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Clinical Factors Associated With Pneumocystis Pneumonia Despite Its Primary Prophylaxis: When to Stop Prophylaxis?
Ju Yeon Kim1, Se Rim Choi2, Jin Kyun Park3
1Division of Rheumatology, Department of Internal Medicine, Chung-Ang University Gwangmyeong Hospital, Gwangmyeong-si, South Korea.
Discontinuing Pneumocystis jirovecii pneumonia (PJP) prophylaxis too early, especially with high-dose glucocorticoids, increases risk in rheumatic disease patients. Tapering to 12.5 mg prednisone equivalent is a safer withdrawal point.
Area of Science:
- Rheumatology
- Infectious Diseases
- Pharmacology
Background:
- Primary prophylaxis against Pneumocystis jirovecii pneumonia (PJP) is recommended for rheumatic disease patients on immunosuppressants.
- Optimal timing for discontinuing PJP prophylaxis remains unclear, posing a risk for patients.
Purpose of the Study:
- To identify risk factors for PJP in rheumatic disease patients despite prophylaxis.
- To provide evidence-based recommendations for an optimal PJP prophylaxis schedule.
Main Methods:
- A case-control study involving 1,294 prophylactic episodes in 1,148 rheumatic disease patients.
- Trimethoprim-sulfamethoxazole (TMP-SMX) was used for prophylaxis.
- Cox proportional hazards model with LASSO was employed to assess clinical factors.
Main Results:
- PJP occurred in 10 patients (0.85 per 100 person-years), primarily after TMP-SMX discontinuation.
- Higher glucocorticoid doses (>12.5 mg prednisone equivalent) at prophylaxis withdrawal significantly increased PJP risk (aHR: 13.84).
- Adverse events from TMP-SMX were observed in 15.9% of cases.
Conclusions:
- Initiating PJP prophylaxis withdrawal when glucocorticoid doses are tapered to 12.5 mg/day of prednisone equivalent is a reasonable strategy.
- This approach may help mitigate the risk of PJP in patients with rheumatic diseases.
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