The risk factor analysis and treatment experience in pneumocystis jirovecii pneumonia after kidney transplantation

被引:7
|
作者
Yang, Pengfeng [1 ]
Zhu, Xiaoqiu [2 ]
Liang, Weixiang [1 ]
Cai, Ruiming [3 ]
机构
[1] Guangzhou Med Univ, Affiliated Hosp 3, Dept Ultrasound Med, 63 Duobao Rd, Guangzhou 510150, Peoples R China
[2] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Dept Anesthesiol, Guangzhou, Peoples R China
[3] Guangzhou Med Univ, Affiliated Hosp 3, Dept Renal Transplantat, 63 Duobao Rd, Guangzhou 510150, Peoples R China
关键词
kidney transplantation; pneumocystis jirovecii pneumonia; prophylaxis; risk factors; treatment; ANTIBODY-MEDIATED REJECTION; CARINII-PNEUMONIA; CYTOMEGALOVIRUS-INFECTION; RECIPIENTS; CLASSIFICATION; PROPHYLAXIS; PROSPECTS; OUTBREAK; DISEASE;
D O I
10.1111/myc.13235
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background Pneumocystis jirovecii pneumonia (PJP) is an opportunistic infection among solid organ transplantation. The occurrence of PJP is dangerous and fatal if there is no early identification and sufficient treatment. Objective The aim of this study was to evaluate the risk factors and provide appropriate strategies of prophylaxis and treatment for PJP after kidney transplantation in our centre. Patients/Methods From January 2009 to December 2018, a total of 167 kidney transplantation recipients with pneumonia were enrolled, including 47 PJP patients as PJP group and 120 non-PJP patients as control group. The clinical characteristics of the two groups were analysed retrospectively. Results Multivariate analysis showed that high total dosage of ATG [OR, 2.03; 95% CI, 1.12-3.68] and cytomegalovirus (CMV) infection were independent risk factors for PJP. Trimethoprim-sulfamethoxazole (TMP-SMX) (1.44 g q6h)-based treatment was used for 2 weeks, and its dosage and course were adjusted according to the therapeutic effect and side effects. Forty-five cases were recovered after 3 months of follow-up, and two patients died of respiratory failure. TMP-SMX (0.48 g/day) prophylaxis was used for 3-6 months and prolonged to 7-8 months after treatment for acute rejection, which reduced the incidence of PJP compared with those without prophylaxis. Conclusion Our study suggests that the high total dosage of ATG and CMV infection indicate the increased risk of PJP. The strategies of prophylaxis and treatment for PJP after kidney transplantation in our centre were effective.
引用
收藏
页码:495 / 502
页数:8
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