دورية أكاديمية
Pharmacological treatment for attention deficit hyperactivity disorder: functional outcomes in children and adolescents from non-Western countries.
العنوان: | Pharmacological treatment for attention deficit hyperactivity disorder: functional outcomes in children and adolescents from non-Western countries. |
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المؤلفون: | Altin M; Eli Lilly Neuroscience, Eli Lilly & Company Turkey, Lilly İlaç Ticaret Ltd. Şti. Kuşbakişi Caddesi, Rainbow Plaza No:4 Kat:3,34662; Altunizade, İstanbul, Turkey;, El-Shafei AA; Eli Lilly, 1229 El Sheikh Aly Gad El Haq St., Floor 6 Sheraton Bldgs, Heliopolis, Cairo, Egypt;, Yu M; Eli Lilly Canada, 3650 Danforth Ave, Toronto, Ontario, Canada;, Desaiah D; Lilly Research Laboratories, Lilly Corporate Center, Indianapolis, IN;, Treuer T; Neuroscience Research, Eli Lilly and Company, 1075 Budapest, Madách u. 13-14, Hungary;, Zavadenko N; Dept. of Neurology, Neurosurgery and Medical Genetics of Pediatric Faculty, Russian State Medical University, Ostrovityanova Str. 1, Moscow, Russian Federation;, Gao HY; Dept. of Psychological Medicine, Children's Hospital of Fudan University, 399 Wanyuan Lu, Shanghai, China. |
المصدر: | Drugs in context [Drugs Context] 2013 Sep 13; Vol. 2013, pp. 212260. Date of Electronic Publication: 2013 Sep 13 (Print Publication: 2013). |
نوع المنشور: | Journal Article |
اللغة: | English |
بيانات الدورية: | Publisher: Bioexcel Publishing Ltd Country of Publication: England NLM ID: 101262187 Publication Model: eCollection Cited Medium: Print ISSN: 1745-1981 (Print) Linking ISSN: 17404398 NLM ISO Abbreviation: Drugs Context Subsets: PubMed not MEDLINE |
أسماء مطبوعة: | Publication: 2016- : London : Bioexcel Publishing Ltd. Original Publication: Long Hanborough, Oxon : CSF Medical Communications, c2005- |
مستخلص: | Objective: Functional outcomes were measured over a 12-month period in children and adolescents with attention deficit hyperactivity disorder (ADHD) after they received monotherapy. Design: Prospective, observational, noninterventional study. Setting: Conducted in six non-Western countries. Participants: Outpatients 6 to 17 years of age with a verified diagnosis of ADHD in accordance with the Diagnostic and Statistical Manual, Fourth Edition, Text Revision (DSM-IV-TR), together with their physicians, decided to initiate or switch treatment for ADHD. Patients were prescribed pharmacological monotherapy: methylphenidate (n=221), nootropic agents (n=91), or atomoxetine (n=234). Measurements: Patients were followed for changes in their functional status and quality of life, which were assessed with the Child Health and Illness Profile-Child Edition (CHIP-CE) Achievement domain. Results: At the end of the study, a mean improvement on the CHIP-CE Achievement domain score was observed for all countries and therapies except in Taiwan, where patients received atomoxetine, and in Lebanon, where patients received methylphenidate. No patient experienced a serious adverse event during the study. Four patients discontinued due to a treatment-emergent adverse event. Conclusion: After 12 months of treatment, clinical and functional outcomes were improved in children and adolescents from non-Western countries who initiated and remained on their prescribed pharmacological monotherapy. |
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فهرسة مساهمة: | Keywords: adolescent; adverse drug events; atomoxetine; attention deficit hyperactivity disorder; central nervous system stimulants; child; nootropic agents; treatment outcome |
تواريخ الأحداث: | Date Created: 20140117 Date Completed: 20140116 Latest Revision: 20211021 |
رمز التحديث: | 20231215 |
مُعرف محوري في PubMed: | PMC3884848 |
DOI: | 10.7573/dic.212260 |
PMID: | 24432046 |
قاعدة البيانات: | MEDLINE |
تدمد: | 1745-1981 |
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DOI: | 10.7573/dic.212260 |