Abstract
Purpose
This study compared the clinical benefits of double J (DJ) ureteral stenting with percutaneous nephrostomy (PCN) for the management of acute pyelonephritis (APN) with complicated ureteral stones.
Materials and Methods
The records of 85 patients with complicated APN between December 2006 and July 2017 were reviewed retrospectively. Sixty one patients who underwent DJ or PCN for the management of acute urinary obstruction were enrolled in this study. Some of the participants were excluded for concurrent renal stones, multiple ureteral stones, ureteral stricture, malignancy, and anatomical anomalies. The patient and stone characteristics and peri-procedural laboratory test results of the groups were compared. The success rate, depending on the type of urinary diversion and the presence of immediate complications, were also analyzed.
Results
In this study, 19 patients underwent DJ stenting, and 42 patients underwent PCN as a transient urinary diversion. No failed procedures or immediate complications requiring subsequent intervention were encountered (Clavien–Dindo grade II-V). Urologists preferred PCN to DJ stenting in cases with an elevated serum creatinine level (p=0.001) and higher C-reactive protein (CRP) level (p<0.001). The indicative parameters for renal injury and septic conditions (white blood cell count, segment neutrophil, and creatinine levels) tended to show immediate improvement, whereas CRP did not; however, the differences in markers were not significant (p=0.701, 0.962, 0.288, and 0.360, respectively).
References
1. Hamasuna R, Takahashi S, Nagae H, Kubo T, Yamamoto S, Arakawa S, et al. Obstructive pyelonephritis as a result of urolithiasis in Japan: diagnosis, treatment and prognosis. Int J Urol. 2015; 22:294–300.
2. Kim B, Myung R, Kim J, Lee MJ, Pai H. Descriptive epidemiology of acute pyelonephritis in Korea, 2010–2014: population-based study. J Korean Med Sci. 2018; 33:e310.
3. Lee DG, Jeon SH, Lee CH, Lee SJ, Kim JI, Chang SG. Acute pyelonephritis: clinical characteristics and the role of the surgical treatment. J Korean Med Sci. 2009; 24:296–301.
4. Richter S, Ringel A, Shalev M, Nissenkorn I. The indwelling ureteric stent: a ‘friendly' procedure with unfriendly high morbidity. BJU Int. 2000; 85:408–11.
5. Ku JH, Lee SW, Jeon HG, Kim HH, Oh SJ. Percutaneous nephrostomy versus indwelling ureteral stents in the management of extrinsic ureteral obstruction in advanced malignancies: are there differences? Urology. 2004; 64:895–9.
6. Baishya RK, Dhawan DR, Jagtap J, Sabnis R, Desai MR. Percutaneous nephrostomy under ultrasound guidance. Indian J Nephrol. 2011; 21:67.
7. Preminger GM, Tiselius HG, Assimos DG, Alken P, Buck C, Gallucci M, et al. EAU/AUA Nephrolithiasis Guideline Panel. 2007 guideline for the management of ureteral calculi. J Urol. 2007; 178:2418–34.
8. Goldsmith ZG, Oredein-McCoy O, Gerber L, Bañez LL, Sopko DR, Miller MJ, et al. Emergent ureteric stent vs percutaneous nephrostomy for obstructive urolithiasis with sepsis: patterns of use and outcomes from a 15-year experience. BJU Int. 2013; 112:E122–8.
9. Mokhmalji H, Braun PM, Martinez Portillo FJ, Siegsmund M, Alken P, Kohrmann KU. Percutaneous nephrostomy versus ureteral stents for diversion of hydronephrosis caused by stones: a prospective, randomized clinical trial. J Urol. 2001; 165:1088–92.
10. Pearle MS, Pierce HL, Miller GL, Summa JA, Mutz JM, Petty BA, et al. Optimal method of urgent decompression of the collecting system for obstruction and infection due to ureteral calculi. J Urol. 1998; 160:1260–4.
11. Van Glabeke E, Conort P, Chartier-Kastler E, Desrez G, Boyer C, Richard F. [Treatment of complicated renal colic in patients treated with indinavir: value of double J stents]. Prog Urol. 1999; 9:470–3. French.
Table 1.
Characteristic | Double J stent (n=19) | Percutaneous nephrostomy (n=42) | p-value |
---|---|---|---|
Age (y) | 56.8 (24–86) | 60.3 (21–92) | 0.443 |
Sex | 0.737 | ||
Male (n=13) | 3 (23.1) | 10 (76.9) | |
Female (n=48) | 16 (33.3) | 32 (66.7) | |
Underlying disease | |||
Diabetes mellitus | 2 (10.5) | 12 (28.6) | 0.992 |
Hypertension | 10 (52.6) | 20 (47.6) | 0.180 |
Ischemic heart disease | 0 (0) | 1 (2.4) | 0.530 |
Cerebrovascular disease | 4 (21.1) | 5 (11.9) | 0.415 |
Medical history (Hx.) | |||
Stone Hx. | 3 (15.8) | 14 (33.3) | 0.961 |
Urinary tract infection Hx. | 4 (21.1) | 7 (16.7) | 0.856 |
Stone | |||
Size (mm) | 9.3 (3–23) | 8.9 (1.1–28) | 0.802 |
Proximal/mid/distal | 12 (63.2)/1 (5.3)/6 (31.6) | 27 (64.3)/4 (9.5)/11 (26.2) | – |
Culture | |||
Positive urine culture | 9 (47.4) | 28 (66.7) | 0.153 |
Bacteremia | 4 (21.1) | 19 (45.2) | 0.091 |
Failure | 0 (0) | 0 (0) | – |
Mortality | 0 (0) | 0 (0) | – |
Initial laboratory data | |||
White blood cell (×103/l) | 1.28 (0.68–2.20) | 1.21 (0.18–2.99) | 0.604 |
Segment neutrophil (%) | 78.1 (55.0–95.9) | 82.3 (35.3–94.4) | 0.277 |
Hemoglobin (g/dl) | 12.3 (8.5–13.9) | 12.0 (9.4–16) | 0.040∗ |
Hematocrit (%) | 37.0 (27.1–41.0) | 35.7 (27.5–45.2) | 0.015∗ |
Platelet count (×103/l) | 249 (70–458) | 201 (39–505) | 0.007∗ |
Blood urea nitrogen (mg/dl) | 16.4 (8–30) | 19.2 (9–50) | 0.092 |
Creatinine (mg/dl) | 0.88 (0.48–1.30) | 1.29 (0.32–3.70) | 0.001∗ |
Erythrocyte sedimentation rate (mm/hr) | 38.0 (6–85) | 54.0 (2–108) | 0.099 |
C-reactive protein (mg/dl) | 4.40 (0.2–16.5) | 11.83 (0.02–33.3) | <0.001∗ |
Albumin (g/dl) | 4.12 (2.9–4.9) | 3.87 (2.5–4.8) | 0.081 |
Aspartate transaminase (U/L) | 27.9 (17–74) | 29.6 (12–163) | 0.786 |
Alanine transaminase (U/L) | 27.3 (11–118) | 21.5 (4–97) | 0.301 |
Na (mEq/L) | 136.7 (130–141) | 136.5 (124–143) | 0.875 |
K (mEq/L) | 3.80 (3.1–4.2) | 3.73 (2.4–4.7) | 0.472 |