Hani S. Faidah¹, Ahmed M. Ashshi² , Ghada A. Abou El-Ella², Ahmad K. Al-Ghamdi³ and Amr M. Mohamed²*

¹Department of Microbiology, Faculty of Medicine, Umm Al-Qura University, Makkah, Saudi Arabia.

²Department of Laboratory Medicine, Faculty of Applied Medical Sciences, Umm Al-Qura University, Makkah, Saudi Arabia.

³College of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.

Corresponding Authors E.mail:   amrmohamed2004@yahoo.com.

Abstract

Urinary tract infection represents a serious health problem in pregnant women. Scarce information is available about the profile of urinary tract infections among pregnant women in Makkah, KSA. The aim of the current study was to study the prevalence of UTI among pregnant women in Makkah, KSA and to investigate the most frequent causative agents and drug resistance profiles associated with such infections. A total of 200 pregnant women that visited maternity and children hospital in makkah were investigated. Personal data as well as medical history were collected using a well structured questionnaire. Midstream clean catch urine samples for urinalysis, and urine culture were collected from all investigated cases. The results revealed that 20% of investigated pregnant women were positive for UTI (12% with symptomatic UTI and 8% were asymptomatic). Escherichia coli was the most frequently isolated bacterial agent (25%) from both symptomatic and asymptomatic bacteriuria. Amoxicillin, cefoxitin, celtaxidime, fusidic acid, norfloxacin, ofloxzcin and penicillin showed the least resistance frequency (2.6%). In conclusion, high rate of UTI infection (20%) was recorded among pregnant women with E. coli being the most frequently encountered causative agent. Although symptoms are good markers of UTI during pregnancy, special care has to be directed towards asymptomatic cases. Finally, Amoxicillin, cefoxitin, celtaxidime, norflaoacin, penicillin and fusidic acid are the most useful antibiotics for treatment of UTI as they were able to inhibit most of the currently isolated UTI pathogens

Keywords

UTI; Pregnant women; Makkah

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Copy the following to cite this article: Faidah H. S, Ashshi A. M, Abou El-Ella G. A, Al-Ghamdi A. K, Mohamed A. M. Urinary Tract Infections among Pregnant Women in Makkah, Saudi Arabia. Biomed Pharmacol J 2013;6(1)

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Introduction

Urinary tract infection (UTI) is one of the most common infections where one or more part of urinary system become infected usually after bacteria overcome the natural defence mechanism of urinary tract (Al-Dujiaily, 2000). Although UTI could affect both sexes, women are more frequently affected than men due to short urethra, loss of prostatic secretion, ease of urinary tract contamination by faecal flora and various other reasons. In women however, the incidence of UTI is more frequent in pregnant women as compared to non pregnant ones due to the pregnancy-associated physiological changes, extended abdomen and difficulty of personal hygiene (Awaness et al., 2000).

Clinically, UTI have two principle presentations; symptomatic and asymptomatic bacteriuria (MacLean, 2001; Warren, 1996). Symptomatic UTI could be accompanied with a variety of clinical signs including dysuria, pyuria, strong  urge to urinate frequently, even immediately after the bladder is emptied,  painful burning sensation, discomfortable pressure and bloody urine, which may have a strong smell (Ferry et al., 1988; Ryan, 2004). In asymptomatic bacteriuria, urine culture reveals significant growth of pathogen (greater than10⁵ bacteria/ml) without showing clinical manifestation (Gilbert et al., 2005). Asymptomatic bacteriuria could be found in pregnant and non pregnant women but pregnancy enhances the progression from asymptomatic to symptomatic form which could lead to pylonephritis and adverse obstruction (Connolly and Thorp, 1999).

The diagnosis of UTI may be made on the basis of clinical signs and symptoms in combination with urinalysis results. Urine culture remains an important test in the diagnosis of UTI, because it helps in the documentation of the infection, by determining the identity of infecting bacteria and its antimicrobial susceptibility (Stamm and Hooton, 1993; Wing et al., 2000).

Urinary tract infections are most often caused by a single bacterial pathogen, frequently originating in the patient’s commensally enteric or skin flora. Escherichia coli, which is part of the normal gut flora accounts for approximately 85% of community-acquired UTIs and 50% of hospital acquired UTIs. Other common organisms include Enterococcus faecalis, Klebsiella pneumoniae, and Staphylococcus saprophyticus. (Hooton et al., 1996).

The aim of the current study was to study the prevalence of UTI and to investigate the most frequent causative agents and drug resistance profiles associated with such infections among pregnant women attending Obstetrics and Gynecology clinics at the main Maternity and Children Hospital in Makkah, KSA.

Materials and Methods

Study population and samples

A total of 200 women with age range of 18 – 45 years were subjected to the study after obtaining their consent. Pregnant women were selected from the Clinic of Obstetrics and Gynecology of Maternity and Children Hospital. Mecca, KSA during the period from May 2010 April 2011. Sterile urine samples for urinalysis and urine culture were collected from all studied cases. Urinalysis and urine cultures were used for the detection of UTI.

Sampling

Selected data related to the presence of suspected UTI-related clinical symptoms were collected by using of structured questionnaire. These symptoms included hematuria, dysuria, frequent urination, painful burning sensation, abdominal pain or pressure and abnormal urine smell. All women were instructed how to give a clean-catch midstream urine specimen. Briefly, they were asked to clean the area around urethral opening with clean water and alcohol swab, dry it and then collect a midstream urine sample by discarding the first part of urine and collecting 10-20 ml of the midstream in clean and sterile containers. Each sample of urine was divided into 2 parts and were properly labeled and sent to the laboratory with a request for complete urinalysis and urine culture.

Urine examination

The first part of urine sample was examined by dipstick tests using Comber 10 reagent test strips (Analyticon, Germany) that have panels to detect protein, blood, nitrite and leukocyte esterase in urine (Smith et al., 2003). In addition, wet preparations were made from sediment of each urine sample after centrifugation and were microscopically examined at X40 for detection of white blood cells as an indicator of pyuria. Samples with ≥ 10 WBC/field were regarded as pyuric. The second part of urine sample was cultured on plates of blood, MacConkey and CLED (cystine-lactose-electrolyte-deficient) agar with standard calibrated loop delivering 0.01 mL of urine. After streaking, plates were incubated at 37ºC for 24 to 48 hours. The plates were then examined macroscopically and microscopically for bacterial growth. Urinary tract infection was positive diagnosed by growth of ≥100,000 colony forming unit (CFU) of urinary tract pathogen per ml in culture of midstream urine sample, regardless of the presence or absence of leukocytes (Stamm and Hooton, 1993). Urine cultures with one pathogen were regarded as suspected infections. Cultures with more than one species were considered contaminated, while cultures with no growth of bacteria were said to be negative. Identification of bacterial pathogens was confirmed by observation of Gram staining and biochemical analysis using MicroScan Walk-Away® (DADE BEHRING INC., West Sacramento, CA). In addition Germ tube test was used for identification of Candida albican, which produce germ tubes when placed in liquid nutrient environment. Briefly, small inoculums of yeast cells obtained from an isolated colony were suspended in 0.5 ml of serum. The tubes were incubated at 35ºC for 2.5-3 hours.  A drop of the incubated serum was placed on a microscope slide and examined at X40 objective for the presence of germ tubes (Forbes et al., 2002).

Antibiotic sensitivity testing

The antibiotic sensitivity profile of isolated pathogens was carried out using MicroScan Walk-Away® (DADE BEHRING INC., West Sacramento, CA) as instructed by the manufacturer. Result were reported qualitatively as either Susceptible (S), Intermediate (I), or Resistant (R).

Result

Prevalence of UTI and among pregnant women

Out of 200 pregnant women, 40 women (20%) were positive for UTI. Based on the clinical symptoms, 24 (12%)  UTI-positive cases were associated with symptoms and classified as symptomatic UTI, while 16 (8%) cases were not associated with symptoms and considered as asymptomatic UTI (Table 1).

Table 1: Prevalence of UTI among pregnant women.

Investigated	Symptomatic UTI		Asymptomatic UTI		Total
population
Pregnant women	%	n	%	n	%	n
-200
	12	24	8	16	20	40

 

Frequency of UTI-associated microbial agents

Out of the 24 symptomatic UTI cases, E. coli was the most frequently isolated pathogen (25%) followed by Klebsiella pneumonia (16.7%). On the other hand, E. coli and staph. aureus were the most frequently isolated pathogens (25% each) from the 16 asymptomatic UTI cases (Table 2).

Table 2: Frequency of UTI-associated microbial agents among pregnant women:

UTI cases
Escherichia coli	Microbial agents associated with UTI cases		Symptomatic		Asymptomatic		Total
Klebseilla pneumonia			%	n	%	n	%	n
Staphylococcus aureus			25	6	25	4	25	10
Proteus mirabilis			16.7	4	12.5	2	15	6
Staph. hemolyticus			4.2	1	25	4	12.5	5
Entrobacter gergovi			12.5	3	6.2	1	10	4
Streptococcus aglactia			8.3	2	12.5	2	10	4
Candida spp.			12.5	3	0	0	7.5	3
Acinetobacter loffi			8.3	2	6.2	1	7.5	3
Enterococcus fecalis			4.2	1	6.2	1	5.2	2
Proteus valgaris			4.2	1	0	0	2.5	1
			4.2	1	0	0	2.5	1
			0	0	6.5	1	2.5	1

Anti-bacterial Resistant of Isolated UTI-causative Bacterial Agents

In the current study, antibiotic sensitivity tests were carried out for the recovered bacterial isolated from UTI cases. The outcome of the sensitivity tests were shown in (Table 3). The study revealed that amoxicillin, cefoxitin, celtaxidime, norflaoacin, penicillin and fusidic acid are the most useful antibiotics for treatment of UTI followed by amikacin and azithromycin as they showed the least resistance frequency (2.6% and 5.3%, respectively) and were able to inhibit most commonly isolated UTI pathogens. On the other hand, ampicillin and tetracycyclin, commonly used antibiotics, were poorly effective against the majority of pathogens isolated in the current study with a resistance rate of 55.3% and 34.21%, respectively.

Table 3: Anti-bactarial drug resistance of isolated UTI-causing bacteria:  

	Asymptomatic UTI		Symptomatic UTI		Total
Anti-bacterial Agents	-15		-23		-38
	%	n	%	n	%	n
Amikacin	6.7	1	4.3	1	5.3	2
Amox/K clav	6.7	1	13.04	3	10.5	4
Amoxicillin	6.7	1	0	0	2.6	1
Amp/Sulbactam	20	3	30.4	7	26.3	10
Ampicillin	40	6	65.2	15	55.3	21
Augrnentin	6.7	1	8.7	2	7.9	3
Azithromycin	0	0	8.7	2	5.3	2
Cefazolin	26.7	4	26	6	26.3	10
Cefoxitin	6.7	1	0	0	2.6	1
Ceftriaxone	26.7	4	8.7	2	15.8	6
Cefuroxime	13.3	2	4.3	1	7.9	3
Celtaxidime	6.7	1	0	0	2.6	1
cotrimoxazole	6.7	1	13.04	3	10.5	4
Erthromycin	0	0	13.04	3	7.9	3
Fusidic acid	6.7	1	0	0	2.6	1
Gentamicin	13.3	2	17.4	4	15.8	6
Norfl	6.7	1	8.7	2	7.9	3
Norfloxacin	6.7	1	0	0	2.6	1
Ofloxzcin	6.7	1	0	0	2.6	1
Oxacillin	30	3	8.7	2	13.2	5
Penicillin	6.7	1	0	0	2.6	1
Tetracycline	26.7	4	39.13	9	34.21	13
Ticnam	6.7	1	8.7	2	7.9	3
Trimeth/Sulfa	20	3	30.4	7	26.3	10

        

Discussion

The aim of the present study was to investigate the prevalence of UTI among pregnant women attending Maternity and Children hospital in Makkah along with studying of the frequently associated causative agents and the drug resistance profile of such infections.

Interestingly, the overall prevalence of UTI among pregnant women was (20%), which is relatively higher than what was recorded earlier (14.2%) in Saudi Arabia (Al-Sibaie et al., 1989) despite of the medical advancement and improved health care over the past years. Moreover, lower rates (4.8% and 6.1%) were recorded in neighbor countries as UAE and Iran, respectively (Abdullah and Al-Moslih, 2005; Hazhir, 2007). The high rate reported in the current study could be attributed to the type of the studied population whose ages lie within the most sexually active period of their lives (age mean 29.7 ± 6.5 SD) (Murry et al., 1998). Asymptomatic UTIs were confirmed among 8% out of the investigated cases. The prevalence of asymptomatic bacteriuria varies from one community to another. For example in Asian studies, while the asymptomatic bacteriuria was 4.3% among Filipino pregnant women (Sescon et al., 2003), it reaches up to 12% in rural areas in Bangladesh (Ullah et al., 2007), in Karachi in Pakistan 28.5% (Sheikh et al., 2000). Similarly, in Africans studies the prevalence of asymptomatic bacteriuria in Ethiopia, Ghana and Nigeria was 9.3%, 7.3% and 45.5%, respectively (Okonko et al., 2009; Turpin et al., 2007; Uncu et al., 2002). Also, in western studies the same differences were recorded. For example while the prevalence of asymptomatic bacteriuria in the USA was 2-7% (Delzell and Lefevre, 2000), 4-7% in Canada (Nicolle, 1994), it reached up to 16% among Spanish pregnant women (Akinloye et al., 2006). This variation can be attributed to several factors such as the geographical variation, ethnicity of the subjects, setting of the study (primary care, community based, or hospitals), and the variation in the screening tests (urine dipstick, microscopy and culture). In general, asymptomatic bacteriuria in young women is common but rarely persists; however, it is a strong predictor of subsequent symptomatic urinary tract infection (Hooton et al., 2000).

Regarding the causative agent of UTI, the current study revealed that E. coli was the most frequently (25%) isolated pathogen from all UTI cases followed by Klebseilla pneumonia (15%) and Staphylococcus aureus (12.5%). The current findings is in general agreement with the majority of the reported studies, which reported E. coli as the most common UTI-associated pathogen with a rates of 41.5%, 44%, 47.2%, 63%, 37.5% and 42.1% in Yemen, Ethiopia, Tanzania, Philippines, Ghana and Nigeria, respectively (Al-Haddad, 2005; Assefa et al., 2008; Masinde et al., 2009; Okonko et al., 2009; Sescon et al., 2003; Turpin et al., 2007). The predominance of E. coli is usually attributed to the urinary stasis, which is common in pregnancy (Delzell and Lefevre, 2000). Moreover, the anatomical and the functional changes that occur during pregnancy that results in a high risk of acquiring UTI from E. coli (Abdullah and Al-Moslih, 2005).

The antibiotic sensitivity studies conducted on the isolated UTI-causative bacterial agent during the current study revealed that amoxicillin, cefoxitin, celtaxidime, norflaoacin, penicillin and fusidic acid are the most useful antibiotics for treatment of UTI followed by amikacin and azithromycin as they showed the least resistance frequency (2.6% and 5.3%, respectively) and were able to inhibit most commonly isolated UTI pathogens. On the other hand, ampicillin followed by tetracyclin, which are commonly used antibiotics, were poorly effective against majority of the organisms isolated in this study with a resistance rate of 55.3% and 34.21%, respectively. This differ from the studies and findings in Caucasian women where ampicillin and septrin remain the most useful antimicrobial agents (Ronald, 1987) and the findings by Ebie et al., (2001) among patients in Military Hospital, Jos, Nigeria where the isolates were highly susceptible to nitrofurantoin. The efficacy of amoxicillin, cefoxitin, celtaxidime, norflaoacin, penicillin and fusidic acid as reported in the current study could be attributed to the fact that these drugs are relatively expensive when compared to most antibiotics frequently used. This probably had restricted their procurement and indiscriminate use, therefore making the organisms susceptible to them. This is similar to other reports where expensive antibiotics as quinolones are the most effective choice (Ebie et al., 2001; Ehinmidu, 2003; Mbata, 2007). On the other hand, the high resistance to other drugs may be due to the practices of self medication and indiscriminate use of these antibiotics with the subsequent resistance acquirement.

In conclusion, the current results show that urinary tract infection in pregnancy is a very frequent medical problem in Makkah. Although symptoms are good markers of UTI during pregnancy, antenatal care should include direct questioning and urine examination to discover asymptomatic cases. The important infecting organisms were found to be the commensals of perianal and vaginal regions as E. coli, Staphylococcus and Candida species, which indicate fecal contamination and low personal hygiene. The current findings highlighted the need for constant monitoring of susceptibility of specific pathogens in different populations to commonly used anti-microbial which will significantly assist clinicians in the rational choice of antibiotic therapy to prevent misuse, or overuse of antibiotics.

References

1. Abdullah, A. A. and M. I. Al-Moslih (2005). “Prevalence of asymptomatic bacteriuria in pregnant women in Sharjah, Unite Arab Emirates.” East Mediterr Health J 11(5-6): 1045-1052.
2. Akinloye O, Ogbolu DO, Akinloye OM, Terry Alli OA. (2006). “Asymptomatic bacteriuria of pregnancy in Ibadan, Nigeria: a re-assessment.” Br J Biomed Sci 63(3): 109-112.
3. Al-Dujiaily, AA. (2000). “Urinary tract infection during pregnancy in Tikrit.” J. Tikrit 6: 220-224.
5. Al-Haddad, A. M. (2005). “Urinary tract infection among pregnant women in Al-Mukalla district, Yemen.” East Mediterr Health J 11(3): 505-510.
6. Al-Sibai MH, Saha A, Rasheed P. (1989). “Sociobiological correlates of bacteriuria in Saudi pregnant women.” Public health 103(2): 113-121.
7. Assefa, A., D. Asrat, Woldeamanuel, Y. G. Hiwot Y Abdella, A. Melesse, T. (2008). “Bacterial profile and drug susceptibility pattern of urinary tract infection in pregnant women at Tikur Anbessa Specialized Hospital Addis Ababa, Ethiopia.” Ethiop Med J 46(3): 227-235.
8. Awaness, A., Al-Saadi MG, Aadoas, SA. (2000). “Antibiotics resistance in recurrent urinary tract infection.” Kufa medical journal 3: 159.
9. Connolly, A. and Thorp. J.M. (1999). Urinary Tract Infection in pregnancy. The Urologic Clinics of North America 26(4): 779-787.
10. Delzell, J. E., Jr. and M. L. Lefevre (2000). “Urinary tract infections during pregnancy.” Am Fam Physician 61(3): 713-721.
11. Ebie M, Kandaki-Olukemi YT, Ayanbadejo J Tanyigna KB. (2001). “UTI infections in a Nigerian Military Hospital.” J. Microbiol 15(1): 31-37.
12. Ehinmidu, J. (2003). “Antibiotics Susceptibility Pattern of Urine Bacterial Isolates in Zaria, Nigeria.” J. Pharmaceutical Res 2(2): 223-228.
13. Ferry, S., L. G. Burman, S.E. Holm. (1988). “Clinical and bacteriological effects of therapy of urinary tract infection in primary health care: relation to in vitro sensitivity testing.” J. Infect. Dis. 20: 535-544.
14. Forbes, B. A., A. S. D.F. Sahm, Weissfeld, eds.(2002). “Laboratory Methods in Basic Mycology in Bailey and Scott’s Diagnostic Microbiology, .” (11th ed): 711-797.
15. Gilbert DN, M. J. R., Eliopoulos GN, Sande NA. (2005). “Sanford guide to Antimicro-bial Therapy.” Vermont: Antimicrobial Therapy, Inc Hyde Park (32nd ed): 22-23.
16. Hazhir, S. (2007). “Asymptomatic bacteriuria in pregnant women.” Urol J 4(1): 24-27.
17. Hooton, T. M., D. Scholes, Hughes, J. P.Winter, C.Roberts, P. L.Stapleton, A. E.Stergachis, A.Stamm, W. E. (1996). “A prospective study of risk factors for symptomatic urinary tract infection in young women.” N Engl J Med 335(7): 468-474.
18. Hooton, T., D. Scholes, Stapleton, AE, Roberts, PL, Winter, C, Gupta, K, Samadpour, M, Stamm, WE.. (2000). “A prospective study of asymptomatic bacteriuria in sexually active young women.” N Engl J Med 343(14): 992-997.
19. MacLean, A. B. (2001). “Urinary tract infection in pregnancy.” Int J Antimicrobial Agents 17(4): 273-276; discussion 276-277.
20. Masinde, A., B. Gumodoka, Kilonzo, A. Mshana, S. E. (2009). “Prevalence of urinary tract infection among pregnant women at Bugando Medical Centre, Mwanza, Tanzania.” Tanzan J Health Res 11(3): 154-159.
21. Mbata, T. (2007). “Prevalence and Antibiogram of UTIs Among Prisons Inmates in Nigeria.” J. Microbiol 3(2).
22. Murry RR, Rosseenthal KS, Kobayashi GS, Pfaller MA (1998). Medical Microbiology, third Edition, Mosby Publishers. p. 186.
23. Nicolle, L. (1994). ” Screening for asymptomatic bacteriuria in pregnancy. Canadian Guide on preventive health care.” Ottawa Health, Canada: 100-106.
24. Okonko, I. O., Ijandipe, L. A., Ilusanya, O. A., Donbraye-Emmanuel, O. B., Ejembi J., and E. O. C. Udeze A. O., Fowotade A. and Nkang A. O. (2009). “Incidence of urinary tract infection (UTI) among pregnant women in Ibadan, South-Western Nigeria.” African Journal of Biotechnology 8(23): 6649-6657.
25. Ryan, K. J. (2004). Urinary Tract Infections. Sherries MEDICAL MICROBIOLOGY: An Introduction to Infectious Diseases. Kenneth J. Ryan and C. G. Ray. USA. 979: 867-872.
26. Sescon , M. D., Felice D.Garingalao-Molina, M.D., Carla Elena J. Ycasiano, and M. C. S. M.D., M.D., and Ricardo M. Manalastas, M.D. (2003). “Prevalence of Asymptomatic Bacteriuria and Associated Risk Factors in Pregnant Women.” Phil J Microbiol infect Dis 32(2): 63-69.
27. Sheikh M.A. , Khan M. S. , Khatoon A. and Arain G. M. (2000). “Incidence of urinary tract infection during pregnancy.” East Mediterr Health J 6(2-3): 265-271.
28. , P., A. Morris., Reller., LB. (2003). ” Predicting Urine Culture Results by Dipstick Testing and Phase Contrast Microscopy.” Pathol 35(2): 161-165.
29. Turpin, C., B. Minkah, B. Danso, K. Frimpong, E. (2007). “Asymptomatic bacteriuria in pregnant women attending antenatal clinic at komfo anokye teaching hospital, kumasi, ghana.” Ghana Med J 41(1): 26-29.
30. Ullah MA, Barman A, Siddique MA, Haque AK. (2007). “Prevalence of asymptomatic bacteriuria and its consequences in pregnancy in a rural community of Bangladesh.” Bangladesh Med Res Counc Bull 33(2): 60-64.
31. Uncu Y, Uncu G, Esmer A, Bilgel N. (2002). “Should asymptomatic bacteriuria be screened in pregnancy?” Clin Exp Obstet Gynecology 29(4): 281-285.
32. Warren, J. (1996). Clinical Presentations and Epidemiology of Urinary Tract Infections. Urinary Tract Infections Molecular Pathogenesis and Clinical Managmant. H. L. T. M. a. J. W. Warren. Washington 439: 3-27.
33. Wing, D. A., A. S. Park, et al. (2000). “Limited clinical utility of blood and urine cultures in the treatment of acute pyelonephritis during pregnancy.” Am J Obstet Gynecology 182(6): 1437-1440.

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