Impact of Pediatric Dermatologic Conditions on Child and Parent Quality of Life

Mildred Min1, Jasminder K Malhi2, Cindy J Chambers1

  • 1Dermatology, California Northstate University College of Medicine, Elk Grove, USA.

Cureus
|August 21, 2023
PubMed

Insights

Parents of children with skin conditions experience greater quality of life impairment than their children. This study highlights the significant psychosocial impact of pediatric dermatoses on families, emphasizing the need for comprehensive support.

Area of Science:

  • Pediatric Dermatology
  • Psychosocial Impact of Diseases
  • Quality of Life Research

Background:

  • Dermatologic conditions significantly affect the well-being of pediatric patients and their families.
  • Understanding the psychosocial burden of childhood skin diseases is crucial for effective management.
  • Previous research indicates a link between dermatoses and reduced quality of life.

Purpose of the Study:

  • To investigate the relationship between child and parent quality of life in pediatric dermatologic conditions.
  • To quantify the psychosocial impact of various skin diseases on patients and their caregivers.
  • To identify specific dermatoses that disproportionately affect family quality of life.

Main Methods:

  • A cross-sectional study involving 100 pediatric patients (aged 7-18) and 98 parents.
  • Data collected at the Pacific Skin Institute between November 2020 and January 2022.
  • Utilized the Children's Dermatology Life Quality Index (CDLQI) and Family Dermatology Life Quality Index (FDLQI) for assessment.

Main Results:

  • Family Dermatology Life Quality Index (FDLQI) scores were higher than Children's Dermatology Life Quality Index (CDLQI) scores across most dermatoses.
  • Acne vulgaris was the exception, with higher CDLQI scores (9.2) than FDLQI scores (8.8).
  • Psoriasis showed the largest disparity, with significantly higher FDLQI scores (10.4) compared to CDLQI scores (5.9).

Conclusions:

  • Parents of children with dermatologic conditions generally experience a greater negative impact on their quality of life.
  • Parental burden may stem from extensive involvement in condition management and associated costs.
  • Clinical practice should adopt a more holistic approach, expanding resources for both pediatric patients and their families.

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