Gastrointestinal manifestations in pediatric and adult patients with Rett syndrome: an analysis of US claims and physician survey data

Author:

May Damian M1ORCID,Neul Jeffrey2,Piña-Garza Jesús Eric3,Kponee-Shovein Kalé4,Satija Ambika4,Mahendran Malena5,Downes Nathaniel4,Sheng Kristy6,Lema Neema6,Boca Andra4,Lefebvre Patrick5,Abler Victor1,Youakim James M1,Cheng Wendy Y4

Affiliation:

1. Acadia Pharmaceuticals Inc., San Diego, CA 92130, USA

2. Vanderbilt University Medical Center, Nashville, TN 37232, USA

3. Centennial Children's Hospital, Nashville, TN 37203, USA

4. Analysis Group, Inc., Boston, MA 02199, USA

5. Analysis Group, Inc., Montréal, H3B 0G7, Canada

6. Analysis Group, Inc., Menlo Park, CA 94025, USA

Abstract

Aim: Patients with Rett syndrome (RTT) experience gastrointestinal (GI) manifestations. This study aimed to describe the prevalence of GI manifestations and the associated medical costs in patients with RTT in the USA. Patients & Methods: The study combined an insurance claims database analysis with a survey of 100 physicians experienced in RTT management. Results: GI manifestations affected 43.0% of 5940 patients, with increased prevalence in pediatric patients (45.6%) relative to adult patients (40.2%). Annualized mean medical cost of managing GI manifestations was $4473. Only 5.9–8.2% of neurologists and pediatricians ranked GI symptom management among the five most important treatment goals. Conclusion: Patients with RTT experience a high burden of GI manifestations, which translate to considerable medical costs. Importantly, the prevalence of GI manifestations was likely underestimated in this study, as only those symptoms which resulted in a healthcare encounter were captured.

Publisher

Becaris Publishing Limited

Subject

Health Policy

Reference17 articles.

1. National Institutes of Health (Nih). Rett Syndrome Fact Sheet (2022). www.ninds.nih.gov/health-information/patient-caregiver-education/fact-sheets/rett-syndrome-fact-sheet

2. Rett syndrome: insights into genetic, molecular and circuit mechanisms;Ip JPK;Nat. Rev. Neurosci.,2018

3. Twenty years of surveillance in Rett syndrome: what does this tell us?;Anderson A;Orphanet. J. Rare Dis.,2014

4. The changing face of survival in Rett syndrome and MECP2-related disorders;Tarquinio DC;Pediatr. Neurol.,2015

5. Survival with Rett syndrome: comparing Rett's original sample with data from the Australian Rett Syndrome Database;Freilinger M;Dev. Med. Child Neurol.,2010

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