Related Experiment Video
Updated: Jan 28, 2026

Preparation and Pathogen Inactivation of Double Dose Buffy Coat Platelet Products using the INTERCEPT Blood System
Published on: December 7, 2012
Protocol for a systematic review and meta-analysis of fractional dose compared with standard dose inactivated polio
Thandiwe Runyararo Mashunye1, Duduzile Edith Ndwandwe2, Kopano Rebaona Dube2
1Department of Epidemiology and Biostatistics, School of Public Health and Family Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, Western Cape, South Africa.
Insights
Fractional inactivated polio vaccine (IPV) doses offer a viable strategy to address global IPV shortages. This review compares fractional IPV doses against standard doses to inform vaccination policies and improve access.
Area of Science:
- Public Health
- Vaccinology
- Epidemiology
Background:
- The World Health Organization (WHO) recommends inactivated polio vaccine (IPV) in routine immunization schedules.
- Global demand for IPV has led to significant supply shortages worldwide.
- Fractional dosing is being explored as a strategy to increase vaccine availability.
Purpose of the Study:
- To compare the efficacy and safety of fractional doses of IPV versus standard full doses.
- To provide evidence for decision-making regarding IPV dosage strategies.
- To inform policies aimed at improving global access to IPV.
Main Methods:
- Systematic review and meta-analysis of randomized trials, non-randomized trials, case-control, and cohort studies.
- Inclusion of studies comparing fractional versus full IPV doses in children aged 5 years or younger.
- Data extraction and risk of bias assessment by two independent reviewers, with stratified and sensitivity analyses.
Main Results:
- The review will pool outcome data using random-effects meta-analyses for each poliovirus type.
- Heterogeneity will be assessed and investigated through subgroup and sensitivity analyses.
- Findings will be stratified by study design, poliovirus type, outcome measure, and number of doses administered.
Conclusions:
- The findings will guide decisions on IPV dosage, potentially improving vaccine accessibility.
- Stretching vaccine supplies through fractional dosing can help mitigate global shortages.
- Results will be disseminated through publication in a peer-reviewed journal and the University of Cape Town online library.
Introduction:
WHO recommends the introduction of at least one single dose of inactivated polio vaccine (IPV) in routine immunisation schedules. Thus, there has been an increased demand and concurrent supply shortages of IPV worldwide. One of the strategies to improve access is the use of fractional instead of full doses of IPV. We aim to compare the effects of fractional with standard doses of IPV.
Methods And Analysis:
We will include randomised trials, non-randomised trials, case-control studies and cohort studies that compared fractional with full doses of IPV among children aged 5 years or younger. We will search for eligible studies among published and grey literature. Two authors will independently screen the results of the search, select studies, extract data and assess risk of bias. We will stratify analyses by study design, type of poliovirus, type of outcome measure and number of IPV doses given. For each type of poliovirus, we will pool the outcome data from studies using random-effects meta-analyses. Statistical heterogeneity will be assessed using the χ2 test of homogeneity and quantified using the I2 statistic. To investigate statistical heterogeneity, subgroup analyses will be performed based on the timing of the first fractional dose, age of administration, immunisation schedules and country income status. Sensitivity analyses will be used to assess if the effect of IPV fractional dosing is affected by study design, risk of bias and methods of meta-analysis.
Ethics And Dissemination:
We obtained approval from the University of Cape Town Human Research Ethics Committee (HREC REF: 412/2018). The findings of this review will provide evidence for decision-making with regards to IPV dosage, eventually improving access to the vaccine by stretching vaccine supplies. The results will be published in the University of Cape Town online library and in a peer reviewed journal.
Prospero Registration Number:
CRD42018092647.
More Related Videos
09:37Detection of Polyfunctional T Cells in Children Vaccinated with Japanese Encephalitis Vaccine via the Flow Cytometry Technique
Published on: September 23, 2022
06:20Irradiator Commissioning and Dosimetry for Assessment of LQ α and β Parameters, Radiation Dosing Schema, and in vivo Dose Deposition
Published on: March 11, 2021
Related Concept Videos
Drug Dosing: Infants and Children
Dose Size and Dosing Frequency: Determination Methods
Determination of Multiple Dosing Parameters: Loading and Maintenance Doses
Rational Dosage Regimen: Maintenance Dose and Loading Dose
In most cases, drugs are administered repetitively or infused continuously to maintain a steady-state concentration in the body. At a steady...
Dose-Response Relationship: Overview
Drug Dosing: Geriatric Patients