TY - JOUR
T1 - Effects of financial support on treatment of adolescents with growth hormone deficiency
T2 - A retrospective study in Japan
AU - Maeda, Eri
AU - Higashi, Takahiro
AU - Hasegawa, Tomonobu
AU - Yokoya, Susumu
AU - Mochizuki, Takahiro
AU - Ishii, Tomohiro
AU - Ito, Junko
AU - Kanzaki, Susumu
AU - Shimatsu, Akira
AU - Takano, Koji
AU - Tajima, Toshihiro
AU - Tanaka, Hiroyuki
AU - Tanahashi, Yusuke
AU - Teramoto, Akira
AU - Nagai, Toshiro
AU - Hanew, Kunihiko
AU - Horikawa, Reiko
AU - Yorifuji, Toru
AU - Wada, Naohiro
AU - Tanaka, Toshiaki
N1 - Publisher Copyright:
© 2016 The Author(s).
PY - 2016/10/21
Y1 - 2016/10/21
N2 - Background: Treatment costs for children with growth hormone (GH) deficiency are subsidized by the government in Japan if the children meet clinical criteria, including height limits (boys: 156.4 cm; girls: 145.4 cm). However, several funding programs, such as a subsidy provided by local governments, can be used by those who exceed the height limits. In this study, we explored the impacts of financial support on GH treatment using this natural allocation. Methods: A retrospective analysis of 696 adolescent patients (451 boys and 245 girls) who reached the height limits was conducted. Associations between financial support and continuing treatment were assessed using multiple logistic regression analyses adjusting for age, sex, height, growth velocity, bone age, and adverse effects. Results: Of the 696 children in the analysis, 108 (15.5 %) were still eligible for financial support. The proportion of children who continued GH treatment was higher among those who were eligible for support than among those who were not (75.9 % vs. 52.0 %, P < 0.001). The odds ratios of financial support to continuing treatment were 4.04 (95 % confidence interval [CI]: 1.86-8.78) in boys and 1.72 (95 % CI: 0.80-3.70) in girls, after adjusting for demographic characteristics and clinical factors. Conclusions: Financial support affected decisions on treatment continuation for children with GH deficiency. Geographic variations in eligibility for financial support pose an ethical problem that needs policy attention. An appropriate balance between public spending on continuation of therapy and improved quality of life derived from it should be explored.
AB - Background: Treatment costs for children with growth hormone (GH) deficiency are subsidized by the government in Japan if the children meet clinical criteria, including height limits (boys: 156.4 cm; girls: 145.4 cm). However, several funding programs, such as a subsidy provided by local governments, can be used by those who exceed the height limits. In this study, we explored the impacts of financial support on GH treatment using this natural allocation. Methods: A retrospective analysis of 696 adolescent patients (451 boys and 245 girls) who reached the height limits was conducted. Associations between financial support and continuing treatment were assessed using multiple logistic regression analyses adjusting for age, sex, height, growth velocity, bone age, and adverse effects. Results: Of the 696 children in the analysis, 108 (15.5 %) were still eligible for financial support. The proportion of children who continued GH treatment was higher among those who were eligible for support than among those who were not (75.9 % vs. 52.0 %, P < 0.001). The odds ratios of financial support to continuing treatment were 4.04 (95 % confidence interval [CI]: 1.86-8.78) in boys and 1.72 (95 % CI: 0.80-3.70) in girls, after adjusting for demographic characteristics and clinical factors. Conclusions: Financial support affected decisions on treatment continuation for children with GH deficiency. Geographic variations in eligibility for financial support pose an ethical problem that needs policy attention. An appropriate balance between public spending on continuation of therapy and improved quality of life derived from it should be explored.
KW - Children with special health care needs
KW - Health insurance
KW - Japan
KW - Public funding
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U2 - 10.1186/s12913-016-1854-z
DO - 10.1186/s12913-016-1854-z
M3 - Article
C2 - 27769307
AN - SCOPUS:84992153345
SN - 1472-6963
VL - 16
JO - BMC Health Services Research
JF - BMC Health Services Research
IS - 1
M1 - 602
ER -