Skip to main content

Advertisement

Download PDF

Correlation of anti-fungal susceptibility with clinical outcomes in patients with cryptococcal meningitis

BMC Infectious Diseases volume 12, Article number: 361 (2012) Cite this article

Abstract

Background

This study aimed to investigate the correlation of minimum inhibiting concentrations (MICs), obtained by broth micro-dilution, and clinical response in patients with cryptococcal meningitis.

Methods

Using retrospective analyses covering the period 2001–2010, factors affecting clinical therapeutic cure in patients with cryptococcal meningitis 10 weeks after the start of anti-fungal therapy were identified. Specific emphasis was placed on the role of anti-fungal susceptibility.

Results

Of 46 patients with cryptococcal meningitis identified, 21 were cured after 10 weeks of treatment. Overall, 12 strains (26.1%) were resistant to fluconazole (>8 μg/ml) and 8 (17.4%) had an MIC >1 μg/ml for amphotericin B. Twenty-three patients received combination amphotericin B and fluconazole as their initial antifungal therapy, 17 were given amphotericin B only, five received fluconazole only, and one received a combination of amphotericin B and flucytosine. After 2 weeks, all patients received fluconazole (400–600 mg daily for 8 weeks at least, then 200 mg daily thereafter). The presence of isolates resistant to fluconazole (MIC >8 μg/ml; 4.8% vs. 44%, p < 0.01) were statistically significant among patients who were cured. Anti-fungal susceptibility, reflected by fluconazole MIC >8 μg/ml, was an independent predictor of therapeutic cure at 10-week evaluation (OR = 15.7; 95% CI: 1.8-135.9; p = 0.01), but higher MIC of amphotericin B (>1 μg/ml) was not.

Conclusions

The MICs of fluconazole, determined by the CLSI method, may be a potential predictor of therapeutic cure in patients with cryptococcal meningitis.

Peer Review reports

Background

Cryptococcus neoformans is an encapsulated yeast responsible for life-threatening infections, particularly in immuno-compromised patients like those with AIDS [1]. Pharmacologic management usually consists of primary therapy with amphotericin B, with or without flucytosine, followed by maintenance therapy [2]. High rates of fungal persistence and frequent relapse have sparked growing concern among clinicians on the possible emergence of anti-fungal resistance. There are now several published reports of resistance to amphotericin B, fluconazole, or flucytosine in C. neoformans during treatment [3–6]. Most cases involve resistance to fluconazole in the setting of meningitis in AIDS patients after prolonged treatment or prophylaxis [4–6].

Physicians have long sought a laboratory test to predict clinical outcomes in patients with cryptococcosis. The Clinical and Laboratory Standards Institute (CLSI) recently established a reproducible method for testing the susceptibility of C. neoformans to anti-fungal drugs [7]. However, in vitro susceptibility testing methods (including the CLSI method and breakpoints) for Cryptococcus species have not been well-validated [2]. One report concludes that in vitro anti-fungal susceptibility does not predict clinical outcomes in patients with cryptococcosis [8], whereas others report that high minimum inhibiting concentrations (MICs) of fluconazole affect outcomes [9, 10]. Unfortunately, these studies are confounded by selection bias because most of them enrolled AIDS patients and most C. neoformans isolates are susceptible to fluconazole [8–10].

The present study investigated the correlation between the MICs of amphotericin B or fluconazole (obtained by the broth micro-dilution method described in the CLSI document M27-A3) with the clinical responses of cryptococcal meningitis patients, excluding those with AIDS only. In the context of recent emerging non-susceptible strains of C. neoformans, the objective was to validate an in vitro measure that could reliably predict patient response after 10 weeks of initial anti-fungal treatment.

Methods

Patients and setting

Data covering the period January 2001 to December 2010 were retrospectively collected from patients with cerebrospinal fluid (CSF) cultures positive for Cryptococcus neoformans admitted to Kaohsiung Chang Gung Memorial Hospital (KCGMH), a 2300-bed facility serving as a primary care and tertiary referral center in southern Taiwan. If a patient had multiple positive results for C. neoformans, only the first instance was included. Demographic and clinical information, including the anti-fungal treatment used in each case, were obtained. The Chang Gung Memorial Hospital’s Institutional Review Board approved the study [No.99-1408C].

Data on clinical variables, including age, sex, underlying diseases (i.e., AIDS, steroids usage, diabetes mellitus, liver cirrhosis, malignancy, chronic renal failure, chronic obstructive pulmonary disease, and organ transplantation) and use of systemic anti-fungal therapy one month prior to first positive cryptococcal CSF culture were collected. Diabetes mellitus was defined as hemoglobin A1c >7%, with random blood glucose level >200 mg/dl or fasting blood glucose level > 126 mg/dl in repeated tests during the hospital stay, or if the patient had previously been diagnosed with diabetes mellitus.

The severity of illness at the time of CSF sampling was assessed using a modified APACHE II scoring method [11], and stratified based on the need for admission to an intensive care unit (ICU). The APACHE II scoring was modified as follows: zero points were given to the items PaO2 and pH if arterial blood gas analysis was not performed because of the absence of respiratory distress. Increasing intra-cranial pressure (IICP) was defined as an elevated opening pressure >200 mmH20. If there was evidence of high intracranial pressure with obstruction that needed decompression, drainage was done via ventriculo-peritoneal shunt in accordance with IDSA guidelines [12]. Laboratory data collected included lumbar puncture findings (opening pressure, India ink smear, and CSF levels of cryptococcal antigen), initial serum level of cryptococcal antigen, and results of blood fungal cultures.

Forty-six patients with cryptococcal meningitis were identified during the 10-year study period, including 32 men and 14 women, with age range between 18 and 85 years. Forty-two (91.3%) were tested for HIV and six were infected.

Clinical evaluation

The 46 patients were divided into 4 groups based on their initial anti-fungal treatment regimen used during the first 2 weeks. Twenty-three patients received a combination of amphotericin B and fluconazole as their initial anti-fungal therapy; 17 had amphotericin B only; 5 received fluconazole (400–800 mg daily) only; and 1 received a combination of amphotericin B and flucytosine. After 2 weeks, patients in all groups received fluconazole (400–600 mg daily for 8 weeks at least, then 200 mg daily thereafter). Follow-up was conducted after 2 weeks of treatment to assess the early outcomes of the disease.

Due to the sub-acute nature of the infection, the primary outcome measure was the clinical outcome after 10 weeks of treatment. Therapeutic cure was defined as improvement or disappearance of symptoms, negative clinical findings (i.e., fever, meningitis, neurological disorder, and abnormal mental status) and sterile CSF culture at the time of evaluation. Therapeutic failure was defined as either 1) clinical deterioration during hospitalization, including progressive hydrocephalus from comparison with initial cranial computed tomography (CT) study; new onset CNS vasculitis demonstrated by brain CT; seizure or status epilepticus with progressive disturbed conscious state; and a modified Barthel Index score <12 [13]; or 2) presence of C. neoformans in the patient’s CSF at the time of evaluation. Death resulting from any cause was recorded at the time of evaluation.

Fungal strain

The processing of specimens and isolate identification were performed by conventional methods and with the YBC identification card (bioMerieux, Marcy l’Etoile, France). The isolated strains were preserved at −70°C until the experiments.

Isolation of genomic DNA and PCR amplification

Each strain was grown on SDA plates at 35°C for 2 days. Cells were collected and suspended in a TE buffer (100 mM Tris–HCl; pH 8.0, 1 mM EDTA) containing lyticase (Sigma, St. Louis, MO, USA). Glass beads (Sigma) were then added to the micro-tubes, and the samples were incubated at 37°C for 4 h, and mixed in an end-over-end mixer to digest cell walls. Genomic DNA was extracted from the cells with the High Pure PCR template preparation kit (Roche Applied Science, Mannheim, Germany) according to the manufacturer’s instructions.

The serotype of Cryptococcus neoformans was identified by multiplex PCR [14]. Briefly, four primers for cloning LAC116 and 2 for CAP64 were used. The amplified products were electrophoretically separated and stained with ethidium bromide. The DNA bands were extracted using a gel extraction kit (QIAquick, QIAGEN Sciences, Germantown, MD, USA) and sequenced directly using a BigDye Terminator Cycle-sequencing kit (ABI PRISM 310NT Genomic Analyzer, Perkin-Elmer Applied Biosystems, Foster, CA, USA).

Anti-fungal susceptibility testing

Anti-fungal susceptibilities were determined using the broth micro-dilution method according to the CLSI M27-A3 methodology [7]. The anti-fungal agents tested were fluconazole (Pfizer, New York, NY, USA), voriconazole (Pfizer), and amphotericin B deoxycholate (Sigma). Stock solutions were prepared in dimethyl sulfoxide (voriconazole and amphotericin B) or water (fluconazole), and were further diluted in RPMI 1640 medium (Sigma) buffered to a pH level of 7 with 0.165 M 3-(N-morpholino) propanesulfonic acid buffer (Sigma). Aliquots of each agent (0.1 ml) at 2× concentrations were dispensed into 96-well micro-dilution trays. Inocula containing 0.5 × 103 to 2.5 × 103 cells/ml were then added to each well and the trays were incubated at 35°C. The final anti-fungal concentrations ranged from 0.06 to 8 μg/ml for voriconazole and amphotericin B, and from 0.25 to 64 μg/ml for fluconazole.

The MICs for voriconazole and fluconazole were read as concentrations causing a 50% reduction in turbidity compared to the growth of the control at 72 h. For amphotericin B, the MICs were read as the concentrations resulting in 100% inhibition relative to that of the growth of controls. Candida krusei ATCC 6258 and Candida parapsilosis ATCC 22019 were used as quality controls. The interpretative criteria for susceptibility to fluconazole was as published by the CLSI as ≤8 μg/ml [7]. Because there were no established interpretative criteria for amphotericin B and voriconazole, isolates with MICs that were both ≤1 μg/ml were considered susceptible, as suggested by Nguyen and Yu [15] and Lozano-Chiu et al. [16].

Statistical analysis

Statistical analysis was conducted using the SPSS statistical analysis system. If 2 or more C. neoformans strains were isolated from a patient, the first isolated strain was included in the analysis. When C. neoformans was isolated from a patient’s blood and CSF, the isolate from the CSF specimen was included in the analysis. Forty-six C. neoformans isolates were analyzed. In the univariate analysis, a comparison of contingency data was performed using the Chi-squared test or Fisher’s exact test, as appropriate. Factors with p < 0.1 in univariate analyses were separately entered into a multiple logistic regression model to identify independent predictive factors for the successful cure of cryptococcal meningitis at the time of evaluation. Variables with a two-tailed p < 0.05 were considered statistically significant.

Results

The serotype of C. neoformans was serotype A in 41 isolates and serotype B in 5 isolates. The susceptibilities of the 46 strains to fluconazole, amphotericin B, and voriconazole were determined by CLSI (Table 1). The widest ranges and highest MICs were for fluconazole (2–32 μg/ml), whereas the lowest MIC was for voriconazole (≤0.5 μg/ml). Overall, 12 strains (26.1%) were not susceptible to fluconazole (>8 μg/ml) and 8 (17.4%) had an MIC >1 μg/ml for amphotericin B.

Table 1 Inhibitory activities of amphotericin B, fluconazole, and voriconazole against clinical isolates of Cryptococcus neoformans (n = 46) from initial cerebro-spinal fluid culture
Full size table

Fifteen patients exhibited worsening symptoms of cryptococcal meningitis and five died from cryptococcal infection on or before the end of the 2-week therapy. Compared to the 20 patients who were not cured, the 26 patients who were cured after 2 weeks of initial therapy showed some statistically significant characteristics, including age <60 years (76.9% of cured patients versus 45% of uncured patients were younger than 60 years; p = 0.04). There was no relationship between anti-fungal susceptibility or induction treatment modality and therapeutic cure at the two-week interim analysis (Table 2). Multivariate logistic regression analysis indicated that patient age >60 years (OR = 4.1; 95% CI: 1.1-14.5; p = 0.03) was an independent predictive factor for poor clinical outcome (failure and death) of cryptococcal meningitis at the two-week interim evaluation.

Table 2 Demographic characteristics, laboratory results, and treatment modalities of patients with cryptococcal meningitis (n = 46) at two-week evaluation
Full size table

Seventeen patients exhibited worsening symptoms of cryptococcal meningitis, and 8 died from cryptococcal infection on or before the end of the 10-week therapy. Compared to the 25 patients who were not cured, the 21 patients who were cured after 10 weeks of initial therapy showed the presence of isolates resistant to fluconazole (MIC >8 μg/ml) was significantly associated with non-cure (4.8% of cured patients versus 44% of uncured patients had resistant isolates; p < 0.01) (Table 3). There was no relationship between initial induction treatment modality and therapeutic cure at the 10-week evaluation. Multivariate logistic regression analysis indicated that the presence of isolates resistant to fluconazole (OR = 15.7; 95% CI: 1.8-135.9; p = 0.01) was an independent predictive factor of poor clinical outcome (failure and death) of cryptococcal meningitis at the 10-week evaluation.

Table 3 Demographic characteristics, laboratory results, and initial treatment modalities of patients with cryptococcal meningitis (n = 46) at 10-week evaluation
Full size table

Clinical outcomes, initial induction treatment modality, and their relation to the susceptibility of amphotericin B and fluconazole were shown in Table 4. Among 12 C. neoformans isolates with high fluconazole MIC (>8 μg/ml), one patient received combined amphotericin B and flucytosine therapy in the first 2 weeks, but died before the 10-week evaluation. Seven patients received combined amphotericin B and fluconazole therapy in the first 2 weeks, of which only one was cured, five failed to respond, and one died. Three patients who received amphotericin B therapy only in the first 2 weeks all failed to respond. One patient who received fluconazole therapy alone in the first 2 weeks died at the 10-week evaluation. For eight isolates with high amphotericin B MICs (>1 μg/ml), five patients received combined amphotericin B and fluconazole therapy in the first 2 weeks, but only one was cured and 4 failed to respond at the 10-week evaluation. Two patients received amphotericin B therapy only in the first 2 weeks, and both died before the 10-week evaluation. One patient received fluconazole alone in the first 2 weeks and was cured. For susceptibility to fluconazole, there was a trend for resistance (MIC >8 μg/ml) to be associated with poor clinical outcome (failure and death), irrespective of initial treatment modality, at the 10-week evaluation.

Table 4 Susceptibility testing results (CLSI method) for Cryptococcus neoformans isolates from patients, with subsequent clinical outcomes after 10 weeks of antifungal therapy
Full size table

Discussion

Cryptococcal meningitis is described as an opportunistic infection in immuno-compromised patients such as people infected with HIV, but it can also affect apparently healthy people [17]. In the present study, only 6 (13%) of the 46 patients identified with cryptococcal meningitis were documented as having AIDS. Sun et al. [18] reported a mortality rate of 20.7% for HIV-infected patients within 10 weeks of hospitalization with cryptococcosis. Similarly, the overall mortality rate in the present study after 10 weeks of initial anti-fungal therapy for cryptococcal meningitis was 17.4% (8 patients died). The similarity in the mortality rates of these two studies suggests that mortality rates caused by cryptococcal meningitis may not be different for HIV-positive and HIV-negative patients.

Factors predictive of poor prognosis and mortality in patients with cryptococcal meningitis include (i) cryptococcus growth from sites other than CSF; (ii) alteration in mental status; (iii) IICP; (iv) CSF glucose <40 mg/dL; (v) CSF cell count <20 cells/mm3; (vi) high CSF cryptococcal antigen titer [19]; and (vii) positive India ink smear [20]. The goal of treatment includes both cure of the infection and prevention of long-term CNS system sequelae [2]. Prognostic factors for mortality may be overlooked because death may not be attributed to cryptococcosis itself. Therefore, cure of the infection is the endpoint of outcome evaluation in the current study.

High CSF cryptococcal antigen titer and the isolation of cryptococci from extra-neural sites indicate increased fungal load in patients with cryptococcal meningitis [21]. Although these clinical characteristics do not affect the clinical outcomes used to determine therapeutic cure in the current study, there is a consistent trend wherein patients who failed were more likely to have co-morbidities and that severity of illness that would predispose them to a poorer clinical outcome. The cured patients were younger at 2-week interim analysis (Table 2). Other negative results in this study may have been due to low statistical power, rather than a true lack of association between the clinical characteristic and therapeutic cure.

Differing approaches exist for the in vitro measurement of C. neoformans susceptibility to anti-fungal agents. Anaissie et al. [22] evaluated YNB, RPMI 1640 medium broth, and Eagle’s minimum essential medium broth, and found that RPMI 1640 broth was a suitable medium to test the susceptibility of C. neoformans. Franzot and Hamdan [23] corroborated these findings. RPMI 1640 medium is the standard broth recommended by CLSI [7]. When using this medium, MIC determinations require 72 h of incubation. Accordingly, the current study evaluated in vitro activities of C. neoformans by the broth micro-dilution method, as described in the CLSI document M27-A3 [7].

For in vitro anti-fungal susceptibility testing of C. neoformans[7], no breakpoint is currently available for any drug [2] and the role of the susceptibility of the initial isolate as a predictor of both early and late clinical treatment failure remains controversial [8–10]. One study with a sample of 74 patients with cryptococcosis (60 of whom had AIDS) found that in vitro anti-fungal susceptibility cannot predict the outcome two weeks after the start of anti-fungal therapy [8]. However, the fluconazole MICs of these isolates, which include C. neoformans strains, are all ≤4 μg/ml [8]. Witt et al. explored the utility of MICs as predictors of 2-week treatment failure in patients receiving fluconazole for acute AIDS-associated cryptococcal meningitis, and found that the low MIC of fluconazole was independently associated with successful treatment [9]. Aller et al. also reported that the clinical outcomes of 25 patients (24 with AIDS) after 10 weeks of fluconazole maintenance therapy might be better when the infecting C. neoformans strain was inhibited by lower concentrations of fluconazole for eradication (MICs ≤8 μg/ml) than when patients were infected with strains that required higher fluconazole concentrations (MICs >8 μg/ml) [10]. These two studies both report reduced treatment efficacies when the fluconazole MIC is >8 μg/ml [9, 10].

As in the present study, the MIC of fluconazole is associated with early clinical outcome due to the very few patients who receive fluconazole alone as induction therapy. The use of combined therapy makes this problematic. Rather than focusing on early outcome, it may make more sense to focus on the 10-week outcome when the patients receive fluconazole as maintenance therapy.

In the present study, only 13% patients had AIDS and strains with higher fluconazole MICs (>8 μg/ml) were specifically investigated. Despite using different testing parameters, an association between high fluconazole MICs (>8 μg/ml) and lack of therapeutic cure is evident. One explanation is that strains with high MIC for fluconazole (≥32 μg/ml) are more virulent than strains that have low MIC for fluconazole (≤8 μg/ml) [24]. To date, two studies has demonstrated a strong correlation between quantitative measures of in vitro amphotericin B susceptibility and the quantitative response observed in patients [25, 26]. In the current study, the discrepancies in susceptibilities to amphotericin B or fluconazole, and clinical outcomes may be due to the small number of patients infected by strains with high MICs of amphotericin B. Further investigation is necessary on the correlation between amphotericin B susceptibility and outcomes in patients with cryptococcosis.

In a previous study, C. neoformans were collected from the CSF specimens of patients with cryptococcal meningitis between 1998 and 2002 [27]. By comparison, the current study found that the MIC90 of fluconazole had increased from 4 μg/ml [27] to 16 μg/ml for the CSF specimens collected between 2001 and 2010 (Table 1). Non-susceptibility to fluconazole was also an emerging problem, according to surveillance data. This is especially true in certain global regions, notably Africa, where prophylactic fluconazole is prescribed widely and the drug is often used alone as the primary therapy for cryptococcosis [4–6]. Initial treatment modality was not associated with clinical outcome in either univariate or multivariate analysis. Only one patient infected by strains with higher fluconazole MICs (>8 μg/ml) received fluconazole therapy alone in the first 2 weeks, and this patient died before the end of the 2-week evaluation. Only two patients infected by strains with higher amphotericin B MICs (>1 μg/ml) received amphotericin B therapy alone in the first 2 weeks, and both died before the end of the 2-week evaluation. Thus, early mortality (first 2 weeks) from cryptococcal meningitis is more likely elated to severity of disease at presentation than treatment response.

Moreover, 12 patients infected by strains with higher fluconazole MICs (> 8 μg/ml) received fluconazole treatment after 2 weeks initial antifungal therapy, and only one was cured at the end of the 10-week evaluation. This suggests that high fluconazole MIC is associated with 10-week treatment failure when fluconazole is used for maintenance therapy after induction therapy.

This study was subject to certain limitations. First, the sample size was relatively small and made retrospective use of patients’ medical records, which usually meant that some data were missing or misclassified. Thus, the findings may underestimate the “true” independent predictor of outcome in this study. Furthermore, the numbers of variables considered for the multiple logistic regression analysis was small. Based on the stepwise procedures, only one variable was selected as the important variable predicting the outcomes. The maximum likelihood estimates of the coefficients are valid in the analysis. Not all the patients were checked for HIV because two patients died before they could be screened for HIV and another two patients did not accept HIV screening. Second, flucytosine was unavailable at the study institution during the 10-year study period and only one patient received the most rapidly fungicidal regimen (amphotericin B plus flucytosine) [28]. Third, the start of induction anti-fungal therapy was different for each patient according to the preference of his/her doctor, which might cause potential bias in statistical analysis. Lastly, no standardization was conducted for certain aspects of data collection, such as amphotericin B or fluconazole levels in serum and CSF. This limits the ability to delineate the relationship between drug dosage, resulting serum and CSF levels, and treatment outcomes.

Conclusions

The present study suggests that primary non-susceptibility to amphotericin B and fluconazole is common. The MICs determined at the time of diagnosis of cryptococcal meningitis by the CLSI M27-A3 broth micro-dilution method may potentially predict the likelihood of therapeutic cure. Further large-scale studies are required to corroborate the findings.

References

  1. 1.

    Mitchell TG, Perfect JR: Cryptococcosis in the era of AIDS-100 years after the discovery of Cryptococcus neoformans. Clin Microbiol Rev. 1995, 8: 515-548.

  2. 2.

    Perfect JR, Dismukes WE, Dromer F, Goldman DL, Graybill JR, Hamill RJ, Harrison TS, Larsen RA, Lortholary O, Nguyen MH, Pappas PG, Powderly WG, Singh N, Sobel JD, Sorrell TC: Practice guidelines for the management of cryptococcal disease: 2010 update by the Infectious Diseases Society of America. Clin Infect Dis. 2010, 50: 291-322. 10.1086/649858.

  3. 3.

    Brandt ME, Pfaller MA, Hajjeh RA, Hamill RJ, Pappas PG, Reingold AL, Rimland D, Warnock DW, Cryptococcal Disease Active Surveillance Group: Trends in anti-fungal drug susceptibility of Cryptococcus neoformans isolates in the United States: 1992 to 1994 and 1996 to 1998. Antimicrob Agents Chemother. 2001, 45: 3065-3069. 10.1128/AAC.45.11.3065-3069.2001.

  4. 4.

    Armengou A, Porcar C, Mascaró J, García-Bragado F: Possible development of resistance to fluconazole during suppressive therapy for AIDS-associated cryptococcal meningitis. Clin Infect Dis. 1996, 23: 1337-1338.

  5. 5.

    Paugam A, Camet-Dupouy J, Blanche P, Gangneux JP, Tourte-Schaefer C, Sicard D: Increased fluconazole resistance of Cryptococcus neoformans isolated from a patient with AIDS and recurrent meningitis. Clin Infect Dis. 1994, 19: 975-976.

  6. 6.

    Berg J, Clancy CJ, Nguyen MH: The hidden danger of primary fluconazole prophylaxis for patients with AIDS. Clin Infect Dis. 1998, 26: 186-187.

  7. 7.

    Clinical and Laboratory Standards Institute (CLSI): Reference method for broth dilution anti-fungal susceptibility testing of yeasts; approved standard. 2008, CLSI document M27–A3, CLSI, Wayne, PA, 3

  8. 8.

    Dannaoui E, Abdul M, Arpin M, Michel-Nguyen A, Piens MA, Favel A, Lortholary O, Dromer F, French Cryptococcosis Study Group: Results obtained with various anti-fungal susceptibility testing methods do not predict early clinical outcome in patients with cryptococcosis. Antimicrob Agents Chemother. 2006, 50: 2464-2470. 10.1128/AAC.01520-05.

  9. 9.

    Witt MD, Lewis RJ, Larsen RA, Milefchik EN, Leal MA, Haubrich RH, Richie JA, Edwards JE, Ghannoum MA: Identification of patients with acute AIDS-associated cryptococcal meningitis who can be effectively treated with fluconazole: the role of anti-fungal susceptibility testing. Clin Infect Dis. 1996, 22: 322-328. 10.1093/clinids/22.2.322.

  10. 10.

    Aller AI, Martin-Mazuelos E, Lozano F, Gomez-Mateos J, Steele-Moore L, Holloway WJ, Gutiérrez MJ, Recio FJ, Espinel-Ingroff A: Correlation of fluconazole MICs with clinical outcome in cryptococcal infection. Antimicrob Agents Chemother. 2000, 44: 1544-1548. 10.1128/AAC.44.6.1544-1548.2000.

  11. 11.

    American College of Chest Physicians/Society of Critical Care Medicine Consensus Conference: Definitions for sepsis and organ failure and guidelines for the use of innovative therapies in sepsis. Crit Care Med. 1992, 20: 864-874. 10.1097/00003246-199206000-00025.

  12. 12.

    Liliang PC, Liang CL, Chang WN, Chen HJ, Su TM, Lu K, Lu CH: Shunt surgery for hydrocephalus complicating cryptococcal meningitis in human immuno-deficiency virus-negative patients. Clin Infect Dis. 2003, 37: 673-678. 10.1086/377208.

  13. 13.

    Lan SH, Chang WN, Lu CH, Lui CC, Chang HW: Cerebral infarction in chronic meningitis: a comparison of tuberculous meningitis and cryptococcal meningitis. QJM. 2001, 94: 247-253. 10.1093/qjmed/94.5.247.

  14. 14.

    Ito-Kuwa S, Nakamura K, Aoki S, Vidotto V: Serotype identification of Cryptococcus neoformans by multiplex PCR. Mycoses. 2007, 50: 277-281. 10.1111/j.1439-0507.2007.01357.x.

  15. 15.

    Nguyen MH, Yu CY: In vitro comparative efficacy of voriconazole and itraconazole against fluconazole-susceptible and -resistant Cryptococcus neoformans isolates. Antimicrob Agents Chemother. 1998, 42: 471-472.

  16. 16.

    Lozano-Chiu M, Paetznick VL, Ghannoum MA, Rex JH: Detection of resistance to amphotericin B among Cryptococcus neoformans clinical isolates: performances of three different media assessed by using E-test and National Committee for Clinical Laboratory Standards M27-A methodologies. J Clin Microbiol. 1998, 36: 2817-2822.

  17. 17.

    Yu YL, Lau YN, Woo E, Wong KL, Tse B: Cryptococcal infection of the nervous system. Q J Med. 1988, 66: 87-96.

  18. 18.

    Sun HY, Chen MY, Hsiao CF, Hsieh SM, Hung CC, Chang SC: Endemic fungal infections caused by Cryptococcus neoformans and Penicillium marneffei in patients infected with human immuno-deficiency virus and treated with highly active anti-retroviral therapy. Clin Microbiol Infect. 2006, 12: 381-388. 10.1111/j.1469-0691.2006.01367.x.

  19. 19.

    Saag MS, Powderly WG, Cloud GA, Robinson P, Grieco MH, Sharkey PK, Thompson SE, Sugar AM, Tuazon CU, Fisher JF, Hyslop N, Jacobson JM, Hafner R, Dismukes WE, The NIAID Mycoses Study Group and the AIDS Clinical Trials Group: Comparison of amphotericin B with fluconazole in the treatment of acute AIDS-associated cryptococcal meningitis. N Engl J Med. 1992, 326: 83-89. 10.1056/NEJM199201093260202.

  20. 20.

    Zuger A, Louie E, Holzman RS, Simberkoff MS, Rahal JJ: Cryptococcal disease in patients with the acquired immunodeficiency syndrome. Ann Intern Med. 1986, 104: 234-240.

  21. 21.

    Clark RA, Greer D, Atkinson W, Valainis GT, Hyslop N: Spectrum of Cryptococcus neoformans infection in 68 patients infected with human immuno-deficiency virus. Rev Infect Dis. 1990, 12: 768-777. 10.1093/clinids/12.5.768.

  22. 22.

    Anaissie E, Shawar R, Paetznick V, Ensign LG, Witte Z, LaRocco M: Two-site comparison of broth micro-dilution and semi-solid agar dilution methods for susceptibility testing of Cryptococcus neoformans in three media. J Clin Microbiol. 1993, 31: 1370-1372.

  23. 23.

    Franzot SP, Hamdan JS: In vitro susceptibilities of clinical and environmental isolates of Cryptococcus neoformans to five anti-fungal drugs. Antimicrob Agents Chemother. 1996, 40: 822-824.

  24. 24.

    Sionov E, Chang YC, Garraffo HM, Kwon-Chung KJ: Hetero-resistance to fluconazole in Cryptococcus neoformans is intrinsic and associated with virulence. Antimicrob Agents Chemother. 2009, 53: 2804-2815. 10.1128/AAC.00295-09.

  25. 25.

    Larsen RA, Bauer M, Brouwer AE, Sanchez A, Thomas AM, Rajanuwong A, Chierakul W, Peacock SJ, Day N, White NJ, Rinaldi MG, Harrison TS: In vitro clinical correlation for amphotericin B susceptibility in AIDS-associated cryptococcal meningitis. Antimicrob Agents Chemother. 2007, 51: 343-345. 10.1128/AAC.00742-06.

  26. 26.

    Larsen RA, Bauer M, Pitisuttithum P, Sanchez A, Tansuphaswadikul S, Wuthiekanun V, Peacock SJ, Simpson AJ, Fothergill AW, Rinaldi MG, Bustamante B, Thomas AM, Altomstone R, Day NP, White NJ: Correlation of susceptibility of Cryptococcus neoformans to amphotericin B with clinical outcome. Antimicrob Agents Chemother. 2011, 55: 5624-5630. 10.1128/AAC.00034-11.

  27. 27.

    Chang WN, Huang CR, Lei CB, Lee PY, Chien CC, Chang HW, Chang CS, Lu CH: Serotypes of clinical cerebrospinal fluid Cryptococcus neoformans isolates from southern Taiwan and their in vitro susceptibilities to amphotericin B, fluconazole, and voriconazole. Jpn J Infect Dis. 2004, 57: 113-115.

  28. 28.

    Brouwer AE, Rajanuwong A, Chierakul W, Griffin GE, Larsen RA, White NJ, Harrison TS: Combination anti-fungal therapies for HIV-associated cryptococcal meningitis: a randomised trial. Lancet. 2004, 363: 1764-1767. 10.1016/S0140-6736(04)16301-0.

Pre-publication history

  1. The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/12/361/prepub

Download references

Acknowledgements

This study was supported by a grant from Pfizer, New York, NY, USA. None of the authors have potential conflicts of interest.

Author information

Affiliations

  1. Division of Infectious Diseases, Department of Internal Medicine, Chang Gung University College of Medicine, Kaohsiung, Taiwan
    • Chen-Hsiang Lee
    • , Tzu-Yao Chang
    • , Jien-Wei Liu
    •  & Fang-Ju Chen
  2. Department of Laboratory Medicine, Kaohsiung, Taiwan
    • Chun-Chih Chien
    •  & Ya-Fen Tang
  3. Department of Neurology, Kaohsiung Chang Gung Memorial Hospital, Chang Gung University College of Medicine, 123 Ta-Pei Road, Kaohsiung, Niao-Sung District, 833, Taiwan
    • Cheng-Hsien Lu
  4. Department of Biological Science, National Sun Yat-Sen University, Kaohsiung, Taiwan
    • Cheng-Hsien Lu
Authors
  1. Chen-Hsiang Lee
    View author publications
    You can also search for this author in
  2. Tzu-Yao Chang
    View author publications
    You can also search for this author in
  3. Jien-Wei Liu
    View author publications
    You can also search for this author in
  4. Fang-Ju Chen
    View author publications
    You can also search for this author in
  5. Chun-Chih Chien
    View author publications
    You can also search for this author in
  6. Ya-Fen Tang
    View author publications
    You can also search for this author in
  7. Cheng-Hsien Lu
    View author publications
    You can also search for this author in

Corresponding author

Correspondence to Cheng-Hsien Lu.

Additional information

Competing interests

This study was sponsored by Pfizer funded, which was acquired in May 2010. The authors declare that they have no competing interests.

Authors’ contributions

CHL, JWL and CHL took the initiative to develop the research project. TYC, FJC, CCC, and YFT participated in reviewing the clinical data and analysis. CHL and CHL contributed to the manuscript writing. All authors read and approved the final manuscript.

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Lee, C., Chang, T., Liu, J. et al. Correlation of anti-fungal susceptibility with clinical outcomes in patients with cryptococcal meningitis. BMC Infect Dis 12, 361 (2012). https://doi.org/10.1186/1471-2334-12-361

Download citation

Keywords

  • Cryptococcal meningitis
  • Fluconazole
  • Outcome
  • Susceptibility

BMC Infectious Diseases

ISSN: 1471-2334

Contact us