Abstract:Up to now one of the major problems for successful organ transplantation has been the reaction of the immune system of the recipient against the donor organ. This could lead to acute and chronic rejection, and in cases of unsuccessful treatment to the loss of the transplant. In organ graft recipients, immunosuppressive agents are used to prevent or treat rejection episodes and to maintain graft function. Although there is an increasing number of immunosuppressive substances, the immunosuppressive therapy curre… Show more
“…I n adults, urinary tract infection (UTI) after renal transplantation has been associated with significant morbidity (1). The use of postoperative antibiotic prophylaxis has reduced dramatically the incidence of UTI after renal transplantation in the past few decades (2,3).…”
Urinary tract infection (UTI) is the most common infection after kidney transplantation.A previous analysis showed that late (>6 mo after transplantation) UTI is associated with earlier graft loss in adults. It was hypothesized that children who are younger than 18 yr would be at higher risk to develop UTI and develop graft loss after both early and late UTI. The US Renal Data System database was analyzed from 1996 to 2000 for Medicare claims (composite of inpatient and outpatient) for UTI up to 36 mo after transplantation. SPSS software and Cox regression models were used to determine association of UTI and age after adjustment for covariates. Early UTI was defined as occurring <6 mo after transplantation, and late UTI was defined as occurring >6 mo after transplantation. The risk for graft loss after early UTI was elevated in all children (adjusted hazard ratio [AHR] 5.47; 95% confidence interval [CI] 1.93 to 15.4; P < 0.001) but not after late UTI (AHR 2.09; 95% CI 0.56 to 7.80; P ؍ 0.27). Risk for posttransplantation death was not increased significantly after either early UTI (AHR 1.23; 95% CI 0.37 to 4.08) or late UTI (relative risk 2.22; 95% CI 0.90 to 5.44). Boys aged 2 to 5 (versus age 13 to <18 years) were at significantly higher risk for UTI. In girls, only those in the youngest age category (0 to 1) had higher risk for UTI. Children are at greater risk for graft loss after early but not necessarily late UTI. UTI was not an independent predictor of death in this population.Clin J Am Soc Nephrol 2: 100 -106, 2007. doi: 10.2215/CJN.01820506 I n adults, urinary tract infection (UTI) after renal transplantation has been associated with significant morbidity (1). The use of postoperative antibiotic prophylaxis has reduced dramatically the incidence of UTI after renal transplantation in the past few decades (2,3). Nevertheless, the rates of serious posttransplantation complications that are associated with UTI, such as bacterial septicemia, remain high for patients even in the modern era (4). Most centers generally stop antibiotic prophylaxis within 3 to 6 mo after kidney transplantation in adult and pediatric recipients (5). Late posttransplantation UTI (occurring Ͼ6 mo after transplantation) is widely considered to be "benign" on the basis of data from relatively small studies (6,7). However, more recent studies suggest that even late UTI after renal transplantation has definite risks (8). In adults, we demonstrated from a recent large data analysis of the US Renal Data System (USRDS) that late UTI in adult renal transplant recipients is associated with a higher risk for both graft loss and patient death (8); late UTI may not be as benign as previously believed. However, the impact of posttransplantation UTI on outcomes in children may not be identical to the impact in adults.Children have a different distribution of causes of ESRD, such as a high proportion of congenital lesions such as reflux nephropathy or posterior urethral valves. In addition, primary bladder dysfunction frequently is associated wi...
“…I n adults, urinary tract infection (UTI) after renal transplantation has been associated with significant morbidity (1). The use of postoperative antibiotic prophylaxis has reduced dramatically the incidence of UTI after renal transplantation in the past few decades (2,3).…”
Urinary tract infection (UTI) is the most common infection after kidney transplantation.A previous analysis showed that late (>6 mo after transplantation) UTI is associated with earlier graft loss in adults. It was hypothesized that children who are younger than 18 yr would be at higher risk to develop UTI and develop graft loss after both early and late UTI. The US Renal Data System database was analyzed from 1996 to 2000 for Medicare claims (composite of inpatient and outpatient) for UTI up to 36 mo after transplantation. SPSS software and Cox regression models were used to determine association of UTI and age after adjustment for covariates. Early UTI was defined as occurring <6 mo after transplantation, and late UTI was defined as occurring >6 mo after transplantation. The risk for graft loss after early UTI was elevated in all children (adjusted hazard ratio [AHR] 5.47; 95% confidence interval [CI] 1.93 to 15.4; P < 0.001) but not after late UTI (AHR 2.09; 95% CI 0.56 to 7.80; P ؍ 0.27). Risk for posttransplantation death was not increased significantly after either early UTI (AHR 1.23; 95% CI 0.37 to 4.08) or late UTI (relative risk 2.22; 95% CI 0.90 to 5.44). Boys aged 2 to 5 (versus age 13 to <18 years) were at significantly higher risk for UTI. In girls, only those in the youngest age category (0 to 1) had higher risk for UTI. Children are at greater risk for graft loss after early but not necessarily late UTI. UTI was not an independent predictor of death in this population.Clin J Am Soc Nephrol 2: 100 -106, 2007. doi: 10.2215/CJN.01820506 I n adults, urinary tract infection (UTI) after renal transplantation has been associated with significant morbidity (1). The use of postoperative antibiotic prophylaxis has reduced dramatically the incidence of UTI after renal transplantation in the past few decades (2,3). Nevertheless, the rates of serious posttransplantation complications that are associated with UTI, such as bacterial septicemia, remain high for patients even in the modern era (4). Most centers generally stop antibiotic prophylaxis within 3 to 6 mo after kidney transplantation in adult and pediatric recipients (5). Late posttransplantation UTI (occurring Ͼ6 mo after transplantation) is widely considered to be "benign" on the basis of data from relatively small studies (6,7). However, more recent studies suggest that even late UTI after renal transplantation has definite risks (8). In adults, we demonstrated from a recent large data analysis of the US Renal Data System (USRDS) that late UTI in adult renal transplant recipients is associated with a higher risk for both graft loss and patient death (8); late UTI may not be as benign as previously believed. However, the impact of posttransplantation UTI on outcomes in children may not be identical to the impact in adults.Children have a different distribution of causes of ESRD, such as a high proportion of congenital lesions such as reflux nephropathy or posterior urethral valves. In addition, primary bladder dysfunction frequently is associated wi...
“…The incidence of bacterial infection in renal transplant recipients is directly related to the net immunosuppressive effect achieved and the duration of time over which this therapy is administered. Bacterial urinary tract infections (UTIs) are frequently associated with the early onset of chronic rejection and may also lead to reduced transplant survival (15,18). Studies have shown that in 40 to 60% of transplant recipients the urinary tract is the source of septicemia and that in patients with urosepsis the recurrence rate was approximately 40% (1,13).…”
Renal transplant recipients are predisposed to urinary tract infections caused by both common uropathogens and opportunistic bacteria resulting frequently in significant polymicrobial infections. In this study, a culture-independent 16S rRNA-based approach was established to identify unusual, fastidious, or anaerobic bacteria and to investigate bacterial diversity in urinary tract specimens. Similarly sized amplicons encompassing the V6 to V8 region of the 16S rRNA were analyzed with denaturing high-performance liquid chromatography (DHPLC) (WAVE System). Artificial mixtures of single amplicons from commonly encountered uropathogenic bacteria produced distinct peak profiles whose identities were confirmed by sequencing individually collected peak products. We evaluated the application of the method on 109 urinary tract specimens from renal transplant recipients; 100% correlation was found for culture-positive specimens, and DHPLC generated peak profiles. However, for culture-negative specimens, DHPLC facilitated the detection of novel peak profiles. DNA sequencing of these individual peaks was used to identify the bacteria involved. Thus, in PCR-positive but culture-negative samples the method allowed detection of previously known uropathogens such as Corynebacterium urealyticum and Gardnerella vaginalis, but also unusual agents including Anaerococcus lactolyticus, Bacteroides vulgatus, Dialister invisus, Fusobacterium nucleatum, Lactobacillus iners, Leptotrichia amnionii, Prevotella buccalis, Prevotella ruminicola, Rahnella aquatilis, and Streptococcus intermedius were detected as single pathogens or as constituents of polymicrobial infections. The method described is reproducible and rapidly and enables both DHPLC-based profiling and sequence-based investigation of microbial communities and polymicrobial infections. A detailed understanding of infections found in recipients of renal transplants will guide antibiotic therapy regimens and provide new perspectives for decreasing the risk of graft rejection.Currently, one of the major problems for successful kidney transplantation is the reaction of the immune system of the recipient against the donor organ, which in the case of unsuccessful immunosuppressive treatment can result in the loss of the transplant. In order to prevent or treat such rejection episodes and to maintain graft function the application of immunosuppressive agents is standard practice. The incidence of bacterial infection in renal transplant recipients is directly related to the net immunosuppressive effect achieved and the duration of time over which this therapy is administered. Bacterial urinary tract infections (UTIs) are frequently associated with the early onset of chronic rejection and may also lead to reduced transplant survival (15,18). Studies have shown that in 40 to 60% of transplant recipients the urinary tract is the source of septicemia and that in patients with urosepsis the recurrence rate was approximately 40% (1, 13).
“…Differences in the definition of UTI, follow-up period, time of testing and the use of antimicrobial prophylaxis may explain this wide range 3 . Previously bacterial agents isolated from renal transplant recipients with UTI were almost similar to those causing UTI in the general population 4 . In Bangabandhu Sheikh Mujib Medical University (BSMMU) over a period of 2 years from January 2002 to December 2003 Islam et al 5 studied 31 post renal transplant patients of which 51 episodes of bacterial infection occur.…”
Abstract:Urinary tract infection (UTI) is the most common infectious complications after renal transplantation. Recently many researchers reported that the bacterial agents of UTI in renal allograft recipients changed and demonstrated increased antimicrobial resistance to commonly used cephalosporins. This study was undertaken to isolate the bacteria which are responsible for UTI and their susceptibility pattern for appropriate antibiotic therapy in renal allograft recipients. This was an observational study conducted in the Department of Microbiology Bangabandhu Sheikh Mujib Medical University (BSMMU) from December 2010 to 2011. Twenty one renal allograft recipients from Department of Nephrology were evaluated for UTI after surgery up to six weeks. Microscopic examination, culture and sensitivity of urine specimen were performed. Out of 21 renal allograft recipients, 13(61.90%) patients developed UTI during initial post transplant period. Of 69 urine specimens collected from them 22(31.88%) yielded positive results for culture. Enterococcus spp. (50%) was the major bacterial pathogen isolated and showed 100% resistance to Cefuroxime, Ceftriaxone and Ceftazidime. Enterococcus spp. is an emerging pathogen responsible for development of UTI in renal allograft recipients which showed 100% resistance to 2nd and 3rd genaration cephalosporin group.
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