Abstract
Background:
Worldwide, pneumonia is the leading cause of mortality in children under the age of five. An expanded program on immunization (EPI) is one kind of evidence-based tool for controlling and even eradicating infectious diseases.
Objectives:
This study aimed to explore the impact of EPI vaccination, including BCG, DPT-Hib-Hep B, OPV, IPV, and PCV-10, among children from the age of 4 to 59 months hospitalized for pneumonia and severe pneumonia. Additionally, we evaluated the role of 10 valent pneumococcal conjugate vaccines alone on clinical outcomes in such children.
Methods:
In this retrospective chart review, children from the age of 4 to 59 months with WHO-defined pneumonia and severe pneumonia admitted to the Dhaka Hospital of the International Centre for Diarrheal Disease Research, Bangladesh (icddr,b) between August 2013 and December 2017 who had the information on immunization as per EPI schedule by 4 months of age were included in the analysis. A comparison was made between the children who were fully immunized (immunization with BCG, DPT-Hib-Hep B, OPV, and IPV from 2013 to 2015 and PCV-10 from 2015 to 2017) and who were not immunized (consisting of partial immunization and no immunization) during the study period.
Results:
A total of 4,625 children had pneumonia and severe pneumonia during the study period. Among them, 2,605 (56.3%) had received the information on immunization; 2,195 (84.3%) were fully immunized by 4 months of age according to the EPI schedule and 410 were not immunized. In the log-linear binomial regression analysis, immunization of children from 4 to 59 months of age was found to be associated with a lower risk of diarrhea (p = 0.033), severe pneumonia (p = 0.001), anemia (p = 0.026), and deaths (p = 0.035). Importantly, the risk of developing severe pneumonia (1054/1,570 [67%] vs. 202/257 [79%], p < 0.001) and case-fatality rate (57/1,570 [3.6%] vs. 19/257 [7.4%], p = 0.005) was still significantly lower among those who were immunized with PCV-10 than those who were not.
Conclusion:
Children immunized as per the EPI schedule were at a lower risk of diarrhea, severe pneumonia, anemia, and death, compared to unvaccinated children. In addition, PCV-10 was found to be protective against severe pneumonia and deaths in vaccinated children. The overall results underscored the importance of the continuation of immunization, scrupulously adhering to the EPI schedule to reduce the risk of morbidities and mortalities in children, especially in resource-limited settings.
Introduction
Since the late eighties, pneumonia has been leading at the top among the infectious etiologies of global deaths of children under five (1, 2) and accounting for an estimated 12·8% of annual deaths beyond the neonatal period (3). In lower- and middle-income countries like Bangladesh, 13% of 100,000 regional deaths occur in children below five years of age (4). The majority of deaths occur in developing countries, in part, due to limited access to healthcare and public health interventions (5, 6). A substantial reduction in the past few decades of estimated pneumonia deaths (0·9 million in 2015 vs.1·7 million deaths in 1990) reflects not only economic development, improved nutrition, and reduced household crowding but also the use of pneumonia-specific interventions, such as improved case management, including empirical antibiotic treatment and effective vaccines against leading pneumonia pathogens (7, 8). Despite these advances, continued progress to reduce pneumonia mortality is constrained by the absence of vaccines against the remaining common pathogens. Pneumococcus pneumoniae is a major cause of childhood pneumonia and other invasive pediatric diseases, including meningitis and sepsis, accounting for approximately 14.5 million cases of invasive pneumococcal disease (IPD) and 826,000 child deaths worldwide. Among these estimated deaths, 741,000 are pneumonia deaths and 60,500 are deaths from meningitis. Bangladesh is one of the 10 countries with the highest number of IPD cases and IPD-related deaths among children under 5 years of age (9). Globally, 8 million episodes of serious disease are caused by Haemophilus influenzae type b (Hib) among children each year leading to an estimated one-half a million deaths (10). Both Pneumococcus pneumoniae and Haemophilus influenzae type B accounted for 5% or more of the etiological distribution of pneumonia in developing countries (11). The mortality rate from childhood pneumonia was much higher before 2,000 (12). By this period, the World Health Organization (WHO) identified several risk factors for deaths from childhood pneumonia on the basis of a good number of evidence generated from resource-limited settings and came up with a set of recommendations, including the incorporation of vaccines, appropriate antibiotics, oxygen therapy, and other routine clinical care (13) to reduce pneumonia-related deaths in children. As a result, between 2,000 and 2018, global pneumonia-related deaths among children under 5 were reduced by 54% (4).
Importantly, the introduction of Haemophilus influenzae type B (Hib) conjugate vaccine and pneumococcal conjugate vaccine 10 (PCV-10) in the EPI schedule by many governments in developing countries has had an enormous impact on the reduction of the pneumonia-related global burden of pneumonia caused by Pneumococcus pneumoniae and Haemophilus influenzae type B, as well as mortality in children under five years of age (14). It is also important to note that if immunization following the EPI schedule is ensured, Hib and PCV-10 as part of this schedule are simultaneously ensured (14).
EPI vaccination includes immunization against tuberculosis with Bacillus Calmette-Guerin (BCG) at birth, immunization against Diphtheria, Pertussis, Tetanus, Hepatitis B, Haemophilus influenzae type B with DPT-Hib-Hep B, Poliomyelitis with oral polio vaccine and inactivated polio vaccine, and Pneumococcus pneumoniae with PCV-10 at the 6th week, 10th week, and 14th week of birth (15). However, despite the WHO-recommended vaccines, antibiotics, oxygen therapy, and other supportive care, deaths from childhood severe pneumonia exceed 10% in many hospitals in developing countries (16, 17).
Among the 30 pneumonia-high-burden countries, Bangladesh has incorporated Hib and PCV-10 vaccines in the EPI schedule in 2009 and 2015, respectively which is considered to be on track along with Indonesia and China in order to achieve the Global Action Plan for Pneumonia and Diarrhea (GAPPD) with the goal to end pneumonia and diarrhea-related deaths by 2025 (14). Thus, Bangladesh needs to continue to keep its highly achieved 8.1% average annual rate of reduction in pneumonia-related deaths (14) to attain GAPPD by 2025. Although immunization coverage following the EPI schedule is still high in Bangladesh (18), we need to understand whether immunization has any role in the reduction of the severity of pneumonia and co-morbidities and thereby increasing the survival benefit among children from 4 to 59 months of age hospitalized for pneumonia and severe pneumonia. Thus, we sought to evaluate the impact of immunization following the EPI schedule as well as the role of PCV-10 alone on clinical outcomes in such children.
Materials and methods
Ethical statement
De-identified data were analyzed in this chart analysis; therefore, informed consent was not taken from the parents or guardians of the study participants. We have taken a waiver of approval by the Ethical Review Committee of the International Centre for Diarrheal Disease Research, Bangladesh (icddr,b) to use the de-identified data.
Study site
The study was conducted in the Dhaka Hospital of icddr,b. It's an urban tertiary care hospital situated in the capital city of Bangladesh and provides both inpatient and outpatient care to diarrheal patients associated with or without co-morbidities, like pneumonia and severe pneumonia. The other descriptions of the hospital have been provided somewhere else (19).
Study population
Children of either sex from the age of 4 to 59 months with WHO-defined pneumonia and severe pneumonia admitted into the Dhaka Hospital of icddr,b between August 2013 and December 2017 who had received the information on immunization captured from electronic medical records were enrolled in the study. Among the enrolled children, those who were fully immunized [children who received a single dose of BCG and three doses of DPT-Hib-Hep B (Diphtheria, Pertussis, Tetanus, Haemophilus influenzae type B, and Hepatitis-B), OPV (oral polio vaccine), and IPV (inactivated polio vaccine) during the period from 2013 to 2017 and PCV-10 (pneumococcal conjugate vaccine-10) during the period from 2015 to 2017] or not immunized (combination of partial immunization and no immunization) as per the EPI schedule by 4 months of age were selected for this analysis.
Study design
The data were extracted from the electronic database of the Dhaka Hospital of icddr,b. We purposefully excluded children below 4 months since we needed at least 14 weeks after birth to accomplish EPI scheduled vaccination, including vaccination against Pneumococcus pneumoniae and Haemophilus influenzae. Thus, we anticipated that by 4 months of age, all the children should have received vaccination against Pneumococcus pneumoniae and Haemophilus influenzae type B. The comparison was made between children who were fully immunized as per the EPI schedule and those who were not. We didn't consider children whose vaccination records were unavailable in the electronic database for the analysis.
As Bangladesh incorporated the PCV-10 against Pneumococcus pneumoniae in 2015, we also compared the characteristics of children who received the PCV-10, compared to those who did not receive the same vaccine between March 2015 and December 2017.
Measurements
We developed the case report forms which were pretested and finalized for the acquisition of the study as relevant data by the research team. The data extracted from the hospital's electronic database were routinely audited by the expert panel of the hospital's clinicians for better clarity before analysis. We evaluated the clinical and laboratory characteristics of children who were immunized, compared to those who were not (Table 1). Among the variables, diarrhea, severe acute malnutrition, hypoxemia, bacteremia, and anemia were defined following the WHO definition (13). We also used the evidence-based definition of severe sepsis (19). Finally, log-linear binomial regression analysis was done to see the independent impact of immunization.
Table 1
| Parameters | Immunized (n = 2195) (%) | Not immunized (n = 410) (%) | RR | 95% CI | p-value |
|---|---|---|---|---|---|
| Female | 747 (34) | 153 (37) | 1.05 | 0.97–1.14 | 0.199 |
| Age in months (median, IQR) | 9.23 (6.49, 13.23) | 8.07 (5.63, 12.00) | – | – | <0.001 |
| Presence of severe acute malnutrition on admission | 911 (42) | 209 (51) | 0.81 | 0.73–0.91 | <0.001 |
| Presence of hypoxemia (SpO2 < 90%) on admission | 611 (28) | 130 (32) | 0.88 | 0.75–1.03 | 0.111 |
| Presence of severe sepsis on admission | 188 (9) | 50 (12) | 0.70 | 0.52–0.94 | 0.019 |
| Presence of convulsion on admission | 298 (14) | 57 (14) | 0.98 | 0.75–1.27 | 0.859 |
| Presence of bacteremia on admission | 144 (7) | 33 (8) | 0.93 | 0.66–1.32 | 0.693 |
| Presence of diarrhea on admission | 1,830 (84) | 368 (90) | 0.93 | 0.89–0.97 | 0.002 |
| Presence of severe pneumonia on admission | 1,487 (68) | 322 (79) | 0.86 | 0.81–0.91 | <0.001 |
| Presence of anemia on admission | 416 (22) | 99 (29) | 0.77 | 0.64–0.92 | 0.008 |
| Duration of hospital stay (days) (median, IQR) | 6.00 (4.00, 9.00) | 6.00 (4.00, 9.00) | – | – | 0.121 |
| Death during hospitalization | 91 (4) | 34 (8) | 0.50 | 0.34–0.73 | <0.001 |
Characteristics of children hospitalized for pneumonia and severe pneumonia and had immunization following EPI schedule, compared to those who were not immunized.
RR, relative risk; CI, confidence interval; IQR, inter-quartile range.
Data analysis
We analyzed the data using SPSS for Windows (version 20.0) and STATA (version 12.0). Differences in proportion were compared by the Chi-square test. Initially, we did a bivariate analysis using a 2/2 table for the Chi-square test, and those who had significant associations between the groups by the Chi-square test like age, severe acute malnutrition, severe sepsis, diarrhea, severe pneumonia, anemia, and death were put into the log-linear binomial regression model. In the model, vaccination was the dependent variable, whereas the other significant variables in the bivariate analysis were considered independent variables. Among those variables, potential confounders like age, severe acute malnutrition, and severe sepsis were adjusted using the regression model to find out the ultimate significant risk factors having a probability of less than 0.05. The strength of the association was determined by calculating the risk ratio and their 95% confidence intervals.
Results
A total of 4,625 children were hospitalized with pneumonia and severe pneumonia during the study period. Among them, 2,605 (56.3%) had immunization records; 2,195 (84.3%) were fully immunized by 4 months of age according to the EPI schedule and 410 were not immunized. The study found that children who were immunized more often grew to an older age and less often had severe acute malnutrition, severe sepsis, diarrhea, severe pneumonia, and anemia, compared to those who were not immunized (Table 1). Co-morbidities like hypoxemia, convulsion, and bacteremia were also comparable between the groups (Table 1). The case-fatality rate was also significantly lower among the children who were immunized than those who were not immunized (Table 1). After adjusting with potential confounders such as age, severe acute malnutrition, and severe sepsis using log-linear binomial regression analysis, immunization was found to be associated with a lower risk of diarrhea, severe pneumonia, anemia, and deaths (Table 2). Our sub-analysis found that from March 2015 to December 2017, 1,570 children received the PCV-10 and 257 did not receive the PCV-10. We also found that the risk of developing severe pneumonia (1054/1,570 [67%] vs. 202/257 [79%], p < 0.001) and case-fatality rate (57/1,570 [3.6%] vs. 19/257 [7.4%], p = 0.005) was still significantly lower among those who were immunized with PCV than those who did not receive this vaccine.
Table 2
| Parameters | RR | 95% CI | p-value |
|---|---|---|---|
| Age | 0.98 | 0.97–1.00 | 0.093 |
| Severe acute malnutrition | 0.97 | 0.79–1.20 | 0.783 |
| Severe sepsis | 0.98 | 0.71–1.38 | 0.914 |
| Diarrhea | 0.69 | 0.50–0.97 | 0.033 |
| Severe pneumonia | 0.60 | 0.44–0.80 | 0.001 |
| Anemia | 0.79 | 0.64–0.97 | 0.026 |
| Death | 0.67 | 0.46–0.97 | 0.035 |
Results of log-linear binomial regression analysis to understand the real impact of immunization among children from the age of 4 to 59 months hospitalized for pneumonia and severe pneumonia.
Discussion
Tremendous progress has been made over the last 20 years toward the development of an effective national immunization program throughout the world. The major contributor to this success is the EPI of the WHO usually implemented through UNICEF (20). It is not only associated with the reduction of disease burden but also the severity of the diseases and fatal outcomes. With the support of the GAVI Alliance (formerly known as the Global Alliance for Vaccines and Immunization), the Bangladesh government introduced the Hib and PCV-10 vaccines in the EPI schedule in 2009 and 2015, respectively, which were significant milestones for our nation. In order to understand the impact of the routine EPI vaccination by 4 months of age that includes the Hib and the PCV vaccines, we found that the vaccination was not only associated with a lower risk of morbidities but also with a lower risk of mortality, even after adjusting with potential confounders. In this study, we identified four main findings among the children from the age of 4 to 59 months who were immunized according to the EPI schedule, compared to those who were not immunized: these findings were significantly lower risk of deaths, severe pneumonia, anemia, and diarrhea.
The study's key observation was the significantly lower risk of mortality during hospitalization after immunization following the EPI schedule by 4 months of age. All the EPI vaccines either produced antibodies or activated immunologically competent cells through the stimulation of the body`s immune system and thus protected the children from vaccine-preventable diseases (21). However, all the children in our study had pneumonia with different severity and the significant reduction in deaths in these children may be attributed to the intake of Hib and PCV-10 vaccines, which were also consistent with previous observations (10, 22). Both vaccines effectively reduced the burden of pneumonia by targeting two of the most common bacterial etiologies (23). It is important to note that the PCV-10 vaccine was introduced in 2015, which was during our study period. The sub-analysis of the data during this specific period found that the children who were vaccinated with the PCV-10 also had a significantly lower risk of death, compared to those who did not receive the vaccine. This observation also bolsters the impact of PCV-10 in lowering deaths in the children in our study, which was also observed in a previous study (6, 9). PCV-10 had been documented to be safe and effective in reducing illnesses and deaths caused by Pneumococcus pneumoniae in numerous studies. In most high-income countries, PCV-10 was used routinely with a concomitant, and there was a substantial reduction of pneumococcal diseases, which is consistent with our study findings (24–26). Although we don`t have data on the use of empirical antibiotic therapy and effective vaccines against major pathogens causing pneumonia, we can still speculate that these might lead to a substantial reduction of mortality in our study population (7, 8).
Moreover, the heterogeneous impact of BCG in lowering deaths in children with pneumonia was also well recognized (27).
The observation of a lower risk of severe pneumonia among the immunized children, compared to the unimmunized children is also understandable. We have further identified that the children who received PCV-10 had a significantly lower risk of developing severe pneumonia, compared to those who did not receive the vaccine (21). The vaccination against pertussis might have a confounding effect in reducing pneumonia-related mortality among children who were vaccinated with PCV-10 (28, 29).
The observation of a lower risk of anemia among the immunized children, compared to the unimmunized children is really notable here. To our knowledge, this is the first study that identified the independent lower risk of anemia among immunized children. This might be the impact of an overall improved immunity potentially caused either by the production of antibodies or activation of immunologically competent cells through the stimulation of the body`s immune system among the vaccinated children (21). There was also a persistence of immunity in children who had the PCV vaccination as was observed in a previous study (30). The observation of a lower risk of diarrhea among the immunized children, compared to unimmunized children is also consistent with the previous study (31).
The main limitation of the study was its retrospective nature which potentially limited our ability to identify the association of other variables of interest. The lack of information on full vs. partial immunization was one of the limitations of our study. Another limitation was the lack of availability of 44% of information on immunization in the electronic database which led to a potential selection bias that might have evaded stronger associations. Another important limitation was that the impact of immunization in our analysis might be confounded by other WHO-recommended interventions such as antibiotics, oxygen therapy, and other routine care. The main strength of this study is the reasonably large sample from an electronic database that increases the reliability of our observation.
Conclusion
The results of our data suggested that the children from 4 to 59 months of age who were immunized according to the EPI schedule and hospitalized for pneumonia and severe pneumonia had significantly lower case-fatality-rate, compared to those who were not immunized. The immunized children also had a lower risk of developing severe pneumonia, anemia, and diarrhea than their contemporaries. The overall results underscored the importance of increasing the national immunization coverage as high as 100%, scrupulously following the EPI schedule in order to reduce morbidities and pneumonia-related mortality in children, especially in resource-constrained settings.
Statements
Data availability statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Ethics statement
The studies involving human participants were reviewed and approved by Ethical Review Committee. Written informed consent for participation was not required for this study in accordance with the national legislation and the institutional requirements.
Author contributions
Conceptualization: AS and MC; Formal analysis: AS and MC; Investigation: AR and MC; Methodology: AS, AR, KS, and MC; Supervision: AS and MC; Data collection, analysis, and interpretation: AS, AR, and MC; Writing—original draft: AS, AR, KS, FA, MS, SN, TA, FC, MS, MA, IP, HS, SI, LS, TA, and MC; Writing—review and editing: AS, AR, and MC. All authors contributed to the article and approved the submitted version.
Acknowledgments
We gratefully acknowledge core donors of icddr,b for their support and commitment to research efforts. icddr,b receives unrestricted support from the Government of the People's Republic of Bangladesh, Canada, Sweden, and the UK. We would like to express our sincere thanks to all clinical fellows, nurses, members of the feeding team, and cleaners of the hospital for their invaluable support and contribution to patient care.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
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Summary
Keywords
Bangladesh, children, immunization, pneumonia, hospitalization
Citation
Shahid ASMSB, Rahman AE, Shahunja KM, Afroze F, Sarmin M, Nuzhat S, Alam T, Chowdhury F, Sultana MS, Ackhter MM, Parvin I, Saha H, Islam SB, Shahrin L, Ahmed T and Chisti MJ (2023) Vaccination following the expanded programme on immunization schedule could help to reduce deaths in children under five hospitalized for pneumonia and severe pneumonia in a developing country. Front. Pediatr. 11:1054335. doi: 10.3389/fped.2023.1054335
Received
26 September 2022
Accepted
06 March 2023
Published
27 March 2023
Volume
11 - 2023
Edited by
Houdouin Veronique, Assistance Publique Hopitaux De Paris, France
Reviewed by
Montse Soriano Gabarro, Bayer, Germany Andrea Orsi, Università di Genova, Italy
Updates
Copyright
© 2023 Shahid, Rahman, Shahunja, Afroze, Sarmin, Nuzhat, Alam, Chowdhury, Sultana, Ackhter, Parvin, Saha, Islam, Shahrin, Ahmed and Chisti.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Mohammod Jobayer Chisti chisti@icddrb.org
Specialty Section: This article was submitted to Pediatric Pulmonology, a section of the journal Frontiers in Pediatrics
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.