Quantifying the Impact of Acute Hepatic Porphyria on Well-Being via Patient-Reported Outcomes: Results from the Porphyria Worldwide Patient Experience Research (POWER) Study

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Publication Details

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JIMD Reports

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October 2022

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Author(s)

Amy Dickey1, Kristen Wheeden2, Desiree Lyon2, Sue Burrell3, Sean Hegarty3, Rocco Falchetto4, Edrin R Williams2, Jasmin Barman-Aksözen4 5, Marc DeCongelio6, Alison Bulkley6, Joana E Matos7, Tarek Mnif8, Jordanna Mora9, John J Ko9, Stephen Meninger9, Stephen Lombardelli10, Danielle Nance11

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Affiliations

Affiliations

1Division of Pulmonary and Critical Care Medicine, Department of Medicine Massachusetts General Hospital Boston Massachusetts USA; 2American Porphyria Foundation Bethesda Maryland USA; 3Global Porphyria Advocacy Coalition Durham City UK; 4Swiss Society for Porphyria Zürich Switzerland; 5Institute of Laboratory Medicine, Department of Medical Institutes Stadtspital Zürich, Triemli Zürich Switzerland; 6Cerner Enviza (formerly Kantar Health) New York New York USA; 7Cerner Enviza (formerly Kantar Health) Kansas City Missouri USA; 8Cerner Enviza (formerly Kantar Health) Paris France; 9Alnylam Pharmaceuticals Cambridge Massachusetts USA; 10Alnylam Pharmaceuticals Maidenhead UK; 11Banner Health Gilbert Arizona USA

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abstract

Abstract

Acute hepatic porphyria (AHP) is a group of rare genetic diseases of heme biosynthesis resulting in severe neurovisceral attacks and chronic complications that negatively impact patients' well-being. This study evaluated the impacts of AHP on patients' physical and emotional health from a global perspective. Adult patients from the United States, Italy, Spain, Australia, Mexico, and Brazil with AHP with >1 porphyria attack within the past 2 years or receiving intravenous hemin and/or glucose for attack prevention completed an online survey assessing demographics, health characteristics, and patient-reported outcomes. Results were analyzed collectively and by patient subgroups. Ninety-two patients with AHP across the six countries completed the survey. More than 70% of patients reported that their physical, emotional, and financial health was fair or poor. Among patients who reported pain, fatigue, and muscle weakness, 94.3%, 95.6%, and 91.4%, respectively, reported that these symptoms limited daily activities. Moderate to severe depression was present in 58.7% of patients, and moderate to severe anxiety in 48.9% of patients. Of the 47% of patients who were employed, 36.8% reported loss in productivity while at work. Among patients, 85.9% reported that they had to change or modify goals that were important to them because of AHP. Aside from differences in healthcare utilization and pain severity, scores did not significantly vary with attack rate or use of hemin or glucose prophylactic treatments. AHP substantially impacts patients' physical and emotional well-being, regardless of hemin or glucose prophylactic treatment or frequency of attacks. This multinational study demonstrates that there is substantial disease burden for patients with AHP, even among those experiencing sporadic attacks or using prophylactic treatment.

Conclusions:

These multinational results demonstrate that AHP disease burden, even among those experiencing sporadic attacks or using prophylactic hemin/glucose, is substantial. Similarly, the present results indicate that the disease burden not only affects patients' physical health, but also their emotional, social, and financial well-being. These findings highlight the need for therapeutic strategies that can reduce attacks, alleviate chronic disease manifestations, and improve patient well-being over time.

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abstract

PMID

36636593

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abstract

DOI

10.1002/jmd2.12343

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