Limb lengthening in achondroplasia: a cost-effectiveness analysis using a Markov model

BACKGROUND: Disproportionate short stature is one of the most characteristic clinical traits of achondroplasia, a condition with a significant impact on patients' autonomy that results in a series of limitations leading to poorer health-related quality of life. Limb lengthening surgery is an effective therapeutic alternative for increasing the stature of persons with achondroplasia. The purpose of this study was to evaluate the cost-effectiveness of bone lengthening in patients with achondroplasia and to estimate the economic impact of the procedure on the Spanish health system by means of a Markov model. RESULTS: Patients with achondroplasia who undergo a limb lengthening procedure gain, on average, 5.954 quality-adjusted life years (QALYs) more than unoperated patients (27.197 vs. 21.243 QALYs). As the procedure entails a mean incremental cost of €49,480, the resulting incremental cost-effectiveness ratio (ICER) is €8,310/QALY. The probabilistic sensitivity analysis (PSA) performed yielded a mean quality of life gain of 6.287 QALYs and a mean cost increase of €49,131, which translates into an ICER of €7,814/QALY. The budget impact analysis was based on the hypothesis that all patients with achondroplasia born every year in the country used as a reference (Spain, n = 15) undergo the procedure. Under this assumption, a cumulative cost increase of €8,896,196 can be estimated over a 15-year period (€8,836,931 following the PSA). CONCLUSIONS: Limb lengthening surgery in patients with achondroplasia can be considered a cost-effective intervention according to the most commonly accepted willingness-to-pay thresholds in Spain and other Western countries.

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Journal
Orphanet Journal of Rare Diseases
Published
2026-05-27
DOI
https://doi.org/10.1186/s13023-026-04397-0
Primary Topic
Connective tissue disorders research
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article
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article

Limb lengthening in achondroplasia: a cost-effectiveness analysis using a Markov model

Pablo Roberto Miguel, Antonio Leiva‐Gea, María Rabanal Rubio, Eduardo González Fidalgo et al.
Orphanet Journal of Rare Diseases
Connective tissue disorders research
article

Limb lengthening in achondroplasia: a cost-effectiveness analysis using a Markov model

Pablo Roberto Miguel, Antonio Leiva‐Gea, María Rabanal Rubio, Eduardo González Fidalgo, Nuria García-Rodríguez
article en

Abstract

BACKGROUND: Disproportionate short stature is one of the most characteristic clinical traits of achondroplasia, a condition with a significant impact on patients' autonomy that results in a series of limitations leading to poorer health-related quality of life. Limb lengthening surgery is an effective therapeutic alternative for increasing the stature of persons with achondroplasia. The purpose of this study was to evaluate the cost-effectiveness of bone lengthening in patients with achondroplasia and to estimate the economic impact of the procedure on the Spanish health system by means of a Markov model. RESULTS: Patients with achondroplasia who undergo a limb lengthening procedure gain, on average, 5.954 quality-adjusted life years (QALYs) more than unoperated patients (27.197 vs. 21.243 QALYs). As the procedure entails a mean incremental cost of €49,480, the resulting incremental cost-effectiveness ratio (ICER) is €8,310/QALY. The probabilistic sensitivity analysis (PSA) performed yielded a mean quality of life gain of 6.287 QALYs and a mean cost increase of €49,131, which translates into an ICER of €7,814/QALY. The budget impact analysis was based on the hypothesis that all patients with achondroplasia born every year in the country used as a reference (Spain, n = 15) undergo the procedure. Under this assumption, a cumulative cost increase of €8,896,196 can be estimated over a 15-year period (€8,836,931 following the PSA). CONCLUSIONS: Limb lengthening surgery in patients with achondroplasia can be considered a cost-effective intervention according to the most commonly accepted willingness-to-pay thresholds in Spain and other Western countries.

Orphanet Journal of Rare DiseasesVol. 21(1)
Universidad San Pablo CEU (ES), Universidad de Oviedo (ES), Biomechanics Institute of Valencia (ES), Hospital Clínico Universitario Virgen de la Victoria (ES), Instituto de Investigación Biomédica de Málaga (ES)
No poverty
Openalex Percentile: Top 6%
Connective tissue disorders research
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