Cost effectiveness of pediatric pneumococcal conjugate vaccines: a comparative assessment of decision-making tools

Nathorn Chaiyakunapruk1, Ratchadaporn Somkrua, Raymond Hutubessy

  • 1Center of Pharmaceutical Outcomes Research, Faculty of Pharmaceutical Sciences, Naresuan University, Phitsanulok, Thailand.

BMC Medicine
|May 17, 2011
PubMed

Insights

This study compared cost-effectiveness tools for pneumococcal conjugate vaccine (PCV) adoption. Understanding these tools aids policymakers in making informed decisions for national immunization programs.

Area of Science:

  • Health Economics
  • Vaccine Policy
  • Decision Science

Background:

  • Numerous decision support tools exist for pneumococcal conjugate vaccine (PCV) adoption in national immunization programs.
  • A critical appraisal of these tools is lacking, hindering informed decision-making by policymakers.
  • This study aimed to guide policymakers by comparing available PCV decision-making tools.

Purpose of the Study:

  • To critically assess and compare publicly available cost-effectiveness (CE) tools for PCV adoption.
  • To analyze the methods, influential parameters, and results of these CE tools.
  • To provide guidance for policymakers on the optimal use of these decision-making tools.

Main Methods:

  • The World Health Organization (WHO) accessed publicly available CE tools for PCV.
  • Tools were critically assessed using the WHO's guide for economic evaluations of immunization programs.
  • Sensitivity analyses were performed, and results were compared using standardized input parameters.

Main Results:

  • Three CE tools were compared: PAHO ProVac Initiative TriVac, PneumoADIP (cohort-based), and GlaxoSmithKline's SUPREMES (population-based).
  • Models differed in structure and data requirements but covered similar diseases; herd effects varied.
  • Key drivers identified were vaccine efficacy, price, coverage, serotype coverage, and disease burden.

Conclusions:

  • Vaccine cost, efficacy, and disease epidemiology significantly influence CE model outcomes.
  • Comparing CE tools enhances transparency and aids policymakers in efficient decision-making for PCV adoption.
  • Standardized data sets and adherence to WHO guidelines improve the utility of these tools for research and policy.
Abstract

Related Concept Videos

Impact of Pharmacokinetic–Pharmacodynamic Models: Regulatory Decisions01:15

Impact of Pharmacokinetic–Pharmacodynamic Models: Regulatory Decisions

PK–PD modeling has significantly influenced FDA regulatory decisions, particularly drug approval, dosage optimization, and labeling. These models integrate pharmacokinetics (PK) and pharmacodynamics (PD) to predict drug behavior and effects, aiding in optimizing dosing regimens and enhancing the probability of clinical trial success.One notable example is Nesiritide (Natrecor®), a recombinant human brain natriuretic peptide for treating acute decompensated congestive heart failure (CHF).
Pharmacokinetic Models: Comparison and Selection Criterion01:26

Pharmacokinetic Models: Comparison and Selection Criterion

Physiological and compartmental models are valuable tools used in studying biological systems. These models rely on differential equations to maintain mass balance within the system, ensuring an accurate representation of the dynamic processes at play.
Physiological models take a detailed approach by considering specific molecular processes. They can predict drug distribution, metabolism, and elimination changes, providing a comprehensive understanding of how drugs interact with the body.
Drug Dosing: Infants and Children01:29

Drug Dosing: Infants and Children

Pediatric patient dosages diverge from adults due to disparities in body surface area, total body water, and extracellular fluid per kilogram of body weight. The dosing regimen considers the variations in pharmacokinetics and pharmacology across distinct age groups, encompassing preterm newborns, infants, young children, older children, and adolescents. Calculation of pediatric patient doses is predicated on determining body surface area, which exhibits a superior correlation with the child's...
Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches01:23

Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches

Biopharmaceutical studies constitute a vital field aiming to enhance drug delivery methods and refine therapeutic approaches, drawing upon diverse interdisciplinary knowledge. In research methodologies, the choice between controlled and non-controlled studies significantly influences the study's reliability and accuracy.
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast, controlled...
Pneumonia III: Complications and Assessment01:30

Pneumonia III: Complications and Assessment

Pneumonia poses the potential for numerous complications that warrant consideration. These complications include the following:
Decision Making: P-value Method01:09

Decision Making: P-value Method

The process of hypothesis testing based on the P-value method includes calculating the P- value using the sample data and interpreting it.
First, a specific claim about the population parameter is proposed. The claim is based on the research question and is stated in a simple form. Further, an opposing statement to the claim  is also stated. These statements can act as null and alternative hypotheses:  a null hypothesis would be a neutral statement while the alternative hypothesis can have a...