Abstract
Background
Puerperal sepsis is any bacterial infection of the genital tract that occurs after childbirth. It is among the leading causes of maternal morbidity and mortality especially in low-income countries including Ethiopia. The aim of this study was to determine the proportion of bacterial isolates, their antimicrobial susceptibility profile and factors associated with puerperal sepsis among post-partum/aborted women at a Referral Hospital in Bahir Dar, Northwest Ethiopia.
Methods
A cross sectional study was conducted from January to May 2017 among 166 post-partum/aborted women admitted to Felege Hiwot Referral Hospital for medical services and suspected for puerperal sepsis.. Socio-demographic data and associated factors were collected using structured questionnaire. Bacteria were isolated and identified from blood samples on Trypton soya broth, blood, Chocolate and MacConkey agars following standard bacteriological procedures. The VITEK 2 identification and susceptibility testing system was used to determine the antimicrobial susceptibility profiles of bacterial isolates. Data were entered and analyzed using SPSS version 20. Factors associated with puerperal sepsis were considered statistically significant at P-value < 0.05.
Results
The overall proportion of bacterial isolates among post-partum/aborted women was 33.7% (56/166); of which 55.4% was caused by Gram-negative and 44.6% was by Gram-positive bacteria. The most frequently isolated bacteria were Escherichia coli (32.1%) from Gram-negatives and Staphylococcus aureus (33.9%) from Gram-positives. The proportion of other isolates was (7.2%) for Coagulase Negative Staphylococci (CoNS), (12.5%) for Klebsiella pneumoniae, (10.7%) for Acinetobacter baumanni and (3.6%) for Raoultella ornithinolytica. All isolates of Gram-positive and Gram-negative bacteria were resistant to tetracycline (100%). The gram negatives show resistance to Cefazolin (72.7%), Tetracycline (93.9%) and Ampicillin (100%). The overall prevalence of multidrug resistance (MDR) was 84%. Women having multiparous parity were more likely to develop puerperal sepsis than primiparous parity (AOR 4.045; 95% CI: 1.479–11.061; P < 0.05). Other socio-demographic and clinical factors had no significant association with puerperal sepsis.
Conclusion
About one third of post-partum/aborted women suspected for puerperal sepsis were infected with one or more bacterial isolates. Significant proportion of bacterial isolates showed mono and multi-drug resistance for the commonly prescribed antibiotics. Women with multiparous parity were more likely to develop puerperal sepsis than primiparous parity.
Keywords: Puerperal sepsis, Gram-positive bacteria, Gram-negative bacteria, Antimicrobial susceptibility, Felege Hiwot referral hospital, Women, Ethiopia
Background
Puerperal sepsis is any bacterial infection of the genital tract that occurs after child birth usually in the first 24 h [1] or at any time between the rupture of membranes or labor and the 42nd days of postpartum [2]. Following vaginal delivery, approximately 6–7% of women experience puerperal sepsis. Home birth in unhygienic conditions, poor nutrition, prim parity, anemia, prolonged rupture of membranes (PROM), prolonged labor, multiple vaginal examinations, caesarean section, instrumental deliveries, and postpartum hemorrhage are some of the risk factors for puerperal sepsis [3].
World Health Organization (WHO) estimated that about 350,000 maternal deaths occur during labor and childbirth of which 15% were associated with puerperal sepsis [4]. Puerperal sepsis causes at least 75,000 maternal deaths every year and mostly occurs in low-income countries with a distribution of 11.6% in Asia, 9.7% in Africa, 7.7% in Latin America and the Caribbean compared to the 2.1% in developed countries [5, 6]. In Nigeria, puerperal sepsis accounted for 12% of maternal deaths [7] In Ethiopia, puerperal sepsis accounted for about 13% of all maternal deaths and became one of the top four causes of mortality [8].
Antibiotics are among the successful interventions developed to treat bacterial diseases including puerperal sepsis, but bacteria could develop resistance [9]. Resistance to antimicrobial agents has emerged as a public health problem at an alarming rate. Infecting agents capable of developing resistance to multiple drugs (MDR) have enhanced rate of morbidity and mortality [10]. The dynamic nature of bacteria resistant to antimicrobial agents can lead to prolonged illness, increased health care expenditures and risk of death.
Ethiopia has adopted the sustainable development goals (SDGs) to reduce maternal mortality to < 70/100,000 by the year 2030. To achieve this target and significantly reduce maternal mortality, identifying the causes and contributors of puerperal sepsis is paramount. Therefore, this study was aimed to determine the proportion of bacterial isolates, their antimicrobial susceptibility profile and factors associated with puerperal sepsis among post-partum/aborted women suspected for puerperal sepsis at Felege Hiwot Referal Hospital, Northwest Ethiopia.
Methods
Study design, area, and period
A cross sectional study was conducted from January to May 2017 among postpartum/aborted women admitted to Felege Hiwot Referral Hospital for medical services and suspected of puerperal sepsis.. The Hospital is found in Bahir Dar; the capital city of the Amhara Regional State. In the city, there were 14 healthcare serviceinstitutions (one government referral hospital, one primary hospital, two general private hospitals and ten health centers) during data collection.
Study populations
Postpartum/aborted women (any type of abortion) admitted to Felege Hiwot Referral Hospital during the study period. Women were suspected for puerperal sepsis if they develop fever of > 38.5 0c, pelvic pain, abnormal genital discharge with offensive smell and delay in the reduction of the size of uterus to the 42nd day of postpartum/abortion.
Inclusion and exclusion criteria
Women with sign and symptoms of puerperal sepsis at the time of admission or who developed sepsis during their stay in the hospital during the study period were included in the study. However, women with puerperal sepsis but started antibiotic therapy and those unable to give the interview were excluded.
Sample size and sampling technique
The sample size was determined using a single population proportion formula: n = z2 p (1-p)/ d2; where: n = the number of postpartum/aborted women; z = standard normal distribution value at 95% CI (z = 1.96); p = the prevalence of puerperal sepsis. Taking p at 8.4% from study conducted in Addis Ababa, Ethiopia [11]; d = the margin of error, taken as 5%. Accordingly, the sample size was () estimated at 119. Additional 47 women who fulfilled the inclusion and exclusion criteria were admitted to the hospital during the study period and included in the study. Hence, the final total sample size was 166. Convenient sampling was used to select the study participants.
Data collection
Socio-demographic and clinical data
Socio-demographic characteristics of the study participants was collected using a pretested and structured questionnaire by BSc nursing graduates. The questionnaire was prepared in English and translated to the local Amharic language. The questionnaire was pretested on a sample of 5% of study participants at University of Gondar specialized Hospital and amended accordingly. The questionnaire was prepared based on the WHO education material on puerperal sepsis and customized to this study [1]. The clinical data of each woman was retrieved from their medical records.
Nutritional status assessment
The nutritional status of each woman was measured by mid upper arm circumference (MUAC using tape meter. MUAC less than 23 cm were considered as under nutrition [12].
Assessment of anemia
Postpartum/aborted women were screened for anemia using automated hematology analyzer (Cell-DYN 1800, Abbott diagnostic, USA). Each blood sample was investigated for total hemoglobin (Hgb) concentration. The Hgb thresholds were used to classify anemia. Anemia was categorized as mild (Hgb level 10 to 10.9 g/dl), moderate (Hgb level 7.0 to 9.9 g/dl) and severe (Hgb level < 7.0 g/dl) per WHO criteria [13].
HIV screening
The HIV status of each woman was collected from the medical record of each patient. Screening for HIV in the hospital was done with the First Response (Premier Medical Corporation, India), Unigold (Trinity Biotech Manufacturing, Ireland) and Vikia (bioMerieux SA, France) test algorithm.
Blood collection and processing
Blood was collected from each woman to detect the presence and frequency of bacteria.. Two bottles of blood (5 ml for each bottle) was collected aseptically from two different sites of peripheral veins. Blood was inoculated directly into Trypton soya broth (Oxoid Ltd. Basingstoke, Hampshire, UK) and incubated aerobically at 37 °C. The growth of visible colonies were observed daily for the first 3 days. Subcultures were made on blood agar, Chocolate agar, and MacConkey agar (Oxoid Ltd. Basingstoke, Hampshire, UK) and examined for growth after 24–48 h of incubation. The procedure was repeated and negative blood cultures were reported after the 7th day of incubation. Blood cultures positive for bacterial growth were further analyzed for colony isolation. Bacterial isolates were identified by gram stain and VITEK 2 identification and susceptibility testing system (bioMerieux, Inc., Hazelwood, USA). Standard biochemical tests were also used as backup identification modalities [14].
Antimicrobial susceptibility testing
Antimicrobial susceptibility tests were done for each identified bacteria using the VITEK 2 identification and susceptibility testing system. The VITEK 2is an automated, walkway system that works on the principle of photometry. Briefly, pure colony of the isolated bacteria was emulsified in 2 ml of 0.85% normal saline. Bacterial suspensions with an optical density of 0.5–0.63 was taken as acceptable bacterial concentration. Reagents were then immersed to the suspension and transferred to VITEK 2 system for antimicrobial susceptibility testing [15].
Quality control
Training for data collectors and supervisors about the study and data collection procedures was given. Consistency and completeness of data was also checked on daily bases. The working standards of materials, equipment, culture media and procedures were strictly followed. The sterility of culture media was ensured by incubating 5% of each batch at 37 °C for 24 h. The performance of each media was checked by inoculating standard strains of E. coli (ATCC 25922) for Gram-negative bacteria, S. aureus (ATCC 25923) for Gram-positive bacteria and N. gonorrhoeae (ATCC49226) for fastidious bacteria [16]. The VITEK 2 system was also verified using known strains.
Data processing and analysis
Socio-demographic and laboratory data were entered and analyzed using SPSS version 20. Descriptive statistics was presented as frequencies and percentages in tables and figures. Logistic regressions were used to assess factors associated with puerperal sepsis. Odds ratio with its 95% CIs was used to assess the presence of association and its significances was declared at P-values < 0.05.
Results
Socio-demographic and clinical characteristics
During the study period, a total of 756 women were admitted for postpartum/abortion medical services. Of these, 166 women suspected for puerperal sepsis and enrolled in the study. The mean age of the study participants was 27.3 years (SD ± 6.2). Data on educational status showed that 42.2% were unable to read and write, 36.7% had secondary school and above while 21.1% attended only elementary school. Majority (134, 80.7%) of cases of puerperal sepsis was related with labor while 32 (19.3%) was related with abortion. Of the laboring mothers, 91 (67.9%) gave birth through caesarean section (CS) and 43 (32.1%) through spontaneous vaginal delivery (SVD). Half (83, 50%) of the study participants were living in rural areas and the remaining were urban residents (Table 1). Twenty (12%) of women did not follow antenatal care. Among the 134 laboring mothers, eleven women (6.6%) were found to be HIV positive.
Table 1.
Variable | Frequency N, (%) | Bacterial isolates | ||
---|---|---|---|---|
Yes, N (%) | No, N (%) | |||
Age | 18–24 | 68 (41) | 22 (32.4) | 46 (67.6) |
25–34 | 69 (41.6) | 17 (24.6) | 52 (75.4) | |
35–42 | 29 (17.5) | 17 (58.6) | 12 (41.4) | |
Educational Status | Illiterate | 70 (42.2) | 29 (41.4) | 41 (58.6) |
1–4 grade | 14 (8.4) | 8 (57.1) | 6 (42.9) | |
5–8 Grade | 21 (12.7) | 6 (28.6) | 15 (71.4) | |
Secondary and Above | 61 (36.7) | 13 (21.3) | 38 (78.7) | |
Occupation | Government Employee | 36 (27.7) | 7 (19.4) | 29 (80.6) |
Farmer | 65 (39.2) | 26 (40) | 39 (60) | |
Merchant | 17 (10.2) | 8 (47) | 9 (53) | |
House Wife | 37 (22.2) | 13 (35.1) | 24 (64.9) | |
Other | 11 (6.7) | 2 (18.2) | 9 (81.8) | |
Residence | Rural | 86 (51.8) | 26 (30.2) | 60 (69.8) |
Urban | 80 (48.2) | 30 (37.5) | 50 (62.5) | |
Religion | Orthodox | 148 (89.2) | 48 (32.4) | 100 (67.6) |
Muslim | 18 (10.8 | 8 (44.4) | 10 (55.6) |
Proportion of bacterial isolates
The overall prevalence of bacterial isolates among women suspected of puerperal sepsis was 33.7% (56/166). The proportion of Gram-negative bacteria was 58.9% (33/56) and that of Gram-positive was 41.1% (23/56). Overall, S. aureus was the dominant isolate (33.9%; 19/56) followed by E. coli (32.1%; 18/56) (Fig. 1). The proportion of Gram-negative isolates was 54.5% (18/33) for E. coli, 21.2% (7/33) for K. pneumonaie 18.2% (6/33) for A. baumannii and that of Raoultella orinthinolytica was 3.6% (2/33). On the other hand, the proportion of Gram-positive isolates was 82.6% (19/23) for S. aureus and 17.4% (; 4/23) for CoNS.
Antimicrobial susceptibility profiles of gram-positive bacteria
Gram-positive bacteria demonstrated high rate of resistance to Tetracycline (100%), Erythromycin (87%) and Penicillin (61%). However, gram positive bacteria showed low rate of resistance to Ciprofloxacin (4.3%), Vancomycin (13%) and Ceftriaxone (13%). S. aureus isolates were susceptible to Vancomycin (100%) but resistant to Cefoxitin (47.4%), Erythromycin (84.2%) and Tetracycline (100%). The drug susceptibility profile of CoNS isolates showed resistance to Penicillin (100%), Ampicillin (100%), Tetracycline (100%) and Erythromycin (100%). None of the Gram-positive bacteria were susceptible for all antimicrobials tested (Table 2).
Table 2.
Bacterial Isolates | Resistance Rate, N (%) | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
P | AMP | VAN | CXT | SXT | CIP | CRO | TE | CAF | E | DA | |
S.aureus (n = 19) | 10 (52.6) | 8 (42.1) | 0 | 9 (47.4) | 6 (31.6) | 2 (10.5) | 2 (10.5) | 19 (100) | 7 (36.8) | 16 (84.2) | 5 (26.3) |
CoNs (n = 4) | 4 (100) | 4 (100) | 3 (75) | 3 (75) | 2 (50) | 1 (25) | 2 (50) | 4 (100) | 1 (25) | 4 (100) | 3 (75) |
Total (n = 23) | 14 (61) | 12 (52) | 3 (13) | 12 (52) | 8 (35) | 3 (13) | 4 (17) | 23 (100) | 8 (35) | 20 (87) | 8 (35) |
CoNS Coagulase negative Staphylococcus, DA Clindamycin, CXT Cefoxitin, E Erythromycin, P Penicillin, SXT Trimethoprim-sulfamethoxazole, TE Tetracycline, AMP Ampicillin, CRO Ceftriaxone, CAF Chloramphenicol, CIP Ciprofloxacin
Antimicrobial susceptibility profiles of gram-negative bacteria
Gram-negative bacteria showed high rate of sensitivity to Gentamicin (78.8%) and Ciprofloxacin (75.8%) while high rate of resistance was observed for Cefazolin (72.7%), Tetracycline (93.9%) and Ampicillin (100%). Species specific resistance of Gram-negative bacteria showed that E. coli were resistant to Ampicillin (100%) and Tetracycline (100%). Nevertheless, all isolates of E .coli were susceptible to Ciprofloxacin and Gentamicin. K. pneumoniae isolates were highly resistant to Ampicillin (100%) andTetracycline (100%). However; relatively sensitive isolates were observed for Trimethoprim/Sulfamethoxazole (57.1%), Ceftriaxone (57.1%) and Gentamicin (57.1%). A. boumanni isolates were resistant to trimethoprim/Sulfamethoxazole (100%) and Ampicillin (100%). Isolates of Raoultella orinthinolytica were resistant for most antibiotics tested except to Tetracycline (Table 3).
Table 3.
Bacterial isolates | Resistance rate, N (%) | |||||||||
---|---|---|---|---|---|---|---|---|---|---|
SXT | AMC | TE | CIP | GEN | CRO | CZN | AMP | CAZ | CAF | |
E.coli (n = 18) | 6 (33.3) | 7 (38.8) | 18 (100) | 0 | 0 | 7 (38.8) | 10 (55.5) | 1 8 (100) | 6 (33.3) | 2 (11.1) |
K.pneumoniae (n = 7) | 3 (42.8) | 4 (57.1) | 7 (100) | 4 (57.1) | 3 (42.8) | 4 (57.1) | 7 (100) | 7 (100) | 4 (57.1) | 3 (42.8) |
A.baumannii (n = 6) | 6 (100) | 5 (83.3) | 6 (100) | 2 (33.3) | 2 (33.3) | 3 (50) | 5 (83.3) | 6 (100) | 3 (50) | 2 (33.3) |
R.orinthinolytica (n = 2) | 1 (50) | 2 (100) | 0 | 2 (100) | 2 (100) | 2 (100) | 2 (100) | 2 (100) | 2 (100) | 2 (100) |
Total = 33 | 16 (48.5) | 18 (54.5) | 31 (93.9) | 8 (24.2) | 7 (21.2) | 16 (48.5)) | 24 (72.7) | 33 (100) | 15 (45.5) | 9 (27.2) |
SXT Trimethoprim-Sulfamethoxazole, AMC Amoxicillin-clavulanate, TE Tetracycline, Amp Ampicillin, CIP Ciprofloxacin, GEN Gentamicin, CRO Ceftriaxone, CAZ Ceftazidam and CAF Chloramphenicol
The proportion of multidrug resistant (MDR) bacterial isolates
Among the 56 isolates tested for susceptibility, 84% showed resistance to 3 or more classes of antibiotics. The proportion of bacteria resistant to 3 different antimicrobials was 21.4% while 55.4% were resistant to more than three classes of antibiotics. The proportion of MDR S. aureus was 52.6% (10/19). The study also showed high rate of MDR CoNS (Table 4).
Table 4.
Bacterial pathogens | Patterns of drug resistance | Total MDR (%) | |||||||
---|---|---|---|---|---|---|---|---|---|
R0 (%) | R1 (%) | R2 (%) | R3 (%) | R4 (%) | R5 (%) | R6 (%) | R7 (%) | ||
S. aureus (n = 19) | 0 | 3 (15.8) | 6 (31.6) | 1 (5.3) | 1 (5.3) | 1 (5.3) | 1 (5.3) | 6 (31.6) | 10 (52.6) |
CoNS (n = 4) | 0 | 0 | 0 | 0 | 1 (25) | 0 | 0 | 3 (75) | 4 (100) |
E. coli (n = 18) | 0 | 0 | 0 | 8 (44.4) | 3 (16.6) | 0 | 1 (5.5) | 6 (33.4) | 18 (100) |
K.pnuemonaie (n = 7) | 0 | 0 | 0 | 3 (42.9) | 0 | 0 | 0 | 4 (57.1) | 7 (100) |
A.baumannii (n = 6) | 0 | 0 | 0 | 0 | 1 (16.6) | 1 (16.6) | 0 | 4 (66.7) | 6 (100) |
R.orinthinolytica (n = 2) | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 (100) | 2 (100) |
Total (n = 56) | 0 | 3 (5.4) | 6 (10.7) | 12 (21.4) | 5 (8.9) | 2 (3.6) | 2 (3.6) | 22 (39.3) | 47 (84) |
Key: R0: susceptible to all antimicrobials; R1–7: resistance to 1, 2, 3, 4, 5, 6 & 7 antimicrobials
The antimicrobial susceptibility profile of Gram-negative isolates showed significant rate of MDR. The proportion of MDR E. coli was 44.4% and that of K. pnemonaie was 42.9%. In addition, 66.7% of A. baumanii and all R. ornithinolytica isolates were MDR (Fig. 2).
Factors associated with puerperal sepsis
In this study; parity, HIV status, antenatal care, duration of labour, membrane rupture, mode of delivery, diabetes mellitus, method of placenta removal, hypertension, anemia and place of delivery were evaluated as possible factors associated with puerperal sepsis. In the binary analysis; multiparous parity, antenatal care, diabetes mellitus and anemia showed s association with puerperal sepsis (P < 0.05). The multivariable regression analysis showed that only being multiparous parity had statistically significant association with puerperal sepsis. Women that had multiparous parity were four times more likely to develop puerperal sepsis compared to primiparous women (AOR = 4.045; 95% CI: 1.479–11.061; P = 0.006). Other socio-demographic and clinical variables had no significant association with puerperal sepsis (Table 5).
Table 5.
Variable | Bacterial isolate | ||||||
---|---|---|---|---|---|---|---|
No | Yes | COR (95% CI) | P –Value | AOR (95%CI) | P-value | ||
Parity | Primiparous | 60 | 20 | 1 | 0.023a | 1 | 0.006a |
Multiparous | 50 | 36 | 2.160 (1.113–4.192) | 4.045 (1.479–11.061) | |||
HIV | No | 104 | 51 | 1 | 0.399 | ||
Yes | 6 | 5 | 1.699 (0.495–5.833) | ||||
ANC | Booked | 92 | 54 | 1 | 0.030a | 1 | |
Un booked | 18 | 2 | 0.189 (0.042–0,848) | 0.000 | |||
Duration of labor | < 18 h | 59 | 29 | 1 | 0.094 | 1 | 0.101 |
> = 18 h | 24 | 22 | 1.865 (0.899–3.868) | 2.058 (0.868–4.879) | |||
Membrane rupture | 0–8 h | 59 | 29 | 1 | 0.094 | 1 | 0.761 |
> 8 h | 24 | 22 | 1.865 (0.899–3.868) | 1.151 (0.464–2.859) | |||
Mode of delivery | Vaginal | 28 | 15 | 1 | 0.603 | ||
CS | 55 | 36 | 1.220 (0.574–2.599) | ||||
Placenta removal | Spontaneous | 19 | 3 | 1 | 0.703 | ||
Cord Traction | 8 | 0 | 0.000 | ||||
Manual | 1 | 2 | 2.923 (0.239–35.68) | ||||
Diabetes mellitus | No | 107 | 49 | 1 | 1 | 0.117 | |
Yes | 3 | 7 | 5.095 (1.264–20.54) | 0.022a | 3.471 (0.733–16.433) | ||
Hypertension | No | 104 | 55 | 1 | 0.291 | ||
Yes | 6 | 1 | 0.315 (0.037–2.684) | ||||
Anemia | None | 50 | 33 | 1 | 0.040a | 1 | 0.36 |
Mild | 23 | 4 | 0.264 (0.084–0.832) | 0.111 (0.020–0.608) | |||
Moderate | 20 | 15 | 1.136 (0.510–2.531) | 0.846 (0.287–2.494) | |||
Sever | 17 | 4 | 0.357 (0.110–1.154) | 0.229 (0.045–1.155) | |||
Place of delivery | Heath institute | 81 | 47 | 1 | 1 | 0.729 | |
Home | 29 | 9 | 0.535 (0.233–1.226) | 0.139 | 0.816 (0.179–3.707) |
a Significant at p < 0.05
Discussion
Puerperal sepsis is one of the leading causes of preventable maternal morbidity and mortality [17]. In the present study, about one third of women suspected of puerperal sepsis were infected with one or more bacterial isolates with an overall proportion of 33.7%. Previous study from Ethiopia reported similar findings (33.3%) [18]. On the other hand, the proportion of bacterial isolates causing puerperal sepsis was lower than reports from Nigeria (82.7%), Sudan (72.9%), and Bangladesh (84%) [16, 19, 20]. These discrepancies might be attributable to cultural, health seeking behavior, health care coverage, period of studies conducted and other socioeconomic factors.
In this study, the proportion of bacterial isolates causing puerperal sepsis was higher than reports from Nepal (19.7%) and Uganda (17%) [21, 22]. This difference can be explained by fact that two-third (67.9%) of women gave birth through caesarean section (CS). Postnatal infections (pyrexia, endometritis, and puerperal sepsis), thrombosis and excessive blood loss are indeed higher after caesarean section [23].
The prevalence of Gram-positive bacteria causing puerperal sepsis was 41.1% and S. aureus was the dominant isolate (33.9%). This is consistent with previous study that report S. aureus as one of the major bacteria isolated from puerperal septic patients [16, 19]. S. aureus is frequently found on the skin and can be easily acquired during delivery [24].
The prevalence of Gram-negative bacteria was 58.9% and E coli was the dominant isolate (32.1%). This finding is higher than reports isolated from women with puerperal sepsis in Bangladesh (14.5%) [20] and Nigeria (15.8%) [25]. It is known that E. coli are among the commonest bacterial isolates causing blood stream infections, wounds and other complications in humans [26, 27]. K. pnemonaie with a prevalence of (12.5%) was found to be the third frequently isolated bacteria among women with puerperal sepsis in our study. It is recently emerged as a significant cause of hospital acquired infections (urinary tract infection, pneumonia and septicemia) especially among immune compromised individuals [28, 29] which can be sources of infection for puerperal sepsis.
Two very uncommon bacterial pathogens namely A. baumannii and R. orinthinolytica were isolated from the blood culture of women suspected of puerperal sepsis. A. baumannii is an opportunistic bacteria affecting people with compromised immune systems and increasingly important hospital acquired infection [30]. It has been noted for its apparent ability to survive on artificial surfaces for extended period of time that can allow it to persist in the hospital environment as a source of puerperal sepsis [31].
This study revealed that E. coli isolates were susceptible to Ciprofloxacin (100%) and Gentamicin (100%). Similar susceptibility profiles were reported form Ethiopia around Jimma and Gondar [32, 33]. On the other hand, resistance to Ampicillin (100%) was observed among E. coli isolates consistent with reports from India and Ethiopia [20, 32]. This is because; E. coli has resistant genes for beta-lactam agents including ampicillin [34–36] and has selective pressure excreted by overuse of the antibiotics.
Multiple drug resistance (MDR) is an emerging public health threat that has been reported in different countries [37]. In our study, the overall proportion of MDR isolates was 84%. Similar finding were reported from Uganda (80%) that majority of puerperal sepsis were caused by MDR bacteria [22]. S. aureus were highly resistant to Tetracycline (consistent with other studies) [30] and unusually to Erythromycin. Similarly, 47.4% of S. aureus isolates showed resistance to Cefoxtin which is relatively lower than reports from India (53.2%) [38, 39]. More than half (52.6%) of S. aureus isolates were resistant to three or more tested antimicrobials (MDR) This can be explained by its unique features to adapt antimicrobial pressures and genetic competence to acquire antibiotic resistant genes from other strains.
Relatively high proportion of MDR was observed among E .coli, A. baumannii, and K. pneumonaie isolates. K. pneumonaie has chromosomal and plasmid encoded beta-lactam hydrolyzing enzymes [40]. A. baumannii is clinically important pathogen and causes septicemia with widespread resistance to various antibiotics [41]. There are reports that showed resistance of R. ornithinolytica to ampicillin and other commonly used antibiotics which can be associated with the presence of β-lactamases [42, 43].
Puerperal sepsis can be associated with different socio-demographic and clinical factors. In the present study, statistically significant association was observed between multiparous parity and puerperal sepsis. Women that had multiparous parity were four times more likely to develop puerperal sepsis compared to primiparous women (AOR = 4.045; 95% CI: 1.479–11.061; P = 0.006). Similar finding was reported from Pakistan that high prevalence of puerperal sepsis was observed among women of multiparous parity (78.29%) [44].
Although it is not significantly associated, women with age greater than 34 years had high proportion of culture positive bacterial infection (58.6%). This is supported by previous study from Pakistan indicating that majority (65.11%) of women admitted with puerperal sepsis were above 30 years of age [44]. Previous study reported that rural residence, educational level, family monthly income, prolonged labour (> 24 h), delivery by caesarean section, ANC follow up, ruptured membrane (> 24 h before delivery), frequent vaginal examination and being referred were reported as significant factors associated with puerperal sepsis [45]. But in our study HIV status, antenatal care, duration of labour, membrane rupture, mode of delivery, diabetes mellitus, method of placenta removal, hypertension, anemia and place of delivery had significant association with puerperal sepsis.
Limitation of the study
The limitation of the study include: investigation for anaerobic bacteria that can cause significant puerperal sepsis was not done. The study was conducted only in a public referral hospital that lacks representativeness and difficult to generate generalized conclusions. Convenient sampling was used to select study participants that can allow missing of cases. In addition, the nutritional status of post-partum/aborted women was measured by MUAC that may not be enough to determine nutritional status as a single measurement.
Conclusion
About one third of post-partum/aborted women suspected for puerperal sepsis were infected with one or more bacterial isolates. E. coli and S. aureus were the most dominant bacteria isolated from post-partum/aborted women. Significant proportion of bacterial isolates showed mono and multi-drug resistance rates. Relatively high rate of resistance was observed to Tetracycline and Ampicillin. The very uncommon bacterial isolates of A. baumanni and R. ornithinolytica showed high rate of resistance to the commonly prescribed antibiotics. Post-partum/aborted women with multiparous parity were more likely to develop puerperal sepsis than primiparous parity. Systematic surveillance for the commonly prescribed antibiotics and uncommon bacterial isolates is recommended to maintain the emergence and spread of antimicrobial resistance. In addition; awareness about post-partum/abortion complications and available cares are needed.
Acknowledgements
We would like to thank the Department of Medical Microbiology, College of Medicine and Health Sciences, University of Gondar for their support for this study. We also thank staffs of Felege Hiwot Referral Hospital laboratory and maternity ward in general for all the support during data collection and processing of samples. All women involved in this study are also acknowledged.
Abbreviations
- AIDS
Acquired Immune Deficiency Syndrome
- ATCC
American Type Cell Culture
- CLSI
Clinical Laboratory Standard Institute
- CoNS
Coagulase Negative Staphylococcus
- CS
Cesarean Section
- DM
Diabetic Mellitus
- HIV
Human Immune Deficiency Virus
- MDR
Multi Drug Resistance
- MUAC
Mid Upper Arm Circumference
- PROM
Prolonged rupture of membranes
- SDGs
Sustainable Developmental Goals
- SVD
Spontaneous vaginal delivery
- TMP/SMX
Trimethoprim/Sulphametaxone
- VRE
Vancomycin Resistance Enterococci
- WHO
World Health Organization
Authors’ contributions
AA: Designed the study, collected and analyzed the data and participated in the draft and final write up of the manuscript; BG: Participated in conception and design of the study, data analysis and interpretations and preparation of the draft and final write up of the manuscript; BT: participated in proposal writing, data analysis and interpretation of results; AW: involved in data collection, clinical diagnosis and characterization of patients; AM: interpret results and prepared the manuscript. All authors read and approved the manuscript.
Funding
Not applicable; no funding was received for this study.
Availability of data and materials
Data were collected from puerperal sepsis suspected women admitted to Felege Hiwot Referral Hospital, Bahir Dar, Northwest Ethiopia. The datasets are available from the corresponding author upon reasonable request through alemalea@gmail.com but will not be shared publicly to ensure patient confidentiality.
Ethics approval and consent to participate
Ethical clearance was obtained from the Ethical Review Committee of School of Biomedical and Laboratory Sciences, College of Medicine and Health Sciences, University of Gondar with Ref. No SBMLS/62/5/09 Letter of co-operation was given to Felege Hiwot Referral Hospital prior to data collection. After explaining the purpose and objective of the study, informed consent was obtained from each woman. Any woman who was not willing to participate in the study was not forced to participate. All data obtained were kept confidential by using codes and no personal identifiers were used. Blood samples collected were used only for the purpose of the study. The laboratory results were communicated to their attending physicians for appropriate intervention.
Consent for publication
Not applicable
Competing interests
The authors declare that they have no competing interests.
Footnotes
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Contributor Information
Alemale Admas, Email: alemalea@gmail.com.
Baye Gelaw, Email: tedybayegelaw@gmail.com.
BelayTessema, Email: bt1488@yahoo.com.
Amsalu Worku, Email: amsalework4@gmail.com.
Addisu Melese, Email: addisum22@gmail.com.
References
- 1.World Health Organization . Education material for teachers of midwifery: midwifery education modules. 2 2008. [Google Scholar]
- 2.World Health Organization (WHO). The prevention and management of puerperal infections : report of a technical working group. Geneva: World Health Organization; 1992. https://apps.who.int/iris/handle/10665/59429.
- 3.Maharaj D. Puerperal pyrexia: a review. Part I. Obstet Gynecol Surv. 2007;62(6):393–399. doi: 10.1097/01.ogx.0000265998.40912.5e. [DOI] [PubMed] [Google Scholar]
- 4.Buddeberg BS, Aveling W. Puerperal sepsis in the 21st century: progress, new challenges and the situation worldwide. Postgrad Med J. 2015;91(1080):572–578. doi: 10.1136/postgradmedj-2015-133475. [DOI] [PubMed] [Google Scholar]
- 5.Van Dillen J, Zwart J, Schutte J, van Roosmalen J. Maternal sepsis: epidemiology, etiology and outcome. Curr Opin Infect Dis. 2010;23(3):249–254. doi: 10.1097/QCO.0b013e328339257c. [DOI] [PubMed] [Google Scholar]
- 6.Kehoe S, Neilson J, Norman J. Maternal and infant deaths: chasing millennium development goals 4 and 5. London: RCOG; 2010. p. 433. [Google Scholar]
- 7.Dare F, Bako A, Ezechi O. Puerperal sepsis: a preventable post-partum complication. Trop Dr. 1998;28(2):92–95. doi: 10.1177/004947559802800212. [DOI] [PubMed] [Google Scholar]
- 8.Berhan Y, Berhan A. Causes of maternal mortality in Ethiopia: a significant decline in abortion related death. Ethiop J Health Sci. 2014;24:15–28. doi: 10.4314/ejhs.v24i0.3S. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Martinez JL. General principles of antibiotic resistance in bacteria. Drug Discov Today Technol. 2014;11:33–39. doi: 10.1016/j.ddtec.2014.02.001. [DOI] [PubMed] [Google Scholar]
- 10.Van der Tak J. Abortion, fertility, and changing legislation: an international review: Lexington books. 1974. [Google Scholar]
- 11.Fikremelekot T. Incidence and determinants of puerperal fever among Parturients who gave birth in a tertiary teaching hospital. Addis Ababa: AAU; 2014. [Google Scholar]
- 12.Tang AM, Dong K, Deitchler M, Chung M, Maalouf-Manasseh Z, Tumilowicz A, et al. Use of cutoffs for mid-upper arm circumference (MUAC) as an indicator or predictor of nutritional and health-related outcomes in adolescents and adults: a systematic review. 2013. [Google Scholar]
- 13.World Health Organization (WHO) Haemoglobin concentrations for the diagnosis of anemia and assessment of severity. Vitamin and Mineral Nutrition Information System. Geneva: WHO; 2011. [Google Scholar]
- 14.Cheesbrough M. District laboratory practice in tropical countries-part 2. 2. New York: Cambridge University press; 2006. p. 442. [Google Scholar]
- 15.Romero-Gómez M-P, Gómez-Gil R, Paño-Pardo JR, Mingorance J. Identification and susceptibility testing of microorganism by direct inoculation from positive blood culture bottles by combining MALDI-TOF and Vitek-2 compact is rapid and effective. J Infect. 2012;65(6):513–520. doi: 10.1016/j.jinf.2012.08.013. [DOI] [PubMed] [Google Scholar]
- 16.Ahmed MI, Alsammani MA. Babiker RA. Puerperal Sepsis in a rural Hospital in Sudan. Mater Sociomed. 2013;25(1):19–22. doi: 10.5455/msm.2013.25.19-22. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Maharaj D. Puerperal pyrexia: a review. Part II. Obstet Gynecol Surv. 2007;62(6):400–406. doi: 10.1097/01.ogx.0000266063.84571.fb. [DOI] [PubMed] [Google Scholar]
- 18.Duncan M, Perine P, Krause D, Awoke S, Zaidi A. Pelvic inflammatory disease and puerperal sepsis in Ethiopia: II. Treatment. Am J Obstet Gynecol. 1980;138(7):1059–1063. doi: 10.1016/0002-9378(80)91108-4. [DOI] [PubMed] [Google Scholar]
- 19.Bako B, Audu BM, Lawan ZM, Umar JB. Risk factors and microbial isolates of puerperal sepsis at the University of Maiduguri Teaching Hospital, Maiduguri, North-Eastern Nigeria. Arch Gynecol Obstet. 2012;285(4):913–917. doi: 10.1007/s00404-011-2078-4. [DOI] [PubMed] [Google Scholar]
- 20.Tamboli SS, Tamboli SB, Shrikhande S. Puerperal sepsis: predominant organisms and their antibiotic sensitivity pattern. Int J Reprod Contracept Obstet Gynecol. 2017;5(3):762–765. [Google Scholar]
- 21.Pradhan B, Shrestha SD, Bhandary S, Singh A, Shrestha R. Puerperal Sepsis and its cause in Patan hospital. Nepal J Obstet Gynaecol. 2015;10(1):33–35. doi: 10.3126/njog.v10i1.13192. [DOI] [Google Scholar]
- 22.Lisa M, Joseph N, Joel B, Yarine F, Adeline A, Mark J, et al. Antimicrobial-resistant infections among postpartum women at a Ugandan referral hospital. PLoS One. 2017;12(4):e0175456. doi: 10.1371/journal.pone.0175456. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Zarko A, Stephen M, Stefania L. Caesarean section versus vaginal delivery for preterm birth in singletons. Cochrane Database Syst Rev. 2012. 10.1002/14651858.CD000078.pub2. [DOI] [PMC free article] [PubMed]
- 24.Naber CK. Staphylococcus aureus bacteremia: epidemiology, pathophysiology, and management strategies. Clin Infect Dis. 2009;48(Supplement 4):S231–S2S7. doi: 10.1086/598189. [DOI] [PubMed] [Google Scholar]
- 25.Bako B, Ibrahim UN, Umar JB, Zamo AB. Microbial Isolates in Puerperal Sepsis and their in vitro Antibiotic Sensitivity in North Eastern Nigeria. Women’s Health Care. 2012;1(107):2167–0420. [Google Scholar]
- 26.Biedenbach DJ, Moet GJ, Jones RN. Occurrence and antimicrobial resistance pattern comparisons among bloodstream infection isolates from the SENTRY antimicrobial surveillance program (1997–2002) Diagn Microbiol Infect Dis. 2004;50(1):59–69. doi: 10.1016/j.diagmicrobio.2004.05.003. [DOI] [PubMed] [Google Scholar]
- 27.Gebre-Sealsssie S. Antimicrobial resistance patterns of clinical bacterial isolates in southwestern Ethiopia. Ethiop Med J. 2007;45(4):363–370. [PubMed] [Google Scholar]
- 28.Zaidi AK, Thaver D, Ali SA, Khan TA. Pathogens associated with sepsis in newborns and young infants in developing countries. Pediatr Infect Dis J. 2009;28(1):S10–SS8. doi: 10.1097/INF.0b013e3181958769. [DOI] [PubMed] [Google Scholar]
- 29.Ghotaslou R, Ghorashi Z, Nahaei M. Klebsiella pneumoniae in neonatal Sepsis: a 3-year-study in the pediatric hospital of Tabriz Iran. Jpn J Infect Dis. 2007;60(2/3):126. [PubMed] [Google Scholar]
- 30.Biadglegne F, Abera B, Alem A, Anagaw B. Bacterial isolates from wound infection and their antimicrobial susceptibility pattern in Felege Hiwot referral Hospital North West Ethiopia. Ethiop J Health Sci. 2009;19(3):173–7.
- 31.Antunes LC, Visca P, Towner KJ. Acinetobacter baumannii: evolution of a global pathogen. Pathog Dis. 2014;71(3):292–301. doi: 10.1111/2049-632X.12125. [DOI] [PubMed] [Google Scholar]
- 32.Beyene G, Tsegaye W. Bacterial uropathogens in urinary tract infection and antibiotic susceptibility pattern in Jimma University specialized hospital, Southwest Ethiopia. Ethiop J Health Sci. 2011;21(2):141–146. doi: 10.4314/ejhs.v21i2.69055. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Tiruneh M, Yifru S, Gizachew M, Molla K, Belyhun Y, Moges F, et al. Changing trends in prevalence and antibiotics resistance of uropathogens in patients attending the Gondar University hospital, Northwest Ethiopia. Int J Bacteriol. 2014;2014:629424. doi: 10.1155/2014/629424. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Shehab El-Din EMR, El-Sokkary MMA, Bassiouny MR, Hassan R. Epidemiology of Neonatal Sepsis and Implicated Pathogens: A Study from Egypt. Biomed Res Int. 2015;2015:509484. doi: 10.1155/2015/509484. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Aamir MM, Ali AE, Hamouda HM, Mourad FE. Prevalence of multidrug resistant Bacteria causing late-onset neonatal Sepsis. Int J Curr Microbiol App Sci. 2015;4(5):172–190. [Google Scholar]
- 36.Gebrehiwot A, Lakew W, Moges F, Anagaw B, Yismaw G, Unakal C. Bacterial profile and drug susceptibility pattern of neonatal sepsis in Gondar University hospital, Gondar Northwest Ethiopia. Der Pharmacia Lettre. 2012;4(6):1811–1816. [Google Scholar]
- 37.Walsh AL, Phiri AJ, Graham SM, et al. Bacteremia in febrile Malawian children: clinical and microbiologic features. Pediatr Infect Dis J. 2000;19:312–318. doi: 10.1097/00006454-200004000-00010. [DOI] [PubMed] [Google Scholar]
- 38.Ge T. Bacterial etiologic agents causing neonatal sepsis, their antimicrobial susceptibility pattern and associated risk factors at University of Gondar Hospital, North -West Ethiopia. 2016. [Google Scholar]
- 39.Singh L, Cariappa M, Das N. Drug sensitivity pattern of various Staphylococcus species isolated at a tertiary care hospital. Med J Armed Forces India. 2016;72:S62–SS6. doi: 10.1016/j.mjafi.2016.07.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Thenmozhi S, Moorthy M, Sureshkumar B, Suresh M. Antibiotic resistance mechanism of ESBL producing Enterobacteriaceae in clinical field: a review. Int J Pure Appl Biosci. 2014;2:207–226. [Google Scholar]
- 41.Mindolli PB, Salmani MP, Vishwanath G, Manumanthappa A. Identification and speciation of Acinetobacter and their antimicrobial susceptibility testing. Al Ameen J Med Sci. 2010;3(4):345–349. [Google Scholar]
- 42.Hostacká A. Antibiotic susceptibility, serum response and surface properties of Klebsiella species. Microbios. 2000;104(408):115–124. [PubMed] [Google Scholar]
- 43.Walckenaer E, Poirel L, Leflon-Guibout V, Nordmann P, Nicolas-Chanoine M-H. Genetic and biochemical characterization of the chromosomal class a β-lactamases of Raoultella (formerly Klebsiella) planticola and Raoultella ornithinolytica. Antimicrob Agents Chemother. 2004;48(1):305–312. doi: 10.1128/AAC.48.1.305-312.2004. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Khaskheli M-N, Baloch S, Sheeba A. Risk factors and complications of puerperal sepsis at a tertiary healthcare Centre. Pak J Med Sci. 2013;29(4):972. doi: 10.12669/pjms.294.3389. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Demisse GA, Sifer SD, Kedir B, Fekene DB, Bulto GA. Determinants of puerperal sepsis among post-partum women at public hospitals in west SHOA zone Oromia regional STATE, Ethiopia (institution BASEDCASE control study) BMC Pregnancy and Childbirth. 2019;19:95. doi: 10.1186/s12884-019-2230-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
Data were collected from puerperal sepsis suspected women admitted to Felege Hiwot Referral Hospital, Bahir Dar, Northwest Ethiopia. The datasets are available from the corresponding author upon reasonable request through alemalea@gmail.com but will not be shared publicly to ensure patient confidentiality.