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Abstract

Objective

Urinary tract infections (UTI) are common during pregnancy. Identification of antimicrobial susceptibility patterns of microorganisms in pregnant women is important to select the most appropriate antimicrobial. We assessed common uropathogens in pregnant women with UTI and antimicrobial susceptibility, to guide empirical antibiotic selection.

Methods

In this retrospective study, we analyzed mid-stream urine culture and antibiotic susceptibility data from pregnant women who attended Jordan University Hospital during 2014 to 2018. Data were collected from patients’ charts and urine cultures, and sensitivity results were extracted from the laboratory electronic system. We calculated descriptive statistics and determined correlations among pathogens and antibiotics.

Results

We examined 612 positive urine cultures from 559 pregnant women, including 163 (29.2%) inpatients. Escherichia coli (29.4%) was the most frequently identified microorganism, followed by coagulase-negative staphylococci (CoNS) (21.6%). All bacterial isolates were sensitive to aztreonam, chloramphenicol, fosfomycin, ofloxacin, pefloxacin, piperacillin, and colistin sulfate; 87.5% were sensitive to amikacin. Only 15.79%, 18.93%, and 17.91% were sensitive to oxacillin, nalidixic acid, and erythromycin, respectively.

Conclusion

E. coli and CoNS were the most commonly identified microorganisms in this study. We found increased antibiotic resistance in Enterobacter species. The chosen antimicrobial therapy in pregnancy should be determined by sensitivity/resistance and fetomaternal safety.

Keywords

Antimicrobial culture pregnancy resistance sensitivity urine

Introduction

Pregnant women are at increased risk of urinary tract infections (UTIs) owing to physiological changes. Infections can cause pregnancy complications and may be transmissible to the fetus.¹ UTIs are the most common type of infection during pregnancy, affecting up to 10% of pregnant women, and all UTIs during pregnancy, including asymptomatic infections, require treatment.² Asymptomatic or symptomatic bacteriuria occurs in 5% to 10% and 1% to 3% of pregnant women, respectively.³ Screening for and treatment of asymptomatic bacteriuria in pregnancy is standard obstetric care, and most antenatal guidelines include routine screening for asymptomatic bacteriuria.⁴ Antimicrobial resistance represents a major global challenge that is largely attributed to widespread misuse and overuse of antimicrobials by physicians or by other health care workers in some countries and self-medication practices among individual patients to treat infections.^1,2 The identification of frequently isolated pathogens in UTIs among pregnant women and antimicrobial susceptibility patterns of such microorganisms will help in guiding physicians with selecting the appropriate antimicrobial therapy, which will improve management outcomes and will help in reducing the emergence of resistant microbial strains.^5–7 The presence of asymptomatic bacteriuria and antibiotic susceptibility testing results should be taken into consideration during the management of pregnant women who are visiting an antenatal care clinic.⁸

Although infection with uropathogens among pregnant women is a common medical problem, there is a little information on these microorganisms in pregnancy, and very little is known about their antimicrobial susceptibility patterns. Investigation of this issue is needed, to identify the etiologic agents involved for subsequent treatment with the proper antimicrobial agent.

In this study, we aimed to determine the most frequent UTI pathogens and their antimicrobial susceptibility among pregnant women who attended Jordan University Hospital (JUH) from 2014 to 2018. The results will help guide the management of UTIs in pregnancy.

Methods

Study design

In this retrospective study, we collected urine culture and sensitivity results for pregnant women who were seen at JUH from 2014 to 2018. The pregnancy status of patients was confirmed in urine or blood pregnancy testing and ultrasound scan examination. Urine cultures were requested on the clinical grounds of suspected UTI, with symptoms of frequency, urgency, incontinence, suprapubic pain, low back pain, renal angle tenderness, fever, chills or rigors or in patients with asymptomatic bacteriuria in routine urinalysis as evidenced by white blood cell count more than 10 to 12/high power field.

This study was approved by the institutional review board at JUH (decision number 112/2019, dated 14 May 2019). The requirement for informed consent was waived as the study was retrospective and data were collected using patients' files, and confidentiality and anonymity were maintained throughout the study process.

Study sample collection

The microbiological and antimicrobial susceptibility data in this study were obtained from records of the clinical microbiology laboratory and JUH electronic databases. Data from 2014 to 2018 were extracted using a data extraction sheet. The clinical microbiology laboratory of JOH uses a predefined procedure for culturing, bacterial identification, and susceptibility testing.

Urine sample collection, primary inoculation, and analysis

About 10 mL of mid-stream urine was collected by pregnant women, after appropriate instruction was given. Urine samples were delivered immediately to the microbiological laboratory. Women were given specific instructions to avoid contamination and avoid using of any kind of antiseptics on the vulva, vagina, and urethral orifice. Only mid-stream samples were taken.

Urine samples were cultured on 5% blood agar and MacConkey agar using calibrated loops in semi-quantitative assessment and incubated in aerobic conditions at 35 to 37°C for 18 to 24 hours. Isolates were identified and confirmed using standard methods including Gram staining; colony morphology on media; growth on selective media; lactose and mannitol fermentation; hydrogen sulfide production; catalase, oxidase, coagulase, and indole tests; citrate utilization; and urease testing. Urine infection cultures were considered positive with bacterial counts ≥10⁵/mL. All patients with positive urine cultures were treated.

Antimicrobial susceptibility testing

For reliable detection, laboratories may use conventional, quantitative susceptibility testing methods or specially developed, single concentration agar screening tests for some resistant species, as previously described.⁹ The antibiotic discs consisted of antibiotics, according to the type of bacteria; for gram-positive bacteria, the antimicrobials listed in Table 1 were tested; for gram-negative bacteria, antimicrobials listed in Table 2 were tested.

Table 1.

Antimicrobials for gram-positive bacteria.

Ring A (for gram-positive bacteria)

Ampicillin

Levofloxacin

Chloramphenicol

Clindamycin

Erythromycin

Gentamycin

Oxacillin

Vancomycin

*Tigecycline

*Provided as single discs.

Table 2.

Antimicrobials for gram-negative bacteria.

Ring B (for gram-negative bacteria)

Augmentin

Cefuroxime

Cotrimoxazole

Gentamicin

Nalidixic acid

Nitrofurantoin

Norfloxacin

Cefixime

Amikacin

Cefepime

Cefoxitin

Ceftazidime

Ceftriaxone

Ciprofloxacin

*Imipenem

*Ertapenem

Tetracycline

*Tigecycline

Ampicillin

Cefalotin

Cefpodoxime

Meropenem

Piperacillin/tazobactam

Tobramycin

Colistin sulphate

Cefotaxime

*Provided as single discs.

Antimicrobial susceptibility testing for UTIs in the laboratory is performed using two groups of antimicrobial discs for cascade reporting, a strategy recommended by the Clinical and Laboratory Standards Institute. In this strategy, the reporting of antimicrobial susceptibility test results for the second group of agents (e.g., broader-spectrum, more costly) may only be reported if an organism is resistant to primary agents within a particular drug class. If a pathogen shows resistance to all of these, the laboratory will move to the second stage for testing broad-spectrum antibiotics.

Identification and sensitivity testing were done if the culture was pure and growth was significant (≥10⁵ CFU/mL). If the culture growth involved a mix of two pathogens and no isolate was dominant, or more than two types of colonies were grown, then it was reported as a mixed growth and clinical correlation was needed to make a determination. In such cases, no sensitivity testing was carried out.

Statistical analysis

Data were analyzed using IBM SPSS software version 22 (IBM Corp., Armonk, NY, USA). Chi-square or Fisher’s exact tests were used to identify any significant association between the most frequent pathogens and their antimicrobial susceptibility in pregnant women.

Results

A total of 612 urine samples from pregnant women with suspected UTI were selected for isolation and identification of bacteria and antimicrobial susceptibility testing. Among these, 11 patients showed recurrent infections. The mean age of patients who underwent urine testing was 32.3± 6.5 years. Of 559 patients, 29.2% (163/559) were inpatients and 70.8% (396/559) were outpatients (Table 3).

Table 3.

Demographic profile of the study population.

Characteristics
Age (years), mean ± SD	32.3 ± 6.5
Recurrent infection, frequency, %	11, 1.96
Admission status, number, %
Inpatient	163, 29.2
Outpatient	396, 70.8

SD, standard deviation.

The most frequently identified microorganism identified was Escherichia coli (29.4%) followed by coagulase-negative staphylococci (CoNS; 21.7%); Candida was identified in 48 samples (7.8%) (Table 4).

Table 4.

Number and percentage of microorganisms isolated from pregnant urine samples between 2014 and 2018.

Microorganism	Number	Percent
Escherichia coli	180	29.4
Coagulase-negative staphylococci	132	21.7
Enterococcus spp.	80	13.1
Streptococcus agalactiae (Group B)	48	7.8
Candida	48	7.8
Klebsiella	43	7.0
Staphylococcus spp, (other non-CoNS or S. aureus)	15	2.4
Group D streptococci (Enterococcus faecalis)	14	2.3
Staphylococcus aureus	14	2.3
Proteus	6	0.9
Enterobacter spp.	6	0.9
Acinetobacter	4	0.7
No bacterial growth	4	0.7
Other microorganisms (Corynebacterium, Pseudomonas)	12	2.0
Coliforms, unlabeled, broken, contaminated samples	6	1.0

CoNS, coagulase-negative staphylococci.

All isolate were sensitive to aztreonam, chloramphenicol, fosfomycin, ofloxacin, pefloxacin, piperacillin, and colistin sulphate; 87.5% were sensitive to amikacin. Only 15.79%, 18.93%, and 17.91% of cultures were sensitive to oxacillin, nalidixic acid, and erythromycin, respectively (Table 5).

Table 5.

Overall sensitivity of antimicrobial agents.

Antimicrobial agent	Sensitive		Resistant		Intermediate		Total
Antimicrobial agent	No.	%	No.	%	No.	%	Total
Amikacin	98	87.5	14	12.5			112
Ampicillin	66	48.18	70	51.09	1	0.73	137
Augmentin	321	68.3	137	29.15	12	2.55	470
Aztreonam	1	100					1
Benzylpenicillin	37	48.05	40	51.95			77
Cefalotin	41	41.41	41	41.41	17	17.17	99
Cefepime	41	36.28	72	63.72			113
Cefixime	129	41.88	179	58.12			308
Cefotaxime	132	60	88	40			220
Cefoxitin	179	84.83	29	13.74	3	1.42	211
Cefpodoxime	61	62.24	37	37.76			98
Ceftazidime	133	62.74	79	37.26			212
Ceftriaxone	73	59.35	50	40.65			123
Cefuroxime	260	64.52	142	35.24	1	0.25	403
Chloramphenicol	6	100					6
Ciprofloxacin	218	80.15	50	18.38	4	1.47	272
Clindamycin	22	39.29	31	55.36	3	5.36	56
Co-trimoxazole	283	62.47	170	37.53			453
Colistin Sulphate	2	100					2
Ertapenem	110	98.21	2	1.79			112
Erythromycin	12	17.91	47	70.15	8	11.94	67
Fosfomycin	1	100					1
Gentamicin	358	70.06	152	29.75	1	0.2	511
Imipenem	203	96.67	7	3.33			210
Levofloxacin	66	84.62	7	8.97	5	6.41	78
Linezolid	68	98.55	1	1.45			69
Meropenem	101	98.06	2	1.94			103
Minocycline	1	50			1	50	2
Moxifloxacin	44	88	2	4	4	8	50
Nalidixic acid	71	18.93	304	81.07			375
Nitrofurantoin	417	76.65	102	18.75	25	4.6	544
Norfloxacin	273	57.96	198	42.04			471
Ofloxacin	1	100					1
Oxacillin	6	15.79	32	84.21			38
Pefloxacin	1	100					1
Piperacillin	1						1
Piperacillin/tazobactam	99	96.12	2	1.94	2	1.94	103
Quinupristin	21	72.41	8	27.59			29
Tetracycline	80	47.06	90	52.94			170
Ticarcillin	1	33.3	2	66.7			3
Ticarcillin/clavulanic acid	1	50	1	50			2
Tigecycline	59	95.16	3	4.84			62
Tobramycin	82	84.54	9	9.28	6	6.45	97
Vancomycin	89	97.8	2	2.2			91

More than three-quarters (76.65%) of isolates were sensitive to nitrofurantoin (Table 5). Regarding E. coli, most cultures were sensitive to meropenem, ertapenem, imipenem, piperacillin/tazobactam, and cefoxitin. However, approximately two-thirds were resistant to nalidixic acid and ampicillin. All Klebsiella cultures were sensitive to amikacin, ertapenem, and imipenem. Nearly half of Klebsiella isolates were sensitive to different cephalosporins whereas only 20.9% were sensitive to nitrofurantoin. Enterobacter species showed 100% sensitivity to amikacin, ciprofloxacin, co-trimoxazole, ertapenem, and imipenem. These cultures were most resistant to augmentin, cefoxitin, and cefuroxime (Table 6).

Table 6.

Antimicrobial sensitivity in gram-negative bacterial isolates.

	Escherichia coli (180)						Klebsiella (43)						Enterobacter (6)						Proteus (6)						Acinetobacter (4)
	S		R		I		S		R		I		S		R		I		S		R		I		S		R		I
	No.	%	No.	%	No.	%	No.	%	No.	%	No.	%	No.	%	No.	%	No.	%	No.	%	No.	%	No.	%	No.	%	No.	%	No.	%
Amikacin	71	84.5	13	15.5			14	100					4	100					4	100					1	50	1	50
Augmentin	86	48	85	47.6	6	3.4	23	56.1	12	29.3	6	14.6	1	16.7	5	83.3			4	66.7	2	33.3					2	100
Cefepime	53	63.8	30	36.2			7	50	7	50			3	75	1	25			4	100							2	100
Cefixime	68	59.7	46	40.3			10	52.6	9	47.4			1	25	3	75			5	100							2	100
Cefotaxime	88	57.9	62	42.1			17	47.2	19	52.8			4	66.7	2	33.3			5	100					2	50	2	50
Cefoxitin	132	86.8	18	11.8	2	1.3	35	94.6	2	5.4			1	16.7	5	83.3			5	100					1	50	1	50
Ceftazidime	95	62.1	68	37.9			18	48.6	19	51.4			5	83.3	1	16.7			4	100					2	50	2	50
Ceftriaxone	45	52.9	40	47.1			8	53.3	7	46.7			2	50	2	50			4	100					2	50	2	50
Cefuroxime	107	60.5	69	39	1	0.5	21	50	21	50			1	16.7	5	83.3			6	100							2	100
Ciprofloxacin	116	75.8	38	31.2			36	97.3	1	2.7			6	100					5	100					1	25	3	75
Co-trimoxazole	101	55.1	79	43.9			35	58.1	18	41.9			6	100					5	83.3	1	16.7			3	75	1	25
Ertapenem	83	98.8	1	1.2			15	100					4	100					4	100					1	50	1	50
Gentamicin	152	84.4	27	15.0	1	0.6	35	81.4	8	16.6			5	83.3	1	16.7			6	100					3	75	1	25
Imipenem	150	98.7	1	1.3			36	100					6	100					4	80	2	20			1	50	1	50
Nalidixic acid	42	37.8	69	62.2			13	95	7	35			3	75	1	25			4	80	2	20					2	100
Nitrofurantoin	133	75.0	36	20.0	9	5.0	9	20.9	19	44.2		34.9	1	16.7	4	66.7	1	16.7			6	100					2	100
Norfloxacin	132	73.9	46	26.1			40	95.2	2	4.8			5	83.3	1	16.7			6	100							2	100
Tetracycline	41	64.6	22	35.4			11	64.7	6.0	35.3				33.3		66.7					1	100			1	50	1	50
Tigecycline	3	60.0	2	40.0			3	75	1	25									1	100
Ampicillin	25	35.7	42	62.8	1	1.4			23	100									1	100
Cefalotin	28	35.7	33	35.7	17	24.3	11	47.8	12	52.2					2	100			1	100
Cefpodoxime	46	65.7	22	34.3			11	47.8	12	52.2			2	100					1	100
Meropenem	68	100					22	100					2	100					1	100					1	50	1	50
Piperacillin/tazobactam	65	95.7	1	1.4	2	2.9	24	100					2	100					1	100					1	50	1	50
Tobramycin	45	88.5	4	7.7	1	2	14	77.8	3	22.2			2	100					1	100
Colistin sulphate																									1	100

S, sensitive; R, resistant; I, intermediate.

All Proteus species were sensitive to most tested antibiotics. Nevertheless, these cultures showed high resistance of nearly 100% to ceftriaxone and tetracycline (Table 6).

All Acinetobacter species showed resistance to augmentin, cefepime, cefixime, cefuroxime, nalidixic acid, nitrofurantoin, and norfloxacin. These microorganisms were sensitive to colistin sulphate. Of these species, 75% were sensitive to co-trimoxazole and gentamycin (Table 5). All CoNS isolates were sensitive to tigecycline, vancomycin, ampicillin, and linezolid, and most were sensitive to quinupristin (93.3%), gentamicin (91.4%), and augmentin (86.7%). These microorganisms were less sensitive to cefixime, nalidixic acid, benzylpenicillin, and oxacillin, compared with other antibiotics (Table 7). Staphylococcus aureus isolates were 100% sensitive to ciprofloxacin, levofloxacin, linezolid, moxifloxacin, tigecycline, vancomycin, and quinupristin. Enterococcus species were sensitive to augmentin, cefixime, nitrofurantoin, linezolid, oxacillin, tetracycline, and vancomycin (Table 7); all were resistant to nalidixic acid, benzylpenicillin, and oxacillin. All Enterococcus faecalis cultures were sensitive to augmentin, nitrofurantoin, linezolid, tigecycline, vancomycin, and ampicillin, but all isolates were resistant to cotrimoxazole, nalidixic acid, norfloxacin, tetracycline, and quinupristin (Table 7). Most Streptococcus agalactiae (Group B) isolates were sensitive to augmentin, cefixime, cefuroxime, nitrofurantoin, benzylpenicillin, levofloxacin, linezolid, moxifloxacin, tigecycline, vancomycin, ampicillin, and quinupristin (Table 7). All Candida isolates were sensitive to micafungin and voriconazole, and most were sensitive to amphotericin B, fluconazole, flucytosine, and caspofungin (Table 8).

Table 7.

Antimicrobial sensitivity in gram-positive bacterial isolates.

Gram-positive bacteria	Coagulase-negative staphylococci (98)						Enterococcus spp.						Streptococcus agalactiae (Group B)						Staphylococcus spp.						Enterococcus faecalis						Staphylococcus aureus
	S		R		I		S		R		I		S		R		I		S		R		I		S		R		I		S		R		I
	No	%	No	%	No	%	No	%	No	%	No	%	No	%	No	%	No	%	No	%	No	%	No	%	No	%	No	%	No	%	No	%	No	%	No	%
Augmentin	85	86.7	13	13.3			80	100					30	100					7	46.7	8	53.3			2	100					6	60	4	40
Cefixime	11	11.2	87	88.8			4		100				26	96.3	3	3.7			1	6.7	14	83.3			1	50	1	50			1	10	9	90
Cefuroxime	80	81.6	18	18.4			1	25	3	75			29	100					6	40	9	60			1	50	1	50			3	30	7	70
Ciprofloxacin	28	80	4	11.4	3	8.6	7	77.8	1	11.1	1	11.1													9	75	3	25			4	100
Cotrimoxazole	88	68.2	41	31.8			1	25	3	75			29	76.3	9	23.7			10	66.7	5	33.3					2	100			9	64.3	5	35.7
Gentamycin	117	91.4	9	8.6			2	2.8	68	97.2			13	41.4	17	58.6			6	46.7	8	53.3			2	66.7	1	33.3			8	57.1	6	42.9
Nalidixic acid	2	2	96	98			1	1.4	70	98.6			1	3.4	28	96.6			1	6.7	14	83.3					2	100					10	100
Nitrofurantoin	115	87.9	16	12.1			76	95	4	5			38	95	2	5			14	93.3	1	6.7			14	100					10	71.4	4	28.6
Norfloxacin	61	62.2	38	37.8			2	3	65	97			4	13.3	26	86.7			10	66.7	5	33.3					2	100			4	40	6	60
Benzylpenicillin	2	5.7	34	94.3			8	88.9	1	11.1			18	100											9	75	3	25						100

Table 8.

Anti-fungal sensitivity and resistance patterns.

Anti-fungal	Candida (48), % (n)
Anti-fungal	S	R	I
Amphotericin B	95.8% (46)		4.2% (2)
Caspofungin	87.5% (42)	4.2% (20)	8.3% (4)
Fluconazole	90% (43)	10% (5)
Flucytosine	90.1% (43)	9.9% (5)
Voriconazole	100% (48)
Micafungin	100% (48)

S, sensitive; R, resistant; I, intermediate.

A history of antibiotic therapy was the only variable that remained an independent factor for the occurrence of multi-drug resistant bacterial infection among pregnant women (odds ratio [OR] 5.461, 95% confidence interval [CI] 1.622–17.578; p < 0.05) (Table 9).

Table 9.

Multi-drug resistance among pregnant women.

	MDR
Variable	Yes	No	COR (95% CI)	AOR (95% CI)
No. of pregnancies
Primigravida	31	10	1
Multigravida	17	17	0.318 (0.114–1.011)	0.441 (0.019–1.558)
History of UTI
Yes	24	10	2.578 (0.955–8.615)	2.513 (0.565–12.250)
No	20	20	1
Antibiotic therapy
Yes	25	8	5.375 (1.760–18.20)	5.461 (1.622–17.578)*
No	20	25	1

* p-value < 0.05.

COR, crude odds ratio; AOR, adjusted odds ratio; CI, confidence interval; MDR, multi-drug resistant; UTI, urinary tract infection.

Discussion

Pregnant women are at increased risk of developing UTI, mainly because of a shift in the position of the urinary tract and hormonal changes throughout pregnancy, making it easier for bacteria to reach the kidney and leading to both symptomatic and asymptomatic bacteriuria. UTIs can adversely affect both the woman and her fetus, without timely intervention.^1–3 Initial screening and antimicrobial treatment are the preferred interventions. The findings of this study showed that E. coli was the most commonly identified pathogen, which was in line with the findings of previous studies, such as that by Tandan et al.¹⁰ in which E. coli was found to be the commonest UTI-causing organism. In addition, Gessese et al.⁵ found that E. coli was the most frequently identified pathogen in 46.4% of study participants with mean age 25 years. Those authors also identified S. aureus in 14.3% of participants, CoNS in 14.3%, and Proteus in 10.6%. Souza et al.¹¹ found that E. coli and S. aureus were the most commonly identified species, and 89% of isolates were sensitive to fosfomycin. All cultures in this study were sensitive to fosfomycin. Assefa et al.¹² also found high susceptibility to amoxicillin/clavulanic acid (70%), chloramphenicol (83.3%), gentamicin (93.3%), kanamycin (93.3%), nitrofurantoin (87.7%), and co-trimoxazole (73.3%).

Regarding E. coli susceptibility and resistance, Kibret et al.¹³ found results similar to the findings of this study. Those authors identified high resistance rates to amoxicillin (86.0%) and tetracycline (72.6%) and a high degree of sensitivity to nitrofurantoin (96.4%), gentamicin (90.6%), and ciprofloxacin (79.6%). Most E. coli isolates in this study were susceptible to norfloxacin, which is relatively safe for use in pregnancy and breastfeeding.^14–18 E. coli is considered to be the predominant uropathogenic bacteria because of a number of virulence factors related to invasion and colonization of the urinary epithelium. E. coli is also related to ascent from periurethral regions contaminated by fecal flora because of the close proximity of the perianal area. Chloramphenicol, tetracyclines, and cotrimoxazole should be avoided in pregnancy.¹⁹ However, during early pregnancy chloramphenicol treatment presents little, if any, teratogenic risk to the fetus in humans.²⁰

Regarding use of nitrofurantoin in pregnancy, there is no increased risk for cardiovascular malformations, oral cleft, or craniosynostosis but the risk of hypoplastic left heart syndrome has been demonstrated (OR 3.07, 95% CI 1.59–5.93).²⁰ Muanda et al.²¹ found that exposure in utero to clindamycin, doxycycline, quinolones, macrolides, and phenoxymethylpenicillin was linked to organ-specific malformations whereas exposure to amoxicillin, cephalosporins, and nitrofurantoin was not associated with major congenital malformations. Bookstaver et al.²² concluded that beta-lactams, vancomycin, nitrofurantoin, metronidazole, clindamycin, and fosfomycin were generally considered safe and effective in pregnancy whereas fluoroquinolones and tetracyclines should generally be avoided in pregnancy. Among gram-positive bacteria, CoNS showed higher resistance rates to ciprofloxacin, norfloxacin, kanamycin, gentamicin, nitrofurantoin, erythromycin, and amoxicillin/clavulanic acid. The resistance to nitrofurantoin of gram-positive and gram-negative bacteria was comparatively low in this study. The reason might be owing to less frequent use of nitrofurantoin in the study area. In the present study, gram-negative Enterobacter species showed significant resistance to cefuroxime, cefoxitin, and cefalotin. This finding indicates that the recognized practice of oral empirical treatment with these agents should be abandoned. Emerging resistant Enterobacter species have also been identified in other studies.^23–26

Napier et al.²⁷ identified colistin-heteroresistant Enterobacter cloacae in the United States. In the present study, all bacterial isolates were sensitive to colistin sulphate. Ceftazidime–avibactam, colistin, polymyxin B, fosfomycin, aztreonam, aminoglycosides, and tigecycline are treatment options for UTIs caused by carbapenem-resistant Enterobacteriaceae.²⁸

Contrary to Enterobacter, Proteus species were very sensitive to most cephalosporins, except ceftriaxone. Resistance to tetracycline is of little importance in our study as this antibiotic is contraindicated in pregnancy. For better management, detection of extended-spectrum beta-lactamases (ESBL) should be conducted routinely for Proteus isolates and the genotype surveyed periodically.²⁹ A high prevalence of ESBL and AmpC β-lactamases has been found in Proteus infections.³⁰ Phenotypic methods could be implemented in routine diagnostic laboratories along with susceptibility testing, to help in the control of infections.³¹ The low resistance levels observed in the present study might be associated with the relative inaccessibility and high prices of these drugs compared with other antimicrobials. Thus, these drugs can be used as adjunct medications in the management of UTIs.

The second most common uropathogen identified in our study was Staphylococcus species. The findings of the antimicrobial resistance profile are supported by the findings of numerous previous studies^5,10 showing that Staphylococcus species are highly resistant gram-negative bacteria. In addition, most isolated gram-negative bacteria are sensitive to gentamicin, ceftazidime, and ciprofloxacin whereas these bacteria are resistant to ampicillin, chloramphenicol, and amoxycillin.^32,33

CoNS are sensitive to a wide range of antimicrobials but are resistant to benzylpenicillin and oxacillin. Taponen et al.³⁴ found that penicillin resistance was the most common type of antimicrobial resistance in CoNS, and Staphylococcus epidermidis was the most resistant among the four major species. Those authors also found that phenotypic oxacillin resistance was found in all four main species. CoNS are challenging owing to the large proportion of methicillin-resistant strains and increasing number of isolates with less susceptibility to glycopeptides.³⁵ Our study findings indicated high sensitivity of CoNS to gentamicin, vancomycin, and linezolid, which was in agreement with the findings of Cui et al.³⁶ The virulent nature of this infection justifies the use of such agents in pregnancy.

Enterococcus species were susceptible to augmentin, nitrofurantoin, linezolid, tigecycline, vancomycin, and ampicillin. According to Fallah et al.,³⁷ linezolid, chloramphenicol, and nitrofurantoin are the most effective agents against Enterococcus species. All E. faecalis cultures were sensitive to a wide range of antimicrobials; they were all resistant to cotrimoxazole, nalidixic acid, norfloxacin, tetracycline, and quinupristin. Hussain et al.³⁸ found that 90.09% of E. faecalis strains exhibited resistance to gentamicin, 86.95% to norfloxacin, and 85.71% exhibited multi-drug resistance. Among the urine cultures tested, 7.8% were Streptococcus agalactiae (Group B), and recto–vaginal swab samples showed a 25.5% carriage rate in the third trimester, as reported by Slotved et al.³⁹

Most Streptococcus agalactiae (Group B) cultures were sensitive to a wide range of antibiotics including augmentin, cefuroxime, and benzylpenicillin. Among 481 recto–vaginal cultures from pregnant women in a study by Shore et al.,⁴⁰ all were sensitive to penicillin and 19% were resistant to clindamycin. The rate of recurrent infection in this study was 1.8%. In a national sample of non-pregnant women in the United States with uncomplicated UTI, the overall incidence of recurrence was 102/100,000 women.⁴¹

Candida accounted for only 7.8% of all infections in this study. Candida showed sensitivity to most antifungals tested. Pregnancy is a risk factor for UTIs owing to Candida species.⁴² Pregnant women are mainly treated with fluconazole and amphotericin B deoxycholate because other drugs have extremely low concentrations in urine.⁴³

There are some limitations to this study. Routine screening and treatment are still a matter of debate and depend on the prevalence of pathogens. Antimicrobial treatment has not yet shown any benefit for the outcomes of pregnancy,^44,45 and overtreatment with antibiotics should be prevented owing to the development of resistance. Our choice of the study period of 2014 to 2018 was owing to JUH having begun using an electronic database in 2014. Additionally, this study was only conducted in one hospital. These may be possible sources of bias in this study. Bacterial resistance is currently at a very high rate, which is often associated with the misuse or inappropriate use of antimicrobial drugs, the absence of stringent drug control and monitoring, and failure to follow standard treatment guidelines.

Conclusion

E. coli and CoNS were the most common microorganisms identified in this study. Empirical therapy with meropenem, ertapenem, imipenem, piperacillin/tazobactam, cefoxitin, tigecycline, vancomycin, ampicillin, amikacin, or linezolid are very appropriate. Most of these antibiotics are relatively safe to be used in pregnancy and breastfeeding. We found increased antibiotic resistance in Enterobacter species. Oxacillin, nalidixic acid, tetracycline, and erythromycin should not be used empirically owing to increased resistance. The choice of antimicrobial therapy in pregnancy should be determined according to sensitivity/resistance and fetomaternal safety.

Footnotes

Declaration of conflicting interest

The authors declare that there is no conflict of interest.

Funding

The authors received no financial support for the research, authorship, and/or publication of this article.

ORCID iDs

Naser Al-Husban

Mohammad S Elmuhtaseb

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Spectrum of uropathogens and their susceptibility to antimicrobials in pregnant women: a retrospective analysis of 5-year hospital data

Abstract

Objective

Methods

Results

Conclusion

Keywords

Introduction

Methods

Study design

Study sample collection

Urine sample collection, primary inoculation, and analysis

Antimicrobial susceptibility testing

Statistical analysis

Results

Discussion

Conclusion

Footnotes

Declaration of conflicting interest

Funding

ORCID iDs

References