Research article | Open | Open Peer Review | Published:
Invasive fungal infection among hematopoietic stem cell transplantation patients with mechanical ventilation in the intensive care unit
BMC Infectious Diseasesvolume 12, Article number: 44 (2012)
Invasive fungal infection (IFI) is associated with high morbidity and high mortality in hematopoietic stem cell transplantation (HSCT) patientsThe purpose of this study was to assess the characteristics and outcomes of HSCT patients with IFIs who are undergoing MV at a single institution in Taiwan.
We performed an observational retrospective analysis of IFIs in HSCT patients undergoing mechanical ventilation (MV) in an intensive care unit (ICU) from the year 2000 to 2009. The characteristics of these HSCT patients and risk factors related to IFIs were evaluated. The status of discharge, length of ICU stay, date of death and cause of death were also recorded.
There were 326 HSCT patients at the Linkou Chang-Gung Memorial Hospital (Taipei, Taiwan) during the study period. Sixty of these patients (18%) were transferred to the ICU and placed on mechanical ventilators. A total of 20 of these 60 patients (33%) had IFIs. Multivariate analysis indicated that independent risk factors for IFI were admission to an ICU more than 40 days after HSCT, graft versus host disease (GVHD), and high dose corticosteroid (p < 0.01 for all). The overall ICU mortality rate was 88% (53 of 60 patients), and was not significantly different for patients with IFIs (85%) and those without IFIs (90%, p = 0.676).
There was a high incidence of IFIs in HSCT patients requiring MV in the ICU in our study cohort. The independent risk factors for IFI are ICU admission more than 40 days after HSCT, GVHD, and use of high-dose corticosteroid.
Hematopoietic stem cell transplantation (HSCT) is a treatment option for malignant and non-malignant hematological disorders such as leukemia, lymphoma, myelodysplastic syndrome, and aplastic anemia. Despite improvements in HSCT, its widespread adoption has been limited due to the high rate of severe complications associated with the toxicity of the conditioning regimen, immunosuppression, and graft-versus-host disease (GVHD) . These complications are commonly related to the underlying illness and often require admission to an intensive care unit (ICU) [2, 3]. More than 60% of HSCT recipients are admitted to an ICU, and these patients have very poor prognosis [4, 5]. Although the mortality rate of HSCT recipients admitted to the ICU has declined in the past two decades, it still exceeds 80% for patients on mechanical ventilation (MV) .
Invasive fungal infections (IFIs) are increasingly diagnosed in critically ill HSCT patients. The main risk factors for an IFI are advanced age, use of an unmatched donor, neutropenia, acute GVHD, underlying disease, corticosteroid therapy, and duration of fungemia . Other risk factors for serious fungal infection are the nature of the critical illness, use of immunosuppressive therapy, presence of neutropenia, use of multiple broad-spectrum antibiotics, use of total parenteral nutrition, and presence of an indwelling catheter . Despite advances in HSCT procedures, improved prophylactic antifungal agents, and better ICU care, mortality and morbidity remain major concerns for HSCT patients with IFIs .
HSCT recipients with respiratory failure who need MV have increased risk of transplant-related morbidity and mortality, but few reports have examined the association of IFI and in these patients. The purpose of this study was to assess the characteristics and outcomes of HSCT patients with IFIs who are undergoing MV at a single institution in Taiwan.
Patient information and data collection
A total of 326 adult patients underwent HSCT in Linkou Chang-Gung Memorial Hospital (Taipei, Taiwan) between January 2000 and December 2009. Four patients whose families declined ICU admission and two patients who died before ICU admission were excluded. For patients with multiple ICU admissions during the study period, only the first admission episode was analyzed. Ultimately, a total of 60 HSCT patients who were undergoing mechanical ventilation (MV) and admitted to the medical ICU during the study period were enrolled. The Institutional Review Board and the Chang Gung Medical Foundation (IRB no. 99-2134B) approved this study. Consent was waived due to the retrospective nature of the study.
The medical records of 60 patients were retrospectively reviewed. On the first day of ICU admission, we recorded patient age, gender, underlying disease, date and type of transplantation (autologous or allogeneic), stem cell source (bone marrow or peripheral blood stem cells), laboratory analyses, hemodynamic status, renal and hepatic function, episodes of concurrent GVHD, cytomegalovirus (CMV) infection, and corticosteroid use. The acute physiology and chronic health evaluation (APACHE) II score and the sequential organ failure assessment (SOFA)  score were calculated for each patient within the first 24 h of ICU admission.
For patients with IFIs, we recorded the clinical characteristics, cytological or histological results, mean duration of diagnosis after ICU admission, and treatment. We also evaluated the stem cell source, donor type, presence of acute or chronic GVHD, CMV infection, neutrophil count, bacteremia, and corticosteroid use in all patients. The status of discharge, length of ICU stay, date of death, and cause of death were also recorded.
Each IFI patient was classified as having "proven IFI", "probable IFI", or "possible IFI" based on criteria of the European Organization for Research and Treatment of Cancer/Mycoses Study Group (EORTC/MSG) . In brief, proven IFI was diagnosed by serologic analysis, microscopic analysis, and culture; probable IFI was diagnosed by host, clinical criteria, and mycological criteria; and possible IFI was diagnosed by the same criteria as probable IFI, except that mycological criteria were not used. The day on which the second positive diagnostic test was performed was defined as the day of IFI diagnosis. When an IFI was diagnosed by surgical lung biopsy or trans-bronchial lung biopsy, the day of diagnosis was defined as the day of the first clinical suspicion of IFI. IFI was defined as an early infection if it occurred within 40 days after HSCT, and was otherwise defined as a late infection. Previous studies have used this cutoff date as an indication of the immediate post-engraftment period .
Acute GVHD was defined as GVHD that occurred within 100 days after myeloablative chemotherapy . The severity of acute GVHD in the three main target organs (skin, liver, gastrointestinal tract) was assigned stage 1 to 4 based on accepted criteria . Chronic GVHD is determined by a 0- to 3-point score (none, mild, moderate, severe) that reflects the clinical effect in various organs including skin, liver, eyes, mouth, respiratory tract, and esophagus .
Cytomegalovirus (CMV) infection was diagnosed by positive culture and characteristic pathological findings in specimens from a surgical lung biopsy or bronchoalveolar lavage. Neutropenia was diagnosed as a neutrophil count less than 500 cells/mL for more than 10 days. Concurrent bacteremia was diagnosed if bacteria were isolated from blood culture within one week of the diagnosis of IFI. High dose corticosteroid use was defined as more than 0.3 mg/kg/day prednisolone for more than three weeks.
Data were analyzed with SPSS 13.0 (SPSS Inc. Chicago, II, USA). The characteristics of with and without IFIs were compared by a Chi-square test for categorical variables and by an independent t-test for continuous variables. If the cells of a 2 × 2 table had an expected count less than five, Fisher's Exact Test was used. Risk factors for IFI were initially assessed by univariate analysis. Variables that were statistically significant (p < 0.05) in the univariate analysis were included in a multivariate analysis by a multiple logistic regression based on the backward elimination of data. All statistical tests were two-tailed and a p-value less than 0.05 was considered statistically significant.
A total of 326 patients underwent HSCT at our institution during the study period, and 66 of these patients had respiratory failure before ICU admission that necessitated MV. Six of those patients were excluded because they declined ICU admission or died before admission. Table 1 shows the baseline characteristics of the 60 enrolled patients.
A total of 20 of these 60 HSCT patients undergoing MV had IFIs (33%). Table 2 shows the basic characteristics of patients with and without IFIs. Five of the 20 patients diagnosed with IFIs were diagnosed within 30 days after HSCT, four patients were diagnosed between 30 and 100 days after HSCT, and 11 patients were diagnosed more than 100 days after HSCT. Patients with IFIs were significantly younger than those without IFIs (30 vs. 37 yrs., p = 0.024). IFI patients were significantly more likely to be diagnosed with GVHD and to have received high dose corticosteroid therapy (94% vs. 52%, p = 0.003 and 65% vs. 25%, p = 0.003, respectively). In addition, the APACHE II and SOFA scores were significantly lower in patients with IFIs (21.6 vs. 26.7, p = 0.014 and 10.5 vs. 12.8, p = 0.02, respectively). The overall ICU mortality rate was 88% (53/60), and was not significantly different between the two groups (85% vs. 90%).
Table 3 shows the results of our multivariate analysis of variables associated with IFIs. The results indicate that ICU admission more than 40 days after HSCT, diagnosis of GVHD, and use of high dose corticosteroid were significantly and independently associated with IFIs.
The average time of IFI diagnosis was four days after ICU admission and the range was one to seven days. Figure 1 shows the diagnostic categories and characteristics of the 20 IFI patients. Four patients had proven IFIs, and 3 of these patients had Aspergillus and 1 patient had Candida. Eleven patients had probable IFIs, and 4 of these patients had Aspergillus, 5 patients had Candida, and 2 patients had other fungi. Five patients had possible IFIs, and all 5 patients had Aspergillus.
All 20 patients with IFIs had lung involvement, and two patients had concurrent central nervous system infection by Aspergillus. All 60 of the HSCT patients received empiric treatment with fluconazole if neutropenia was diagnosed. Aspergillus spp. was the most common isolate (12 of 20 patients). All patients with proven IFI and possible IFI died. Only three of the 20 patients with probable IFI survived, one with probable Aspergillus who was treated with amphotericin B, and two with probable Candida who were treated with fluconazole. For the three IFI patients who survived, one had Aspergillus flavus and the other two had Candida spp. other than C. tropicalis or C. albicans. Among the 17 IFI patients who died, the causes of death were multiple organ failure (12 patients), septic shock (3 patients), and profound hypoxemia (2 patients).
The major findings of this study were that HSCT patients undergoing MV in the ICU had a high incidence of IFI (33%) and high ICU mortality (88%). Patients with IFIs had a significantly longer duration from HSCT to ICU admission, higher percentage of GVHD, and greater use of high-dose corticosteroid use than patients without IFIs. Although univariate analysis indicated that IFI patients had lower APACHE II and SOFA scores, multivariate analysis indicated that these were not independently associated with IFI. Moreover, the ICU mortality rate was similar for patients with and without IFIs.
Several previous studies have reported high mortality rates in HSCT recipients who were admitted to ICUs. In particular, Soubani reported that intubated HSCT patients had an ICU mortality rate of nearly 100% before 1990, but that the mortality rate decreased to 61-67% in more recent years . The mortality rate of these patients was directly related to the number of organ system failures and use of MV rather than their status as HSCT recipients [4, 6]. Other research reported that early initiation of noninvasive positive ventilation decreased the likelihood of invasive endotracheal intubation, and can improve the survival rate of HSCT patients with respiratory failure . The high ICU mortality rate in the present study (88%) may be partially explained by the fact that all enrolled patients were receiving invasive MV upon ICU admission.
Previous reports indicated that impaired cell-mediated immunity and use of immunosuppressants to treat GVHD led to CMV reactivation in HSCT patients [14, 15]. In particular, CMV reactivation was identified as a significant independent risk factor for HSCT patients with IFIs during the early post-engraftment phase [14, 15]. The HSCT patients undergoing MV with IFIs in the present study also had higher percentage of CMV infection than those without IFIs (7 of 20, 35% vs. 6 of 40, 15%, respectively), although this difference was not statistically significant.
Previous studies reported that the risk factors for IFI in HSCT recipients were presence of an underlying disease, advanced age, donor type, GVHD, and use of corticosteroids [16–18]. Moreover, higher grade GVHD and higher dose of corticosteroid were associated with increased likelihood of an IFI [19, 20]. Other studies reported that neutropenia and use of immunosuppressants to treat GVHD were associated with IFI [21, 22]. The presence of neutropenia increases the risk of developing bacterial or fungal infections. During the neutropenic period, HSCT patients have increased risk of developing severe sepsis, septic shock, and multiple organ failure, making it necessary for more intensive care that includes MV. However, the present study of HSCT patients undergoing MV indicated that significant risk factors for IFI were GVHD and use of high-dose corticosteroid, but not neutropenia. The very high overall rate of neutropenia in our severely ill patients (80%) may partially explain why there was no significant difference in neutropenia between patients with and without IFIs.
During our study period, 7 of 326 HSCT patients were admitted to the ICU without MV. Among these 7 non-ventilated critically ill patients, 4 patients had IFIs (57%) and all 4 of these patients were diagnosed with possible IFI by Aspergillus spp. following ICU admission more than 40 days after HSCT. Two of these 4 patients died. Clearly, a larger number of patients are needed to establish the influence of IFI on the outcome of non-ventilated critically ill HSCT patients. A previous study reported that IFIs in HSCT patients differed according to the time of infection after HSCT . IFI cases that occurred within 40 days of HSCT were predominantly Candida infections and were more common in patients with active hematological disease, longer duration of neutropenia, and severe GVHD [6, 14]. IFI cases that occurred more than 40 days after HSCT were predominantly Aspergillus infections, and were more common in patients with mismatched related donor transplants, severe GVHD, and use of high-dose corticosteroid [6, 14]. In the present study, IFI was diagnosed a mean of 209 days after HSCT, during the late post-engraftment phase. The use of a non-myeloablative conditioning regimen and granulocyte-colony stimulation factor (G-CSF) may improve the transplantation success and reduce the duration of neutropenia. Furthermore, these improvements appeared to decrease the incidence of early IFI, but increase the incidence of late IFI.
The GITMO (Gruppo Italiano Trapianto di Midollo Osseo) study reported that Aspergillosis accounted for 80% of invasive fungal infections in HSCT patients . In our patients with IFIs, 60% (12 of 20 patients) had Aspergillosis, and Aspergillus flavus was the most common species (3 of 11 patients). In the early 1990s, Candida albicans accounted for about two-thirds of Candida infections, but this decreased to about 50% by the end of the last decade . Our results indicated that Candida albicans was the most isolated species of Candida (50%, 3 of 6 patients).
HSCT patients who have IFIs have poor prognosis, and the overall mortality rate of our HSCT patients undergoing MV was 88%. Our results also indicated similar ICU mortality rates in patients with and without IFIs. Thus, the presence of an IFI had no further impact on the already dismal prognosis of HSCT patients undergoing MV.
There were three major limitations in our study. First, we included patients who were diagnosed with "possible IFI" because of the difficulty in establishing a proven or probable diagnosis. It is possible that some of these "possible IFI" patients did not actually have IFIs. If so, then the differences between the two groups may have been reduced. Second, our study was retrospective and was performed at a single tertiary care medical center, so the findings have limited generalizability. Third, antifungal azoles and echinocandins have only been available in the last five years at our institute, so other populations with longer histories of azole and echinocandin use may have different results.
HSCT patients undergoing MV in the ICU had a high rate of IFI and had an extremely high rate of mortality. The risk factors for IFI in HSCT patients undergoing MV were long time from HCST to ICU admission, presence of GVHD, and use of high-dose corticosteroid. Recognition of risk factors for an IFI and early use of effective antifungal agents that can treat Aspergillus and fluconazole-resistant Candida spp. may provide better outcomes for HSCT patients with IFIs.
Hematopoietic stem cell transplantation (HSCT) patients undergoing mechanical ventilation (MV) in the intensive care unit (ICU) had a high rate of invasive fungal infection (IFI) and an extremely high rate of mortality.
The risk factors for IFI in HSCT patients undergoing MV were late ICU admission after HSCT, GVHD, and use of high dose corticosteroid.
In our study cohort, Aspergillus was the primary cause of IFI in and infection mostly occurred during the late post-engraftment phase.
Acute Lymphoid Leukemia
Acute Myeloid Leukemia
- APACHE II:
Acute Physiology and Chronic Health Evaluation II
Bone Marrow Transplantation
Chronic Myeloid Leukemia
European Organization for Research and Treatment of Cancer/Mycoses Study Group
Granulocyte-Colony Stimulation Factor
GRUPPO Italiano Trapianto di Midollo Osseo
Hematopoietic Stem Cell transplantation
Invasive Fungal Infection
Intensive Care Unit
Peripheral Blood Stem Cell transplantation
Sequential Organ Failure Assessment.
Aksu G, Ruhi MZ, Akan H, Bengisun S, Ustun C, Arslan O, Ozenci H: Aerobic bacterial and fungal infections in peripheral blood stem cell transplants. Bone Marrow Transplant. 2001, 27: 201-205. 10.1038/sj.bmt.1702739.
Yang TM, Wang PN, Kao KC, Huang CC, Tsai YH, Hsieh MJ: Outcome of hematopoietic stem cell recipients who were mechanically ventilated and admitted to intensive care units. J Formos Med Assoc. 2007, 106: 295-301. 10.1016/S0929-6646(09)60255-2.
Afessa B, Azoulay E: Critical care of the hematopoietic stem cell transplant recipient. Crit Care Clin. 2010, 26: 133-150. 10.1016/j.ccc.2009.09.001.
Huaringa AJ, Leyva FJ, Giralt SA, Blanco J, Signes-Costa J, Velarde H, Champlin RE: Outcome of bone marrow transplantation patients requiring mechanical ventilation. Crit Care Med. 2000, 28: 1014-1017. 10.1097/00003246-200004000-00017.
Hilbert G, Gruson D, Vargas F, Valentino R, Gbikpi-Benissan G, Dupon M, Reiffers J, Cardinaud JP: Noninvasive ventilation in immunosuppressed patients with pulmonary infiltrates, fever, and acute respiratory failure. N Engl J Med. 2001, 344: 481-487. 10.1056/NEJM200102153440703.
Soubani AO: Critical care considerations of hematopoietic stem cell transplantation. Crit Care Med. 2006, 34: S251-S267. 10.1097/01.CCM.0000231886.80470.B6.
Marr KA: Fungal infections in hematopoietic stem cell transplant recipients. Med Mycol. 2008, 46: 293-302. 10.1080/13693780701885552.
Vincent JL, Moreno R, Takala J, Willatts S, De Mendonca A, Bruining H, Reinhart CK, Suter PM, Thijs LG: The SOFA (Sepsis-related Organ Failure Assessment) score to describe organ dysfunction/failure. On behalf of the Working Group on Sepsis-Related Problems of the European Society of Intensive Care Medicine. Intensive Care Med. 1996, 22: 707-710. 10.1007/BF01709751.
De Pauw B, Walsh TJ, Donnelly JP, Stevens DA, Edwards JE, Calandra T, Pappas PG, Maertens J, Lortholary O, Kauffman CA, et al: Revised definitions of invasive fungal disease from the European Organization for Research and Treatment of Cancer/Invasive Fungal Infections Cooperative Group and the National Institute of Allergy and Infectious Diseases Mycoses Study Group (EORTC/MSG) Consensus Group. Clin Infect Dis. 2008, 46: 1813-1821. 10.1086/588660.
Bjorklund A, Aschan J, Labopin M, Remberger M, Ringden O, Winiarski J, Ljungman P: Risk factors for fatal infectious complications developing late after allogeneic stem cell transplantation. Bone Marrow Transplant. 2007, 40: 1055-1062. 10.1038/sj.bmt.1705856.
Glucksberg H, Storb R, Fefer A, Buckner CD, Neiman PE, Clift RA, Lerner KG, Thomas ED: Clinical manifestations of graft-versus-host disease in human recipients of marrow from HL-A-matched sibling donors. Transplantation. 1974, 18: 295-304. 10.1097/00007890-197410000-00001.
Martin PJ, Nelson BJ, Appelbaum FR, Anasetti C, Deeg HJ, Hansen JA, McDonald GB, Nash RA, Sullivan KM, Witherspoon RP, et al: Evaluation of a CD5-specific immunotoxin for treatment of acute graft-versus-host disease after allogeneic marrow transplantation. Blood. 1996, 88: 824-830.
Filipovich AH, Weisdorf D, Pavletic S, Socie G, Wingard JR, Lee SJ, Martin P, Chien J, Przepiorka D, Couriel D, et al: National Institutes of Health consensus development project on criteria for clinical trials in chronic graft-versus-host disease: I. Diagnosis and staging working group report. Biol Blood Marrow Transplant. 2005, 11: 945-956. 10.1016/j.bbmt.2005.09.004.
Pagano L, Caira M, Nosari A, Van Lint MT, Candoni A, Offidani M, Aloisi T, Irrera G, Bonini A, Picardi M, et al: Fungal infections in recipients of hematopoietic stem cell transplants: results of the SEIFEM B-2004 study-Sorveglianza Epidemiologica Infezioni Fungine Nelle Emopatie Maligne. Clin Infect Dis. 2007, 45: 1161-1170. 10.1086/522189.
Garnacho-Montero J, Amaya-Villar R, Ortiz-Leyba C, Leon C, Alvarez-Lerma F, Nolla-Salas J, Iruretagoyena JR, Barcenilla F: Isolation of Aspergillus spp. from the respiratory tract in critically ill patients: risk factors, clinical presentation and outcome. Crit Care. 2005, 9: R191-R199. 10.1186/cc3488.
Alangaden GJ, Wahiduzzaman M, Chandrasekar PH: Aspergillosis: The most common community-acquired pneumonia with gram-negative Bacilli as copathogens in stem cell transplant recipients with graft-versus-host disease. Clin Infect Dis. 2002, 35: 659-664. 10.1086/342061.
Cornillet A, Camus C, Nimubona S, Gandemer V, Tattevin P, Belleguic C, Chevrier S, Meunier C, Lebert C, Aupee M, et al: Comparison of epidemiological, clinical, and biological features of invasive aspergillosis in neutropenic and nonneutropenic patients: a 6-year survey. Clin Infect Dis. 2006, 43: 577-584. 10.1086/505870.
Patterson TF, Kirkpatrick WR, White M, Hiemenz JW, Wingard JR, Dupont B, Rinaldi MG, Stevens DA, Graybill JR: Invasive aspergillosis. Disease spectrum, treatment practices, and outcomes. I3 Aspergillus Study Group. Medicine (Baltimore). 2000, 79: 250-260. 10.1097/00005792-200007000-00006.
Ascioglu S, Rex JH, de Pauw B, Bennett JE, Bille J, Crokaert F, Denning DW, Donnelly JP, Edwards JE, Erjavec Z, et al: Defining opportunistic invasive fungal infections in immunocompromised patients with cancer and hematopoietic stem cell transplants: an international consensus. Clin Infect Dis. 2002, 34: 7-14. 10.1086/323335.
Enoch DA, Ludlam HA, Brown NM: Invasive fungal infections: a review of epidemiology and management options. J Med Microbiol. 2006, 55: 809-818. 10.1099/jmm.0.46548-0.
Soubani AO, Kseibi E, Bander JJ, Klein JL, Khanchandani G, Ahmed HP, Guzman JA: Outcome and prognostic factors of hematopoietic stem cell transplantation recipients admitted to a medical ICU. Chest. 2004, 126: 1604-1611. 10.1378/chest.126.5.1604.
Garcia-Vidal C, Upton A, Kirby KA, Marr KA: Epidemiology of invasive mold infections in allogeneic stem cell transplant recipients: biological risk factors for infection according to time after transplantation. Clin Infect Dis. 2008, 47: 1041-1050. 10.1086/591969.
Girmenia C, Barosi G, Aversa F, Bacigalupo A, Barbui T, Baronciani D, Bosi A, Candoni A, Locasciulli A, Locatelli F, et al: Prophylaxis and treatment of invasive fungal diseases in allogeneic stem cell transplantation: results of a consensus process by Gruppo Italiano Trapianto di Midollo Osseo (GITMO). Clin Infect Dis. 2009, 49: 1226-1236. 10.1086/605665.
Pfaller MA, Diekema DJ: Epidemiology of invasive candidiasis: a persistent public health problem. Clin Microbiol Rev. 2007, 20: 133-163. 10.1128/CMR.00029-06.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/12/44/prepub
We thank the nursing staff of the medical ICUs in Linkuo Chang Gung Memorial Hospital for their help in completing this study.
The authors declare that they have no competing interests.
CYH and KCK conceived and designed the study and wrote the article. PNW recruited patients. The study was performed by HCH, CCH, MJH, CHC, JYF, LFL, and YHT. The data was coordinated and analyzed by CTY. All the authors contributed to, read, and approved the final manuscript.
Chen-Yiu Hung, Kuo-Chin Kao contributed equally to this work.
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About this article
- Invasive fungal infection (IFI)
- Hematopoietic stem cell transplantation (HSCT)
- Intensive care unit (ICU)
- Outcome assessment
- Risk factor