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Abstract
Objectives The aim of this study was to elicit the willingness-to-pay (WTP) for genomic testing, using contingent valuation, among people with lived experience of genetic conditions in Australia.
Methods Parents of children with suspected mitochondrial disorders, epileptic encephalopathy, leukodystrophy, or malformations of cortical development completed a dynamic triple-bounded dichotomous choice (DC) contingent valuation. Adult patients or parents of children with suspected genetic kidney disease or complex neurological and neurodegenerative conditions completed a payment card (PC) contingent valuation. DC data were analyzed using a multilevel interval regression and a multilevel probit model. PC data were analyzed using a Heckman selection model.
Results In total, 360 individuals participated in the contingent valuation (CV), with 141 (39%) and 219 (61%) completing the DC and PC questions, respectively. The mean WTP for genomic testing was estimated at AU$2830 (95% confidence interval [CI] 2236-3424) based on the DC data and AU$1914 (95% CI 1532-2296) based on the PC data. The mean WTP across the six cohorts ranged from AU$1879 (genetic kidney disease) to AU$4554 (leukodystrophy).
Conclusions Genomic testing is highly valued by people experiencing rare genetic conditions. Our findings can inform cost-benefit analyses and the prioritization of genomics into mainstream clinical care. While our WTP estimates for adultonset genetic conditions aligned with estimates derived from discrete choice experiments (DCEs), for childhood-onset conditions our estimates were significantly lower. Research is urgently required to directly compare, and critically evaluate, the performance of CV and DCE methods.
1Introduction
Rare diseases are an emerging global public health priority [1], with an estimated 263-446 million people globally being affected by nearly 7000 rare diseases [2]. Despite being heterogeneous in nature and geographically disparate, most rare diseases have identified genetic origins [3]. The challenges faced by families are often similar regardless of the underlying condition [4], including lack of access to correct and timely diagnosis [5], slow progress in sharing of genetic and clinical information and scientific knowledge [6], as well as inequitable access to diagnostic opportunities and medical care [7]. These challenges have a significant effect on the quality of life of affected families [8], and substantial economic consequences to health systems [9].
Genomic testing has changed the landscape associated with the diagnosis and management of rare genetic conditions [2]. It has the...