Abstract:Colonization of multidrug resistant (MDR) bacteria is associated with subsequent invasive infections in children with comorbidities. This study aimed to determine the resistance profile and factors associated with MDR pathogen colonization among HIV−and HIV+ children below five years of age in Mwanza, Tanzania. A total of 399 (HIV− 255 and HIV+ 144) children were enrolled and investigated for the presence of MDR bacteria. The median [IQR] age of children was 19 (10–36) months. Out of 27 Staphylococcus aureus c… Show more
“…Among the three groups, isolates from children with a HIV infection showed significantly high resistance to ampicillin, trimethoprim/sulfamethoxazole, and tetracycline. Similar findings in the same region reported that HIV-infected children had significantly higher multidrug resistance than non-HIV infected children [ 6 ]. The level of resistance reflects the high use of these antibiotics in the healthcare system and the community [ 37 ].…”
Section: Discussionsupporting
confidence: 80%
“…Rectal carriage of ESBL-producing bacteria is a potential endogenous source of infections and an independent risk of developing subsequent infections due to ESBL-producing bacteria [ 3 , 4 , 5 ]. Furthermore, the colonization of ESBL-producing bacteria was found to be high in individuals with comorbidities such as Human Immunodeficiency Virus (HIV) [ 6 ], diabetes mellitus (DM), organ transplant, and sickle cell disease (SCD) due to the fact that these patients are often in long-term antibiotic prophylaxis [ 7 , 8 ].…”
Rectal carriage of extended spectrum β-lactamase-lactose fermenters (ESBL-LF) is the major risk factor for the development of subsequent endogenous infections. This study determined the patterns and factors associated with the rectal carriage of ESBL-LF among children with Human Immunodeficiency Virus (HIV), Diabetes Mellitus (DM), and Sickle Cell Disease (SCD) attending clinics at different health care facilities in the city of Mwanza, Tanzania. A cross-sectional study was conducted among children living with HIV (n = 236), DM (n = 42) and SCD (n = 126) between July and September 2021. Socio-demographic and clinical data were collected using a structured questionnaire. Rectal swabs/stool samples were collected and processed to detect the rectal carriage of ESBL-LF following laboratory standard operating procedures (SOPs). Descriptive statistical analysis was conducted using STATA 13.0. The overall prevalence of ESBL-LF carriage was 94/404 (23.3%). Significantly higher resistance was observed to ampicillin, trimethoprim-sulfamethoxazole, and tetracycline among Enterobacteriaceae isolated from HIV infected children than in non-HIV infected children (p < 0.05). The commonest ESBL allele 45/62 (72.6%) detected was blaCTX-M. Generally, a parent’s low education level was found to be associated with ESBL-LF colonization among children living with HIV; (OR 4.60 [95%CI] [1.04–20], p = 0.044). A higher proportion of ESBL-LF from DM 10/10 (100%) carried ESBL genes than ESBL-LF from HIV 37/56 (66.1%) and SCD 15/28 (53.6%), p = 0.02. There is a need to collect more data regarding trimethoprim-sulfamethoxazole (SXT) prophylaxis and antibiotic resistance to guide the decision of providing SXT prophylaxis in HIV-infected children especially at this time, when testing and treatment is carried out.
“…Among the three groups, isolates from children with a HIV infection showed significantly high resistance to ampicillin, trimethoprim/sulfamethoxazole, and tetracycline. Similar findings in the same region reported that HIV-infected children had significantly higher multidrug resistance than non-HIV infected children [ 6 ]. The level of resistance reflects the high use of these antibiotics in the healthcare system and the community [ 37 ].…”
Section: Discussionsupporting
confidence: 80%
“…Rectal carriage of ESBL-producing bacteria is a potential endogenous source of infections and an independent risk of developing subsequent infections due to ESBL-producing bacteria [ 3 , 4 , 5 ]. Furthermore, the colonization of ESBL-producing bacteria was found to be high in individuals with comorbidities such as Human Immunodeficiency Virus (HIV) [ 6 ], diabetes mellitus (DM), organ transplant, and sickle cell disease (SCD) due to the fact that these patients are often in long-term antibiotic prophylaxis [ 7 , 8 ].…”
Rectal carriage of extended spectrum β-lactamase-lactose fermenters (ESBL-LF) is the major risk factor for the development of subsequent endogenous infections. This study determined the patterns and factors associated with the rectal carriage of ESBL-LF among children with Human Immunodeficiency Virus (HIV), Diabetes Mellitus (DM), and Sickle Cell Disease (SCD) attending clinics at different health care facilities in the city of Mwanza, Tanzania. A cross-sectional study was conducted among children living with HIV (n = 236), DM (n = 42) and SCD (n = 126) between July and September 2021. Socio-demographic and clinical data were collected using a structured questionnaire. Rectal swabs/stool samples were collected and processed to detect the rectal carriage of ESBL-LF following laboratory standard operating procedures (SOPs). Descriptive statistical analysis was conducted using STATA 13.0. The overall prevalence of ESBL-LF carriage was 94/404 (23.3%). Significantly higher resistance was observed to ampicillin, trimethoprim-sulfamethoxazole, and tetracycline among Enterobacteriaceae isolated from HIV infected children than in non-HIV infected children (p < 0.05). The commonest ESBL allele 45/62 (72.6%) detected was blaCTX-M. Generally, a parent’s low education level was found to be associated with ESBL-LF colonization among children living with HIV; (OR 4.60 [95%CI] [1.04–20], p = 0.044). A higher proportion of ESBL-LF from DM 10/10 (100%) carried ESBL genes than ESBL-LF from HIV 37/56 (66.1%) and SCD 15/28 (53.6%), p = 0.02. There is a need to collect more data regarding trimethoprim-sulfamethoxazole (SXT) prophylaxis and antibiotic resistance to guide the decision of providing SXT prophylaxis in HIV-infected children especially at this time, when testing and treatment is carried out.
“…Furthermore, the prevalence of ciprofloxacin and gentamicin resistance among ESBL E. coli is higher than the reported prevalence of ciprofloxacin and gentamicin reported in non-ESBL E. coli in our setting, which ranges from 48.6% to 62.7% and from 14.4% to 17% for ciprofloxacin and gentamicin, respectively (Msanga et al, 2022;Mtemisika et al, 2022). This relatively high resistance rate to fluroquinolones and aminoglycosides to ESBLproducing bacteria compared with non-ESBL-producing bacteria might be due to the co-existence of the ESBL genes with those conferring resistance to fluroquinolones and aminoglycosides in the same large plasmid (Lee et al, 2012).…”
BackgroundAdditional antimicrobial resistance to extended-spectrum β-lactamase (ESBL)-producing E. coli exhausts treatment options. We investigated allele distribution and resistance to ciprofloxacin and gentamicin among ESBL-producing E. coli isolates from the urine, stool, animals, and environments of presumptive urinary tract infection (UTI) patients, in order to gain a crucial insight toward devising prevention and control measures and treatment guidelines.MethodsArchived ESBL-producing E. coli isolates from the urine, stool, animals, and surrounding environments of presumptive UTI patients were retrieved. Antimicrobial susceptibility profiles for ciprofloxacin and gentamicin were done followed by multiplex Polymerase chain reaction (PCR) for blaCTX-M, blaTEM, and blaSHV, to determine ESBL allele distribution. Data were analyzed using STATA version 17.ResultsA total of 472 confirmed ESBL-producing E. coli isolates from Mwanza 243 (51.5%), Kilimanjaro 143 (30.3%), and Mbeya 86 (18.2%) were analyzed. Of these, 75 (15.9%) were from urine, 199 (42.2%) from stool, 58 (12.3%) from rectal/cloaca swabs of animals, and 140 (29.7%) from surrounding environments. Out of the 472 ESBL-producing E. coli, 98.9% (467) had at least one ESBL allele. The most frequent allele was blaCTX-M, which was detected in 88.1% (416/472) of isolates, followed by the blaTEM allele, which was detected in 51.5% (243/472) of isolates. A total of 40.7% (192/472) of isolates harbored dual blaCTX-M + blaTEMalleles and only 0.2% (1/472) of isolates had dual blaCTX-M + blaSHValleles, whereas 2.3% (11/472) of isolates had a combination of all three alleles (blaCTX-M + blaTEM + blaSHV). None of the isolates harbored a combination of blaTEM + blaSHVonly. Resistance to ciprofloxacin and gentamicin was observed in 70.8% (334/472) and 46.0% (217/472) of isolates, respectively. There was a significant difference in the distribution of resistance to ciprofloxacin as well as gentamicin among ESBL-producing E. coli isolated from various sources (p-value < 0.001 and 0.002, respectively).ConclusionAlmost all ESBL-producing E. coli isolates carry blaCTX-M, blaTEM, and blaSHV either alone or in combination, with the most common allele being blaCTX-M.The resistance to ciprofloxacin and gentamicin, which are frontline antibiotics for UTIs among ESBL-producing E. coli, is high. This implies the need to continually revise the local guidelines used for optimal empirical therapy for UTIs, and for continual research and surveillance using one health approach.
“…1 for reasons for exclusion). This left 40 studies, 19 , 20 , 21 , 22 , 23 , 24 , 25 , 26 , 27 , 28 , 29 , 30 , 31 , 32 , 33 , 34 , 35 , 36 , 37 , 38 , 39 , 40 , 41 , 42 , 43 , 44 , 45 , 46 , 47 , 48 , 49 , 50 , 51 , 52 , 53 , 54 , 55 , 56 , 57 , 58 involving a total of 9408 children, that reported on the carriage prevalence of Enterobacterales resistant to third-generation cephalosporins or carbapenems. …”
Section: Resultsmentioning
confidence: 99%
“…The risk of ESCR-E carriage also increased significantly among patients who had received antibiotics in the previous three months, with an OR of 3.20 (95% CI: 2.10–4.88) in the eight studies (2580 children) that examined this issue ( Table 3 , Appendix pp 13). 25 , 37 , 42 , 43 , 46 , 48 , 50 , 51 …”
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