PMID- 32820678 OWN - NLM STAT- MEDLINE DCOM- 20210610 LR - 20220422 IS - 1439-7609 (Electronic) IS - 1439-7595 (Linking) VI - 31 IP - 3 DP - 2021 May TI - The efficacy and safety of reduced-dose sulfamethoxazole-trimethoprim for chemoprophylaxis of Pneumocystis pneumonia in patients with rheumatic diseases. PG - 629-635 LID - 10.1080/14397595.2020.1812834 [doi] AB - OBJECTIVES: Pneumocystis pneumonia (PCP) is a life-threatening opportunistic infection. Sulfamethoxazole-trimethoprim (SMX/TMP) is the first-line drug for PCP prophylaxis. However, adverse events (AEs) force clinicians to alter or reduce the drug dosage. METHODS: We retrospectively reviewed all patients with rheumatic diseases who received SMX/TMP for prophylaxis and glucocorticoid therapy between April 2004 and March 2018. The rates of AEs, SMX/TMP discontinuation, and incidence of PCP were analyzed. Patients were divided into the conventional group and the dose-reduction group. RESULTS: One hundred forty-five patients and 75 patients were included in the conventional group and the dose-reduction group, respectively. Compared to the dose-reduction group, the conventional group had a significantly high frequency of AEs (10.7% vs. 24.1%; p = .017); however, the rate of discontinuing SMX/TMP was not significantly different (8.0% vs. 14.5%; p = .165). Thirteen conventional group patients required a reduced SMX/TMP dose because of AEs; no patient developed PCP. The conventional SMX/TMP dose and renal dysfunction were associated with AEs in multivariate analysis. CONCLUSION: Patients who received a reduced SMX/TMP dose did not have PCP and had a lower frequency of AEs. A reduction in SMX/TMP for PCP prophylaxis is effective and safe in patients with rheumatic disease. FAU - Harada, Tomoya AU - Harada T AUID- ORCID: 0000-0002-6820-4814 AD - Division of Respiratory Medicine and Rheumatology, Faculty of Medicine, Tottori University, Tottori, Japan. FAU - Kato, Ryohei AU - Kato R AD - Division of Respiratory Medicine and Rheumatology, Faculty of Medicine, Tottori University, Tottori, Japan. FAU - Sueda, Yuriko AU - Sueda Y AD - Division of Respiratory Medicine and Rheumatology, Faculty of Medicine, Tottori University, Tottori, Japan. FAU - Funaki, Yoshihiro AU - Funaki Y AD - Division of Respiratory Medicine and Rheumatology, Faculty of Medicine, Tottori University, Tottori, Japan. FAU - Takata, Miki AU - Takata M AD - Division of Respiratory Medicine and Rheumatology, Faculty of Medicine, Tottori University, Tottori, Japan. FAU - Okazaki, Ryota AU - Okazaki R AD - Division of Respiratory Medicine and Rheumatology, Faculty of Medicine, Tottori University, Tottori, Japan. FAU - Hasegawa, Yasuyuki AU - Hasegawa Y AD - Division of Rheumatology, Tottori Prefectural Central Hospital, Tottori, Japan. FAU - Yamasaki, Akira AU - Yamasaki A AD - Division of Respiratory Medicine and Rheumatology, Faculty of Medicine, Tottori University, Tottori, Japan. LA - eng PT - Journal Article DEP - 20200909 PL - England TA - Mod Rheumatol JT - Modern rheumatology JID - 100959226 RN - 0 (Anti-Bacterial Agents) RN - 8064-90-2 (Trimethoprim, Sulfamethoxazole Drug Combination) SB - IM MH - Adult MH - Anti-Bacterial Agents/administration & dosage/adverse effects/*therapeutic use MH - Chemoprevention/adverse effects/*methods MH - Female MH - Humans MH - Incidence MH - Male MH - Middle Aged MH - Pneumonia, Pneumocystis/complications/drug therapy/*prevention & control MH - Retrospective Studies MH - Rheumatic Diseases/*complications MH - Trimethoprim, Sulfamethoxazole Drug Combination/administration & dosage/adverse effects/*therapeutic use OTO - NOTNLM OT - Dose reduction OT - efficacy OT - pneumocystis pneumonia OT - prophylaxis OT - sulfamethoxazole-trimethoprim EDAT- 2020/08/22 06:00 MHDA- 2021/06/11 06:00 CRDT- 2020/08/22 06:00 PHST- 2020/08/22 06:00 [pubmed] PHST- 2021/06/11 06:00 [medline] PHST- 2020/08/22 06:00 [entrez] AID - 10.1080/14397595.2020.1812834 [doi] PST - ppublish SO - Mod Rheumatol. 2021 May;31(3):629-635. doi: 10.1080/14397595.2020.1812834. Epub 2020 Sep 9.