those of the order Mucorales, Fusarium spp., and Scedosporium spp.


Study personnel based at each TRANSNET center reviewed records of patients who had undergone solid organ transplantation (SOT) or hematopoietic cell transplantation (HCT). Each IFI was evaluated to determine whether it met the criteria for a proven or probable IFI as defined by the European Organization for Research and Treatment of Cancer and Mycoses Study Group (EORTC-MSG) (8). Trained personnel at each site completed a detailed case report form for each identified proven and probable IFI. Data included demographics, clinical characteristics, clinical involvement, underlying diseases and conditions, and use of antifungal drugs. Investigators collected clinical data on all HCT recipients in whom an IFI developed, regardless of transplant date. Surveillance began in March 2001 and concluded in March 2006.

Cultures and histopathologic specimens were processed at the participating hospitals. Species were identified by using routine methods at the local laboratories. Fungal isolates were forwarded to the University of Alabama at Birmingham Fungal Reference Laboratory (Birmingham, AL, USA) and the Mycotic Diseases Branch at the Centers for Disease Control and Prevention (Atlanta, GA, USA), where species identification was confirmed by using morphologic and DNA-based methods. Patients in this analysis had an IFI and 1) a culture or histopathologic specimen consistent with Mucorales mold or 2) a culture from a clinical specimen positive for Fusarium spp. or Scedosporium spp. We excluded patients with invasive mold infection for whom diagnostic evidence was inconclusive.

All detected cases, regardless of transplant date, were described (surveillance cohort). In addition, the subset of cases in persons receiving transplants during the surveillance period was included for determination of the incidence of these infections (incidence cohort). Denominator data collected on identified patients undergoing transplant at each site during the surveillance period included date and type of transplant and date of last follow-up and clinical status at that time (alive, had undergone retransplant, IFI, dead). These data were used to calculate transplant-associated 12-month cumulative incidence. Estimated cumulative incidence was based on time to first infection after transplant and accounted for the competing risks for death, relapse of underlying disease, and retransplant. For HCT recipients, overall and transplant-specific 12-month cumulative incidence was calculated for mucormycosis and for fusariosis and scedosporiosis combined. For SOT patients, overall and transplant-specific incidence was estimated only for mucormycosis because of low numbers of scedosporiosis and fusariosis. We estimated cumulative incidence using the cmprisk risk package version 2.2-1 in R version 2.11.1 (

We also explored the change in incidence of mold infections over time among HCT recipients. Because case counts can vary due to increases or decreases in the size of the denominator, we measured the changing epidemiology by estimating the incidence, according to transplant date. To do this, we classified the denominator of all transplant patients into 9 sequential subcohorts according to the 4-month period when the transplant was performed, as described (5,7). Twelve-month cumulative incidence for each of the 9 time periods (i.e., subcohorts) was calculated for mucormycosis and for fusariosis and scedosporiosis combined.

In addition, we attempted to estimate whether the underlying risk for infection in the overall population was changing because of changes in the numbers of allogeneic HCTs. To do this, we calculated the total follow-up time (in person-days) for each transplant type and plotted it for each period. Analysis was limited to the 21 sites that contributed data consistently during May 2002-April 2005, the last period for which complete data were available.


Clinical Description of Cases

Of the 1,208 cases of proven or probable IFI in SOT recipients (7) and the 983 cases in HCT recipients (5) in TRANSNET, we detected 169 cases of Mucorales, Fusarium spp., or Scedosporium spp. infection in 166 transplant recipients, making these molds the most frequently identified molds, after Aspergillus within this patient population. The Mucorales (105 patients) were the most common of these molds, followed by Fusarium spp. (37 patients), and Scedosporium spp. (27 patients). Most cases occurred among HCT recipients (124 [73.4%] patients), compared with 45 (26.6%) cases in SOT recipients (Table 1).

Among the Mucorales, Rhizopus was the most common genus (55 [52.4%] of 105 cases), followed by Mucor (19 [18.1%]) and unspecified Mucorales (10 [9.5%]) (Table 1). F. solani (10 [27.0%] cases) was the most common Fusarium species; however, we detected a large number of unspecified Fusarium spp. (22 [59.5%]). S. apiospermum (19 [70.4%]) and S. prolificans (8 [29.6%]) were the most common Scedosporium species (27 cases).

Site Distribution

Numbers of cases varied by hospital and by region (Table 2). The 3 northeastern hospitals collectively reported 12 (7.1%) cases of non-Aspergillus mold infections during the surveillance period; 7 were caused by Mucorales. The 11 hospitals in the South reported 80 (47.3%) cases, of which 46 were caused by Mucorales. In the Midwest, the 5 participating hospitals detected 51 (30.2%) cases, and the 3 western hospitals detected 26 (15.4%) cases. The total number of Mucorales, Fusarium spp., or Scedosporium spp. infections varied substantially by site, ranging from 0 cases (3 sites) to 31 cases (1 site [18.3% of total cases]). The total number of transplants at each site for which follow-up was conducted as part of TRANSNET also varied widely, ranging from 89 to 2,551 HCTs and from 239 to 2,111 SOTs (Table 2). The median number of cases at a site was 8 (interquartile range 2-11 cases).

Patient Characteristics (Surveillance Cohort)

Of the 169 case-patients, 96 (56.8%) were male, and 141 (91.6%) were white (Table 3); median age was 49 years (range 36-57 years). Proven IFIs comprised 95 (56.2%) cases. Active diabetes at the time of infection, either glucocorticoid-associated or as a preexisting condition, was present among 46 (43.8%) mucormycosis patients, 9 (56.8%) fusariosis patients, and 7 (25.9%) scedosporiosis patients. The overall crude mortality rate at 90 days was 56.6% (90/169).

The lower respiratory tract was the most commonly involved site for all mold illnesses (53.1% of mucormycosis, 38.9% of fusariosis, and 59.3% of scedosporiosis) (Table 3). Disseminated disease (17.4% of all cases) was also frequent (13.3% of mucormycosis, 22.2% of fusariosis, and 25.9% of scedosporiosis).

Of the 124 HCT recipients with 1 of these infections, the most common indication for HCT was acute myelogenous leukemia (35 [28.2%] cases), followed by non-Hodgkin lymphoma (26 [21.0%] cases) (Table 3). Most HCT recipients received a human leukocyte antigen (HLA)-matched, allogeneic graft from a related donor (54 [43.5%] patients), followed by HCT recipients with an unrelated donor (47 [37.9%] patients) (Table 3). In the 60 days before diagnosis of infection, neutropenia was reported in 4 (25.0%) patients with scedosporiosis, 39 (50.6%) with mucormycosis, and 17 (54.8%) with fusariosis. Acute graft-versus-host disease was present in 32 (41.6%) patients with mucormycosis, 7 (22.6%) with fusariosis, and 6 (37.5%) with scedosporiosis.

Of the 45 transplant patients with mold infections who had received an SOT, 19 (42.2%) had received a lung and 12 (26.7%) had received a kidney (Table 3). Twenty-four (54.5%) patients experienced organ rejection in the 30 days before infection occurred.

Many cases occurred early after transplant, but late-onset infection was also prevalent. Among HCT recipients, 67 (54.4%) infections occurred <6 months after transplant; 17 (13.8%) occurred [greater than or equal to] 2 years after transplant (Figure 1). Among SOT recipients, 17 (37.8%) infections occurred within the first 6 months; 15 (33.3%) occurred [greater than or equal to] 2 years after transplant. Median time to IFI for liver transplant recipients was 81 days, compared with 533 for non-liver SOT recipients (p = 0.035).


Exposure to Antifungal Drugs

Voriconazole was the most frequently administered antifungal agent before infection in mucormycosis patients (47 [44.7%]) (Table 4). In contrast, fewer patients with fusariosis (27.0%) or scedosporiosis (11.1%) had received voriconazole (Table 4). Of the 47 patients with mucormycosis who received voriconazole, 28 (59.6%) were receiving voriconazole as prophylaxis, 15 (31.9%) were receiving it as empiric therapy, and 4 (8.7%) were receiving it as treatment for a suspected or other proven fungal infection.

More mucormycosis patients received an amphotericin B formulation after diagnosis (78.1%) than did fusariosis (51.4%) and scedosporiosis (33.3%) patients (Table 4). Patients with fusariosis (20 [54.1%] of 37) and scedosporiosis (15 [55.6%] of 27) most commonly received voriconazole after IFI diagnosis.

Incidence Cohort

Follow-up data were available for 15,820 HCT recipients from 22 sites. Among these, 17% died, 13% experienced relapse, and 1% underwent retransplant in the first 12 months after transplant. Mucormycosis was diagnosed in 44 (0.3%) persons. Overall 12-month cumulative incidence for mucormycosis in HCT recipients was 0.29% (Figure 2). Recipients of an organ or cells from an allogeneic HLA-unrelated donor had the highest 12-month cumulative incidence of mucormycosis at 0.85%; allogeneic HLA-matched related donors had a cumulative incidence of 0.58%; and allogeneic HLA-mismatched related donors had a 12-month cumulative incidence of 0.25% (Figure 2).

Follow-up data were available for 16,457 SOT recipients from 15 sites. Of these, 6% died; 2% of kidney transplant recipients returned to chronic dialysis; and 2% underwent retransplant within 12 months after the transplant. In 12 (0.07%) persons, mucormycosis was diagnosed within the first 12 months after transplant. In SOT recipients, the overall 12-month cumulative incidence of mucormycosis was 0.07% (Figure 3). Patients receiving lung transplants and liver transplants had the highest incidence of mucormycosis (0.18% and 0.16%, respectively). Four Scedosporium spp. (3 lung SOTs, 1 kidney) and 2 Fusarium spp. (1 lung SOT, 1 liver) infections occurred within the first 12 months after transplant (data not shown).


We estimated cumulative incidence for mucormycosis and for Fusarium spp. and Scedosporium spp. infections combined for the 9 subcohorts from May-August 2002 through January-April 2005 (Figure 4). Cohorts ranged from [approximately equal to]1,200 to 1,400 transplant recipients each. Estimated cumulative incidence of Fusarium spp. and Scedosporium spp. infections in the 9 subcohorts did not increase over time. Incidence ranged from 0% during January-April 2004 and September-December 2004 to a high of 0.30% (4 infections) during May-August 2004.

The incidence of mucormycosis in HCT recipients varied, with generally higher incidences in 2003 and 2004 than in 2002. Initially, the 12-month cumulative incidence for mucormycosis was 0.08% (1 infection) for the cohort receiving transplants during May-August 2002. The cumulative incidence was higher for all subsequent cohorts and peaked at 0.69% (9 infections) in the cohort receiving transplants during September-December 2004. In the subsequent cohort that received transplants during January-April 2005, incidence declined to 0.16% (2 infections). These 39 Mucorales infections occurred at 13 of the 21 sites, with these 13 sites contributing 1-7 infections each. The pattern was similar across the 9 subcohorts when we excluded the site with most cases (site D) and limited the analysis to allogeneic transplants only (data not shown). In addition, the total follow-up time of allogeneic HCTs did not appreciably increase (Figure 4). Mucormycosis incidence rates appeared to decrease for the cohorts receiving transplants during the first 4 months (January-April) of each year in the 2003-2005 surveillance period.


We describe the modern epidemiology of common non-Aspergillus invasive mold infections at multiple tertiary care sites throughout the United States. During the TRANSNET surveillance period, the estimated cumulative incidence of mucormycosis among HCT subcohorts receiving transplants in 2003 and 2004 was generally higher than in 2002. Public health officials and clinicians should be aware of these emerging mold infections, particularly in susceptible hosts, such as transplant recipients.

The worrisome possibility of an increase in mucormycosis incidence has gained attention recently, particularly because this disease has an extremely high case-fatality rate (9,10). Most supporting information about the emergence of this mold has come from compilations of case series (11,12), single-center studies (13-15), or registries (16,17). One national study in France used administrative data to demonstrate an increase over a 10-year period (18). In contrast, our analysis is based on a comprehensive database from a surveillance program that included a large number of centers with a broad geographic distribution. Furthermore, all cases were independently evaluated by using standardized case definitions (EORTC-MSG criteria [8]).


Reasons for higher incidence of mucormycosis during 2003 and 2004 are not clear from these data. It is certainly possible that these are natural variations or that changes in practices (e.g., mold-active prophylaxis or immunosuppressive agents) or changes in the at-risk populations could be contributory factors. Although we did not see an increase in the numbers of transplants from allogeneic donors performed at the participating sites during this period, we did not have data on other conditions that increase risk for mucormycosis, such as diabetes mellitus or iron overload conditions. The higher incidence during certain periods did not result from a single institution; nor was it likely to be attributable to surveillance artifact, in which improved detection methods falsely suggest a changing trend because other common non-Aspergillus mold infections did not also increase during this period.


Another issue that has been reported recently is the frequency of breakthrough mucormycosis in patients receiving voriconazole (3,4,19-21). In these reports, progressive mucormycosis developed in patients who were receiving voriconazole for prophylaxis or treatment for another disease, or these patients were at higher risk for mucormycosis than were control populations (2). In our study, voriconazole was the most frequently reported antifungal drug used before mucormycosis developed, although it was used in fewer than half of all patients. The frequency of voriconazole use before development of mucormycosis is striking, especially in the context of these case reports; however, the implication of the broader use of this antifungal drug to the emergence of this mold is far from clear. Experimental models have demonstrated increased virulence of Mucorales after exposure to voriconazole (22), but other reports have noted an increase of this mold before introduction of voriconazole (14,23). In a randomized trial that used voriconazole as a prophylactic agent, incidence of mucormycosis was not higher among the intervention group than in the group who received fluconazole (24), although patients meeting enrollment criteria may not have been at high risk for mucormycosis (25). The increase might not be evidence of a causal relationship between voriconazole and mucormycosis but might instead reflect a parallel increase related to a changing patient risk profile, including patients at higher risk or increased time at risk, mainly through improved posttransplant survival (25). We did find that 1 factor associated with death in mucormycosis patients on bivariate analysis was prior use of voriconazole (data not shown); this finding could indicate that persons receiving voriconazole are more complicated transplant patients and therefore at higher underlying baseline risk for mucormycosis. Because our study did not collect medication data on uninfected controls or on global antimicrobial drug use practices, we were not able to correlate broader voriconazole use to the higher incidence of mucormycosis in this cohort.

We found a high degree of site-to-site variability in the number of cases reported. One hospital contributed 31 cases, 18 of which were caused by Mucorales; this number was nearly double that of the hospital with the second-highest number. No cases were detected at 3 sites. However, the site with 31 cases was also 1 of the sites with the highest number of HCTs performed per year. Whether this variability is a function of environmental or climate conditions, the underlying transplant population at that site, medical practices (e.g., prophylaxis, diagnostic interventions), or a combination of these factors is not known.

The variability in the incidence of infections from Mucorales in HCT recipients over time was also intriguing, with the lowest incidence in the cohorts who received transplants during the first 4 months of the year. One recent report described a similar finding for aspergillosis among HCT recipients (26). Whether this pattern reflects an underlying seasonal risk for mucormycosis is not known. However, a seasonal pattern is feasible; these molds exist in the environment, and environmental and temperature conditions can greatly influence their growth or sporulation (27). Further study of the seasonal risk for rare mold infections such as these most likely necessitates a larger cohort than that from TRANSNET; large national databases, including those using administrative codes, despite their poor predictive values (28), might be promising for estimating trends for such diseases.

Our data corroborate other reports regarding the clinical features of these mold infections (11,29-33). We found that even though most cases occurred soon after transplant, a large number occurred >6 months after transplant. A similar pattern occurs in other mold infections, such as those caused by Aspergillus spp., indicating the need for clinicians to be vigilant about mold infections, particularly a substantial length of time after transplant. Furthermore, we found that the clinical features of these 3 common non-Aspergillus mold infections were similar (with only bloodstream involvement being associated more often with fusariosis, as would be expected) (30). Not surprisingly, the pulmonary system and sinuses were the most common sites of infection for all molds studied, similar to infections caused by Aspergillus spp. These data highlight the similarities in features among mold infections and illustrate the difficulties in differentiating these infections on the basis of clinical features or organ involvement. Because correct treatment depends on the proper isolate identification, these results reinforce the need for major improvements in diagnostic testing, including development of tissue-based molecular identification methods (34,35) to correctly and efficiently identify the causative organism.

Our study had a few limitations. Because we collected data only on proven and probable IFIs (and omitted possible infections), as defined by EORTC-MSG criteria (8), we are likely to have underestimated disease in these populations. In addition, we were not able to systematically determine which, if any, of these infections resulted from donor-derived infection of the allograft. However, routine posttransplant surveillance conducted by transplant clinical teams, in conjunction with the United Network for Organ Sharing, did not indicate any such clusters.

Our large prospective parallel assessment of the modern epidemiology of these emerging, yet uncommon, non-Aspergillus molds demonstrated a generally higher incidence in mucormycosis in 2003 and 2004 than in 2002 in HCT recipients. More comprehensive and long-term surveillance for these emerging rare molds might be warranted to track trends and assess the changing landscape of these infections.


We thank Pallavi Daram, Robert Warren, Beth Deerman, Pamela DeTullio, Deborah Berg, Christine Kane Sanjeet Dadwal, Bernard Tegtmeier, Jane Kriengkauykiat, Mary Ann Clouser, Margaret O'Donnell, Stephen Forman, Cheryl Shoden, Kathleen Hinkle, Kathleen Speck, Mary E. Brandt, Lynette Benjamin, Karen Stamey, Shirley McClinton, S. Arunmohzi Balajee, Rui Kano, Scott Fridkin, Juliette Morgan, Rana Hajjeh, and David Warnock for assistance with this study.

This study was supported through Centers for Disease Control and Prevention Grant 5U01CI000286-05 and grants from Merck & Co., Inc.; Astellas U.S., Inc.; Pfizer, Inc.; Schering-Plough Research Institute; and Enzon Pharmaceuticals, Inc.

Dr Park is a medical officer in the Mycotic Diseases Branch, Centers for Disease Control and Prevention, and leader of the epidemiology team. His research interests include the prevention and epidemiology of fungal infections.


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CME Questions

1. You are preparing a 35-year-old woman for hematopoietic cell transplantation (HCT) from a related donor, and you are concerned with the possibility of a fungal infection following transplantation. Which of the following infections was most common among the current cohort of transplant recipients?

A. Scedosporiosis

B. Mucormycosis

C. Chromoblastomycosis

D. Fusariosis

2. Which of the following statements regarding patient characteristics of individuals with fungal infection in the current study is most accurate?

A. All cases had proven invasive fungal infection

B. The overall 90-day mortality rate exceeded 50%

C. Nearly all patients had neutropenia before fungal infection

D. The prevalence of mucormycosis was highest among recipients of HCT from allogenic human leukocyte antigen mismatched related donors

3. What else should you consider regarding factors associated with fungal infection in the current study?

A. Most mold infections occurred in the gastrointestinal tract

B. Liver transplant was particularly associated with a higher risk for mucormycosis

C. There were no cases of late-onset infection

D. Voriconazole failed to prevent many infections, especially mucormycosis

4. Which of the following statements regarding mucormycosis in the current study is most accurate?

A. Rhizopus was the most common genus

B. Renal transplants were associated with the highest incidence of mucormycosis

C. The annual incidence rates of mucormycosis remained stable during the study period

D. Mucormycosis was most common in the months from January to April
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Author affiliations: Centers for Disease Control and Prevention, Atlanta, Georgia, USA (B.J. Park, K.A. Wannemuehler); University of Alabama at Birmingham Medical Center, Birmingham, Alabama, USA (P.G. Pappas, J.W. Baddley); Duke University Medical Center, Durham, North Carolina, USA (B.D. Alexander); University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA (E.J. Anaissie); University of Wisconsin- Madison, Madison, Wisconsin, USA (D.R. Andes); Stanford University School of Medicine, Stanford, California, USA (J.M. Brown); Mayo Clinic, Jacksonville, Florida, USA (L.M. Brumble); University of Nebraska Medical Center, Omaha, Nebraska, USA (A.G. Freifeld); Tufts Medical Center, Boston, Massachusetts, USA (S. Hadley); University of Iowa Hospital, Iowa City, Iowa, USA (L. Herwaldt); City of Hope National Medical Center, Duarte, California, USA (J.I. Ito); University of Michigan, Ann Arbor, Michigan, USA (C.A. Kauffman); Veterans Affairs Ann Arbor Healthcare System-Medicine, Ann Arbor (C.A. Kauffman); Emory University School of Medicine, Atlanta (G.M. Lyon); Johns Hopkins Medical Institutions, Baltimore, Maryland, USA (K.A. Marr, T.M. Perl); Fred Hutchinson Cancer Research Center, Seattle, Washington, USA (K.A. Marr); University of Minnesota, Minneapolis, Minnesota, USA (V.A. Morrison); Veterans Affairs Medical Center, Minneapolis (V.A. Morrison); Memorial Sloan Kettering Cancer Center, New York, New York, USA (G. Papanicolaou); University of Texas Health Sciences Center, San Antonio, Texas, USA (T.F. Patterson); South Texas Veterans Healthcare System, San Antonio (T.F. Patterson); Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA (M.G. Schuster); Mayo Clinic, Rochester, Minnesota, USA (R. Walker); University of Florida, Gainesville, Florida, USA (J.R. Wingard); National Institutes of Health, Bethesda, Maryland, USA (T.J. Walsh); and MD Anderson Cancer Center, Houston, Texas, USA (D.P. Kontoyiannis)

DOI: 10.3201/eid1710.110087

Address for correspondence: Benjamin J. Park, Centers for Disease Control and Prevention, 1600 Clifton Rd NE, Mailstop C09, Atlanta, GA 30333, USA; email:

All material published in Emerging Infectious Diseases is in the public domain and may be used and reprinted without special permission; proper citation, however, is required.
Table 1. Distribution of Mucorales, Fusarium, and Scedosporium
organisms causing infection in HCT and SOT recipients, as
detected in TRANSNET, United States, 2001-2006 *

 No. (%) patients

Organism HCT SOT Total

Mucorales 77 (62.1) 28 (62.2) 105 (62.1)
 Rhizopus spp. 39 (50.6) 16 (57.1) 55 (52.4)
 Mucor spp. 12 (15.6) 7 (25.0) 19 (18.1)
 Rhizomucor spp. 7 (9.1) 0 7 (6.7)
 Cunninghamella spp. 5 (6.5) 4 (14.3) 9 (8.6)
 Lichtheimia spp. ([dagger]) 3 (3.9) 0 3 (2.9)
 Apophysomyces spp. 1 (1.3) 0 1 (1.0)
 Syncephalastrum spp. 1 (1.3) 0 1 (1.0)
 Unspecified 9 (11.7) 1 (3.6) 10 (9.5)
Genus Fusarium 31 (25.0) 6 (13.3) 37 (21.9)
 F. solani 9 (29.0) 1 (16.7) 10 (27.0)
 F. oxysporum 0 2 (33.3) 2 (5.4)
 F. proliferatum 2 (6.5) 0 2 (5.4)
 F. verticilloides 1 (3.2) 0 1 (2.7)
 Unspecified 19 (61.3) 3 (50.0) 22 (59.5)
Genus Scedosporium 16 (12.9) 11 (24.4) 27 (16.0)
 S. apiospermum 13 (81.3) 6 (54.5) 19 (70.4)
 S. prolificans 3 (18.8) 5 (45.5) 8 (29.6)
Total 124 (73.4) 45 (26.6) 169 (100)

* HCT, hematopoietic cell transplant; SOT, solid organ transplant;
TRANSNET, Transplant-Associated Infection Surveillance Network.

([dagger]) This genus was formerly Absidia.

Table 2. Regional and hospital variability of Mucorales, Fusarium
spp., and Scedosporium spp. invasive infections, as reported in
TRANSNET, United States, 2001-2006 *

US region, No. transplant
([dagger]) recipients
code HCT SOT

 A 608 1,532
 B 245 377
 C 1,107 NA
 D 2,551 NA
 E 646 549
 F 363 NA
 G 523 1,201
 H 342 1,532
 I 808 377
 J 89 728
 K 2,040 239
 L 110 1,210
 M 449 NA
 N 511 NA
 O 970 2,111
 P 1,028 1,391
 Q 361 1,210
 R 315 2,111
 S 546 755
 T 1,512 NA
 U 854 NA
 V 1,019 NA

US region, No. (%) cases
hospital Mucorales, Fusarium Scedosporium Total,
code n = 105 spp., n = 37 spp., n = 27 N = 169

Northeast 7 (6.7) 3 (8.1) 2 (7.4) 12 (7.1)
 A 5 (4.8) 1 (2.7) 1 (3.7) 7 (4.1)
 B 1 (1.0) 2 (5.4) 1 (3.7) 4 (2.4)
 C 1 (1.0) 0 0 1 (0.6)
South 46 (43.8) 23 (62.2) 11 (40.7) 80 (47.3)
 D 18 (17.1) 12 (32.4) 1 (3.7) 31 (18.3)
 E 6 (5.7) 3 (8.1) 6 (22.2) 15 (8.9)
 F 5 (4.8) 3 (8.1) 1 (3.7) 9 (5.3)
 G 4 (3.8) 2 (5.4) 2 (7.4) 8 (4.7)
 H 5 (4.8) 1 (2.7) 1 (3.7) 7 (4.1)
 I 4 (3.8) 0 0 4 (2.4)
 J 3 (2.9) 0 0 3 (1.8)
 K 1 (1.0) 1 (2.7) 0 2 (1.2)
 L 0 1 (2.7) 0 1 (0.6)
 M 0 0 0 0
 N 0 0 0 0
Midwest 35 (33.3) 9 (24.3) 7 (25.9) 51 (30.2)
 O 8 (7.6) 5 (13.5) 4 (14.8) 17 (10.1)
 P 8 (7.6) 2 (5.4) 0 10 (5.9)
 Q 8 (7.6) 0 0 8 (4.7)
 R 5 (4.8) 0 3 (11.1) 8 (4.7)
 S 6 (5.7) 2 (5.4) 0 8 (4.7)
West 17 (16.2) 2 (5.4) 7 (25.9) 26 (15.4)
 T 9 (8.6) 2 (5.4) 4 (14.8) 15 (8.9)
 U 8 (7.6) 0 3 (11.1) 11 (6.5)
 V 0 0 0 0

* TRANSNET, Transplant-Associated Infection Surveillance Network; HCT,
hematopoietic cell transplant; SOT, solid organ transplant; NA, not
available because of nonparticipation in surveillance for this
transplant type.

([dagger]) Northeast: Massachusetts, New York, Pennsylvania; South:
Alabama, Arkansas, Florida, Georgia, Maryland, North Carolina,
Tennessee, Texas; Midwest: Iowa, Michigan, Minnesota, Nebraska,
Wisconsin; West: California, Washington.

Table 3. Characteristics of HCT and SOT patients * with proven or
probable invasive Mucorales, Fusarium spp., or Scedosporium spp.
infection, as reported in TRANSNET, United States, 2001-2006

 Mucorales, Fusarium spp.,
Characteristic no. (%), no. (%),
([double dagger]) n = 105 n = 37

Male sex 58 (56.9) 26 (70.3)
White race 86 (90.5) 34 (94.4)
Proven IFI 61 (58.1) 21 (56.8)
Diabetes mellitus at time of 46 (43.8) 9 (56.8)
 fungal infection
 Prior IFI 23 (21.9) 8 (19.5)
 Prior aspergillosis 17 (16.2) 1 (2.7)
Antemortem clinical involvement
 Pulmonary only 52 (53.1) 14 (38.9)
 Sinus only 12 (12.2) 2 (5.6)
 Skin only 9 (9.2) 3 (8.3)
 Disseminated 13 (13.3) 8 (22.2)
 Rhinocerebral only 3 (3.1) 1 (2.8)
 Other ([paragraph]) 3 (3.1) 6 (16.7)
Death at 90 d 57 (58.2) 18 (51.4)
HCT 77 (73.3) 31 (24.3)
Underlying condition
 ALL 7 (9.1) 1 (3.2)
 AML 21 (27.3) 11 (35.5)
 CML 7 (9.1) 2 (6.5)
 HL 4 (5.2) 1 (3.2)
 NHL 15 (19.5) 8 (25.8)
 AA 3 (3.9) 1 (3.2)
 MM 5 (6.5) 1 (3.2)
 MDS 10 (13) 1 (3.2)
HCT graft donor
 Autologous 8 (10.4) 4 (12.9)
 Allogeneic matched-related 34 (44.2) 13 (41.9)
 Allogeneic mismatched-related 4 (5.2) 4 (12.9)
 Allogeneic unrelated 30 (39) 10 (32.3)
Other characteristics
 Neutropenia (#) 39 (50.6) 17 (54.8)
 Steroids at diagnosis 59 (76.6) 24 (77.4)
 Myeloablative preconditioning 46 (59.7) 18 (58.1)
 Acute GvHD 32 (41.6) 7 (22.6)
 Chronic GvHD 29 (37.7) 14 (45.2)
 Steroid treatment 58 (75.3) 19 (61.3)
 GvHD grade 1 or 2 18 (23.4) 4 (12.9)
 GvHD grade 3 or 4 35 (45.4) 14 (45.2)
 SOT 28 (26.7) 6 (51.4)
Organ transplanted
 Heart 3 (10.7) 1 (16.7)
 Lung 8 (28.6) 2 (33.3)
 Kidney 9 (32.1) 1 (16.7)
 Liver 9 (32.1) 2 (33.3)
Organ rejection within 13 (48.1) 3 (50)
 previous 30 d

Characteristic spp., no. (%), Total, no. (%),
([double dagger]) n = 27 N = 169

Male sex 12 (44.4) 96 (57.8)
White race 21 (91.3) 141 (91.6)
Proven IFI 13 (48.1) 95 (56.2)
Diabetes mellitus at time of 7 (25.9) 62 (36.7)
 fungal infection
 Prior IFI 10 (24.4) 41 (24.3)
 Prior aspergillosis 4 (14.8) 22 (13.0)
Antemortem clinical involvement
 Pulmonary only 16 (59.3) 82 (50.9)
 Sinus only 1 (3.7) 15 (9.3)
 Skin only 0 12 (7.5)
 Disseminated 7 (25.9) 28 (17.4)
 Rhinocerebral only 0 4 (2.5)
 Other ([paragraph]) 2 (7.4) 11 (6.8)
Death at 90 d 15 (57.7) 90 (56.6)
HCT 16 (59.3) 124 (73.4)
Underlying condition
 ALL 2 (12.5) 10 (8.1)
 AML 3 (18.8) 35 (28.2)
 CML 4 (25) 13 (10.5)
 HL 0 5 (4)
 NHL 3 (18.8) 26 (21)
 AA 0 4 (3.2)
 MM 1 (6.3) 7 (5.6)
 MDS 1 (6.3) 12 (9.7)
HCT graft donor
 Autologous 0 12 (9.7)
 Allogeneic matched-related 7 (43.8) 54 (43.5)
 Allogeneic mismatched-related 2 (12.5) 10 (8.1)
 Allogeneic unrelated 7 (43.8) 47 (37.9)
Other characteristics
 Neutropenia (#) 4 (25) 60 (48.4)
 Steroids at diagnosis 14 (87.5) 97 (78.2)
 Myeloablative preconditioning 11 (68.8) 75 (60.5)
 Acute GvHD 6 (37.5) 45 (36.3)
 Chronic GvHD 7 (43.8) 50 (40.3)
 Steroid treatment 13 (81.3) 90 (72.6)
 GvHD grade 1 or 2 4 (25.0) 26 (21.0)
 GvHD grade 3 or 4 5 (31.3) 54 (43.5)
 SOT 11 (40.7) 45 (26.6)
Organ transplanted
 Heart 0 4 (8.9)
 Lung 9 (81.8) 19 (42.2)
 Kidney 2 (18.2) 12 (26.7)
 Liver 0 11 (24.4)
Organ rejection within 8 (72.7) 24 (54.5)
 previous 30 d

* Includes 3 patients with 2 infections each; 2 patients had separate
Fusarium and Scedosporium infections; 1 person had separate
mucormycosis and scedosporiosis.

([dagger]) Denominators vary because of missing data. HCT,
hematopoietic cell transplant; SOT, solid organ transplant; TRANSNET,
Transplant-Associated Infection Surveillance Network; IFI, invasive
fungal infection; ALL, acute lymphocytic leukemia; AML, acute
myelogenous leukemia; CML, chronic myelogenous leukemia; HL, Hodgkin
lymphoma; NHL, non-Hodgkin lymphoma; AA, aplastic anemia; MM, multiple
myeloma; MDS, myelodysplastic syndrome; GvHD, graft-versus-host

([double dagger]) Median ages (interquartile ranges) are as follows:
patients with Mucorales infection, 51 y (39-57 y); patients with
Fusarium spp. infection, 45 y (32-59 y); patients with Scedosporium
spp. infection, 46 y (38-59 y); and all patients, 49 y (36-57 y).

([section]) Antemortem organ involvement was classified according to
recorded sites of infection; disseminated infection was defined as
infection in noncontiguous organs.

([paragraph]) Esophageal (1 Scedosporium spp.); heart (3 Mucorales);
blood (6 Fusarium spp., 1 Scedosporium sp.).

(#) Defined as an absolute neutrophil count <500/[micro]L, within 60 d
before development of invasive fungal infection.

Table 4. Antifungal medications received before and after diagnosis of
invasive mold infection, TRANSNET data, United States, 2001-2006 *

 Mucorales, no. Fusarium spp.,
Antifungal drug (%), n = 105 no. (%), n = 37

Received before diagnosis
 Amphotericin B ([dagger]) 7 (6.7) 5 (13.5)
 Fluconazole 35 (33.3) 17 (45.9)
 Itraconazole 13 (12.4) 4 (10.8)
 Voriconazole 47 (44.8) 10 (27.0)
 Caspofungin 18 (17.1) 3 (8.1)
 Posaconazole 0 1 (2.7)
Received after diagnosis
 Amphotericin B ([dagger]) 82 (78.1) 19 (51.4)
 Fluconazole 4 (3.8) 0
 Itraconazole 10 (9.5) 2 (5.4)
 Voriconazole 39 (37.1) 20 (54.1)
 Caspofungin 26 (24.8) 12 (32.4)
 Posaconazole 24 (22.9) 3 (8.1)

 Scedosporium spp., Total, no.
Antifungal drug no. (%), n = 27 (%), N = 169

Received before diagnosis
 Amphotericin B ([dagger]) 3 (11.1) 15 (8.9)
 Fluconazole 5 (18.5) 57 (33.7)
 Itraconazole 8 (29.6) 25 (14.8)
 Voriconazole 3 (11.1) 60 (35.5)
 Caspofungin 3 (11.1) 24 (14.2)
 Posaconazole 0 1 (0.6)
Received after diagnosis
 Amphotericin B ([dagger]) 9 (33.3) 110 (65.1)
 Fluconazole 0 4 (2.4)
 Itraconazole 8 (29.6) 20 (11.8)
 Voriconazole 15 (55.6) 74 (43.8)
 Caspofungin 11 (40.7) 49 (29.0)
 Posaconazole 3 (11.1) 30 (17.8)

* TRANSNET, Transplant-Associated Infection Surveillance Network.
Numbers do not total 100% because of concomitant receipt of multiple
antifungal agents.

([dagger]) Any amphotericin B formulation.
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Title Annotation:RESEARCH
Author:Park, Benjamin J.; Pappas, Peter G.; Wannemuehler, Kathleen A.; Alexander, Barbara D.; Anaissie, Eli
Publication:Emerging Infectious Diseases
Date:Oct 1, 2011
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