Longitudinal analysis of health care costs in patients with childhood onset inherited retinal dystrophies compared to healthy controls

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Longitudinal analysis of health care costs in patients with childhood onset inherited retinal dystrophies compared to healthy controls. / Kessel, Line; Kjellberg, Jakob; Ibsen, Rikke; Rasmussen, Annette; Nissen, Kamilla Rothe; la Cour, Morten.

In: BMC Ophthalmology, Vol. 22, No. 1, 466, 2022.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Kessel, L, Kjellberg, J, Ibsen, R, Rasmussen, A, Nissen, KR & la Cour, M 2022, 'Longitudinal analysis of health care costs in patients with childhood onset inherited retinal dystrophies compared to healthy controls', BMC Ophthalmology, vol. 22, no. 1, 466. https://doi.org/10.1186/s12886-022-02708-0

APA

Kessel, L., Kjellberg, J., Ibsen, R., Rasmussen, A., Nissen, K. R., & la Cour, M. (2022). Longitudinal analysis of health care costs in patients with childhood onset inherited retinal dystrophies compared to healthy controls. BMC Ophthalmology, 22(1), [466]. https://doi.org/10.1186/s12886-022-02708-0

Vancouver

Kessel L, Kjellberg J, Ibsen R, Rasmussen A, Nissen KR, la Cour M. Longitudinal analysis of health care costs in patients with childhood onset inherited retinal dystrophies compared to healthy controls. BMC Ophthalmology. 2022;22(1). 466. https://doi.org/10.1186/s12886-022-02708-0

Author

Kessel, Line ; Kjellberg, Jakob ; Ibsen, Rikke ; Rasmussen, Annette ; Nissen, Kamilla Rothe ; la Cour, Morten. / Longitudinal analysis of health care costs in patients with childhood onset inherited retinal dystrophies compared to healthy controls. In: BMC Ophthalmology. 2022 ; Vol. 22, No. 1.

Bibtex

@article{f2f0002f31c64b54afda399ece96664c,
title = "Longitudinal analysis of health care costs in patients with childhood onset inherited retinal dystrophies compared to healthy controls",
abstract = "Background: We evaluated health care costs in patients with childhood onset visual impairment caused by inherited retinal dystrophies (IRD). Methods: The IRD cohort, identified from the Danish Registry of Blind and Partially Sighted Children, was compared to age- and sex-matched controls from the national, Danish population registry. Information on health care expenditures for somatic and psychiatric in- and outpatient services, purchase of prescription medications and paid assistance at home were obtained from national registries for the years 2002–2017. Results: We included 412 in the IRD cohort (6,290 person years) and 1656 (25,088 person years) in the control cohort. Average, annual health care expenditures from age 0–48 years of age were €1,488 (SD 4,711) in the IRD cohort and €1,030 (4,639) in the control cohort. The largest difference was for out-patient eye care (13.26 times greater, 95% confidence interval 12.90–13.64). Psychiatric in-patient expenditures were 1.71 times greater (95% CI 1.66–1.76) in the IRD cohort but psychiatric out-patient health care costs were comparable between groups. Conclusions: Health care costs were approximately 40% greater in the IRD cohort compared to an age- and sex-matched sample from the general Danish population. This is relevant in the current situation with a number of trials aimed at treating IRDs using genetically based therapies. Although eye care expenditures were many times greater, they made up < 10% of the total health care expenditures even in the IRD cohort. The reduced costs related to injuries in the visually impaired cohort was a surprising finding but may reflect a reduced propensity to seek medical care rather than a reduced risk of injuries.",
keywords = "Childhood visual impairment, Health care costs. Injury, Inherited retinal dystrophy",
author = "Line Kessel and Jakob Kjellberg and Rikke Ibsen and Annette Rasmussen and Nissen, {Kamilla Rothe} and {la Cour}, Morten",
note = "Publisher Copyright: {\textcopyright} 2022, The Author(s).",
year = "2022",
doi = "10.1186/s12886-022-02708-0",
language = "English",
volume = "22",
journal = "BMC Ophthalmology",
issn = "1471-2415",
publisher = "BioMed Central Ltd.",
number = "1",

}

RIS

TY - JOUR

T1 - Longitudinal analysis of health care costs in patients with childhood onset inherited retinal dystrophies compared to healthy controls

AU - Kessel, Line

AU - Kjellberg, Jakob

AU - Ibsen, Rikke

AU - Rasmussen, Annette

AU - Nissen, Kamilla Rothe

AU - la Cour, Morten

N1 - Publisher Copyright: © 2022, The Author(s).

PY - 2022

Y1 - 2022

N2 - Background: We evaluated health care costs in patients with childhood onset visual impairment caused by inherited retinal dystrophies (IRD). Methods: The IRD cohort, identified from the Danish Registry of Blind and Partially Sighted Children, was compared to age- and sex-matched controls from the national, Danish population registry. Information on health care expenditures for somatic and psychiatric in- and outpatient services, purchase of prescription medications and paid assistance at home were obtained from national registries for the years 2002–2017. Results: We included 412 in the IRD cohort (6,290 person years) and 1656 (25,088 person years) in the control cohort. Average, annual health care expenditures from age 0–48 years of age were €1,488 (SD 4,711) in the IRD cohort and €1,030 (4,639) in the control cohort. The largest difference was for out-patient eye care (13.26 times greater, 95% confidence interval 12.90–13.64). Psychiatric in-patient expenditures were 1.71 times greater (95% CI 1.66–1.76) in the IRD cohort but psychiatric out-patient health care costs were comparable between groups. Conclusions: Health care costs were approximately 40% greater in the IRD cohort compared to an age- and sex-matched sample from the general Danish population. This is relevant in the current situation with a number of trials aimed at treating IRDs using genetically based therapies. Although eye care expenditures were many times greater, they made up < 10% of the total health care expenditures even in the IRD cohort. The reduced costs related to injuries in the visually impaired cohort was a surprising finding but may reflect a reduced propensity to seek medical care rather than a reduced risk of injuries.

AB - Background: We evaluated health care costs in patients with childhood onset visual impairment caused by inherited retinal dystrophies (IRD). Methods: The IRD cohort, identified from the Danish Registry of Blind and Partially Sighted Children, was compared to age- and sex-matched controls from the national, Danish population registry. Information on health care expenditures for somatic and psychiatric in- and outpatient services, purchase of prescription medications and paid assistance at home were obtained from national registries for the years 2002–2017. Results: We included 412 in the IRD cohort (6,290 person years) and 1656 (25,088 person years) in the control cohort. Average, annual health care expenditures from age 0–48 years of age were €1,488 (SD 4,711) in the IRD cohort and €1,030 (4,639) in the control cohort. The largest difference was for out-patient eye care (13.26 times greater, 95% confidence interval 12.90–13.64). Psychiatric in-patient expenditures were 1.71 times greater (95% CI 1.66–1.76) in the IRD cohort but psychiatric out-patient health care costs were comparable between groups. Conclusions: Health care costs were approximately 40% greater in the IRD cohort compared to an age- and sex-matched sample from the general Danish population. This is relevant in the current situation with a number of trials aimed at treating IRDs using genetically based therapies. Although eye care expenditures were many times greater, they made up < 10% of the total health care expenditures even in the IRD cohort. The reduced costs related to injuries in the visually impaired cohort was a surprising finding but may reflect a reduced propensity to seek medical care rather than a reduced risk of injuries.

KW - Childhood visual impairment

KW - Health care costs. Injury

KW - Inherited retinal dystrophy

U2 - 10.1186/s12886-022-02708-0

DO - 10.1186/s12886-022-02708-0

M3 - Journal article

C2 - 36460996

AN - SCOPUS:85143242580

VL - 22

JO - BMC Ophthalmology

JF - BMC Ophthalmology

SN - 1471-2415

IS - 1

M1 - 466

ER -

ID: 329304906