Global PARITY: Study Design for a Multi-Centered, International Point Prevalence Study to Estimate the Burden of

Qalab Abbas1, Adrian Holloway2, Paula Caporal3,4

  • 1Department of Pediatrics and Child Health, Aga Khan University Karachi, Karachi, Pakistan.

Frontiers in Pediatrics
|February 14, 2022
PubMed

Insights

This study investigates pediatric critical illness in resource-limited settings (RLS), revealing crucial data on prevalence, causes, and resource use to improve child healthcare outcomes globally.

Area of Science:

  • Global Health
  • Pediatric Critical Care
  • Epidemiology

Background:

  • The burden of pediatric critical illness and resource utilization in resource-limited settings (RLS) remains largely unknown.
  • Lack of specific data hinders the development of evidence-based interventions for pediatric critical care in RLS.
  • This study aims to determine the prevalence, etiology, outcomes, and resource utilization of pediatric critical illness in RLS globally.

Purpose of the Study:

  • To address the significant knowledge gap in pediatric critical illness within RLS.
  • To provide data on the prevalence, causes, and hospital outcomes of critically ill children in RLS.
  • To inform the allocation of limited resources and guide clinical management decisions.

Main Methods:

  • A prospective, observational, multicenter, multinational point prevalence study across 61 hospitals in RLS.
  • Enrolled children aged 29 days to 14 years presenting with acute illness or injury.
  • Collected data on critical illness prevalence, etiology, resource utilization, and hospital outcomes over 12 months with four sampling points.

Main Results:

  • The study is expected to quantify the prevalence and characteristics of pediatric critical illness in diverse RLS.
  • It will identify common etiologies and patterns of resource utilization for critically ill children.
  • Data on hospital outcomes, including mortality and length of stay, will be generated.

Conclusions:

  • This research will fill a critical gap in understanding pediatric critical illness in RLS.
  • The findings are essential for informing future research and improving clinical management.
  • The study aims to enhance global pediatric hospital outcomes through evidence-based strategies.
Abstract

Related Concept Videos

Study Designs in Epidemiology01:20

Study Designs in Epidemiology

Epidemiological study designs are fundamental tools for investigating the distribution, determinants, and control of health conditions in populations. They help researchers understand the relationships between exposures and outcomes, and they broadly fall into two categories: "observational" and "experimental" studies.
Observational studies are those where the researcher does not intervene but rather observes natural variations. They include cross-sectional, cohort, and...
475
Bioavailability Study Design: Healthy Subjects Versus Patients01:15

Bioavailability Study Design: Healthy Subjects Versus Patients

Bioavailability studies are essential for evaluating a drug's therapeutic efficacy and understanding its absorption patterns under various physiological conditions. Conducting such studies on target patient populations provides more relevant data by simulating real-world disease states. However, practical challenges often necessitate the use of young, healthy adult volunteers as study subjects.Patients may exhibit altered drug absorption patterns due to the effects of the disease itself,...
8
Bioequivalence Experimental Study Designs: Repeated Measures, Cross-Over, Carry-Over, and Latin Square Designs01:15

Bioequivalence Experimental Study Designs: Repeated Measures, Cross-Over, Carry-Over, and Latin Square Designs

Body:Bioequivalence experimental study designs play a pivotal role in testing the effectiveness of various treatments. Key among these are the repeated measures, cross-over, carry-over, and Latin square designs. In the repeated measures design, each subject receives all treatments, allowing for temporal comparisons. This type of design is useful in reducing variability but requires careful planning to avoid bias.The cross-over design, an economical method, involves sequential administration of...
6
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,...
190
Bioavailability Study Design: Single Versus Multiple Dose Studies01:11

Bioavailability Study Design: Single Versus Multiple Dose Studies

Bioavailability studies are essential for understanding how a drug is absorbed, distributed, metabolized, and excreted in the body. These studies assess the extent and rate at which the active pharmaceutical agent becomes available at the site of action. The design of bioavailability studies can involve single-dose or multiple-dose regimens, each with distinct advantages and limitations.Single-dose studies are the preferred approach due to their simplicity and reduced drug exposure for...
5
Observational Studies01:11

Observational Studies

Observational studies are a type of analytical study where researchers observe events without any interventions. In other words, the researcher does not influence the response variable or the experiment's outcome.
There are three types of observational studies – Prospective, retrospective, and cross-sectional.
Prospective Study
Prospective studies, also known as longitudinal or cohort studies, are carried out by collecting future data from groups sharing similar characteristics. One...
9.9K