Introduction
The urinary tract is second only to the respiratory tract in acquiring microbial infections, especially in females. Urinary tract infections (UTI) are more common in pregnant than non-pregnant women.1,2 Asymptomatic bacteriuria (ASB) is defined as the presence of actively multiplying bacteria in the urinary tract excluding the distal urethra in a patient without any obvious symptoms.3 This is confirmed in the presence of significant bacteriuria based on isolation of ≥105 cfu/ml of same species of bacteria in properly collected and transported midstream urine during a screening test.3-8
Several studies have shown the overall prevalence of asymptomatic bacteriuria in pregnancy to be between 2-7%,3,5,8-13 but may be as high as 10% in high risk populations.9,14,15 It is twice as common in pregnant women with sickle cell trait and three times as common in pregnant women with diabetes mellitus as in normal pregnant women.3,9,14,16 Other conditions associated with increased incidence include low socio-economic status, grandmultiparity and advancing age.10,17 However, several studies have shown that the prevalence of ASB in developing countries is higher than in the developed countries.
The significance of asymptomatic bacteriuria in pregnancy lies in its potential to cause acute pyelonephritis, preterm labor and preterm rupture of membranes. Others include anemia, pre-eclampsia, chronic pyelonephritis and even fetal wastage.5,18-21 It is associated with acute pyelonephritis in 25-30% of pregnant women compared with 1-2% in those without asymptomatic bacteriuria.7,8,22,23
This study assessed the prevalence of ASB among pregnant women attending antenatal care in University of Ilorin Teaching Hospital.
Methods
This was a prospective descriptive study amongst asymptomatic pregnant women attending their first antenatal clinic visit, at the Maternity wing of the University of Ilorin Teaching Hospital, Ilorin between July and October, 2007. Systematic random sampling technique was employed in recruiting 125 subjects who met the stated criteria. A structured profoma containing information on bio-data was administered on all recruited subjects at booking, and physical examination was done by medical personnel on the research team after obtaining informed consent. Subjects were informed of their results and those with positive culture were treated with a course of antibiotics based on the sensitivity pattern and duly followed up in the clinic to ensure bacteriological cure. The study was approved by the Ethical Research Committee of the Hospital.
Laboratory Procedure
About 5 ml of midstream urine was collected into a sterile universal bottle and the sample taken to the microbiology laboratory for microscopy and culture within 2 hours of collection.
Urine Microscopy & Culture
A loop full of well-mixed centrifuged urine was examined under wet preparation procedure to detect pyuria, while noting red cells, casts, parasites and fungi, when present. Urine culture was done with 0.001 ml of well mixed urine delivered by a sterile calibrated wire loop and plated on CLED and blood agar plates, which were incubated aerobically at 35-37oC for 24 hours. Repeat culture was ordered for contaminated specimens. Each significant isolate was identified by colonial morphology, gram staining and biochemical reactions according to standard procedure.24 Antibiotic sensitivity testing was done by emulsifying selected isolates in normal saline at a turbidity compared to 0.5 Mac Farland’s standard. Using sterile swabs, suspensions were inoculated on Muller-Hinton agar in accordance with modified Kirby-Bauer method and incubated at 35-37oC for 18-24 hrs. Single antibiotic impregnated discs including; gentamicin (10 µg), amoxicillin (25 µg), augmentin (30 µg), nalidixic acid (30 µg), nitrofurantoin (300 µg), erythromycin (5 µg), cotrimoxazole (25 µg), ceftazidime (30 µg) and cefuroxime (30 µg) were tested against gram-positive and gram-negative organisms as appropriate. Interpretation was done by comparing the diameter of zone of inhibition with those of a standard table in three grades of susceptibility which are sensitive, intermediate and resistant.
Control strains of Staphylococcus aureus (ATCC 25923) and Escherichia coli (ATCC 25922) were run with the gram-positive and gram-negative isolates, respectively. All procedures were done as recommended by the Clinical Laboratory Standard Institute (CLSI).25 Information obtained were recorded on a data collection sheet designed for the study, and fed into the computer using EPI-INFO version 3.3.2 software package for data analysis.
Results
A total of 125 consenting pregnant women who met the inclusion criteria were studied. The socio-demographic characteristics of the women screened are illustrated in Table 1. Their age ranged between 14 and 40 years with a mean age of 28.5+ 4.95. The median and modal ages were 28 and 30 years respectively. Most of the women, (94.4%) were married, while 5.6% were single. The table also shows that majority (64.8%) of the women had tertiary education. Also, 3.2% of the women had no formal education, while 4% and 28% had primary and secondary education respectively. Forty-seven (37.6%) were Christians while 78 (62.4%) were Muslims. The parity of the women ranged between zero and six, with the modal parity of zero. Forty-nine (39.2%) women were nulliparous, while 47.2% belonged to the para 1-2 group. Three (2.4%) women were grandmultiparous. The gestational age of these women ranged between 9 and 24 weeks with a modal gestational age of 17 weeks. Forty-one (33.3%) had a gestational age between 17 and 20 weeks, while 17.9% had gestational age between 9 to 12 weeks.
Table 1: Sociodemographic characterisctics of women screened for asymptomatic bacteriuria.
Table 2 shows the results of the urine culture of the 125 pregnant women screened. A total of 50 women had asymptomatic bacteriuria on urine culture, giving a prevalence of 40%. Thirty-five (28%) had no growth on culture, while 40 women (32%) had insignificant bacteriuria. Twelve women had mixed growth which was repeated and subsequently were classified into one of the above three groups. None of the women with asymptomatic bacteriuria had any medical illness.
Table 2: Results of urine culture.
The profile of bacteria isolated from cases of significant bacteriuria is shown in Table 3. Staphylococcus aureus constituted the commonest cultured organism, 36 (72%). This was followed by Proteus spp. 7 (14%). Other isolates included Staphylococcus epidermidis 3 (6%), Klebsiella spp. 2 (4%) and Escherichia coli 2 (4%).
Table 3: Profile of bacteria isolated from cases of significant bacteriuria.
The sensitivity pattern of organisms cultured from the cases of significant bacteriuria is illustrated in Table 4. Staphylococcus aureus, the commonest isolate showed good sensitivity to gentamicin and nitrofurantoin with 75% and 77.8% of the organisms respectively. Proteus spp showed good sensitivity to gentamicin, nalidixic acid, ceftazidime and cefuroxime. Most of the organisms showed good sensitivity to Nitrofurantoin and gentamicin.
Table 4: Sensitivity pattern of organisms cultured from cases of significant bacteriuria.
- not tested; S- sensitive; R- resistance; Is-intermidiate sensitivity.
Discussion
The patients involved in the study though recruited randomly at booking were mainly between 21-30 years of age, this being about the peak reproductive period in this environment and most societies. Most of the women (94.4%) were married and this could be associated with the higher chance of pregnancy being planned and thus presentation for antenatal care compared to singles. The literacy rate was quite high with 64.8% having tertiary education and 28% having secondary education. The women were also mainly of low parity (86.4%). These were both in keeping with other studies which found antenatal booking to be high in women with at least secondary school education and low parity.26,27 Of the women recruited, 62.4% were Muslims and 37.6% Christians, Ilorin being a predominantly Muslim community. Fifty-one percent (51%) of the Christians and 33% of the Muslims had positive culture results. The lower prevalence in the Muslims might be attributed to rinsing of the vulva following every episode of urination, practiced in the religion. However Sescon et al. found low socio-economic status, high parity and advancing age to be associated with increased prevalence of asymptomatic bacteriuria in pregnancy.4 McNair et al.28 and Akinloye et al.29 found an increased association of asymptomatic bacteriuria with parity.
This study found 50 cases of significant bacteriuria among the 125 pregnant women at UITH giving a prevalence rate of 40%. This is higher than the reported prevalence from Lagos, Ibadan, Sagamu and Ile-Ife of 4%, 12%, 23.9% and 26%, respectively.22,30-32 This high prevalence might be due to the fact that only women who booked around the peak gestational age for bacteriuria were recruited for the study. It was however lower than the prevalence of 86.6% reported by Akerele in Benin.33 These differences may also be attributed to variation in population characteristics such as age, parity, socio-economic status and bacterial ecology.
The strength of the study lies in the fact that measures were taken to ensure that urine samples were appropriately collected and analyzed within two hours of collection. The most common organism isolated was Staphylococcus aureus which was isolated from 36 (72%) cases. This was followed by Proteus spp. 7 (14%), Staphylococcus epidermidis 3 (6%), Klebsiella 2 (4%) and Escherichia coli 2 (4%). This was consistent with the findings by Akerele in Benin,33 and Oyagade in Ado-Ekiti,34 who also found Staphylococcus aureus as the predominant isolate.
Most of the organisms were very sensitive to nitrofurantoin, gentamicin, cefuroxime and ceftazidime. Resistance to cotrimoxazole and amoxicillin were relatively high. Results showed that 77.8% of Staphylococus aureus, 100% of Staphylococcus epidermidis, Klebsiella and Escherichia coli were sensitive to Nitrofurantoin; while Staphylococcus aereus and Proteus spp. showed 75% and 85.7% sensitivity respectively to gentamicin. Both antibiotics were also found to be highly effective in studies by Mandara in Zaria,12 Ezeome in Enugu,35 and Tupin in Ghana.36 Mezue et al.37 at the University of Nigeria found Cotrimoxazole to be virtually useless against pathogens that cause UTI. Amoxicillin and augmentin were only slightly better. A clear alternative as a first line drug against UTI before culture and sensitivity is Nitrofurantoin.37,38 Gupta et al. stated that nitrofurantoin is relatively safe in pregnancy and is effective against most urinary tract infections but may cause hemolysis in glucose-6-phosphate dehydrogenase deficient infants if used close to term.36 There is some reluctance among doctors to prescribe nitrofurantoin and this may be due to its side effect profile, but it is clearly an important drug for urinary tract infections.
Conclusion
Overall, the prevalence of asymptomatic bacteriuria in our locality at 40% is high. Therefore, screening for and treatment of asymptomatic bacteriuria in pregnancy should be an integral part of obstetric care and should be included in all antenatal guidelines.
Acknowledgements
The Authors are grateful to the University of Ilorin Teaching Hospital for its financial contribution in carrying out the study. The study was approved by the Ethical Research Committee of the Hospital. No conflict of interest exists.
References
1. Kriplani A, Bukshee K, Rafan A. Asymptomatic bacteriuria in pregnant Indian patients at all Indian Institute of Medical Sciences, New Delhi, and Treatment with single dose antimicrobial therapy. J Obstet Gynaecol India 1993;43:489-491.
2. Sharma JB. Prevalence of significant bacteriuria in preterm labour. J Obstet Gynaecol India 1990;40:336-338.
3. Greval M, Biswas KM, Perloff D. Cardiac, Haematologic, Pulmonary, Renal and Urinary Tract Disorders in Pregnancy. In: DeCherney AH, Nathan L(ed), Current Obstetrics and Gynaecologic Diagnosis and Treatment, 9th edition. U.S.A: Lange Medical Books 2003; 387-427.
4. Seseon NI, Garingalo-molina FD, Yeasiano CJ. Prevalence of asymptomatic bacteriuria and associated risk factors in pregnant women. Phil J. Microbial Infect Dis 2003;32:63-69.
5. Patterson TF, Andriole VT. Detection, significance, and therapy of bacteriuria in pregnancy. Update in the managed health care era. Infect Dis Clin North Am 1997 Sep;11(3):593-608.
6. Task Force on Urinary Tract Infection. Philippine Practice Guidelines Group in Infectious Disease. Urinary Tract Infection in Pregnancy 1998;1:16-19.
7. Duff P. Maternal & Perinatal Infection.In: Gubbe SG, Niebyl JR (ed), Obstetrics: Normal & Problem Pregnancies, 3rd edition, U.S.A, Churchill Livingstone, 1996; 1199.
8. Robson SC. Hypertensive and renal disease in pregnancy. In: Edmonds DK(ed), Dewhurst’s Textbook of Obstetrics and Gynaecology for Postgraduates, 6th Edition, U.K, Blackwell Science, 1999; 166-185.
9. Addo VN. Urinary Tract Infection in Pregnancy. In: Kwawukume EY, Emuveyan EE(ed),Comprehensive Obstetrics in the Tropics, first edition, Asante & Hittscher printing press Ltd, 2002; 261-265.
10. Maranchie JK, Capelouto CC, Loughlin KR. Urinary tract infections during pregnancy. Infect Urol 1997;10:152-157.
11. Krieger JN. Complications and treatment of urinary tract infections during pregnancy. Urol Clin North Am 1986 Nov;13(4):685-693.
12. Mandara MU, Shittu SO. Asymptomatic Bacteriuria in Antenatal Patients at Ahmadu Bello University Teaching Hospital, Zaria, Nigeria. Trop J Obstet Gynaecol 1999;16:41-45.
13. Okpere EE. Medical Disorders in Pregnancy. In: Okpere E (ed), Clinical Obstetrics, revised edition, Uniben press, 2003; 131.
14. Whalley P. Bacteriuria of pregnancy. Am. J Obstet Gynaecol 1967;97:723-738.
15. Kacmaz B, Cakir O, Aksoy A, Biri A. Evaluation of rapid urine screening tests to detect asymptomatic bacteriuria in pregnancy. Jpn J Infect Dis 2006 Aug;59(4):261-263.
16. Kiningham RB. Asymptomatic bacteriuria in pregnancy. Am Fam Physician 1993 Apr;47(5):1232-1238.
17. Lucas MJ, Cunningham FG. Urinary infection in pregnancy. Clin Obstet Gynecol 1993 Dec;36(4):855-868.
18. Kunin CM. Urinary tract infection in adults. Urinary Tract Infection 1997; 139-144
19. Smith GW, Brumfit C. Urinary Tract Infection in Pregnancy. P.G. D- Africa 1984; 6: 231-254.
20. Okonofua FF, Adeniran A, Okonofua B. Incidence and Pattern of Asymptomatic Bacteriuria of Pregnancy in Nigerian Women. Niger Med Pract 1989;17:35-38.
21. Onyemelukwe NF, Obi SN, Ozumba BC. Significant Bacteriuria in Pregnancy in Enugu, Nigeria. Jnal College of Medicine 2003;8:20-22.
22. Nnatu S, Essien EE, Akinkugbe A, Odum CU. Asymptomatic bacteriuria in pregnant Nigerian patients. Clin Exp Obstet Gynecol 1989;16(4):126-129.
23. Tincello DG, Richmond DH. Evaluation of reagent strips in detecting asymptomatic bacteriuria in early pregnancy: prospective case series. BMJ 1998 Feb;316(7129):435-437.
24. Cheesbrough M. Medical Laboratory Manual for Tropical Countries. Vol. 11, Microbiology. Cambridge University Press. 2000.
25. As CL. (2006) Performance standards for antimicrobial disk susceptibility tests. Approved standard. 9th Edition, Document M2-A9. Clinical and Laboratory Standards Institute, Wayne, PA.
26. Jimoh AA. Utilisation of antenatal services at the Provincial Hospital, Mongomo, Guinea Equatoria. Afr J Reprod Health 2003 Dec;7(3):49-54.
27. Harrison KA, Bergstrom S. Poverty, deprivation and unsafe motherhood. In: Lawson J, Harrison KA, Bergstrom S. (eds) Maternity Care in Developing Countries. 1st Edition. RCOG Press, London 2001: 1-19.
28. McNair RD, MacDonald SR, Dooley SL, Peterson LR. Evaluation of the centrifuged and Gram-stained smear, urinalysis, and reagent strip testing to detect asymptomatic bacteriuria in obstetric patients. Am J Obstet Gynecol 2000 May;182(5):1076-1079.
29. Akinloye O, Ogbolu DO, Akinloye OM, Alli OA. Asymptomatic bacteriuria of pregnancy in Ibadan, Nigeria: a re-assessment. British Journal of Biochemical science, 2006. Available on http://www.findarticles.com. Extracted on 14/12/2007.
30. Ojo OA, Akinkugbe OO. The significance of asymptomatic bacteriuria in pregnancy in Ibadan. W Afr J Surg 1996;1:23-28.
31. Olusanya O, Ogunledun A, Fakoya TA. Asymptomatic significant bacteriuria among pregnant and non-pregnant women in Sagamu, Nigeria. West Afr J Med 1993 Jan-Mar;12(1):27-33.
32. Aboderin AO, Ako-Nai AK, Zailani SB, Ajayi A, Adedosu AN. A Study of Asymptomatic Bacteriuria in Pregnancy in Ile-Ife, Southwestern Nigeria. Afr J Exper. Microbiol. 2004;5:252-259.
33. Akerele J, Abhulimen P, Okonofua F. Prevalence of asymptomatic bacteriuria among pregnant women in Benin City, Nigeria. J Obstet Gynaecol 2001 Mar;21(2):141-144.
34. Oyagade AO, Smith SI, Famurewa O. Asymptomatic significant bacteriuria among pregnant women in Ado- Ekiti, Ekiti State, Nigeria. Afr J Exper Microbiol 2004;5:64-67.
35. Ezeome IV, Ikeme AC, Okezie OA, Onyebueke EA. Asymptomatic bacteriuria in pregnant women in Enugu, Nigeria. Trop J Obstet Gynaecol 2006;23:12-13 .
36. Turpin C, Minkah B, Danso KA, Frimpong EH. Asymptomatic bacteriuria in pregnant women attending antenatal clinic at komfo anokye teaching hospital, kumasi, ghana. Ghana Med J 2007 Mar;41(1):26-29.
37. Mezue K, Ofong C, Nmezi D, Ugochukwu-Obi G. Antibiotic Sensitivity patterns in urinary tract infections at a Tertiary Hospital. Journal of the University Of Nigeria Medical students, 2006. Available on http://www.1990unecmedclass.com. Extracted on 12/12/2007.
38. Abdul IF, Onile BA. Bacterial Isolates from the urine of Women in Ilorin and their Antibiotic Susceptibility pattern. Trop J Obstet Gynaecol 2001;18:61-65 .
|