Evidence map›Paper›PMID 32070341›Full record

ArticleBMC health services research2020

The societal economic burden of autosomal dominant polycystic kidney disease in the United States.

Martin Cloutier, Ameur M Manceur, Annie Guerin, Myrlene Sanon Aigbogun, Dorothee Oberdhan, Marjolaine Gauthier-Loiselle

Open access · goldAbstract read
In one paragraph

Article in BMC health services research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 2 pooled it
4.5field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 2 syntheses or guidelines pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  12. Consideration for Health Disparities in Value Assessment Frameworks.ClinicoEconomics and outcomes research : CEOR · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Martin CloutierAnalysis Group, Inc., Montréal, QC, Canada.
Ameur M ManceurAnalysis Group, Inc., Montréal, QC, Canada.
Annie GuerinAnalysis Group, Inc., Montréal, QC, Canada.
Myrlene Sanon AigbogunOtsuka Pharmaceutical Development & Commercialization, Inc., Princeton, NJ, USA.
Dorothee OberdhanOtsuka Pharmaceutical Development & Commercialization, Inc., Princeton, NJ, USA.
Marjolaine Gauthier-LoiselleAnalysis Group, Inc., Montréal, QC, Canada. Marjolaine.Gauthier-Loiselle@analysisgroup.com.ORCID http://orcid.org/0000-0002-9439-595X
Otsuka (United States) · USGroup for Research in Decision Analysis · CA

Funding

Otsuka Pharmaceutical Development & Commercialization, Inc. NA
6 · The paper itself

Abstract

backgroundAutosomal dominant polycystic kidney disease (ADPKD) is one of the most common inherited kidney diseases characterized by progressive development of renal cysts and numerous extra-renal manifestations, eventually leading to kidney failure. Given its chronic and progressive nature, ADPKD is expected to carry a substantial economic burden over the course of the disease. However, there is a paucity of evidence on the impact of ADPKD from a societal perspective. This study aimed to estimate the direct and indirect costs associated with ADPKD in the United States (US).

methodsA prevalence-based approach using data from scientific literature, and governmental and non-governmental organizations was employed to estimate direct healthcare costs (i.e., medical services, prescription drugs), direct non-healthcare costs (i.e., research and advocacy, donors/recipients matching for kidney transplants, transportation to/from dialysis centers), and indirect costs (i.e., patient productivity loss from unemployment, reduced work productivity, and premature mortality, caregivers' productivity loss and healthcare costs). The incremental costs associated with ADPKD were calculated as the difference between costs incurred over a one-year period by individuals with ADPKD and the US population. Sensitivity analyses using different sources and assumptions were performed to assess robustness of estimates and account for variability in published estimates.

resultsThe estimated total annual costs attributed to ADPKD in 2018 ranged from $7.3 to $9.6 billion in sensitivity analyses, equivalent to $51,970 to $68,091 per individual with ADPKD. In the base scenario, direct healthcare costs accounted for $5.7 billion (78.6%) of the total $7.3 billion costs, mostly driven by patients requiring renal replacement therapy ($3.2 billion; 43.3%). Indirect costs accounted for $1.4 billion (19.7%), mostly driven by productivity loss due to unemployment ($784 million; 10.7%) and reduced productivity at work ($390 million; 5.3%). Total excess direct non-healthcare costs were estimated at $125 million (1.7%).

conclusionsADPKD carries a considerable economic burden, predominantly attributed to direct healthcare costs, the majority of which are incurred by public and private healthcare payers. Effective and timely interventions to slow down the progression of ADPKD could substantially reduce the economic burden of ADPKD.

Indexed as

Cost of IllnessHealth Care CostsHumansPolycystic Kidney, Autosomal DominantPrevalenceUnited StatesAutosomal dominant polycystic kidney diseaseBurden of diseaseDirect costsIndirect costsSocietal impact

Identifiers

PMID32070341
PMCPMC7029467
OpenAlexW3006965099

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.