TY - JOUR
T1 - Pneumocystis jiroveci pneumonia in patients with rheumatoid arthritis treated with infliximab
T2 - A retrospective review and case-control study of 21 patients
AU - Komano, Yukiko
AU - Harigai, Masayoshi
AU - Koike, Ryuji
AU - Sugiyama, Haruhito
AU - Ogawa, J. U.N.
AU - Saito, Kazuyoshi
AU - Sekiguchi, Naoya
AU - Inoo, Masayuki
AU - Onishi, Ikuko
AU - Ohashi, Hiroyuki
AU - Amamoto, Fujio
AU - Miyata, Masayuki
AU - Ohtsubo, Hideo
AU - Hiramatsu, Kazuko
AU - Iwamoto, Masahiro
AU - Minota, Seiji
AU - Matsuoka, Naoki
AU - Kageyama, Goichi
AU - Imaizumi, Kazuyoshi
AU - Tokuda, Hitoshi
AU - Okochi, Yasumi
AU - Kudo, Koichiro
AU - Tanaka, Yoshiya
AU - Takeuchi, Tsutomu
AU - Miyasaka, Nobuyuki
PY - 2009/3/15
Y1 - 2009/3/15
N2 - Objective. To establish proper management of Pneumocystis jiroveci pneumonia (PCP) in rheumatoid arthritis (RA) patients treated with infliximab. PCP has been observed in 0.4% of patients with RA treated with infliximab in Japan. Methods. Data from patients with RA (n = 21) who were diagnosed with PCP during infliximab treatment and from 102 patients with RA who did not develop PCP during infliximab therapy were collected from 14 rheumatology referral centers in Japan. A retrospective review of these patients and a case-control study to compare patients with and without PCP were performed. Results. The median length of time from the first infliximab infusion to the development of PCP was 8.5 weeks. At the onset of PCP, the median dosages of prednisolone and methotrexate were 7.5 mg/day and 8 mg/week, respectively. Pneumocystis jiroveci was microscopically identified in only 2 patients, although the polymerase chain reaction test for the organism was positive in 20 patients. The patients with PCP had significantly lower serum albumin levels (P < 0.001) and lower serum IgG levels (P < 0.001) than the patients without PCP. Computed tomography of the chest in all patients with PCP revealed ground-glass opacity either with sharp demarcation by interlobular septa or without interlobular septal boundaries. Sixteen of the 21 patients with PCP developed acute respiratory failure, but all survived. Conclusion. PCP is a serious complication that may occur early in the course of infliximab therapy in patients with RA. For the proper clinical management of this infectious disease, physicians need to be aware of the possibility of PCP developing during infliximab therapy.
AB - Objective. To establish proper management of Pneumocystis jiroveci pneumonia (PCP) in rheumatoid arthritis (RA) patients treated with infliximab. PCP has been observed in 0.4% of patients with RA treated with infliximab in Japan. Methods. Data from patients with RA (n = 21) who were diagnosed with PCP during infliximab treatment and from 102 patients with RA who did not develop PCP during infliximab therapy were collected from 14 rheumatology referral centers in Japan. A retrospective review of these patients and a case-control study to compare patients with and without PCP were performed. Results. The median length of time from the first infliximab infusion to the development of PCP was 8.5 weeks. At the onset of PCP, the median dosages of prednisolone and methotrexate were 7.5 mg/day and 8 mg/week, respectively. Pneumocystis jiroveci was microscopically identified in only 2 patients, although the polymerase chain reaction test for the organism was positive in 20 patients. The patients with PCP had significantly lower serum albumin levels (P < 0.001) and lower serum IgG levels (P < 0.001) than the patients without PCP. Computed tomography of the chest in all patients with PCP revealed ground-glass opacity either with sharp demarcation by interlobular septa or without interlobular septal boundaries. Sixteen of the 21 patients with PCP developed acute respiratory failure, but all survived. Conclusion. PCP is a serious complication that may occur early in the course of infliximab therapy in patients with RA. For the proper clinical management of this infectious disease, physicians need to be aware of the possibility of PCP developing during infliximab therapy.
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U2 - 10.1002/art.24283
DO - 10.1002/art.24283
M3 - Article
C2 - 19248121
AN - SCOPUS:62549098205
SN - 2151-4658
VL - 61
SP - 305
EP - 312
JO - Arthritis Care and Research
JF - Arthritis Care and Research
IS - 3
ER -