Table 1 Baseline characteristics of kidney transplant patients according to Pneumocystis jirovecii pneumonia.

From: Comparison of early and late Pneumocystis jirovecii Pneumonia in kidney transplant patients: the Korean Organ Transplantation Registry (KOTRY) Study

Variables

Non-PJP (n = 4,789)

PJP (n = 50)

P value

Age at transplantation (years)

49.1 ± 11.5

51.1 ± 13.6

0.102

Gender (female)

1,945 (40.6%)

20 (40.0%)

0.930

Smoking

  

0.180

Never

3,633 (75.9%)

37 (74.0%)

 

Current

413 (8.6%)

1 (2.0%)

 

Former

691 (14.4%)

11 (22.0%)

 

DM

1,428 (29.8%)

14 (28.0%)

0.780

BMI (kg/m2)

23.1 ± 0.10

21.80 ± 0.48

0.004

Hemoglobin (g/dL)

10.79 ± 2.74

10.63 ± 1.93

0.579

Serum creatinine (mg/dL)

1.29 ± 2.59

1.19 ± 0.39

0.169

eGFR (mL/min/1.73m2)

38.11 ± 36.12

35.60 ± 31.55

0.625

Cause of ESRD

  

0.282

DM, n (%)

1,125 (23.5%)

10 (20.0%)

 

Hypertension, n (%)

757 (15.8%)

6 (12.0%)

 

Glomerulonephritis, n (%)

1,588 (33.2%)

22 (44.0%)

 

Others, n (%)

375 (7.8%)

6 (12.0%)

 

Unknown, n (%)

944 (19.7%)

6 (12.0%)

 

Delayed graft function

176 (3.6%)

4 (8.0%)

0.196

Re-transplantation, n (%)

372 (7.8%)

3 (6.0%)

0.450

Type of donor

  

0.289

Deceased donor, n (%)

3,004 (62.1%)

35 (70.0%)

 

Living donor, n (%)

1,785 (36.9%)

15 (30.0%)

 

Desensitization, n (%)

1,083 (22.5%)

19 (38.0%)

0.011

Number of HLA mismatch

3.2 ± 1.7

3.6 ± 1.4

0.104

Tacrolimus use at discharge, n (%)

4,608 (96.2%)

47 (94.0%)

0.433

Tacrolimus dose at discharge (mg)

5.96 ± 3.44

7.36 ± 4.62

0.014

Tacrolimus dose per body weight at discharge (mg/kg)

0.10 ± 0.00

0.13 ± 0.01

0.001

Tacrolimus level at discharge (ng/mL)

7.83 ± 0.05

8.05 ± 0.45

0.651

Formulation of tacrolimus

  

0.629

Once daily, n (%)

133 (2.7%)

0 (0.0%)

 

Twice daily, n (%)

4,104 (85.69%)

37 (74%)

 

Unknown, n (%)

371 (7.7%)

10 (20%)

 

Tacrolimus conversion (twice to once daily), n (%)

156 (3.87%)

1 (3.03%)

1.000

ATG use, n (%)

998 (20.8%)

7 (14%)

0.236

Steroid use at discharge

4,690 (97.93%)

49 (98.0%)

0.973

MMF use at discharge

4,508 (94.13%)

46 (92.0%)

0.524

mTORi use at discharge

51 (1.06%)

2 (4.0%)

0.047

PJP prophylaxis, n (%)

4,626 (96.60%)

50 (100.0%)

0.184

Dose of prophylactic TMP-SMP, n (%)

  

0.038

Single strength/d or double strength × 3/wk

3,940 (82.27%)

48 (96.0%)

 

Double strength/d

686 (14.32%)

2 (4.0%)

 

Duration of PJP prophylaxis (months)

6.3 ± 2.6

6.0 ± 1.0

0.575

Mean follow up duration (months)

24.93 ± 15.32

8.42 ± 7.57

 < 0.001

  1. Data are presented as mean ± standard deviation, or n (%). Abbreviations: ATG, anti-thymocyte globulin; BMI, body mass index; d, days; DM, diabetes mellitus; eGFR, estimated glomerular filtration rate; ESRD, end stage renal disease; MMF, mycophenolate mofetil; mTORi, mammalian target of rapamycin inhibitor; N/A, not applicable; PJP, pneumocystis jirovecii pneumonia; TMP-SMX, trimethoprim/sulfamethoxazole; w, weeks.