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Pneumococcal pneumonia and carriage in Africa before and after introduction of pneumococcal conjugate vaccines, 2000–2019: protocol for systematic review
  1. Newton L. Kalata1,
  2. Tinashe K. Nyazika1,2,
  3. Todd D. Swarthout1,
  4. Dean Everett1,3,
  5. Neil French1,4,
  6. Robert S. Heyderman1,5,
  7. Stephen B. Gordon1,2,
  8. Kondwani C. Jambo1,2
  1. 1Malawi-Liverpool-Wellcome Trust Clinical Research Programme, University of Malawi College of Medicine, Blantyre, Malawi
  2. 2Department of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK
  3. 3The Queens Medical Research Institute, University of Edinburgh, Edinburgh, UK
  4. 4Centre for Global Vaccine Research, Institute of Infection and Global Health, Liverpool, UK
  5. 5Division of Infection and Immunity, University College London, London, UK
  1. Correspondence to Mr Tinashe K. Nyazika; tknyazika{at}gmail.com

Abstract

Introduction Africa harbours a high burden of pneumococcal disease, with associated high mortality rates. Despite 34 countries introducing the pneumococcal conjugate vaccine, which reduces the risk of pneumococcal carriage (a prerequisite for disease) of some of the most pathogenic pneumococcal serotypes, it remains uncertain whether they will achieve the sustained direct or indirect protection necessary to reduce pneumococcal carriage to levels sufficient to interrupt transmission and disease. We will therefore summarise the available data on the impact of the pneumococcal conjugate vaccine in reducing vaccine serotype carriage and pneumococcal pneumonia in Africa between 2000 and 2019.

Methods and analysis Using a predetermined search strategy, we will conduct a comprehensive search of PubMed, MEDLINE database, the Excerpta Medica Database, the ISI Web of Science (Science Citation Index), Scopus and the African Index Medicus to identify published studies reporting the prevalence of Streptococcus pneumoniae carriage (vaccine type and non-vaccine type), incidence rates of pneumococcal pneumonia and mortality among children, adults and HIV-infected (all-ages) pre-pneumococcal conjugate vaccine (PCV) and post-PCV introduction (published between 1st January 2000 and 31st December 2019) in African countries that have introduced PCVs (PCV7/PCV10/PCV13) in their routine national immunisation programme. The studies retained and data extracted will be assessed for bias using prevalidated tools and checklists. Heterogeneity across studies will be assessed using the χ2 test on Cochrane Q statistic. A random effect meta-analysis will be used to estimate the overall prevalence of pneumococcal carriage and incidence of pneumococcal pneumonia across studies with similar characteristics. Results will be reported in compliance with the Meta-Analysis Of Observational Studies in Epidemiology guidelines. The protocol has been prepared in accordance to the 2015 guidelines on Preferred Reporting Items for Systematic Reviews and Meta-Analyses.

Ethics and dissemination This systematic review will not require ethical approval as we will be using already published data. The final manuscript will be submitted for publication in a peer-reviewed journal and presented at conferences.

PROSPERO registration number CRD42019130976.

  • Streptococcus pneumoniae
  • Carriage
  • Pneumococcal conjugate vaccine
  • Pneumococcal pneumonia
  • mortality
  • Africa

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Strengths and limitations of this study

  • To the best of our knowledge, this study will be the first systematic review that will comprehensively compare and explore the impact of pneumococcal conjugate vaccine (PCV) on carriage, pneumococcal pneumonia (invasive and non-invasive) and mortality associated with the disease prevaccine and postvaccine introduction in adults and other at risk groups living in Africa.

  • Small number of studies eligible across regions could impact the quality of our estimates.

  • Presence of high heterogeneity across studies, particularly in countries where PCV7, PCV10 or PCV13 were in use around the same time and were serotyping was only done for vaccine-type pneumococcal strains.

Introduction

Streptococcus pneumoniae (‘the pneumococcus’) is a common coloniser of the nasopharynx and a major cause of morbidity and mortality among children under the age of 5 years worldwide.1 2 High rates of pneumococcal disease are found in Africa and other low-income and middle-income countries, which harbour an accumulation of factors conducive for high and persistent pneumococcal carriage and transmission including, high-density living conditions, poverty and high HIV seroprevalence.3–5In 2015, pneumococcal pneumonia accounted for 55.4% (95% uncertainty interval: 31.5–79.1) of lower respiratory deaths in all ages.1 Implementation of treatment strategies, which focus on early detection and antimicrobial therapy of suspected pneumonia cases, has been difficult in Africa.6 Therefore, introduction of an effective vaccine against pneumococcal carriage for children is crucial in this region as carriage is a prerequisite for disease.

With support from Gavi (the Vaccine Alliance), 34 African countries introduced the pneumococcal conjugate vaccines (PCV7/PCV10/PCV13) into their extended immunisation programmes between 2009 and 20157 8 in line with WHO recommendations.9 These vaccines have been shown to be highly effective in reducing both incidence of pneumococcal disease and prevalence of carriage by some of the most pathogenic of the 97 known pneumococcal serotypes.10 Furthermore, the vaccine indirectly protects the PCV-unvaccinated population against pneumococcal carriage and disease by reducing pneumococcal transmission from PCV-vaccinated children who are at greater risk of carriage and, therefore, sources of transmission.2 11–13 However, PCV’s indirect protection on other high-risk populations (including HIV-infected individuals) remains to be seen in Africa.11 14 Studies conducted in Africa have demonstrated high nasopharyngeal carriage of pneumococcus among the HIV-infected adults on antiretroviral therapy (ART), with estimated point prevalence ranging between 40% and 80%.12 15 Therefore, it remains uncertain whether the introduction of PCV in Africa will achieve the sustained direct or indirect protection necessary to reduce pneumococcal carriage to levels sufficient to interrupt transmission and disease.16

Systematic reviews that have been done so far on the impact of PCV in Africa have focused on carriage and clinical pneumonia endpoints in children.17 18 None have summarised these data in the adult or important at-risk populations like HIV-infected individuals. We therefore plan to synthesise the available published data and update the evidence on the impact of the PCV introduction on pneumococcal carriage, pneumococcal pneumonia and associated mortality in Africa between 2000 and 2019.

Objectives

General objectives

1. To summarise available data on the impact of the PCV on the prevalence of pneumococcal carriage (vaccine type - VT and non-vaccine type - NVT) and its impact on pneumococcal pneumonia and associated mortality in Africa between 2000 and 2019.

Specific objectives

Using data published between 2000 and 2019, this review will assess the impact of PCV by:

  1. Comparing the trend in pneumococcal carriage prevalence in Africa before and after PCV introduction.

  2. Comparing the trends in the incidence and/or prevalence of pneumococcal pneumonia (invasive and non-invasive) in Africa before and after PCV introduction.

  3. Estimating the mortality associated with pneumococcal pneumonia in Africa.

Methods

​Information sources, search strategy and study identification

We will conduct a comprehensive literature search in PubMed, MEDLINE database, the Excerpta Medica Database, the ISI Web of Science (Science Citation Index), Scopus and the African Index Medicus to identify all studies published between 1st January 2000 to 31st December 2019, meeting our inclusion and exclusion criteria using the literature search strategy outlined in table 1. Using a structured screening guide, we will screen the reference lists for eligible articles and relevant reviews as well as conference abstracts to identify additional sources of information. Search results will be compiled and managed using the EndNote X9 citation software.

Table 1

Search strategy

​Eligibility criteria of relevant studies

​Inclusion criteria

Population

Children (0–15 years), adults (15–64 years), the elderly (>65 years) and HIV-infected individuals (all ages) residing in African countries.

Intervention

PCVs (PCV 7, PCV10 and PCV13) introduction into the country’s routine infant immunisation programmes.

Comparators

Ten-year period (2000–2010) before PCV introduction versus 10-year period (2011–2019) after PCV introduction.

Outcomes

Percentage difference in the pooled point prevalence of pneumococcal carriage post when compared with pre-PCV introduction; adjusted prevalence ratios in the pooled prevalence of pneumococcal pneumonia between post-PCV and pre-PCV introduction; and adjusted mortality rate ratios for post-PCV and pre-PCV introduction.

Type of studies

We will include randomised control trials, non-randomised trials and observational studies reporting prevalence of pneumococcal carriage and/or incidence rates for disease and/or deaths and were published between 1st January 2000 and 31st December 2019 without language restriction.

Serotyping methods

For pneumococcal carriage, identification and serotyping of S. pneumoniae must be from a pernasal swab using culture (as per WHO guidelines,19 PCR (lyt-A gene amplification), microarray or based on whole genome sequencing (WGS).

Pneumococcal pneumonia

For a pneumococcal pneumonia diagnosis among adults, a minimum of either (1) symptoms consistent with an acute chest infection (at least cough or dyspnoea) or (2) new infiltrates on radiograph and (3) pneumococcal antigen detection in either blood, urine or pleural fluid. For children (1–15 years), the case definition is the criteria for adults plus symptoms of fast breathing, chest-indrawing and nasal flaring. These definitions have been adopted in order to increase the specificity of identifying pneumococcal pneumonia but are limited in their sensitivity.

​Study exclusion criteria

  1. Any study reporting impact data of vaccines within 12 months of PCV introduction into routine extended programme of immunisation and data reported in such a way that impact cannot be defined without data from within 12 months of PCV introduction.

  2. Studies with small sample size (less than 50 participants), letters, commentaries, narratives and editorials, will be excluded as they are likely to have biased estimates, and this could affect our estimates.

  3. Studies that did not distinguish between pre-PCV and post-PCV introduction periods in the data presented.

​Data extraction

Three independent reviewers (NLK, TKN and TDS) will assess the articles for inclusion based on a predetermined inclusion and exclusion criteria. Those included after initial screening will be further evaluated for methodological quality and presence of bias. Discordance will be resolved by discussion between reviewers to reach consensus or by a fourth member of the team (KJ). All articles retrieved will be stored and managed using Endnote X9 throughout the review process. A standardised data extraction form designed specifically for each outcome of interest, will be used to collect information on the following parameters:

  1. Study identification: name of first author, year of publication, year of participant inclusion, country, type of publication, language of publication.

  2. Study characteristics: study design (eg, cross-sectional, cohort, case control, clinical trial), setting (hospital, outpatient, population, institution (eg, school or care facility), urban/rural), period of surveillance/recruitment, sample size, age (mean or median, range), proportion of HIV-infected participants and method of confirmation (if any), proportion on ART (if any), proportion PCV-vaccinated (if any), proportion with natural pneumococcal carriage (VT, NVT, total), diagnostic method for pneumococcal carriage detection and serotyping (culture, PCR, DNA microarray, WGS), diagnostic criteria for pneumococcal pneumonia, duration of follow-up for cohort studies and mortality rates.

  3. Epidemiological estimates of pneumococcal carriage: prevalence of VT and NVT carriage.

  4. Epidemiological estimates for pneumococcal pneumonia: prevalence and/or incidence of pneumococcal pneumonia and/or mortality in all subpopulations, where reported (infants below age of 1 year, children 1–4 years, children 5–15 years and adults 16+years), the elderly and HIV infected. When estimates are not available or cannot be computed, the corresponding authors will be contacted to request for any missing information of these estimates.

​Appraisal of quality of reporting and the risk of bias

We will assess the quality of reporting of the studies using either the Strengthening the Reporting of Observational studies in Epidemiology or the Consolidated Standards of Reporting Trials checklist depending on the nature of the study (observational study or clinical trial).20–22

We will use the 10-item risk of bias tool for prevalence studies developed by Hoy et al23 to assess the risk of bias for all the studies included using the full text publications. Bias risk scores will be presented in a table and inter-rater agreement will be assessed using a weighted Cohen’s kappa statistic.24 25

​Data analyses and reporting

We will use the metaprop command provided within the STATA software V.15 to analyse the data.26 Heterogeneity of studies with similar study characteristics will be evaluated by the χ2 test on Cochrane’s Q statistic27 and quantified using I2 values assuming that I2 of 25%, 50% and 75% represent low, medium and high heterogeneity, respectively.28 Study-specific estimates will be pooled through a random effect meta-analysis to obtain an overall summary estimate of the prevalence of S. pneumoniae carriage, incidence of pneumococcal pneumonia and mortality after stabilising the variance of individual studies using the Freeman-Tukey double arcsine transformation.29 For impact of PCV on carriage, the percentage change in point prevalence will be calculated to compare pooled prevalence estimates in the before and after PCV introduction periods. Mortality rate ratios will be calculated to compare pooled mortality rates for the periods before and after PCV introduction. Meta-analysis results will be presented on a forest plot. Visual analysis of funnel plot and Egger’s test will be done to detect small study effect.30 31 All tests will be two-sided and statistical significance will be defined as p<0.05. In case of marked heterogeneity, a descriptive analysis will be done instead of a meta-analysis.

We will report our results according to the Meta-Analysis Of Observational Studies in Epidemiology guidelines.32 The process with which studies were selected will be summarised using a flow diagram. Reasons for study exclusion will be described and quantitative data will be presented in summary tables and graphs (for trends) where appropriate.

​Ethics and dissemination

This systematic review will not require ethical approval as we will be using already published data. The findings will be summarised in a manuscript and submitted in peer-reviewed journals and presented at relevant conferences.

​Patient and public involvement

This systematic review will use published scientific data and will not involve patients or members of the public.

Acknowledgments

The Malawi-Liverpool-Wellcome Trust Clinical Research Programme (MLW) receives a strategic grant from the Wellcome Trust (UK).

References

Footnotes

  • NLK and TKN are joint first authors.

  • NLK and TKN contributed equally.

  • Contributors NLK, TKN, KJ and TDS conceived the study and drafted the manuscript. The manuscript was revised by DE, SBG, NF, RSH and KJ. All authors approved the final version of the manuscript. TKN is the guarantor of the manuscript.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Patient consent for publication Not required.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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