Department of Rehabilitation Medicine, Faculty of Medicine, Chulalongkorn University, b

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Chula Med J Vol. 63 No. 2 April - June 2019; 107-112 DOI : 10.14456/clmj.2019.XX Original article Antimicrobial resistance patterns of bacterial colonization in urine of patients with spinal cord lesion admitted at Thai Red Cross Rehabilitation Center Sutunchalee Sikanjananun a, Sirikwan Panyasriwanit b, Wasuwat Kitisomprayoonkul a, Chusana Suankrata c, Natthiya Tantisiriwat d a Department of Rehabilitation Medicine, Faculty of Medicine, Chulalongkorn University, b Thai Red Cross Rehabilitation Center, Thai Red Cross Society c Division of Infectious Diseases, Department of Medicine, Faculty of Medicine, Chulalongkorn University d Department of Rehabilitation Medicine, King Chulalongkorn Memorial Hospital, Thai Red Cross Society and Department of Rehabilitation Medicine, Faculty of Medicine, Chulalongkorn University Background: The emergence of extended spectrum beta-lactamase (ESBL)-producing Escherichia coli and Klebsiella pneumoniae at the stand-alone Rehabilitation Center of the Thai Red Cross Society has become a concern for treatment of patients with neurogenic bladder. Objective: To identify commonly observed bacterial colonization in urine of patients with spinal cord lesion. Methods: Medical records of all 135 patients with spinal cord lesion and admitted at the Thai Red Cross Rehabilitation Center were retrospectively reviewed for demographic data, type of neurogenic bladder and bladder management, common bacterial colonization in urine specimens with antimicrobial susceptibility reports. Results: Of the 135 spinal cord lesion patients, 100 were male with the median age of 47 years old: 85% of them had neurogenic bladder, 39.8% detrusor overactivity (DO), 35% DO with detrusor sphincter dyssynergia, 24.3% detrusor underactivity, and 1% mixed type. Escherichia coli was the most frequent isolate followed by Klebsiella pneumoniae. Both E. coli and K. pneumoniae were multidrug-resistant (MDR) strains: 100% resistant to penicillin, fluoroquinolones (FQ), trimethoprim/ sulfamethoxazole (TMP-SMZ), and amoxicillin-clavulanic acid (AMC); 66.7% resistant to cephalosporin; 28.6% resistant to carbapenems; and, 28.6% resistant to aminoglycosides. Conclusion: MDR E.coli and K. pneumoniae were the most commonly observed bacterial colonizations in patients with spinal cord lesion who were admitted at our institute. E. coli isolates are highly resistant to almost all antimicrobials except aminoglycosides and carbapenems. K. pneumoniae isolates are highly resistant to all antimicrobials which were firstly found resistant to aminoglycosides and carbapenems in the 2015. Keywords: Bacterial colonization, spinal cord lesion, neurogenic bladder, urinary tract infection, extended spectrum beta-lactamase producing Enterobacteriaceae. The emergence of extended spectrum betalactamase (ESBL)-producing Escherichia coli and Klebsiella pneumoniae at the stand-alone Correspondence to: Tantisiriwat N. Department of Rehabilitation Medicine, King Chulalongkorn Memorial Hospital, Thai Red Cross Society and Faculty of Medicine, Chulalongkorn University, Bangkok10330, Thailand. E-mail: natthiyamd@gmail.com Received : September 12, 2018 Revised : October 11, 2018 Accepted : October 17, 2018 Rehabilitation Center of Thai Red Cross Society has become a concern for treatment of patients with neurogenic bladder due to their spinal cord lesion. (1) Patients with spinal cord lesions who have neurogenic bladder (NGB) have a tendency to develop urinary tract infection (UTI). (2-4) Urinalysis and antimicrobial susceptibility tests were frequently performed among these patients at the Rehabilitation Center of Thai Red Cross Society from 2007 to 2015 because proper antimicrobial prescription is necessary for patients diagnosed with UTI. Bacterial colonizations in urine

108 S. Sikanjananun, et al. Chula Med J and perineum area are considered as the risk factors associated with UTI. (2) The present study is aimed to identify commonly observed bacterial colonization in urine specimens and antimicrobial resistance patterns to implement new strategic approaches for this ESBL-producing Enterobacteriaceae. Methods The medical records of all 135 patients with spinal cord lesion who were admitted at the Thai Red Cross Rehabilitation Center were retrospectively reviewed for demographic data, type of neurogenic bladder and bladder management, common bacterial colonization in urine specimens with antimicrobial susceptibility reports and episodes of UTI. Materials and Methods Operational definition Patients with spinal cord lesions who were admitted at the Rehabilitation Center, the Thai Red Cross Society, were defined as patients with length of hospital stay greater than 48 hours.bacterial colonization was defined as bacteria presented in urine specimen. Pyuria was defined as urinalysis reporting the amount of white blood cell (WBC) counts per high power field (HPF) has been 10 WBC or more. (5) High pyuria level was defined as WBC count greater than 50 WBC count/hpf whereas low pyuria level was defined as WBC count range from 10 50 WBC count/hpf. (6) Urinary tract infection (UTI) was defined as bacteriuria ( 10 2 colony forming units (CFU)/mL for intermittent catheter specimens; ( 10 4 CFU/mL) for condom catheter and any value from indwelling urethral and suprapubic catheter with tissue invasion and resultant tissue response with signs and/or symptoms. Significant bacteriuria was defined as bacteriuria of 10 5 CFU/mL or higher. For patients with spinal cord lesion and NGB, signs and/or symptoms sometimes differed from general patients by the following: fever, discomfort or pain over kidney or bladder increasing in spasticity, new episodes and/or increasing in urinary incontinence and autonomic dysreflexia. (7) Asymptomatic bacteriuria represented bacterial colonization of the urinary tract without symptoms or signs. (7) Uropathogens represented bacterial colonization of the urinary tract resulting in urinary tract infection. Nosocomial urinary tract infection (NUTI) was defined as the infection is acquired in any healthcare institutions. (8) The NUTI in the present study was determined by the onset greater than 3 days as after admission. Reviewed antimicrobial susceptibility reports were defined as reports from urine cultures performed under attending clinician s decision. Study design, setting, and ethical considerations This retrospective study was performed at the Thai Red Cross Rehabilitation Center. Data from January 2013 to May 2015 of the patients with spinal cord lesion were retrospectively reviewed. The data included in-patient records, urinalysis reports and antimicrobial susceptibility reports. Protocol for the study has been approved by the Institutional Review Board (IRB) of the Faculty of Medicine, Chulalongkorn University (IRB. No 289/58). This study was registered in the Thai Clinical Trials Registry (TCTR20160712003). Statistical analysis and data presentation Data were analysed using SPSS Statistics version 22.0 (SPSS, Inc., Chicago, IL, USA). Demographic data were collected and tested for normal distribution. Normal distribution data were demonstrated as mean and percentage whereas non normal distribution data were demonstrated as median and interquartile range; IQR1- IQR3. Resistance patterns to each antimicrobial of most common bacterial colonization were reported as biannual percentage. Results In total, there were 135 patients with spinal cord lesion (male: female = 100:35) in the study; their median age was 47 years old; all together, there were 154 admissions. Eighty-five percent of the patients were diagnosed with NGB. The median length of hospital stay was 39 days. All other demographic data are presented in Table 1. Of 135 patients, all urinalyses revealed pyuria (63%); 87 antimicrobial susceptibility reports were reviewed during the 30-month study period. These reports revealed asymptomatic bacteriuria (49%) and uropathogens (51%). The bacterial colonization in each biannual percentage demonstrated multiple organisms (0 31.6%) and single organisms (68.4 100%). During the 30-month study, out of 135 patients with UTI, 36 patients were with UTI (26.7 %) and 32 patients with NUTI (23.7%). Most patients had a single episode of UTI while 7 patients had recurrent UTI. Escherichia coli was the common isolate

Vol. 63 No.2 April - June 2019 Antimicrobial resistance patterns of bacterial colonization in urine of patients with spinal cord lesion admitted at Thai Red Cross Rehabilitation Center 109 (66.7%, 33.3%, 52.9%, 36.8 and 56.5% in the first half and second half of 2013, 2014 and the first half of 2015, respectively) followed by K. pneumoniae (0 40.0 %) as shown in Table 2. Both organisms are susceptible to cephalosporin, aminoglycosides and carbapenem but demonstrated high resistance to penicillin, fluoroquinolones (FQ), trimethoprim/ sulfamethoxazole (TMP-SMZ) and amoxicillinclavulanic acid (AMC). The antibiotic susceptibility patterns of the two most common isolations are described as details (Table 3). Table 1. Demographic data. Demographic data Value Male (%) 74.0 Age (years) Median, IQR ; IQR 1- IQR3 47.0; 28.0-67.0 Onset of spinal cord lesion (days) Median, IQR ; IQR 1- IQR3 18.0; 7.0-51.0 Length of hospital stay (days) 39.0; 30.0-58.5 Traumatic causes of spinal cord lesion (%) 51.0 Level of spinal cord lesion (%) Cervical 59.0 Thoracic 25.0 Lumbar 13.0 Sacrum 2.0 Cauda equina 1.0 ASIA impairment scale (%) A/B/C/D/E 32.0/12.0/21.0/47.0 Neurogenic bladder (%) 85.0 Detrusor overactivity 40.0 Detrusor overactivity with detrusor sphincter dyssynergia 35.0 Detrusor underactivity 24.0 Mixed type 1.0 Bladder Management Clean intermittent catheterization 41.0 Able to perform void 28.0 Indwelling urethra 27.0 Pampers 3.0 Condom 1.0 Accommodation before admission (%) Home 95.0 Hospital 2.0 Rehabilitation center 1.0 Unspecified 2.0 Table 2. The first four commonly isolated organisms. Organisms 1 st half of 2 nd half of 1 st half of 2 nd half of 1 st half of 2013 2013 2014 2014 2015 Escherichia coli 66.7 33.3 52.9 36.8 56.5 Klebsiella pneumoniae - 40.0 11.8 10.5 4.3 Enterococcus faecalis - 6.7-10.5 - Pseudomonas aeruginosa 22.2 6.7 - - -

110 S. Sikanjananun, et al. Chula Med J Table 3. Antimicrobial susceptibility patterns in two commonly isolated organisms. Organism Antimicrobials 1 st half of 2 nd half of 1 st half of 2 nd half of 1 st half of 2013 2013 2014 2014 2015 E. coli FQ S 0% (0/6) 16.7% (1/6) 40% (4/10) 10% (1/10) 25% (5/20) R 100% (6/6) 83.3% (5/6) 60% (6/10) 90% (9/10) 75% (15/20) TMP-SMZ S 16.7% (1/6) 16.7% (1/6) 10% (1/10) 30% (3/10) 45% (9/20) R 83.3% (5/6) 83.3% (5/6) 90% (9/10) 50% (5/10) 50% (10/20) Penicillin S 0% (0/6) 0% (0/6) 10% (1/10) 0% (0/10) 15% (3/20) R 100% (6/6) 100% (6/6) 90% (9/10) 100% (6/10) 75% (15/20) AMC S 50% (3/6) 16.7% (1/6) 30% (3/10) 10% (1/10) 55% (11/20) R 16.7% (1/6) 66.7% (4/6) 30% (3/10) 50% (5/10) 30% (6/20) Cephalosporin S 66.7% (4/6) 16.7% (1/6) 70% (7/10) 50% (5/10) 70% (14/20) R 33.3% (2/6) 66.7% (4/6) 20% (2/10) 30% (3/10) 25% (5/20) Aminoglycosides S 100% (6/6) 100% (6/6) 90% (9/10) 90% (9/10) 100% (20/20) R 0% (0/6) 0% (0/6) 0% (0/10) 0% (0/10) 0% (0/20) Carbapenems S 100% (6/6) 100% (6/6) 100% (10/10) 100% (10/10) 100% (20/20) R 0% (0/6) 0% (0/6) 0% (0/10) 0% (0/10) 0% (0/20) K. pneumoniae FQ S - 66.7% (4/6) 100% (2/2) 50% (2/4) 28.6% (2/7) R - 33.3% (2/6) 0% (0/2) 50% (2/4) 71.4% (5/7) TMP-SMZ S - 66.7% (4/6) 0% (0/2) 0% (0/4) 57.1% (4/7) R - 33.3% (2/6) 100% (2/2) 75% (3/4) 42.9% (3/7) Penicillin S - 0% (0/6) 0% (0/2) 0% (0/4) 0% (0/7) R - 66.7% (4/6) 50% (1/2) 75% (3/4) 100% (7/7) AMC S - 66.7% (4/6) 0% (0/2) 50% (2/4) 28.6%(2/7) R - 16.7% (1/6) 100% (2/2) 25% (1/4) 42.9% (3/7) Cephalosporin S - 83.3% (5/6) 0% (0/2) 75% (3/4) 71.4% (5/7) R - 16.7% (1/6) 0% (0/2) 25% (1/4) 28.6% (2/7) Aminoglycosides S - 100% (6/6) 50% (1/2) 75% (3/4) 71.4% (5/7) R - 0% (0/6) 0% (0/2) 0% (0/4) 28.6% (2/7) Carbapenems S - 100% (6/6) 100% (2/2) 100% (4/4) 71.4% (5/7) R - 0% (0/6) 0% (0/2) 0% (0/4) 28.6% (2/7) Abbreviation: FQ; Fluoroquinolone, Trimethoprim-sulfamethoxazole; (TMP-SMZ), Penicillin; PCN, Amoxicillin + Clavulanic acid; AMC, S; Sensitive, R; Resistant Table 4. Antimicrobial resistant patterns of isolated bacteria from 2014 to 2016. Antimicrobials Organisms 1 st half of 2 nd half of 1 st half of 2 nd half of 1 st half of 2013 2013 2014 2014 2015 FQ E. coli 100.0 83.3 60.0 90.0 75.0 K. pneumoniae - 33.3-50.0 71.4 TMP-SMZ E. coli 83.3 83.3 90.0 50.0 50.0 K. pneumoniae - 33.3 100.0 50.0 42.9 Penicillin E. coli 100.0 100.0 90.0 100.0 75.0 K. pneumoniae - 66.7 50.0 75.0 100.0 AMC E. coli 16.7 66.7 30.0 50.0 30.0 K. pneumoniae - 16.7 100.0 25.0 42.9 Cephalosporin E. coli 33.3 66.7 20.0 30.0 25.0 K. pneumoniae - 16.7-25.0 28.6 Carbapenems E. coli - - - - - K. pneumoniae - - - - 28.6 Aminoglycosides E. coli - - - - - K. pneumoniae - - - - 28.6 Abbreviation: FQ; Fluoroquinolone, Trimethoprim-sulfamethoxazole; (TMP-SMZ) Penicillin; PCN, Amoxicillin + Clavulanic acid; AMC

Vol. 63 No.2 April - June 2019 Antimicrobial resistance patterns of bacterial colonization in urine of patients with spinal cord lesion admitted at Thai Red Cross Rehabilitation Center 111 Discussion Significant bacterial colonizations were found among all urine specimens. Multidrug-resistant (MDR) E. coli and K. pneumoniae, were commonly presented in urine specimens. These finding were present similiarly as previous studies which were performed at rehabilitation wards of acute hospital care. (9, 10) In the early review period at 12 months, Pseudomonas aeruginosa was as high as 20% in our stand-alone rehabilitation center. It then disappeared for 18 months. In comparison with our setting as a stand-alone rehabilitation center, P. aeruginosa was found significantly higher at 9.1% - 17.3% in rehabilitation wards of acute hospital (9-11) care. The prevalence of UTI in the present study demonstrated lower rates than previous study. For cephalosporin, ESBL-producing E. coli and ESBLproducing K. pneumoniae, our findings revealed higher resistance animicrobial patterns than the previous study performed in 2007 (20% vs. 25%). (1) As for aminoglycosides, E. coli revealed great susceptability that was similar to previous studies, before whereas K. pneumoniae revealed first-half resistance in 2015 with a slightly higher rate than previous studies (20% vs. 28.6%). Moreover these causative organism were found as the new infection. The present study demonstrates that antimicrobial resistance patterns of bacterial colonization in urine specimens among patients with spinal cord lesion is higher than prior studies; moreover, the resistant of K. pneumoniae to carbapenem and aminoglycoside was firstly demonstrated in the first half of 2015. (1) These findings require close monitoring together with controlling the spread of the organism. Nitrofuratoin is recommended as the initial treatment for lower urinary tract infection with proven optimal efficacy when it is prescribed for 5 days. Short-term usage of nitrofurantoin for 14 days or lower revealed low adverse events such as pulmonay fibrosis, gastrointestinal side effect and hepatotoxicity. Moreover, acquisition of resistance to nitrofurantoin is relatively rare. (12) Frequent urine specimen screening by urine analysis and culture for all patients with spinal cord lesion is necessary to identify pyuria and ESBL-producing Enterobacteriaceae might not be a cost-effective strategy, nevertheless an optimal control strategy to restrict the spread of ESBL-producting Enterobacteriaceae seems more appropriate. (13) The present study provides important information for our stand-alone rehabilitation center, the Thai Red Cross Society. Strategic approaches for ESBLproducing Enterobacteriaceae at our setting requires extensive changes. Firstly, managing and control of the spread of ESBL-producing Enterobacteriaceae is required. Secondly, urine specimen screening by urine analysis and urine culture among patients with spinal cord lesion should be terminated because these methods are ineffective. Routine clinical assessement proves more important and beneficial than these tests as urine analysis and culture are only indicated for clinical presentations with suspected UTI before prescribing antimicrobials to patients. Thirdly, initially prescribed antimicrobial for patients diagnosed with UTI should be amikacin for those with high risk of upper tract infection and nitrofuratoin for patients with lower tract infections. Proper antimicrobial medication must then be selected according to the antisusceptility report. The appropriate duration for treating patients with NGB is recommended for at least 14 days. (14-15) Fourthly, cephalosporin usage as antimicrobial prophylaxis before urodynamic (UDM) assessment should be terminated in order to prevent an increasing percentage of cephalosporin resistance. Conclusion Extended spectrum beta-lactamase (ESBL)- producing MDR E. coli and K. pneumoniae are observed as the most common bacterial colonizations in patients with spinal cord lesion admitted at our institute. Regarding the high percentage of resistance, E. coli isolates had high resistance to almost all antimicrobials except aminoglycosides and carbapenems. K. pneumoniae isolates are highly resistant to all antimicrobials which are firstly found resistant to aminoglycosides and carbapenems in the first half of 2015. Conflict of interest None of the authors has any potential conflict of interest to disclose. References 1. Tantisiriwat N, Kittisomprayoonkul W, Sukonthamarn K, Unhasuta C, Suankratay C, Tantisiriwat W, et al. Uropathogens and empiric antibiotics for the treatment of urinary tract infections in spinal cord injured patients at rehabilitation center, Thai Red Cross Society during 2001 to 2005. J Med Assoc Thai 2007;90:2482-6.

112 S. Sikanjananun, et al. Chula Med J 2. McKibben MJ, Seed P, Ross SS, Borawski KM. Urinary tract infection and neurogenic bladder. Urol Clin North Am 2015;42:527-36. 3. Mukai S, Shigemura K, Nomi M, Sengoku A, Yamamichi F, Fujisawa M, et al. Retrospective study for risk factors for febrile UTI in spinal cord injury patients with routine concomitant intermittent catheterization in outpatient settings. Spinal Cord 2016;54:69-72. 4. Stover SL, Lloyd LK, Waites KB, Jackson AB. Neurogenic urinary tract infection. Neurol Clin 1991; 9:741-55. 5. Jahromi MS, Mure A, Gomez CS. UTIs in patients with neurogenic bladder. Curr Urol Rep 2014;15:433. 6. Roghmann MC, Wallin MT, Gorman PH, Johnson JA. Prevalence and natural history of colonization with fluoroquinolone-resistant gram-negative bacilli in community-dwelling people with spinal cord dysfunction. Arch Phys Med Rehabil 2006;87:1305-9. 7. The prevention and management of urinary tract infections among people with spinal cord injuries. National Institute on Disability and Rehabilitation Research Consensus Statement. January 27-29, 1992. J Am Paraplegia Soc 1992;15:194-204. 8. Iacovelli V, Gaziev G, Topazio L, Bove P, Vespasiani G, Finazzi AE. Nosocomial urinary tract infections: A review. Urologia 2014;81:222-7. 9. Pongpipatpaiboon K, Wattanapan P, Arayawichanon P. The use of urine dipstick for screening of urinary tract infection in patients with neurogenic bladder secondary to spinal cord lesion. J Thai Rehabil Med 2013;23:1-6. 10. Siripornmongkhol P, Kharmwan S, Tamnanthong N. Urinary tract infection in neurogenic bladder after Completion of Bladder training. J Thai Rehabil Med 2010;20:58-62. 11. Ploypetch T, Dajpratham P, Assanasen S, Thanakiatpinyo T, Tanvijit P, Karawek J. Epidemiology of urinary tract infection among spinal cord injured patients in rehabilitation ward at Siriraj Hospital. J Med Assoc Thai 2013;96:99-106. 12. Huttner A, Verhaegh EM, Harbarth S, Muller AE, Theuretzbacher U, Mouton JW. Nitrofurantoin revisited: a systematic review and meta-analysis of controlled trials. J Antimicrob Chemother 2015;70: 2456-64. 13. Han JH, Bilker WB, Nachamkin I, Zaoutis TE, Coffin SE, Linkin DR, et al. The effect of a hospital-wide urine culture screening intervention on the incidence of extended-spectrum beta-lactamase-producing Escherichia coli and Klebsiella species. Infect Control Hosp Epidemiol 2013;34:1160-6. 14. Vigil HR, Hickling DR. Urinary tract infection in the neurogenic bladder. Transl Androl Urol 2016;5:72-87. 15. Tungsanga K, Chongthaleong A, Udomsantisuk N, Bejraputra O, Sitprija V. A randomized double-blind compaison of Norfloxacin and Cotrimoxazole in the treatment of upper urinary tract infection. Chula Med J 1988; 32: 727-37