Abstract:
Pseudomonas aeruginosa is a leading cause of hospital infections and is intrinsically
resistant to most antimicrobials. Emergence of multidrug resistant Pseudomonas
aeruginosa has been reported and poses a great challenge in the management of the
resultant infections. While a sizable amount of research has been done on these
infections in developed countries, little is known about the susceptibility profiles and
molecular diversity of strains recovered from wounds in Kenya. This cross-sectional
study conducted in Tigoni District Hospital in rural Kenya sought to determine
susceptibility profiles, molecular diversity of strains and risk factors associated with
carriage of the organism in wound infections. This being a rural area, residents are
presumed to be more likely to get wounds due to the manual nature of their work.
Wound swabs were collected from 299 patients, and transported to the NMRL. Isolation
was done on SBA and MacConkey with salt then drug susceptibility testing for
Pseudomonas aeruginosa isolates using gentamicin, amikacin, ciprofloxacin
,piperacillin-tazobactam, ceftazidine, cefepime and meropenem. PCR was performed
testing for β lactamase genes bla NDM-1, blaSHV and blaTEM. Fingerprinting analysis was
done using the (GTG)5 primer to determine the phylogeny of recovered isolates.
Statistical analysis of age and sex in relation to Pseudomonas aeruginosa carriage and
recorded antimicrobial resistance patterns was done using IBM SPSS version 20
software (SPSS, Inc. Chicago, IL). Chi-square test was used to calculate P-value for
risk factors associated carriage of Pseudomonas aeruginosa in wound infections. Binary
logistic regression analysis was done to generate the adjusted odds ratio with 95%
confidence interval, an alpha of less than 0.05 (P < 0.05) was considered statistically
significant. Of the 299 patients 85 (28%) had positive wound carriage of Pseudomonas
aeruginosa. This was highest among adults (94%) compared to children (6%)(P: 0.001,
C.I:2.1-14.0, O.R:3.4). Wounds in females were more likely to be colonised (67%)
compared to those in males at (33%) (P: 0.19, C.I:0.84-2.4, O.R: 1.42). Patients sourcing
medication from a community chemist were more likely to have bacteria carriage
compared to those who sourced from a hospital pharmacy (P: 0.001, C.1:3.01-8.86,
O.R:5.17). Those who acquired antimicrobials without a doctor’s prescription were more
likely to be colonized compared to those to those had (P: 0.001, C.I:3.01-8.86,
O.R:5.17). Patients who did not complete dosage had a higher carriage (50.6%)
compared to those that completed (49.4%). Highest antimicrobial resistance was
recorded towards Ceftazidime (64%), Cefepime (52%) while Piperacillin-tazobactam
was least resisted (20%). The isolates were more resistant towards Gentamicin (45%)
and Amikacin (40%) compared to Ciprofloxacin (25%). Notable is the high resistance
towards Meropenem (40%). Carriage of blaTEM, blaSHV and blaNDM was most common
among strains showing resistance towards third generation cephalosporins, in addition to
Amikacin and Meropenem for bla NDM-1Tight clustering was noted in isolates from
diverse patients with a similarity of ≥ 80% was noted in 9 clusters based on isolates
banding patterns. This appearance of blaNDM-1 linked to pervasive misuse of carbapenem
is worrying. Strengthening antimicrobial stewardship is recommended