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Study to Evaluate the Clinical Outcome in High Risk Patients Who Received Empirical Antifungal Therapy

Observational, Retrospective Study to Evaluate the Clinical Outcome in High Risk Patients Who Received Empirical Antifungal Therapy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01439646
Enrollment
100
Registered
2011-09-23
Start date
2011-08-31
Completion date
2012-03-31
Last updated
2015-08-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Antifungal Therapy

Keywords

empirical, ICU, high risk patient

Brief summary

Retrospective, observational study To study the effect of Empirical Antifungal therapy on clinical outcome in high risk patients with suspected Invasive Fungal Infection admitted in ICU/Critical care unit, To know the current epidemiology of IFI and management approach in patients at high risk of Invasive fungal infections, Identify the risk factors associated with Invasive fungal infections, To comment on the appropriateness of empirical therapy used based on proven/probable diagnosis

Detailed description

Study Objectives Primary Objective: \- To study the effect of Empirical Antifungal therapy on clinical outcome in high risk patients with suspected Invasive Fungal Infection admitted in ICU/Critical care unit * Secondary Objectives: 1. To know the current epidemiology of IFI and management approach in patients at high risk of Invasive fungal infections 2. Identify the risk factors associated with Invasive fungal infections 3. To comment on the appropriateness of empirical therapy used based on proven/probable diagnosis Inclusion criteria: All Non-neutropenic patients admitted in the intensive care/critical care unit who are prescribed any form of pre-emptive / empirical Antifungal therapy during the specified study duration period Exclusion criteria: Neutropenic patients Patients with proven invasive fungal infections where antifungal therapy was initiated after the confirmation of Invasive fungal infection/Candidemia Patients who received prophylactic antifungal agents Study Design * Multi Center (Dual-center - Fortis Hospital and Apollo Hospital) Retrospective, Observational Study * Study Patients: 100 in number Retrospective data will be collected for all patients admitted in intensive care unit/Critical care unit (under the study investigators) who received any form of Empirical / Preemptive (not prophylactic) Antifungal therapy (of any duration, irrespective of culture positivity) as a suspected case of Invasive Fungal Infection. Following details of patients will be captured Demographics, primary and secondary diagnosis, co-morbidities, grade of infection, severity of sepsis and disease. Daily hemodynamic parameters, routine blood tests including Total count and hematologic profile, renal profile, Liver function tests, electrolyte status, additional tests whatever was done as a course of the therapy. Fungal C/S reports and any other sample culture reports Duration of treatment, Changes in therapy, Adjuvant therapy - for relevant cases, Any Surgical procedures undertaken: e.g., surgical debridement, fasciotomy and dressing (as a part of the standard treatment according to available guidelines) - for relevant cases, Any additional invasive procedure (eg: Mechanical ventilation ), Reported adverse events Recording of Risk factors for invasive fungal infections as detailed but not limited to: 1. Diabetes, 2. Use of immunosuppressants (Eg. steroids) 3. Chronic Hemodialysis , TPN, Mechanical ventilation , 4. Sepsis/Septic shock, Multiorgan dysfunction (more than one organ), 5. Non response to \> 4 days of broad spectrum antibiotics, 6. Structural lung disease, 7. Major abdominal surgery, 8. Multifocal colonization * Study Duration: A period of one year starting backwards from December 2010 till January 2010.( max. 100 patients retrospectively tracking back from Dec 2010 whichever comes first ). Statistical analysis Appropriate statistical tools such as Multiple logistic regressions model will be used to analyze linkages between different parameters recorded in the study Primary Endpoint: 1. Mortality both Short term (while on antifungal therapy) and Long term (within 12 weeks of completion of antifungal therapy) 2. Mean Duration of ICU (Intensive Care Unit) / HDU (High Dependency Unit stay after initiation of Antifungal Therapy Secondary Endpoints: The common pathogens associated with Invasive Fungal Infections The common empirical antifungal agents used in suspected Invasive Fungal Infection The mean time for initiation of Antifungal therapy after suspicion of invasive fungal infection. The mean duration of antifungal therapy The risk factors in patients with proven/probable invasive fungal infections The appropriateness of antifungal agent based on microbiological and/or clinical outcome

Interventions

OTHERit is a retrospective study, hence no active intervention

since it is an observational restrospective study hence no active intervention is planned

Sponsors

Merck Sharp & Dohme LLC
CollaboratorINDUSTRY
Fortis Hospital, India
Lead SponsorOTHER

Study design

Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* All Non-neutropenic patients (18-75yrs) admitted in the intensive care/critical care unit who are prescribed any form of pre-emptive / empirical Antifungal therapy during the specified study duration period

Exclusion criteria

* Neutropenic patients * Patients with proven invasive fungal infections where antifungal therapy was initiated after the confirmation of Invasive fungal infection/Candidemia * Patients who received prophylactic antifungal agents

Design outcomes

Primary

MeasureTime frame
Mortality both Short term (while on antifungal therapy) and Long term (within 12 weeks of completion of antifungal therapy)6 months
Mean Duration of ICU (Intensive Care Unit) / HDU (High Dependency Unit stay after initiation of Antifungal Therapy6 months

Secondary

MeasureTime frame
The mean time for initiation of Antifungal therapy after suspicion of invasive fungal infection6 months
The common pathogens associated with Invasive Fungal Infections6 months
The appropriateness of antifungal agent based on microbiological and/or clinical outcome6 months
The risk factors in patients with proven/probable invasive fungal infections6 months
The common empirical antifungal agents used in suspected Invasive Fungal Infection6 months

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026