ISRN Microbiology

Volume 2014 (2014), Article ID 469758, 5 pages

http://dx.doi.org/10.1155/2014/469758

Research Article

Prevalence, Clinical Features, and Outcome of Pseudomonas Bacteremia in Under-Five Diarrheal Children in Bangladesh

Farhana Akram,¹ Mark A.C. Pietroni,² Pradip Kumar Bardhan,³ Samira Bibi,¹ and Mohammod Jobayer Chisti3,4

¹Pharmacy Department, East West University, Dhaka, Bangladesh

²Public Health for South Gloucestershire, South Gloucestershire, Badminton Road, Yate, BS37 5AF, UK

³Dhaka Hospital, International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), 68 Shaheed Tajuddin Ahmed Sarani, Mohakhali, Dhaka 1212, Bangladesh

⁴Centre for Nutrition and Food Security (CNFS), International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh

Received 16 December 2013; Accepted 5 February 2014; Published 9 March 2014

Academic Editors: P. Di Martino, A. Hamood, and S. J. Suh

Copyright © 2014 Farhana Akram et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

We sought to evaluate the prevalence, associated factors, and outcome of under-five diarrheal children with either sex having Pseudomonas bacteremia. A retrospective chart review of under-five diarrheal children admitted to the Dhaka Hospital of the International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), from January 2011 to December 2011 was performed using an online hospital management system. Children with Pseudomonas bacteremia constituted the cases (n = 31), and the controls (n = 124), without Pseudomonas bacteremia, were randomly selected. The prevalence of Pseudomonas bacteremia was 1% (31/5,179). The Pseudomonas was multidrug resistant but was 84% sensitive to ceftazidime and 100% to imipenem. The case-fatality rate was significantly higher among the cases than the controls (26% versus 5%; P = 0.003). In logistic regression analysis, after adjusting for potential confounders such as severe wasting, severe underweight, severe pneumonia, and young age (11.71 (4.0, 18.0) months), the cases more often presented with absent peripheral pulses in absence of dehydration (95% CI = 2.31–24.45) on admission. This finding underscores the importance of early identification of this simple clinical sign to ensure prompt management including fluid resuscitation and broad spectrum antibiotics to help reduce morbidity and mortality in such children, especially in resource-poor settings.

1. Introduction

Sepsis remains a leading cause of morbidity as well as mortality in the pediatric population [1–5]. Most of these deaths occur in developing countries [6–8]. Pseudomonas, a facultative anaerobe Gram-negative organism that is commonly discovered in soil, water, and plants, seldom causes illness in healthy people. However, Pseudomonas sepsis often occurs in patients with burns, malignancy, or immunodeficiency or in preterm infants. Most of these infections are nosocomially acquired [9, 10]. Pseudomonas infection is clinically indistinguishable from other forms of Gram-negative bacterial infection. For this reason, patients with Pseudomonas infection often receive empirical antibiotics that are not sufficiently active against Pseudomonas, especially before culture results and antibiotic sensitivities become available [11–13]. Despite recent improvements in therapy, Pseudomonas bacteremia remains fatal in more than 20% of cases [14]. In a recent large multicentre study of all age groups, Pseudomonas bloodstream infection (BSI) was multidrug resistant (MDR) and associated with crude mortality rates of 39% in all patients and 48% in intensive care unit patients [15]. Mortality is even higher when children with Pseudomonas bacteremia also have diarrhea [16]. Thus, children with Pseudomonas bacteremia and diarrhea need careful attention. An understanding of the factors associated with Pseudomonas bacteremia in diarrheal children may help clinicians in identifying and managing such children promptly and efficiently in order to reduce morbidity and mortality especially in resource-poor settings. However, there is little data on factors which may predict Pseudomonas bacteremia in children with diarrhea. The aim of our study was to identify the prevalence, clinical predictors, and outcomes of Pseudomonas sepsis in under-five diarrheal children.

2. Materials and Methods

2.1. Ethics Statement

Our research did not involve any interviews with patients or caregivers and it was solely a chart analysis. The data were anonymised before being received by us.

2.2. Type of Study

This study involved a retrospective analysis of data extracted from the hospital management system (SHEBA), an online data base of the Dhaka Hospital of icddr,b.

2.3. Study Population and Site

We conducted our study at the International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b). Every year it deals with around 140,000 patients; most of the patients have diarrhea with or without other complications [17]. After arrival at hospital triage nurses obtain the patient’s medical history and make a rapid assessment, focusing on the severity of disease as well as other health complications. Within half an hour of admission, all patients are evaluated by duty physicians and receive appropriate treatment. Patients with complications of diarrhea or those with respiratory distress, cyanosis, apnea, hypothermia, sepsis shock, impaired consciousness, convulsion, severe pneumonia with hypoxemia, or respiratory failure are admitted to the Intensive Care Unit (ICU) or Longer Stay Ward (LSW) of the Dhaka Hospital of icddr,b. The majority of the patients come from a poor socioeconomic background. In addition to clinical services, the hospital also conducts research on various infectious diseases such as diarrhea, pneumonia, and sepsis and malnutrition.

2.4. Study Design

For this study, we used an unmatched case-control design. Data on diarrheal children of both sexes, aged 0–59 months, admitted to ICU or LSW of icddr,b from January 2011 to December 2011, who had a blood culture, were extracted from SHEBA. Under-five diarrheal children with Pseudomonas bacteremia constituted the cases, and those without Pseudomonas bacteremia constituted controls. Controls were randomly selected from the children without Pseudomonas bacteremia by computer randomization using SPSS (version 17.0; SPSS Inc., Chicago) from the personal computerized data source of this study. A 1 : 3 unmatched case-control ratio was used to increase the statistical power of our analyses.

2.5. Measurements

Case report forms (CRF) were developed, pretested, and finalized for data acquisition. Characteristics analyzed include demographics (age, gender, and place of residence), fever, cough, history of difficulty breathing, acute watery diarrhea, pneumonia, absent peripheral pulses even after correction of dehydration or in absence of dehydration, hospital acquired infection (any new infection documented after 48 hours of admission), severe wasting, severe underweight, severe stunting, abnormal mental status (disorientation or lethargy or convulsion), radial pulse, respiratory rate, temperature and outcome.

2.6. Analysis

All the data were entered into SPSS for Windows (version 17.0; SPSS Inc., Chicago) and Epi-Info (version 6.0, USD, Stone Mountain, GA). Differences in proportions were compared by the chi-square test. In normally distributed data, differences of mean were compared by Student’s -test; the Mann-Whitney test was used for comparison of data that were not normally distributed. A probability of less than 0.05 was considered statistically significant. Strength of association was determined by calculating the odds ratio (OR) and 95% confidence intervals (CIs). In identifying predictors of Pseudomonas sepsis in under-five diarrheal children with pneumonia, variables were initially analyzed in a univariate model, and then independent predictors were identified using logistic regression after controlling for covariates.

3. Results

Among a total of 5,179 under-five diarrheal children who were available for the evaluation, 31 met the case definition (1%) and 124 controls were randomly selected from the rest. The case fatality was significantly higher among the cases than the controls (Table 1). The Pseudomonas was multidrug resistant (Table 3) but was sensitive to imipenem (100%) and ceftazidime (84%). In a logistic regression analysis, after adjusting for potential confounders (such as young age (11.71 (4.0, 18.0) months), severe pneumonia, severe underweight, and severe wasting), an absent peripheral pulse in the absence of dehydration has been revealed as an independent predictor of Pseudomonas bacteremia in diarrheal children (Table 2). The distributions of sex, difficulty in breathing, cough, respiratory rate, abnormal status, and hospital acquired infection among the cases and the controls were comparable (Table 1). There was no bacteremia among the controls that had absent or uncountable peripheral pulses. The monthly distribution of Pseudomonas bacteremia has been shown in Figure 1.

Table 1: Admission characteristics of diarrheal children with (cases) and without Pseudomonas bacteremia (controls).

Variables
Cases

Controls

Unadjusted odds ratio

(95% Cl)

Age (median, IQR)
11.71 (4.0, 18.0)
8.93 (5.03, 19.0)
—
0.354

Respiratory rate/minute (mean ± SD)

0.720 (−5.48–0.92)
0.806

Gender (male)
20 (65)
59 (63)
1.05 (0.42–2.73)
0.914

History of the cough
10 (32)
33 (36)
0.87 (0.33–2.20)
0.913

History of difficulty breathing
8 (26)
21 (23)
1.19 (0.40–3.29)
0.903

Presence of fever
12 (39)
38 (41)
0.91 (0.36–2.26)
0.999

Absent peripheral pulses even after correction of dehydration or in absence of dehydration
10 (32)
6 (7)
6.91 (1.97–25.41)
<0.001

Hospital acquired infection
1 (3)
0 (0)
Undefined
0.562

Severe wasting
11 (36)
17 (18)
2.46 (0.91–6.67)
0.083

Severe underweight
15 (55)
37 (40)
1.83 (0.75–4.55)
0.210

Death
8 (26)
5 (5)
6.12 (1.61–24.22)
0.003

Severe pneumonia
8/28 (29)
19/84 (23)
1.37 (0.45–3.90)
0.702

Abnormal mental status
5/7 (71)
13/17 (76)
0.77 (0.08–11.19)
0.795

Figures represent (%) unless indicated otherwise.

CI: confidence interval; IQR: interquartile range; SD: standard deviation.

Table 2: Results of logistic regression analysis to explore the independent predictors of Pseudomonas bacteremia in under-five diarrheal children.

Clinical parameters
Adjusted OR
95% CI

Age (11.71 (4.0, 18.0) months)
0.99
0.96–1.01
0.312

Absent peripheral pulses
7.51
2.31–24.45
0.001

Severe wasting
1.86
0.63–5.46
0.260

Severe underweight
1.14
0.43–3.06
0.790

Severe pneumonia
1.63
0.58–4.57
0.357

Table 3: Antibiotic sensitivity, resistance and intermediate sensitivity of Pseudomonas species isolated from blood culture in under-five diarrheal children

Drugs
Sensitivity

(%)
Resistance

(%)
Intermediate sensitivity

(%)

Gentamicin
16 (52)
15 (48)
0 (0)

Ciprofloxacin
24 (77)
5 (16)
2 (7)

Ceftazidime
26 (84)
3 (10)
2 (7)

Imipenem
31 (100)
0 (0)
0 (0)

Netilmicin
22 (71)
8 (26)
1 (3)

Amikacin
22 (71)
7 (23)
2 (7)

Meropenem
27 (87)
2 (7)
2 (7)

Figure 1: Monthly distribution of Pseudomonas bacteremia (number) in 2011 in Dhaka Hospital.

4. Discussion

Our observation of a higher case-fatality rate in under-five diarrheal children with Pseudomonas bacteremia is an important finding, although it is not surprising. Treatment of children with Pseudomonas bacteremia often requires prompt adherence to appropriate parental broad spectrum antibiotics. The first line of management of sepsis in our hospital is the combination of parental ampicillin and gentamicin, and the second line is the combination of ceftriaxone and gentamicin. These combinations are used in our hospital as previous studies in Bangladesh have revealed that these combinations are very effective in most children with clinical sepsis [18]. Third and fourth lines of treatment of sepsis in our hospital are the combination of ceftazidime and amikacin or imipenem alone, respectively. In cases of hospital acquired infection, ceftazidime and amikacin together and imipenem are the first and second lines of treatment. Thus, apart from 1 patient with hospital acquired Pseudomonas bacteremia, no other patients with Pseudomonas bacteremia in our series received appropriate antibiotics before the availability of the blood culture report. The culture reports are usually received 72 hours after admission in our hospital. The resulting delay in the use of appropriate antibiotics may contribute to the higher mortality in diarrheal children with Pseudomonas bacteremia. A number of studies have revealed that sensitive but delayed antimicrobial therapy in children with P. aeruginosa bacteremia is often associated with septic shock resulting in higher mortality [10, 19] and underscores the importance of appropriate initial antimicrobial treatment [20, 21].

Our observation of absent or uncountable peripheral pulses in absence of dehydration or after correction of dehydration, as an independent predictor of Pseudomonas bacteremia in under-five diarrheal children, is also understandable. Absent peripheral pulses, after appropriate correction of dehydration and maintenance of hydration, are likely to be due to compromised peripheral circulation secondary to Pseudomonas sepsis-related phenomena, such as impaired vasoregulation and cardiac dysfunction. This finding is consistent with our earlier studies [22]. Thus, our findings suggest that under-five diarrheal children with absent or uncountable peripheral pulses in the absence of dehydration or after full correction of dehydration should be treated aggressively with an antipseudomonal parental cephalosporin (ceftazidime) or with carbapenem (imipenem) in addition to routine rapid fluid resuscitation.

We failed to observe any significant difference in gender, fever, cough, history of difficulty in breathing, hospital acquired infection, abnormal mental status, radial pulse, and respiratory rate among the groups. This might be due to the small sample. However, failure to identify any statistical difference in hospital acquired infection among the groups might be due to the fact that there was a lack of documentation of hospital acquired infection in the digital record system (SHEBA). Our study has potentially two important limitations. First, the retrospective nature of the study in identifying Pseudomonas bacteremia prevented us from collecting information on a broader range of variables that may have been potential additional predictors. Second, the limitation in the number of patients included in this study might have reduced the ability to identify more subtle differences between the groups and identify further relevant predictors of Pseudomonas bacteremia.

In conclusion, the results of our data analyses suggest that the prevalence of Pseudomonas bacteremia is low but is associated with a high case-fatality rate in under-five diarrheal children. Absent peripheral pulse in the absence of dehydration or after full correction of dehydration was the best predictor of Pseudomonas bacteremia in under-five diarrheal children. Identification of this simple clinical predictor of Pseudomonas bacteremia may help prompt as well as aggressive management with rapid fluid infusion and broad spectrum antibiotics in diarrheal children and result in reduced morbidity and mortality especially in resource-poor settings. However, a further study with a larger sample and a prospective design is imperative to confirm our observation.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

This research was funded by International Centre for Diarrhoeal Disease Research, Bangladesh, and its donors which provide unrestricted support to International Centre for Diarrhoeal Disease Research for its operations and research. Current donors providing unrestricted support include Australian Agency for International Development (AusAID), Government of the People’s Republic of Bangladesh, Canadian International Development Agency (CIDA), Swedish International Development Cooperation Agency (Sida), and the Department for International Development, UK (DFID). The authors gratefully acknowledge these donors for their support and commitment to International Centre for Diarrhoeal Disease Research’s research efforts. The authors gratefully acknowledge SHEBA personnel for their relentless support and help.

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