Healthcare resource use and costs of managing children and adults with lysosomal acid lipase deficiency at a tertiary referral centre in the United Kingdom

PLoS One. 2018 Feb 2;13(2):e0191945. doi: 10.1371/journal.pone.0191945. eCollection 2018.

Abstract

Objective: To estimate clinical progression and resource utilisation together with the associated costs of managing children and adults with LAL Deficiency, at a tertiary referral centre in the UK.

Methods: A retrospective chart review was undertaken of patients in the UK with a confirmed diagnosis of LAL Deficiency who were managed at a LAL Deficiency tertiary referral treatment centre. Patients' pathways, treatment patterns, health outcomes and resource use were quantified over differing lengths of time for each patient enabling the NHS cost of patient management in tertiary care to be estimated.

Results: The study population comprised 19 patients of whom 58% were male. Mean age at the time of initial presentation was 15.5 years and the mean age at diagnosis was 18.0 years. 63%, 53% and 42% of patients had hepatomegaly, abnormal lipid storage and splenomegaly at a mean age of presentation of 17.8, 17.1 and 20.9 years, respectively. Over a period of 50 years there were a mean of 48.5 clinician visits and 3.4 hospital admissions per patient. The mean NHS cost of patient management at a LAL Deficiency tertiary referral treatment centre, spanning a period of over 50 years was £61,454 per patient.

Conclusion: This study provides important insights into a number of aspects of the disease that are difficult to ascertain from published case reports. Additionally, it provides the best estimate available of NHS resource use and costs with which to inform policy and budgetary decisions pertaining to managing this ultra-orphan disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Cost of Illness*
  • Female
  • Health Care Rationing*
  • Humans
  • Referral and Consultation*
  • Retrospective Studies
  • State Medicine
  • United Kingdom
  • Wolman Disease / economics
  • Wolman Disease / therapy*
  • Young Adult

Grants and funding

This study was part funded by Synageva Biopharma Corp, Lexington, MA, US, now part of Alexion Pharmaceuticals Inc., Cheshire, CT, US. However, the funders had no role in study design, data collection and analysis or preparation of the manuscript. The funders commissioned Catalyst Health Economics Consultants (Catalyst) to conduct the study. However, the funders did not provide support in the form of salaries for Catalyst employees.