Aetiology of paediatric pneumonia with effusion in the Dominican Republic and the potential impact of pneumococcal conjugate vaccines
© The Author(s) 2014
Received: 22 November 2013
Accepted: 26 March 2014
Published: 2 June 2014
Pleural effusion is a serious complication of pneumonia, and Streptococcus pneumoniae is a leading cause. We describe the aetiology of pneumonia with effusion among children in the Dominican Republic before the introduction of the 13-valent pneumococcal conjugate vaccine (PCV) in 2013 and the performance characteristics of a rapid immunochromatographic test (ICT) for detecting S. pneumoniae in pleural fluid. From July 2009 to June 2011, we enrolled children <15 years old admitted with pneumonia and pleural effusion to Robert Reid Cabral Children’s Hospital, Dominican Republic. Pleural fluid was tested by culture, polymerase chain reaction (PCR) for bacterial (S. pyogenes, S. pneumoniae) and viral (respiratory syncytial virus and human rhinovirus) pathogens, and by ICT for S. pneumoniae. We calculated the performance of ICT and culture compared with PCR. Among 121 cases, the median age was 31 months (range 1 week to 14 years). Pleural fluid culture (n = 121) and PCR testing (n = 112) identified an aetiology in 85 (70.2%) cases, including 62 S. pneumoniae (51.2%) and 19 Staphylococcus aureus (15.7%). The viruses tested were not detected. The most prevalent pneumococcal serotypes were 14 (n = 20), 1 (n = 13), and 3 (n = 12). Serotype coverage of the 10- and 13-valent PCVs would be 70.5% and 95.1%, respectively. The sensitivity of point-of-care ICT was 100% (95% confidence interval [CI] 94.1%–100%), while specificity was 86.3% (95% CI 73.7%–94.3%). S. pneumoniae caused more than half of paediatric pneumonia with effusion cases; introduction of PCV in the Dominican Republic could reduce the burden by 36–49%. ICT is a practical, valid diagnostic tool for clinical care and surveillance in settings with limited laboratory capacity.
Pneumonia is the leading cause of death among children worldwide . Pleural effusion is a serious complication of pneumonia affecting up to 40% of children hospitalised with pneumonia . Parapneumonic effusion, also known as pneumonia with effusion, is associated with longer hospitals stays, more intensive care, and higher rates of morbidity [3, 4]. In the Dominican Republic, pleural effusions are frequent and complicate 38% of admissions for pneumonia at Robert Reid Cabral Children’s Hospital (RRCCH), which is a large referral hospital in the capital city of Santo Domingo; one of every two admissions to the infectious disease service is due to pneumonia with effusion .
While various pathogens can lead to pneumonia with effusion in children, the most common causes are bacterial — particularly Streptococcus pneumoniae . Data on the aetiology of parapneumonic infections can help guide clinical management as well as policies for preventive interventions such as the pneumococcal conjugate vaccine (PCV). Yet establishing the cause of pneumonia with effusion can be challenging. Culture is insensitive, and prior antibiotic use further decreases its yield . While more sensitive diagnostic tests such as polymerase chain reaction (PCR) and antigen detection tests exist, they are not widely available in resource-constrained settings. Consequently there are relatively limited data from low- and middle-income countries on the principle causes of pneumonia with effusion.
The 13-valent PCV was introduced in the routine infant immunisation program in the Dominican Republic in August, 2013. Prior to the introduction, we undertook a study of the epidemiology of pneumonia with effusion among children in the Dominican Republic to inform PCV policy decisions. We used culture, PCR and a rapid Immunochromatographic test (ICT) (BinaxNOW®; Alere Inc, USA) to determine predominant aetiologies and estimate the proportion of disease that would be prevented through PCV introduction in the routine infant immunisation program.
2.1 Patients and sample collection
Surveillance for pneumonia with effusion was conducted at RRCCH from July 2009 to June 2011. All children less than 15 years old admitted with history of fever and/or measured temperature ≥38 °C on admission, tachypnoea (defined as a respiratory rate >30 per minute in children less than 8 years old and >25 in children aged 8 to 16 years), and radiological evidence of pleural effusion large enough to require thoracocentesis as a diagnostic or therapeutic procedure were eligible to participate. After obtaining informed written consent from a parent or guardian (and written assent from children ≥12 years old), clinical and epidemiologic data were gathered from medical records and parental interview using standardised forms, and thoracocentesis was performed. Pleural fluid samples were sent immediately to the microbiology laboratory of RRCCH for Gram stain, culture, antimicrobial susceptibility testing, and point of care ICT for S. pneumoniae. Remaining pleural fluid was frozen at −70 °C and sent to the United States (US) Centers for Disease Control and Prevention (CDC) for molecular testing and repeat of the ICT.
2.2 Laboratory methods
All pleural fluids were cultured on blood, chocolate and MacConkey agar plates for bacterial isolation, followed by identification according to recommendations in the Manual of Clinical Microbiology . S. pneumoniae isolates were identified by alpha-haemolysis, optochin susceptibility and bile solubility. Antimicrobial susceptibility tests were conducted using disc diffusion and E-test for penicillin and cefotaxime . The ICT test S. pneumoniae BinaxNOW® was performed according to manufacturer’s instructions as a point of care test at the hospital laboratory. When available, remaining specimen was frozen at −70 °C and sent to CDC for ICT re-testing and performance of PCR for bacterial (S. pyogenes and S. pneumoniae) and viral (respiratory syncytial virus [RSV] and human rhinovirus) pathogens.
Just before bacterial DNA extraction, 200 µl volumes of the pleural fluid samples were manually transferred into 1.5 ml cryotubes containing 100 µl of Tris-EDTA buffer with 0.04 g/ml lysozyme and 75 U/ml mutanolysin (Sigma Chemical Co., USA). The mixture was incubated for 1 h at 37 °C followed by addition of 20 µl of proteinase K. After mixing briefly with a vortex machine, 400 µl of lysis buffer (Qiagen, USA) was added. After completion of the lysis step, the extraction process followed the manufacturer’s procedures using the NucliSENS® easyMAG® automated nucleic acid extraction system (Biomerieux, USA). Bacterial DNA extracts were eluted in 100 µl of elution buffer. Viral total nucleic acids were recovered from separate 200 µl volumes of pleural fluid placed directly in NucliSens® Lysis Buffer (Biomerieux) and extracted as described above. S. pneumoniae and S. pyogenes DNA was detected using real-time PCR assays targeting the lytA and spy genes, respectively [10, 11]. For lytA-positive specimens, pneumococcal serotype deduction was achieved using a sequential multiplex PCR strategy for clinical samples [12, 13]. RSV  and human rhinovirus  were tested by real-time reverse transcription PCR assays as previously described. Positive controls were run concurrently for each specific PCR assay as well as a control reaction with RNAseP human gene performed independently with each sample to check for the presence of inhibitors .
2.3 Data analysis
Data were analysed using SAS (v 9.3, SAS Institute Inc., Cary NC). We described the frequencies of clinical characteristics and aetiologies, and assessed the proportion of disease preventable by available 7-, 10- and 13-valent PCV formulations. Aetiology was determined based on positive results by culture and/or PCR. To evaluate the performance of the ICT to detect S. pneumoniae in pleural fluid, we calculated sensitivity, specificity, positive and negative predictive values with 95% confidence intervals (CI) using PCR results as the gold standard.
2.4 Ethical approval
The study was conducted in accordance with the Helsinki Declaration. The protocol was reviewed and approved by the Ethics Committee and Institutional Review Board of Fundacion Dominicana de Infectologia, Inc. (Approval reference no: 2008-05). The Human Subject Research Protection Office of the CDC determined that it could rely upon approval of the Institutional Review Board of the Fundacion Dominicana de Infectologia, Inc. (Reliance for approval reference no: 5867).
3.1 Clinical characteristics and aetiology
A total of 121 case-patients were enrolled. The median age was 31 months, with a range from 1 week to 14 years. Among 120 case-patients with available sex, 81 (67.5%) were male. Underlying chronic illness was reported for 16 (13.2%) case-patients, including asthma (n = 7), sickle cell anaemia (n = 6), trisomy 21 (n = 1), anaemia (n = 1), and tuberculosis (n = 1). Two patients were diagnosed with other major illnesses during their hospitalisation (one with Burkitt’s lymphoma and one with a mediastinal tumor). One case-patient died; all others were discharged or remained hospitalised (n = 5) at last follow-up. Among 110 case-patients with data available on prior medication use, 60 (54.5%) had previously received antibiotics for the current illness.
Aetiology of paediatric pneumonia with effusion based on results of pleural fluid testing by culture and polymerase chain reaction
Detected by culturea
Detected by PCRb
Detected by culture and/or PCR
Streptococcus pneumoniae c
Staphylococcus aureus c
No aetiology determined
Serotypes detected in children with pneumococcal pneumonia with effusion, n = 61a
Not typeable for 40 serotypes by PCR
3.2 Detection of S. pneumoniae by ICT and culture
Performance of immunochromatographic test and culture compared with polymerase chain reaction to detect Streptococcus pneumoniae in pleural fluid
Sensitivity (95% CI)
Specificity (95% CI)
Positive predictive value (95% CI)
Negative predictive value (95% CI)
Point of care ICT at RRCCH
All samples (n = 112)
Samples from children with prior antibiotic usea (n = 58)
Repeat ICT at CDC
All samplesb (n = 101)
Samples from children with prior antibiotic usea (n = 53)
All samples (n=112)
Samples from children with prior antibiotic usea (n = 58)
This study has demonstrated an important burden of pneumococcal disease among children with pneumonia with effusion in the Dominican Republic. S. pneumoniae was detected in more than half of all cases. This finding is consistent with other studies that have reported S. pneumoniae to be the leading cause of pneumonia with effusion [16–19]. S. aureus was the second most common aetiology identified in this study. Because S. aureus was detected by culture only (not by PCR), the true contribution of this pathogen was likely greater than what was observed. Some studies of paediatric pneumonia with effusion and empyema have found S. aureus to be the leading cause [20–22], and S. pyogenes, which was found in 2 cases in this study, has also been found to be an important aetiology [16, 17, 22]. We did not identify any cases due to RSV, which is a leading cause of severe respiratory illness among young children , or human rhinovirus, which is among the most commonly detected respiratory pathogens in this age group . Interestingly, a recent paper from Brazil described probable viral aetiologies among 9 of 18 children with pneumonia with effusion ; however the viruses were detected in the nasopharynx or based on serologic tests, and pleural fluid samples (which were available for a minority of case-patients) were tested by culture only, thus the results are not directly comparable to our findings. Other studies have found only bacterial infections to be significantly associated with pleural effusion [26, 27]. Our findings similarly do not support an important role of viruses in paediatric pneumonia with effusion, and highlight the primary role of S. pneumoniae.
These data suggest that the 13-valent PCV, which was introduced in the national immunisation program in the Dominican Republic in August 2013, could reduce the burden of pneumonia with effusion in children by up to 49%. The 7-valent PCV, which has been available since 2000, is highly effective against disease caused by vaccine serotypes  and led to a 39% decline in pneumonia hospitalisation among children <2 years in the United States . Rates of empyema in children, however, have increased in the US and other locations since the 1990s [30, 31] — a trend which has not abated despite the introduction of the 7-valent PCV [30, 32]. Serotype 1, which appears to have been a contributing factor to the rise in pneumonia with effusion in some settings , is not included in the 7-valent vaccine but is included in both the 10- and 13-valent formulations currently available. The results of studies evaluating immunogenic responses to the 10- and 13-valent PCVs suggest that they will protect against serotype 1 [33, 34], but data on effectiveness against clinical outcomes are not yet available. Serotype 1 was the second most common pneumococcal serotype identified in this study. It will be important to continue to monitor trends in pneumonia with effusion and pneumococcal serotype distribution in the Dominican Republic in the post-PCV13 era.
Our findings contribute to a growing body of evidence on the utility of ICT for detecting S. pneumoniae in pleural fluid. The rapid, easy-to-use assay was originally developed for detection of pneumococcal antigen in urine samples from adults ; however, studies have examined its performance when testing other specimens such as middle ear fluid [36, 37], cerebrospinal fluid  and pleural fluid [16, 39–43]. The high sensitivity and specificity we found for ICT performed on pleural fluid specimens are consistent with those reported in the published literature — which both range from 71% to 100% [16, 19, 39–44]. Similar to those studies, we found the sensitivity of ICT to be much greater than that of culture, particularly for samples from patients on antibiotics. We found 6 samples that were positive by ICT when used as a point of care test and negative when the ICT was repeated at CDC. These discrepancies may represent false-positive results on the initial test; false-positive results on ICT have been reported in the presence of other streptococcal species, anaerobes and Enterococcus faecalis [43, 44]. In our study, one case with a false-positive ICT result had a pleural fluid culture that grew S. aureus. Alternatively the discrepancies could be due to errors in point of care testing. Yet overall, there were very few discrepant results, confirming the useful role that ICT can play in measuring the burden of pneumococcal pneumonia.
This study had several limitations. RRCCH is a referral hospital, so children admitted there may represent the more severe or complex end of the spectrum of disease. There is no defined population denominator, so it is not possible to calculate incidence to estimate the population-level burden of paediatric pneumonia with effusion. And while we tested for the most common pathogens as well as some less common causes, there are other causes of pleural effusion that were not tested for (e.g. tuberculosis, other viruses) or that were tested for by culture rather than more sensitive molecular assays.
Nonetheless, this study provides important insight on the burden of pneumonia with effusion in a middle-income Latin American country. It highlights the importance of S. pneumoniae, and provides an estimate of the potential impact of PCV introduction on pneumococcal, and overall, pneumonia with effusion in children. We also demonstrated the utility of ICT for detecting pneumococcal disease in children with pneumonia and pleural effusion. The ICT can play an important role both clinically, as a point of care test, and epidemiologically, as a tool for measuring the burden of pneumococcal disease and evaluating the impact of PCV introduction. Such data can inform policy decisions regarding the introduction and sustained use of PCV, which will ultimately help reduce illness and death due to pneumonia among children in the Dominican Republic and elsewhere.
The authors would like to thank the patients and families that participated in the study.
Disclaimer: The findings and conclusions in the report are those of the authors and do not necessarily represent the views of the Centers for Disease Control and Prevention
Funding: The study was funded primarily by the Infectious Diseases Department of the Roberto Reid Cabral Children’s Hospital with in-kind support from the U.S. Centers for Disease Control and Prevention. Pfizer, Inc. (USA) provided funding to JFI for laboratory materials used at Robert Reid Cabral Children’s Hospital. Pfizer had no role in study design, collection and analysis of data, decision to publish, or writing of the manuscript.
Competing interests: All authors have no competing interests to declare.
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