Abstract

BackgroundThe “Primary Immunodeficiencies (PIDs) principles of care” were published in 2014 as the gold standard for care of patients with PIDs, setting a common goal for stakeholders to ensure that patients with PID have access to appropriate care and good quality of life. Since then, IPOPI (the International Patient Organisation for Primary Immunodeficiencies), has been working with national PID patient organisations as well as collaborating with scientific and medical institutions and experts to bring these principles closer to the day-to-day life of individuals with PIDs.MethodThe six PID Principles of Care were revised to consider advances in the field, as well as political developments that had occurred after their initial publication in 2014. Based on this revision the list was updated, and a new principle was added. The six established principles were: diagnosis, treatment, universal health coverage, specialised centres, national patient organisations and registries. Each principle was structured and measured through a series of criteria, and was given the same weight, as they have been considered to all be equally important. Specific weights were attributed to the criteria depending on their relevance and importance to quantify the principle. The index was translated into a survey for data collection: initially involving data from selected countries for a pilot, followed by integration of data from IPOPI’s national member organisations and key countries.ResultsThe PID Life Index was developed in 2020 to assess the status of the PID environment and the implementation of the 6 principles worldwide. The Index allows for benchmarking countries either according to a set of principles and criteria or based on the user’s preferences. This can be displayed in an interactive map or through a data visualisation system.ConclusionThe PID Life Index has been developed successfully and has potential to become an important source of information for PID stakeholders, to increase awareness and information as well as support advocacy initiatives on PIDs nationally, regionally or globally.

Highlights

  • The “Primary Immunodeficiencies (PIDs) principles of care” were published in 2014 as the gold standard for care of patients with Primary immunodeficiencies (PIDs), setting a common goal for stakeholders to ensure that patients with PID have access to appropriate care and good quality of life

  • The PID Life Index has been developed successfully and has potential to become an important source of information for PID stakeholders, to increase awareness and information as well as support advocacy initiatives on PIDs nationally, regionally or globally

  • The data were fed into the PID Life Index database, allowing for the creation of the PID Life Index

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Summary

Introduction

The “Primary Immunodeficiencies (PIDs) principles of care” were published in 2014 as the gold standard for care of patients with PIDs, setting a common goal for stakeholders to ensure that patients with PID have access to appropriate care and good quality of life. Given the complexity and wide range of components of the immune system involved for the different types of PIDs, the diagnosis and management of these diseases are complex and require experienced medical specialists in this specific field [1]. The paper incorporated the views of medical experts from all the continents, as well as nurses and patient representatives from IPOPI (the International Patient Organisation for Primary Immunodeficiencies) Together they called for the implementation of these principles, as elements of PID care provision that should be available and implemented in each country. The gold-standard framework for care and management of PIDs included six principles of care that IPOPI promoted amongst its national member organisations to support their implementation

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