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Published on: June 28, 2018
Dose-dependent association between opioid administration and ventilator-associated pneumonia in sepsis patients
Shengwei Lin1, Lidan Chi1, Wenbin Lu1
1Faculty of Anesthesiology, Changhai Hospital, Naval Medical University, Shanghai, 200433, China.
Background:
This study aimed to investigate the association between opioid administration and the risk of ventilator-associated pneumonia (VAP) in mechanically ventilated (MV) patients in the intensive care unit (ICU).
Methods:
Using a retrospective cohort design, we extracted data from the Medical Information Mart for Intensive Care IV (MIMIC-IV) database. VAP diagnoses were identified using International Classification of Diseases (ICD) codes. Logistic regression and propensity score matching analyses were performed to evaluate the association between opioid exposure and VAP risk. Subgroup analyses evaluated the influence of comorbidities, including diabetes, congestive heart failure, and chronic pulmonary disease.
Results:
Among 6978 patients, 668 (9.6%) developed VAP. Patients in the high-opioid group (fentanyl equivalent daily dose >2.47 mg/day) exhibited a significantly increased risk of VAP (OR: 2.12, 95% CI: 1.77-2.54, P < 0.001). After propensity score matching, the high-opioid group maintained a higher VAP risk compared to the low-opioid group (OR: 1.86, 95% CI: 1.52-2.27, P < 0.001). Secondary outcomes revealed that the high-opioid group had elevated risks of acute kidney injury (AKI) within 7 days of ICU admission (OR: 1.54, 95% CI: 1.35-1.76, P < 0.001). Additionally, 30-day mortality was higher in the high-opioid group (HR: 2.65, 95% CI: 2.24-3.13, P < 0.001).
Conclusions:
Our findings demonstrate a significant association between opioid administration and an increased risk of VAP, particularly in sepsis patients with specific comorbidities. These results highlight the need for careful opioid dosing strategies in critically ill, mechanically ventilated patients.
Insights
High opioid doses in mechanically ventilated patients significantly increase the risk of ventilator-associated pneumonia (VAP). This association also linked to higher rates of acute kidney injury and 30-day mortality, underscoring the need for cautious opioid management.
Area of Science:
- Critical Care Medicine
- Pharmacology
- Infectious Diseases
Background:
- Ventilator-associated pneumonia (VAP) is a significant concern in intensive care units (ICUs).
- Opioid administration is common in mechanically ventilated (MV) patients.
Purpose of the Study:
- To investigate the association between opioid administration and VAP risk in MV patients.
- To explore the impact of opioid dosing on secondary outcomes like acute kidney injury (AKI) and mortality.
Main Methods:
- Retrospective cohort study using the MIMIC-IV database.
- Identified VAP using ICD codes.
- Employed logistic regression and propensity score matching to analyze opioid exposure and VAP risk.
Main Results:
- Higher opioid doses (fentanyl equivalent daily dose >2.47 mg/day) were associated with a significantly increased risk of VAP (OR: 2.12).
- This association persisted after propensity score matching (OR: 1.86).
- High opioid use also correlated with increased AKI risk (OR: 1.54) and higher 30-day mortality (HR: 2.65).
Conclusions:
- Opioid administration is significantly associated with increased VAP risk in critically ill MV patients.
- Specific comorbidities may influence this association.
- Careful opioid dosing strategies are crucial for managing MV patients to mitigate VAP and other adverse outcomes.
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