skip to Main Content
Special Journals Publisher - SJP - OGP +256700488917 admin@spparenet.org
Excellence beyond expectations

Valentino1 SV, 1Nzambandora E, 2Agwu E

Address: Departments of:  1. Obstetrics and Gynecology, 2. Microbiology and Immunology, Kampala International University, Box 71, Ishaka Bushenyi Uganda.  

Correspondence: agwu@spparenet.org; and onyoomoro1@gmail.com, Tel: +256705719325,

Citation

Valentino1 S Valentino, 1Nzambandora E, 2Agwu Ezera. Pregnancy-related asymptomatic bacteriuria at Kampala International University Teaching Hospital, Bushenyi Uganda. Special Journal of Obstetrics, Gynecology and Pediatrics, 2021, Vol 1, No 2: 1- 16

Abstract

Background: Pregnancy-related asymptomatic bacteriuria remains a potential health danger to women of reproductive age because of the possible emergence of urinary tract infections during pregnancy. Surveillance will generate data for effective intervention to avert the devastating health impact of urinary tract infection in pregnancy, especially in a resource-limited setting.

Objective: This study was designed to assess pregnancy-related asymptomatic bacteriuria as potential pathogens for urinary tract infections. at Kampala International University Teaching Hospital, Bushenyi, Uganda.

Methods:  In this cross-sectional study, 362 aseptically collected midstream urine specimens of pregnant mothers were analyzed using standard bacteriological methods for significant bacteria in urine, and antibacterial sensitivity of isolates recovered from mid-stream urine samples of consenting participants. Structured questionnaires were used to obtain sociodemographic, clinical, and obstetric data. Data were analyzed descriptively using STATA 14.2

Results: The overall prevalence of ASB among the studied pregnant women attending ANC clinic at KIU-TH was 15.5% and out of this 15.5% prevalence, 51.8% were E.coli, 19.6% were Staph aureus 17.9% were Klebsiella, 8.9% were Pseudomonas while 1.8% were Proteus species). Most of the isolates were sensitive to Amikacin, Imipenem, Gentamicin, and Levofloxacin.

The factors that were significantly associated with ASB were gravidity (Gravida 1 or prime gravidas) and WOA of the 1st trimester and 3rd trimester. Prevalence of ASB varied directly with gravidity (p-value=0.015, OR = 2.1, 95% CI =1.15-3.93). Thus pregnant women with gestation of 1-12 weeks were more likely to develop ASB compared to those of 13-28 weeks of pregnancy (OR=4.0, 95% CI=1.64-9.83).

Conclusions The study found that 15.5% of pregnant women attending ANC clinic at KIU-TH had asymptomatic bacteriuria mostly during the 1st or 3rd trimester and 51.8% of the bacteria were Escherichia coli followed by 19.6% Staphylococcus and other enteric bacteria.

Background

While the global struggle to provide minimum healthcare to the needy remains below expectation, people in resource-limited settings are faced with worst-case scenarios where a significant population still falls sick, gets worst, and dies without medical attention (1-5). Skeletal interventions directed towards some vulnerable population in resource-poor settings have highlighted the magnitude of the problem especially in hard-to-reach rural communities of Africa.

Targeting vulnerable populations (6) such as pregnant women for intervention is one way of ensuring equitable distribution of available services with the ultimate goal of impacting the morbidity and mortality index. Reduction of urinary tract infections (7) in pregnancy is one of the objectives of antenatal care because infection in pregnancy is a threat to mother and child and infection can become invasive causing complicated urinary tract infections (8-9).

There is a discrepancy between the population that: needs pregnancy now, does not need pregnancy, and those who need pregnancy at a later time in life. This discrepancy defines the various arguments about abortion laws in different healthcare policies globally (10). However, the population in need of pregnancy remains high and so can do almost anything within their power to keep the pregnancy.

In Africa, people seek healthcare when they know the danger associated with present illness thus making illnesses and associated danger, key in defining the rate at which people seek healthcare (11).  In the absence of illnesses as a driving force for the high rate of healthcare seekers, defining the population of bacteria that are potential dangers to mother and child is difficult (12).

Asymptomatic bacteriuria (ASB) is the presence of a significant quantity of bacteria in the urine without symptoms of a lower or upper urinary tract/kidney infection (13-14). Prevalence of asymptomatic bacteriuria in premenopausal and ambulatory women is 2%–10% (13) but due to anatomical and physiological changes higher rates of ASB during pregnancy are expected and a greater chance of progression to UTI (13, 15).

The physiological and anatomical changes during pregnancy facilitate the growth of bacteria in women both symptomatic and asymptomatic. Numerous risk factors for ASB in pregnancy have been identified to include low socioeconomic status, higher parity, a history of recurrent UTI, diabetes, and anatomical abnormalities of the urinary tract (13, 14, 16). ASB was associated with an increased risk of preterm delivery and it has been found that treating ASB does not only reduce the risk of maternal pyelonephritis but also reduces the risk of preterm birth (17).

Pregnancy is an aggravating factor for the asymptomatic bacteriuria to become symptomatic (18). Hormonal effects particularly increase the risk for urinary tract bacterial colonization throughout pregnancy. Asymptomatic bacteriuria in pregnancy is among the commonest (1.9% to 9.5%) health problems globally and 14% in low-income countries (19-21). In Tanzania, the prevalence of ASB was 15.5% (22), and 13.3% in Uganda (23).

Since pregnancy is itself a health challenge, high index of suspicion is needed to decide the place of asymptomatic bacteruria in pregnancy for better pregnancy management. The concept (24) of preventive medicine guides the decision on what to do with asymptomatic bacteriuria as a potential health hazard or a timed bomd that can explode to endanger the health of mother and child any time

Objective

The objective of this study is therefore to evaluate pregnancy-related asymptomatic bacteriuria at Kampala International University Teaching Hospital, Bushenyi district of Uganda with the ultimate goal of providing a database for use designing the effective future intervention. Again this study will provide the knowledge of asymptomatic bacteriuria burden in pregnancy, needed to predict the potential emergence of future symptomatic urinary tract infection.

Materials and Methods

In this cross-sectional asymptomatic bacteriuria study (24), 362 aseptically collected midstream urine specimens were analyzed for significant bacteria in the urine that may serve as potential pathogens for urinary tract infections. All pregnant women attending antenatal clinics at Kampala International University Teaching Hospital were selected while pregnant (adult and emancipated) mothers attending antenatal clinics without any signs or symptoms of urinary tract infection were selected were included. Pregnant women with a history of antibiotic therapy in the previous two weeks and a history of structural urogenital anomalies were excluded.

The 362 patients samples analyzed were obtained using the formulae n= (zα+zβ) 2P (1-P)/d2 Where α=0.05, Zα =z-static at α=1.96, Power=80%, β=0.2, Zβ=0.84, p=13.3%. Consenting respondents were selected using systematic random sampling (ballots). Pre-tested questionnaires were administered to each participant for information on socio-demographic and gynecological factors. A detailed gynecological history was taken and urine samples were inoculated on a sterile CLED medium, Blood agar, Chocolate agar, and MacConkey agar plates and were incubated at 37º C for 24-48 hours and isolate identification made using standard method

Antibiotics susceptibility test

Susceptibility testing was carried out according to standard clinical laboratory guidelines of Kirby Bauer diffusion methods (25).  Pure colonies of the organisms were tested for their antimicrobial drug susceptibility against six commonly used antibiotics including ceftriaxone (30ug), amikacin (30ug), penicillin G. (30ug), pefloxacin (30ug), nalidixic acid (30ug), gentamycin, Oxacillin, nitrofurantoin and erythromycin using Kirby-Bauer disc diffusion (26) as modified by the clinical laboratory standard institute (27).

Overnight bacterial broth suspension was made to match with 0.5% McFarland turbidity standard. A sterile inoculation glass rod was used to spread the surface of Muller-Hinton agar plates homogenously with the diluted broth suspension of bacterial colonies. Antibiotic discs were placed onto the inoculated Muller-Hinton agar and incubate at 37℃ for 24 hours. The zones of inhibition were measured and compared to a standard chart (28). A pre-tested questionnaire was used to collect data on demographics, obstetric, genetic, and socioeconomic status.

Statistical analysis

Data obtained from the questionnaire were used to determine the Cronbach’s coefficient alpha and an index of more than 0.8, which was considered to indicate that the items of the questionnaire are reproducible and consistent (29).  With the aid of STATA version 14.1, binary logistic regression analysis was done at the bivariate level to report crude odd ratios and at a multivariate level to obtain unbiased adjusted odd ratios for potential predictors. The adjusted odds ratio was reported together with their respective 95% confident intervals and p-values. Variables with p-values ≤ of 0.05 were considered statistically significant.

Results

Socio-demographic findings

Table 1: Majority (79%) of the pregnant women were aged between 20-30 years followed by: 97.2% of the women that we’re married and 2.8% that were single. About 43.1% of the women had secondary education while 23.9% and 22.2% had primary and tertiary education respectively. The majority 46.1% and 37.8% were Protestants and were Catholics respectively. About 42.3% of the men were peasants and 28.2% were unemployed.

Table 1: Socio-demographic characteristic of the study subject
Variable Frequency (n) Percentage (%)

Age

< 20 years

21-30 years

>31years

 

15

289

58

 

4.1

79.9

16.0

Education level

None

Primary

Secondary

Tertiary

 

40

86

156

80

 

11.0

23.8

43.1

22.1

Occupation

Unemployed

Peasant

Professional

Business

 

102

153

57

50

 

28.2

42.3

17.7

13.8

Religion

Protestant

catholic

Moslem

born-again/advent

 

167

137

36

22

 

46.1

37.8

9.9

6.2

Marital status

Married

Single

 

352

10

 

97.2

2.8

 Obstetric and other characteristics

In this asymptomatic bacteriuria study, the majority (56%) of the women were of gravida 2-4, while 32.3% were of gravida 1 and 11% were of gravida 5. Many (82%) of the women had never aborted their previous pregnancies and only 18.4% had aborted their pregnancies before the study.

On the other hand, the majority of women were more than 28weeks (3rd trimester) of gestation age in their pregnancy while 40.6% were 13-28 weeks (2nd trimester) of gestation age in their pregnancy and 10.2% were 0-12 week (1st trimester) of gestation age in their pregnancy. A small proportion 2.9% of the women were HIV positive

Asymptomatic bacteriuria prevalence in the studied population

Of the 362 urine samples in this study, 56 (15.5%) had significant bacteria with a colony count of 105CFU/ml. E.coli was 51% prevalent followed by 19.6% Staph aureus, 17.9% of Klebsiella species 8.9% Pseudomonas species, and lastly 1.8% Proteus species respectively.

Susceptibility status to conventional antibiotics of the bacteria isolated from the urine of study participants

Most bacteria isolate 56 (15.5%) were sensitive to Amikacin, Levofloxacin, Imipenem, and Gentamycin and were higher resistant to Ampicillin, Ceftriaxone, and Ciprofloxacin. E.coli was 100% resistant to Ampicillin, and most 65.5%. Sensitive to Amikacin. Staphylococcus aureus was 100% resistant to Ceftriaxone, Perfloxacin, and Ciprofloxacin but 63.6% sensitive to Amikacin. Klebsiella species were 100% resistant to Ampicillin, Ceftriaxone, Ceftrixine, Gentamycin, and Ciprofloxacin.

But it was most sensitive to Imipemum and Levofloxacin at 40.0% each. Pseudomonas was 100% resistant to Ampicillin, Ceftriaxone, Ceftrixine, Gentamycin, and Perfloxacin. But most sensitive to Amikacin and Imipemim at 70.0% and 60.0% respectively. Proteus was most sensitive to Gentamycin, and Imipemim. It was resistant to all the other antibiotics.

Table 2: Susceptibility status of bacteria to conventional antibiotics
Conventional Antibiotics E. coli (n=29) Staph aureus(n=11) Klebsiella (n=5) Pseudomonas(n=10) Proteus (n=1)
Amikacin 19(65.5%) 7(63.6%) 1 (20.0%) 7 (70.0%) 0 (0.0%)
Ampicillin 0(0.0%) 1 (9.1%) 0 (0.0%) 0 (0.0%) 0 (0.0%)
Levofloxacin 6 (20.7%) 5 (45.5%) 2 (40.0%) 2 (20.0%) 0 (0.0%)
Ceftriaxon 3 (10.3%) 0 (0.0%) 0 (0.0%) 0 (0.0%) 0 (0.0%)
Ceftrixine 2 (6.9%) 2 (18.2%) 0 (0.0%) 0 (0.0%) 0 (0.0%)
Gentamycin 5 (17.2%) 3 (27.3%) 0 (0.0%) 1 (10.0%) 1 (100.0%)
Imipemum 7 (24.1%) 4 (36.4%) 2 (40.0%) 6 (60.0%) 1 (100.0%)
Perfloxacin 2 (6.9%) 0 (0.0%) 1 (20.0%) 0 (0.00%) 0 (0.0%)
Ciprofloxacin 3 (10.3%) 0 (0.0%) 0 (0.0%) 1        (10.0%) 0 (0.0%)

Socio-demographic characteristics

In table 3 below all listed socio-demographic variables were not significantly (p>0.05) impact on the acquisition and urinary tract colonization. The prevalence of ASB varied inversely with age. With education, the uneducated were at low risk of developing ASB compared to those primary, secondary and tertiary. Though those primaries were at high risk to develop ASB than those of secondary and tertiary.

Regarding occupation, comparing the peasants with unemployed they were at equal risk of getting ASB while the professionals were 2 times more likely to develop ASB compared to unemployed. Whereas businesswomen were 20% less likely to develop ASB compared to unemployed. On comparing the protestants with Catholics, Muslims, and born again/adverts, the Muslims were at equal risk of getting ASB compared to protestants though the Catholics and born again/adverts were 2 times more likely to develop ASB compared to protestants.

Table 3: Results of Univariate analysis for social demographic characteristics
Variable

No ASB (negative)

n (%)

ASB (positive)

n(%)

Un adjusted OR (95% CI) P-value

Age

< 20 years

20-30 years

31-50 years

12(80.0)

240(83.0)

54 (93.1)

 

3(20.0)

49 (17.0)

4 (6.9)

 

3.4 (0.67-17.09)

2.8 (0.95-7.96)

1.0

 

0.142

0.061

 

Education level

None

Primary

Secondary

Tertiary

 

37 (92.2)

71 (82.6)

130 (83.3)

68 (85.0)

 

3(20.0)

15 (17.4)

26 (16.7)

12 (15.0)

 

1.0

3.8(0.82-17.54)

3.6 (0.82-15.89)

3.2 (0.67-14.97)

 

 

0.087

0.091

0.144

Occupation

Unemployed

Peasant

Professional

Business

 

87 (85.3)

130 (85.0)

45 (78.9)

44(88.0)

 

15 (14.7)

23 (15.0)

12 (21.1)

6 (12.0)

 

1.0

1.0 (0.49-2.08)

1.7 (0.72-4.05)

0.8 (0.28-2.17)

 

 

0.976

0.219

0.633

Religion

Protestant

Catholic

Moslem

born-again/Advent

 

143 (87.0)

111 (82.2)

30 (85.7)

18 (81.8)

 

21 (12.8)

24 (19.8)

4        (14.3)

4 (18.2)

 

 

1.5 (0.78-2.78)

1.1 (0.39-3.25)

1.5 (0.47-4.91)

 

 

0.233

0.814

0.490

Obstetric and other characteristics

In table 4 below, the distribution of asymptomatic bacteria in the urine of respondents was significantly (p<0.05) dependent on the Gravidity and weeks of gestation. Prevalence of ASB varied directly with gravidity (p-value=0.015, OR = 2.1, 95% CI =1.15-3.93).

Thus pregnant women with gestation of 1-12 weeks were more likely to develop ASB compared to those of 13-28 weeks of pregnancy (OR=4.0, 95% CI=1.64-9.83).  HIV status and blood group were not statically significant. Although the positive HIV case was at higher risk of developing ASB.  In addition, pregnant women of blood group A, B, and AB were protective to develop ASB compared to blood group O.

Table 4: Results of Univariate analysis for obstetric and other characteristics

Variable

No ASB (negative)

n (%)

ASB (positive)

n (%)

Un adjusted OR (95% CI) P-value

Gravidity

1

2-4

5

 

171 (81.0)

91(89.2)

44 (89.8)

 

40 (19.0)

11 (11.8)

5 (10.2)

 

2.1 (1.15-3.93)

1.0

1.0 (0.36-2.85)

 

0.015

 

0.973

WOA

1-12 weeks

More than 28 weeks

13-28 weeks

 

29 (70.7)

137 (91.3)

140 (81.9)

 

12 (29.3)

13 (8.7)

31 (18.1)

 

4.0 (1.64-9.83)

2.0 (1.02-3.93)

1.0

 

0.002

0.043

HIV status

Negative

Positive

 

298 (85.0)

8 (80.0)

 

54 (15.0)

2 (20.0)

 

1.0

1.4 (0.29-6.88)

 

 

0.664

Blood group

A

B

AB

O

 

69 (91.5)

87 (88.8)

32 (80.0)

119 (83.8)

 

13 (15.9)

11 (11.2)

8 (20.0)

24 (16.9)

 

0.4  (0.126-1.00)

0.5  (0.201-1.170)

0.8 (0.278-2.409)

1.0

 

0.050

0.107

0.715

Multivariate binary logistic regression: Factors associated with ASB among the study group

The multivariate analysis was achieved using a backward stepwise selection method of the model. With this model factors which were independently associated with ASB among pregnant women were being prime gravida (Gravida 1), being in either the 1stor 3rd trimester (1-12 weeks or more than 28 weeks). The odds of having ASB were higher among prime gravida mothers as compared to multigravida (OR=2.0, 95% CI= 1.07-3.74).

The odds of having ASB were higher among pregnant women of 1st trimester as compared to those of 2nd trimester (OR=3.8, 95% CI=1.51 – 9.56). Lastly the odds of having ASB were 2 times higher among pregnant women of 3rdtrimester as compared to those of 2nd trimester (OR=2.1, 95% CI=1.06 – 4.27).

Discussion

Prevalence of ASB among the study group

The prevalence of asymptomatic bacteriuria among pregnant women in this study was 15.5%. These findings were relatively consistent with a 10% to 20% range from Cairo, global, East Africa, and other prevalence reports (21, 30-36). The fact that the result of this study is relatively similar to reports from major studies globally shows that Uganda and indeed, Kampala International University Teaching Hospital (KIUTH) are moving in the right direction in medical practice and discharge of their corporate health responsibilities to the general public.

KIUTH is a private not-for-profit tertiary hospital acting as a major referral hospital to five districts of southwestern Uganda including Bushenyi, Shema, Rubiriizi, Mitooma, and Buhweju districts respectively. Its major health policy is a public-private partnership in which the Uganda government built a magnificent edifice at the hospital premises where it provides comprehensive free health services (pediatrics, surgery, medical, obstetrics, and gynecology) to the people with government-employed doctors posted to do this work.

In return, KIUTH trains its undergraduate and postgraduate medical students there. This arrangement gives KIUTH strategic and regional advantage placing it at par with other regional referral hospitals like Mbarara Kabale and Masaka referral hospitals respectively.

On the other hand, the result of this asymptomatic bacteriuria study, was lower, than two reports from Ethiopia, 21.5% and 26% respectively (22, 37), India reports of 25.3%-30.5% (38-39), and Kenya report of 21.5% (40). Ethiopia, Kenya, and many parts of India are underdeveloped, with a severe scarcity of health resources including human resources for health.  The vulnerability of mother and child to poverty-related and neglected tropical disease, in the presence of limited resources is the source of concern and impacts the acceptance and uptake of hospital-directed health services to the general public.

The public-private partnership (PPP) health concept is not common in Africa its advantages over public and/or private healthcare centers are numerous including but not limited to higher acceptance and uptake of hospital services, good health education and promotion, moderately resourced antenatal care services, good inter-hospital referral network system, free services and no stock-out of tools for good healthcare delivery among others.

The above factors underlying the policy of heath delivery at KIUTH must have impacted the lower result of this study compared to the reports of Ethiopia, India, and Kenya respectively. Again Senait et al (41), suggested geographical variations between the regions where the pregnant women live, and social habit of the community vis-à-vis pregnancy affects the microecology of the urinary system and the population structure of colonizing asymptomatic bacteria in pregnancy.

Though 15.5% was lower than Ethiopia, India, and Kenya reports, it hard to accept that 15.5% of pregnancy healthcare seekers harbor potential bacteria pathogens capable of initiating urinary tract symptomatic infections during or after 9 months of pregnancy. Stepping up interventions to reduce this prevalence is recommended.

We also found that gravida-one (Primi-gravida) mothers were more likely to acquire and be colonized with asymptomatic bacteriuria in their urinary tract than multigravida mothers, (OR=2.0, 95% CI= 1.07-3.74). This study result was in agreement with 53.89%  report by Karur, (42) and Ajayi et al., (30). Primi-gravida women are expected to be relatively more exposed to complex genital manipulation including intensive sexual intercourse and most times at younger age compared to their multigravida counterparts.

Thus early and intensive sexual intercourse is known to cause minor urethral trauma and transfer of both resident and contaminating bacteria from the perineum into the bladder raising the stakes for asymptomatic bacteria in the urinary tract of pregnant women in this locality (43). In this study, asymptomatic bacteriuria acquisition and colonization of the urinary tract of consenting participants were significantly (p<0.05) influenced by the trimester of pregnancy.

Thus, participants that were in either the 1st or 3rd trimester (1-12 weeks or more than 28 weeks) of pregnancy were more likely to present with asymptomatic bacteriuria compared to their counterparts in the 2nd trimester. This fact is supported by: Adeliade, (40) in Kenya, Chandel et al., (44) in India, Bankole Oladeinde, (45) in Nigeria, and Tadesse et al, (22) in Ethiopia respectively.

However different from the report of Omer et al,(46) in Sudan (OR=3.8, 95% CI=1.51 – 9.56). Higher ASB in 1st trimester may be due to increasing progesterone and estrogen hormones and compressed bladder due to increasing uterus in the pelvic region which causes urine stasis and ureter dilatation, a factor known to encourage bacteria migration retention and colonization of the urinary tract with the ultimate goal of establishing urinary tract infection in pregnancy (47).

Numerous anatomical and hormonal variations in pregnancy lead to urethral dilation and urinary inertia which encourages bacteria acquisition, migration, and colonization of the urinary tract in the 3rd trimester of pregnancy a fact supported by Bankole, (45), (OR=2.1, 95% CI=1.06 – 4.27). Escherichia coli (51.8%) was the most prevalent bacteria followed by 19.6% Staphylococcus aureus, 17.9% Klebsiella species,  8.9% pseudomonas species, and 1.8%. Proteus species respectively. This result is in line with the reports of Gayathree, (20) in India, Prasanna1, (48) in India, Bankole, (45) in Nigeria, Omer et al,(46) in Sudan, Mike et al,(49) in Cameroon, Senait et al, (41) in Ethiopia, Moses et al, (50) in Tanzania and Adelaide et al, (40) in Kenya respectively.

E coli together with Klebsiella species and other bacteria isolates in this study are entro-bacteria found in stool samples. One explanation of 51.8% E coli predominance and other enterobacteria isolates in the urinary tract is poor hygiene whereby most women passing feces prefer to clean up the anus towards the open vagina thereby loading the stool samples and its bacteria content in the genital and urinary tract. Again, E coli strains which are relatively normal flora of the lower intestine become pathogenic when they gain access to the urinary tract Abdullahi, et al (51).

Though the report of this asymptomatic bacteriuria study was not in line with the report of Amiri, (8) and Manasi, (39) who showed Klebsiella to be the most predominant isolate, E coli and Klebsiella species can contaminate the genital and urinary tract due to poor hygiene. The concept of low immunity induced by pregnancy could also explain the observed predominance of staff and enteric bacteria in pregnancy Mor and Cardenas, (52)

Generally, there was greater sensitivity of bacterial isolates to Amikacin, levofloxacin, pefloxacin, and imipenem which were similar to a study by Prasanna, (48), but different from nitrofurantoin, gentamicin, cefuroxime, and ceftazidime reported by Ajayi (30). Klebsiella species and E. coli showed resistance against Penicillin, Ampicillin, Pefloxacin, and Amoxicillin. This may be because in our setting these drugs are overused routinely (31). Asymptomatic bacteria resistance can be explained by exposure to a sub-lethal dose of antimicrobial agents especially when treating other symptomatic bacteria disease.

Limitation: It was difficult to convince pregnant mothers to participate in this asymptomatic bacteriuria study as they found it hard to consent since there was no sign or symptoms to generate the fear factor central in driving patients to seek healthcare. It was also hard to define the status of asymptomatic bacteriuria, normal flora, contaminants, and opportunistic bacteria as well as the resistance profile of bacterial isolates in an asymptomatic pregnant population.

However, the mothers were educated on the dangers of risking the emergence of disease by asymptomatic bacteria during the nine months of pregnancy. Standard aseptic protocols and significant bacteria in urine were used to minimize spurious laboratory results about contaminants and resistance to contaminating bacteria. A primary school teacher of the locally spoken language (Runyankole language) who also works as a social worker was recruited to overcome the language barrier and reduce the magnitude of the problem enabling us to get all information we needed

Conclusion.

In asymptomatic bacteriuria study, 15.5% of pregnant women attending ANC clinic at KIU-TH had asymptomatic bacteriuria mostly during the 1st or 3rd trimester and 51.8% of the bacteria were Escherichia coli followed by 19.6% Staphylococcus and other enteric bacteria. Even though in pregnancy, asymptomatic bacteriuria isolates are considered potential agents of emerging urinary tract infection, a high index of suspicion is needed to decipher how to administer sensitive antimicrobial agents outlined in this study to pregnant women with the ultimate goal of protecting mother and child unexpected complications.

Competing interests

The authors declare that they have no competing interests.

Reference

  1. Kasule A and Agwu E. Health budget shortfalls and inefficient communication systems as a setback to efficient management/control of infectious disease in Bushenyi district, Uganda. Spec Pathog Rev J. 2015; 1(1): 12-17.
  2. Kasule A and Agwu E. Review of health workers attrition and microbial disease endemicity in Bushenyi, Ntungamo and Rukungiri Districts of South Western Uganda. Spec Pathog Rev J. 2015; 1 (1): 1-11.
  3. Kasule A and Agwu E. Low immunization coverage and Viral/Bacterial disease outbreaks among children in Nyakivare and Rukinga Internally Displaced People (IDP) camp, Uganda. Spec Vir Pathog J. 2017; 1 (1): 01-07
  4. Olufunke AV, Agwu E. Uptake of hospital-based delivery services in Bushenyi District, Uganda. Spec Pathog Rev J. 2016;1(1):40-50.
  5. Igbinovia O, Agwu E, Atuanya EI. Epidemic potentials of septic tank sewage systems in Benin-city Edo state, Nigeria. Spec Back Pathog J. 2016; Vol 2, No 1&2: p 01-06.
  6. Shivayogi P. Vulnerable population and methods for their safeguard. Perspect Clin Res. 2013 Jan-Mar;4(1):53-7. doi:10.4103/2229-3485.106389.
  7. Odoki M,  Aliero AA,  Tibyangye J, Mangia, JN  Wampande E,  Kato CD Agwu E, JoelBazira J.  “Prevalence of Bacterial Urinary Tract Infections and Associated Factors among Patients Attending Hospitals in Bushenyi District, Uganda,” International Journal of Microbiology, vol. 2019, Article ID 4246780, 8 pages,
  8. Odoki M,  Aliero AA,  Tibyangye J, Mangia, JN  Wampande E,  Kato CD,  Agwu E, JoelBazira J.  “Prevalence of Bacterial Urinary Tract Infections and Associated Factors among Patients Attending Hospitals in Bushenyi District, Uganda,” Intern J Microbiol, vol. 2019, Article ID 4246780, 8 pages,
  9. Amiri M, Lavasani Z, Norouzirad R, Najibpour R, Mohamadpour M, Nikpoor AR, Raeisi M, Zare Marzouni H. Prevalence of Urinary Tract Infection Among Pregnant Women and its Complications in Their Newborns During the Birth in the Hospitals of Dezful City, Iran, 2012 – 2013. Iran Red Crescent Med J. 2015 Aug 24;17(8):e26946. doi: 10.5812/ircmj.26946.
  10. Lee ACC, Mullany CL, Quaiyum M, Mitra DP, Labrique A, Christian P, Ahmed P, Uddin J, Rafiqullah I, DasGupta S, Rahman M, Koumans EH, Ahmed S, Saha SK,  Baqui AH, for the Projahnmo Study Group in Bangladesh. Effect of population-based antenatal screening and treatment of genitourinary tract infections on birth outcomes in Sylhet, Bangladesh (MIST): a cluster-randomized clinical trial. Lancet Glob Health 2019; 7: e148–59
  11. Johnson BR Jr, Mishra V, Lavelanet AF, Khosla R, Ganatra B. A global database of abortion laws, policies, health standards, and guidelines. Bull World Health Organ. 2017;95:542–4.
  12. Cheraghi, P. P.-S. Effect of educating mothers on injury prevention among children aged <5 years using the Health Belief Model: a randomized controlled trial. Public Health, 2014, 128(9), 825-830. doi:10.1016/j.puhe.2014.06.017
  13. Akinloye O, Ogbolu DO, Akinloye OM, Terry Alli OA. Asymptomatic bacteriuria of pregnancy in Ibadan, Nigeria: a re-assessment. Br J Biomed Sci.2006;63(3):109-12.
  14. Glaser AP,  Schaeffer AJ. . Urinary tract infection and bacteriuria in pregnancy. Urol Clin North Am 2015;42:547–60.
  15. Schnarr J, Smaill F. . Asymptomatic bacteriuria and symptomatic urinary tract infections in pregnancy. Eur J Clin Invest 2008;38(Suppl 2):50–7.
  16. Ipe DS, Sunday L, Benjamin WH, et al. . Asymptomatic bacteriuria: prevalence rates of causal microorganisms, etiology of infection in different patient populations, and recent advances in molecular detection. FEMS Microbiol Lett 2013;346:1–10
  17. Smaill FM, Vazquez JC. Antibiotics for asymptomatic bacteriuria in pregnancy. Cochrane Database Syst Rev2015:CD000490.
  18. Golden berg RL. prevention of premature birth. New Eng.J. 1998, 339(5), 20-313
  19. City DA. Prevalence of Urinary Tract infection among pregnant women and its complications in their Newborns During Birth in the Hospital. IRCMJ, 2015, 17(8), 12-177.
  20. Matsuzkiewicz LJ. An epidemiological study of bacteriuria and blood. 2011, 278(12), 42-635.
  21. Gayathree LSS. Screening for Asymptomatic Bacteriuria in Pregnancy: An evaluation of various screening Tests in Hassan District Hospital. Journal of clinical and Diagnostic Research, 2010, 4(4), 2702-2706
  22. Kani YAUU. Asymptomatic bacteriuria in pregnant women in the antenatal booking clinic at Aminu Kano Teaching Hospital. J Obstetrics and Gynecology, 2015, 5, 286-297
  23. Tadesse E, Teshome M, Merid Y, Kibret B, Shimelis T. Asymptomatic urinary tract infection among pregnant women attending the antenatal clinic of Hawassa Referral Hospital, Southern Ethiopia. BMC Res Notes. 2014 Mar 17;7:155.
  24. Scientific and Technical Advisory Council (STAC) of the Special Journals Publisher (SJP): Research design innovations in Obstetrics, Gynecology, and Pediatrics. Special Journal of Obstetrics, Gynecology, and Pediatrics [SJ-OGP], 2020; 1 (1):1-21
  25. Micheal J and Leboffe BE. A Photographic Atlas for the Microbiology Laboratory (4 ed.). (D. Ferguson, Ed.) Morton Publishing Company 2011
  26. Thornsberry C. NCCLS standards for antimicrobial susceptibility Tests. AJCP, 1993, 39(12), 4283-4287.
  27. Clijical Laboratory Standard Institute. Breakpoints eliminated from CLSI document M100 since 2010.
  28. Agwu E, Ihongbe JC, Okogun GRA, Ezeonwumelu JOC, Igbinovia O. Chromobacterium violation associated with recurrent vaginal discharge among apparently healthy females in Ekpoma Nigeria. OJHAS, 2007, 1: 2.
  29. Tavakol M and Dennik R. Making sense of Cronbach’s alpha. International Journal of Medical Education. 2011; 2:53-55 Editorial ISSN: 2042-6372 DOI: 10.5116/ijme.4dfb.8dfd 53
  30. Ajayi AB, Nwabuisi C, Aboyeji AP, Ajayi NS, Fowotade A, Fakeye OO. Asymptomatic bacteriuria in antenatal patients in Ilorin, Nigeria. Oman Med J. 2012 Jan;27(1):31-5.
  31. Elzayat MA. Prevalence of Undiagnosed asymptomatic bacteriuria and associated risk factors during pregnancy: a cross-sectional study at two tertiary centers. BMJ open, 2017, 7, 1-6.
  32. Widmer MGA. Duration of treatment for asymptomatic bacteriuria during pregnancy. Cochrane Database System rev, 2011, 7(12)
  33. WHO antenatal care randomized trial: a manual for the implementation of new model WHO programme to map best reproductive health practices. WHO, 2016
  34. Nicolle LEBS. Infectious Diseases Society of America guidelines for the diagnosis and treatment of asymptomatic bacteriuria in adults. IDSA Guidelines, 2010, 643-652
  35. Manyanja RKC. Prevalence Asymptomatic bacteriuria and associated factors among women attending antenatal clinics in lower Mulago Hospital. American Scientific Research Journal for Engineering, Technology, and Sciences, 2016, 25(1).
  36. Halder GMA. Risk factors of urinary tract infection in pregnancy. J Pakistan Med Assoc, 2010, 60(3), 6-213
  37. Alaali KY. Prevalence of Asymptomatic Bacteriuria in pregnant Women, Western Region. International Journal of health care service, 2015, 17, 331-339
  38. Udayagiri V and Rohini GS. Prevalence and associate risk factors of asymptomatic bacteriuria in pregnancy with bacterial pathogens and their antimicrobial susceptibility in tertiary care hospital. International Journal of Reproduction, contraception, obstetrics and Gynecology, 2016, 16(2), 223-227
  39. Manasi PKP. Prevalence, risk factors, and causative organisms of asymptomatic bacteriuria in pregnancy. International Journal of Advances in medicine, 2017, 2(4), 213-216
  40. Adeliade OA, Gideon K, Christine B, Samuel K. Prevalence, etiology and antibiotic sensitivity profile of asymptomatic bacteriuria isolates from pregnant women in the selected antenatal clinic. The Pan African Medical Journal, 2017, 12 (4), 221-345
  41. Senait T, Tsega K,  Gebre A,  Getachew K,  Haftom L,   Aderajew Gw , and Awoke D. Prevalence, antimicrobial susceptibility profile and predictors of asymptomatic bacteriuria among pregnant women in Adigrat General Hospital, Northern Ethiopia. BMC Res Notes, 2018, 11, 740
  42. Karure SSR. Asymptomatic bacteriuria among pregnant women. Int J Reprod Contracept Obset Gynecol, 2013, 3(2), 437-441
  43. Onwuezobe IA. Associated Risk Factors of Asymptomatic Urinary Tract Infection among Pregnant Women Attending Antenatal Care in a Secondary Health Care Facility in a South-South Nigerian City. J.Curr.Microbiol.App.Sci, 2015, 4(8), 223-230
  44. ChandelLata RKA. Prevalence of pregnancy-associated bacteriuria. A study was done in a tertiary care Hospital. The J Obstet Gynecol India, 2012, 62(5), 511-514
  45. Oladeinde BH, Omoregie R, Oladeinde OB. Asymptomatic urinary tract infection among pregnant women receiving ante-natal care in a traditional birth home in Benin City, Nigeria. Ethiop J Health Sci. 2015 Jan;25(1):3-8.
  46. Omer Mohammed Ali Ibrahim et al, ME. Asymptomatic Bacteriuria in Pregnant Women at Kosti Teaching Hospital, Kosti-White Nile State (Sudan). International Journal of Current Microbiology and Applied Sciences, 2018, 7(6), 925-930
  47. Musbau S, Muhammad Y. Prevalence of Asymptomatic Bacteriuria among Pregnant Women Attending Antenatal clinic at Federal Medical Centre. Scholars Journal of Applied Medical Sciences(SJAMS), 2013, 1(5), 658-660
  48. Prasanna1, BMN. Prevalence of Asymptomatic Bacteriuria in Pregnant Women, Isolates and their Culture Sensitivity Pattern. J.Curr.Microbiol.App.Sci, 2015, 4(8), 28-35.
  49. Mokube MN, Atashili J, Halle-Ekane GE, Ikomey GM, Ndumbe PM. Bacteriuria amongst Pregnant Women in the Buea Health District, Cameroon: Prevalence, Predictors, Antibiotic Susceptibility Patterns and Diagnosis. PLoS ONE 2013, 8(8): e71086.
  50. Moses KM , Bariki M, Beatrice J, Eusebious M. Asymptomatic bacteriuria among pregnant women attending antenatal clinic at Kilimanjaro Christian Medical Centre in Northern Tanzania. Pract., 2018, 15(6), 917-922
  51. Abdullahi HI, Thairu Y. Asymptomatic Bacteriuria among Pregnant Women Attending Antenatal: Evaluation of Screening Test. IOSR Journal Of Pharmacy, 2015, 5(8), 41-47.
  52. Mor G, Cardenas I. The immune system in pregnancy: a unique complexity. Am J Reprod Immunol. 2010 Jun;63(6):425-33.

Ethics Declaration

Ethics approval and consent to participate

The present study was approved by the Research and Ethical Committee of Kampala International University Teaching Hospital (KIUTH) and also by the Uganda Council for Science and Technology. Participation in this study was completely anonymous and based on written informed consent.

Pregnancy-related asymptomatic bacteriuria at Kampala International University Teaching Hospital, Bushenyi Uganda

Back To Top
We use cookies in order to give you the best possible experience on our website. By continuing to use this site, you agree to our use of cookies.
Accept