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About JMDC

JMDC (TYO: 4483) aims to improve medical disparities and actively invests in human resources to change the development of healthcare initiatives.

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2-5-5 Shiba Daimon, Minato-ku Sumitomo Shiba Daimon Building 12F

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Risk factors for low adherence to methylphenidate treatment in pediatric patients with attention-deficit/hyperactivity disorder

Jan 18, 2021

Abstract Poor adherence is a major concern in the treatment of attention-deficit/hyperactivity disorder (ADHD). The objective of this study was to evaluate factors linked to early interruption of and low adherence to treatment with osmotic-release oral system methylphenidate hydrochloride (OROS-MPH) in pediatric patients with ADHD. A total of 1353 young people (age 6–17 years) with a diagnosis of ADHD who newly started OROS-MPH were extracted from the pharmacoepidemiological data of 3 million people in Japan. The cohort was retrospectively surveyed every month for 12 months. Ten possible risk factors were extracted from the data and analyzed by multivariable logistic regression. Sensitivity analysis was conducted to ensure the robustness of the analysis. The results revealed that treatment adherence was generally poor, with a tendency for discontinuation in the early stage. Multivariable logistic regression results showed that adherence is reduced by female sex, lower starting dose, and concomitant atomoxetine or hypnotics. These findings may help clinicians to predict the risk of poor adherence in the early stage of treatment and improve not only patients’ symptoms, but also their quality of life. Introduction Attention-deficit/hyperactivity disorder (ADHD) is a common chronic neurodevelopmental disorder characterized by symptoms of inattention, hyperactivity, and impulsivity. Individuals with ADHD are at high risk of comorbid psychiatric disorders, such as oppositional defiant disorder, conduct disorders, depression, bipolar disorders, and anxiety disorders 1 . The onset of ADHD occurs mostly in childhood, but 50% to 80% of diagnosed children continue to demonstrate ADHD symptoms into adolescence or adulthood 2 , 3 , 4 , 5 . The symptoms of ADHD and comorbid disorders can impair an individual’s ability to function in social circumstances, resulting in academic, familial, and social problems 6 , 7 . In the latest Japanese guidelines for the diagnosis and treatment of ADHD, released in 2016 8 , the management of children with ADHD should begin with psychosocial treatment. Additional administration of pharmacological therapy should be considered when psychosocial treatments are insufficient. However, as shown by fact-finding surveys on pharmacotherapy for ADHD, most physicians support the need for pharmacotherapy 9 . Four types of ADHD medication are currently available in Japan: osmotic-release oral system methylphenidate hydrochloride (OROS-MPH, CONCERTA), atomoxetine (ATX, STRATTERA), guanfacine hydrochloride (INTUNIV), and lisdexamfetamine dimesylate (VYVANSE). Of these medications, OROS-MPH is the most prescribed. Due to its addictive profile, the circulation management committee strictly controlled its prescription by limiting prescribers’ certification and the prescription duration until the ADHD proper distribution management system is established in December 2019. Accordingly, there is a high likelihood of proper prescription of OROS-MPH in Japan. The latest Japanese guidelines 8 recommended that termination of medication be considered when patients are stable for more than 1 year after they obtain a score of 61 or above on the Global Assessment of Functioning (GAF) scale. Therefore, patients need to adhere to the prescribed treatment regimens for at least 1 year. Despite the high reliability of proper prescription of OROS-MPH medication in Japan because of its strict control, there is an issue with patients’ unstable patterns of outpatient visits and oral intake in clinical practice. This leads to poor adherence or discontinuation of the treatment in the early stage, which could limit treatment effects and increase the risk of comorbid psychiatric disorders. There is a considerable need to understand the prescription patterns of ADHD medications and to identify risk factors associated with poor adherence in order to help patients to adhere to their recommended treatment regimen and to facilitate proper intervention. However, to our knowledge, no study has examined the actual prescription patterns of OROS-MPH and analyzed the possible factors associated with poor adherence in Japan. Therefore, in this study, we evaluated the current prescription trend of OROS-MPH in pediatric ADHD patients in Japan. We also analyzed the factors that could predict poor adherence in the early stage of the treatment, based on data from the claims database. Methods All procedures were performed in accordance with the ethical guidelines for epidemiological research issued by the Japanese Ministry of Health, Labour and Welfare. This study was approved by the Ethics Committee of Akita University Graduate School of Medicine, Akita, Japan, which waived the requirement for obtaining written informed consent. Data source The data used in this research were provided by JMDC Inc. (Tokyo, Japan). JMDC Inc. has been collecting claims information from occupation-based health insurance agencies for corporate employees and their dependents since 2005 10 . All health insurance data included in the JMDC database are anonymized, and permission for secondary use of the data has been obtained from the subscriber. The number of individuals registered in JMDC is about 3 million, which is approximately 2.5% of the entire Japanese population as of June 2016. Each record includes an encrypted personal identifier, age, sex, diagnoses, and prescriptions. The diagnoses are based on International Statistical Classification of Diseases and Related Health Problems, 10th revision (ICD-10) diagnostic codes. The prescription information includes WHO Anatomical Therapeutic Chemical (WHO-ATC) classification system codes, drug name, days of supply, dosage information, and mode of prescription. The date of service is specified up to the month and year. Study population We selected outpatients who were 6 to 17 years when they were first prescribed OROS-MPH between December 2007 and May 2015. We selected only new users who had not been prescribed MPH within 1 year prior to their first prescription during our observation period. Then, we extracted individuals who could be observed for at least 1 year. We also excluded individuals who had a diagnosis of narcolepsy because they are prescribed methylphenidate hydrochloride and not OROS-MPH. A total of 1353 children were included in this study (Fig. 3 ). Study variables Patient persistence and adherence Medication compliance has two indicators: “persistence” and “adherence”. Persistence is usually calculated by the period until the discontinuation of the initial treatment. In this study, the discontinuation of the medication was defined as the beginning of a gap of more than 3 months in prescriptions for OROS-MPH. We named this gap period GAP3M in this study. On the other hand, adherence was assessed using the MPR, which reflects the proportion of months that patients were in possession of the medication within a specific period. We calculated the MPR by summing the number of months in which patients received their prescription and dividing it by the follow-up period in months (12 months). The conventional 50% cutoff was used. Risk factors We selected the possible risk factors that might interfere with medication adherence. As mentioned in previous studies, many factors are related to medication continuation and adherence. These include specific child and adolescent characteristics, such as age 11 , 12 , 13 , 14 , 15 , 16 , male sex 11 , and ethnic background 13 , clinical characteristics, such as symptom severity 13 , 14 , 16 and amount of symptom reduction 17 , 18 , quality of ADHD care, such as medication doses 15 , 17 , 18 , adverse events 19 , and concomitant medication 11 , and factors related to parents or families, such as belief in treatment 12 , poor family support 20 , and family history of ADHD 14 . In this study, we selected sex, age at first OROS-MPH prescription, clinician specialties, mean daily dosage prescribed in the first 3 months, and concomitant medication in the first 3 months. Patient were divided into three age groups as follows: 6–12 years of age (elementary school students), 13–15 years of age (junior high school students), and 16–17 years of age (high school students or junior high school graduates) according to the Japanese school system. The mean daily dosage prescribed in the first 3 months was calculated by dividing the sum of the total prescription in the first 3 months by 90 days. The results were divided into three groups: a low-dose group (< 18 mg), middle-dose group (18–27 mg), and high-dose group (≥ 27 mg) according to the dosing schedule based on approvals granted by the Japanese regulatory authority 21 . Clinician specialties were divided into three groups as follows: psychiatry/psychosomatic medicine, pediatrics, and others. The reasoning for this division of departments is that only members of the Japan Pediatric Society or the Japanese Society of Psychiatry are under the control of the circulation management committee. The types of concomitant medications were divided into six groups: ATX, antipsychotics, hypnotics, antidepressants, antiepileptics, and anxiolytics (see Supplementary Table S2 online). Statistical analysis The estimated prescription rate of OROS-MPH was calculated, as well as the actual prescription rate in the target group, which was the population who received the prescription from December 2007 to April 2016. The estimated prescription rate for the whole population (from 6 to 17 years) was calculated by correction for the population statistics issued by the statistics bureau of Japan 22 . Kaplan–Meier survival curves were used to estimate the continuing prescription of OROS-MPH. We used multivariable logistic regression analysis to assess the association between risk factors and poor adherence. We identified ten possible risk factors (Table 1 ) and divided patients into two groups: poor adherence (MPR below 0.5) and good adherence (MPR above 0.5). The logistic regression analysis was conducted using IBM SPSS Statistics version 22 (IBM, Armonk, NY, USA). The analyses were two-tailed, and P values < 0.05 were considered statistically significant. Table 1 Demographic characteristics of the participants. We also conducted sensitivity analysis to ensure the robustness of the analysis. We identified two factors from the literature: ADHD severity and adverse events. ADHD severity was thought to interfere with the mean daily dosage prescribed in the first 3 months, whereas adverse events are thought to interfere with concomitant hypnotic use. The OR for reduced adherence and the ratio of patients who might have possible confounding factors were determined from the literature 16 , 19 , 23 , 24 . Sensitivity analysis was performed using the method provided by Fox et al. 25 . Results Estimated prescription rate During the period from the launch of OROS-MPH in Japan (December 2007) to the last month of data acquisition from the Japan Medical Data Center (JMDC; April 2016), the estimated prescription rate gradually increased from 0.003 to 0.23% (Fig. 1 ). Figure 1 Prevalence estimates of OROS-MPH in the Japanese population aged 6–17 years. Prevalence estimates were corrected with population statistics issued by the statistics bureau of Japan (27). OROS-MPH, osmotic-release oral system methylphenidate hydrochloride. Regarding the mean daily dosage prescribed in the first 3 months, adherence was likely to be poor if patients were prescribed doses lower than 18 mg per day and was significantly worse than if they were prescribed 18–27 mg per day and ≥ 27 mg per day (OR, 1.986; 95% CI, 1.554–2.536; P = 0.000; OR, 2.499; 95% CI, 1.731–3.608; P = 0.000, respectively). In terms of the types of concomitant medication in the first 3 months, concomitant use of ATX (OR, 0.376; 95% CI, 0.273–0.517; P = 0.000) or hypnotics (OR, 0.536; 95% CI, 0.291–0.985; P = 0.045) was significantly associated with poor adherence. Sensitivity analysis The results of the sensitivity analysis are shown in Supplementary Table S1 online. Considering the calculated original risk ratio of 1.54, ADHD severity was not considered to have a significant effect on the relationship between adherence and the mean daily dosage, even in the most plausible pattern (1.6 for the estimated risk ratio of the confounding factor, about 60% for the proportion of patients who use OROS-MPH more than 18 mg per day and about 50% for the proportion of patients who use OROS-MPH less than 18 mg per day). Therefore, the severity of ADHD was not considered to interfere with the results. Regarding the effect of adverse events on the relationship between adherence and concomitant hypnotic use, the adjusted risk ratio was 1.46 in the most plausible pattern (1.5 for the estimated risk ratio of the confounding factor, 70% for the proportion of the patients in the concomitant hypnotic use group, and 60% in the non-concomitant group). Considering the original risk ratio of 1.52, it is necessary to be cautious about the risk of the occurrence of adverse events in relation to adherence and the concomitant use of hypnotics, and further consideration of this aspect is needed. Discussion First, this study revealed the actual status of OROS-MPH prescription. The trend for a gradual increase in prescription rates is similar to that of other countries 26 , 27 , 28 , 29 . However, the prevalence of ADHD drug use in pediatric patients was lower in Japan (0.4%) 30 than in Norway and the United States (1.4–5.3%) 31 , 32 but similar to that in Italy, France, and the UK (0.2–0.5%) 33 , 34 , 35 . In addition, the share of OROS-MPH in 2014 is lower in Japan (64%) 30 than in Germany, the UK, and Norway (75–100%) 32 , 33 , 36 . Thus, both the prescription of ADHD drug and the share of OROS-MPH are low in Japan. One of the reasons for this situation in Japan could be the strict control of OROS-MPH prescription by the circulation management committee to limit the qualification of prescribers and the prescription period. Another possible reason is the indication for the first-line drug of ADHD medication in the Japanese guidelines 8 . Both OROS-MPH and ATX are equally listed as first-line drugs, in contrast to other guidelines that recommend psychostimulants as first choice 37 , 38 , 39 . Although there are differences in efficacy and tolerability among ADHD medications 40 , 41 , Japanese physicians may prefer ATX for the initial drug because it has no restriction. Second, we revealed the erratic prescription patterns of OROS-MPH and analyzed the possible factors that could predict the risk of low adherence in the early stage of the OROS-MPH prescription. This erratic pattern could be caused by patients forgetting to take the medication, intentional discontinuation, or “drug holidays”. The term “drug holiday” refers to the deliberate interruption of pharmacotherapy for a defined period and for a specific clinical purpose 42 . Although guidelines recommend patients take “drug holidays” when the use is extended over a long period 8 , 39 , some patients take these holidays on weekends or during school holidays from the early stage of the treatment. The mean MPR in this study was 0.51 ± 0.32. This is similar to the mean MPR of 0.52 ± 0.30 for extended-release stimulants in Texas 11 but less than the mean MPR of 0.64 found in the Netherlands 43 . Common adherence thresholds in previous studies were 0.8 11 , 43 , 44 or 0.7 45 . However, as shown in our results, 90.8% of those with an MPR greater than 0.5 continued to take their medication until the end of the follow-up period. Therefore, we defined an MPR greater than 0.5 as an indication of adherence. Among possible risk factors for low adherence detected in our study, sex differences had a statistically significant influence on adherence. Compared with girls, boys with ADHD have a tendency to show more externalized symptoms 46 . Although OROS-MPH can reduce both externalized and internalized symptoms 19 , improvements in externalized symptoms are more readily noticed by caregivers. Therefore, boys may more easily perceive the effects of the medication and thus be more likely to continue to take it, as shown in our results. Regarding a mean daily dosage lower than 18 mg per day, an insufficient treatment effect due to an insufficient dose might be the reason for lower adherence 47 . Although the occurrence of adverse events might affect adherence, the adverse events that occur in the short term are mostly non-serious 48 , 49 and lead to withdrawal in less than 10% of the patients who experience them 49 . In addition, lower doses are usually less likely to cause adverse events compared with higher doses. In terms of concomitant medication, only ATX and hypnotics were linked to adherence. The common reasons for the prescription of concomitant ADHD medications are an inadequate response and intolerance to the previous treatment 50 . Therefore, the patients who were prescribed ATX in the early stage could be in the process of treatment switching or augmentation. Patients undergoing switching or augmentation are likely to have lower adherence because of the risk of additive adverse effects caused by the combination use. Therefore, it is understandable that the patients with concomitant ATX use had lower adherence. Patients with concomitant psychotropic use had lower MPRs in our study. However, only hypnotics exhibited a statistically significant association with adherence. Sleep disturbances can appear as ADHD symptoms 51 , 52 , 53 . Therefore, patients with concomitant hypnotic use in the early stage are presumed to originally have had moderate or severe sleep problems. OROS-MPH may worsen sleep status as an adverse effect 54 , 55 , which may negatively affect adherence. There are limitations to the use of the JMDC dataset. It is one of the largest claims databases in Japan but includes only 1–2% of all Japanese inhabitants. Additionally, all participants were recipients (or the family members of recipients) of employee’s health insurance (Kenkō-Hoken). Therefore, there is a potential for bias in socioeconomic and family backgrounds, which could affect adherence 12 , 14 , 20 . In addition, there is a lack of clinical detail in the database, such as ADHD symptoms and severity, incidence of adverse events, and coexisting psychiatric diseases. Therefore, it was not possible to determine whether adherence was due to remission of ADHD, ineffectiveness of medication, or aggravated coexisting psychiatric diseases. Thus, we evaluated the effect of these factors by conducting sensitivity analysis. Another limitation is that this database represents the prescription records and not the actual oral intake records. Thus, there is a possibility that patients did not take the medication, even with the prescription. These limitations should be considered in future studies. Despite these limitations, the findings of our study reveal the current state of pharmacotherapy for ADHD using OROS-MPH in Japan and provide useful insights into its resolution. Due to the increased prevalence of ADHD and use of psychostimulants, the inappropriate use of and low adherence to psychostimulants have been major problems in Japan. Appropriate medications for young ADHD patients are important not only to improve ADHD symptoms, but also to prevent the resultant disabilities and difficulties in their daily lives. This is the first study to provide clinically important evidence of the relationship between adherence and the possible risk factors in OROS-MPH treatment for children and adolescents with ADHD in Japan using a large-scale claims database. These results can help clinicians to predict the risk of poor adherence in the early stage of treatment and improve not only patients’ symptoms, but also their quality of life. Data availability The data that support the findings of this study are available from JMDC but restrictions apply to the availability of these data. The data were used under license for the current study and thus are not publicly available. However, the data are available from the authors upon reasonable request and with permission of JMDC. References 1. Acknowledgements This study was partly supported by research grants from the Japanese Ministry of Health, Labour and Welfare (H29-Seishin-Ippan-001, 19GC1012). Author information Affiliations Department of Psychiatry and Behavioral Neurosciences, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan Asami Ishizuya, Hidehiko Takahashi & Genichi Sugihara Department of Neuropsychiatry, Akita University Graduate School of Medicine, Hondo 1-1-1, Akita-city, Akita, 010-8543, Japan Asami Ishizuya & Kazuo Mishima Department of Sleep-Wake Disorders, National Center of Neurology and Psychiatry, National Institute of Mental Health, Kodaira, Tokyo, Japan Asami Ishizuya, Shingo Kitamura & Kazuo Mishima Department of Medical Technology, School of Health Sciences, Tokyo University of Technology, Tokyo, Japan Minori Enomoto Competing interests SK has received research support from the Japanese Ministry of Education, Sports, Science and Technology (17K07597). SK has received lecture fees from Otsuka Pharmaceutical Co., Ltd., and research funding from Boehringer Ingelheim Japan, Inc., VELDT Inc., and Tsubota Laboratory Inc. HT received a joint research grant from FUJIFILM Corporation. KM has received research support from the Japanese Ministry of Health, Labour and Welfare (H29-Seishin-Ippan-001, 19GC1012), the Japanese Ministry of Education, Sports, Science and Technology (19H03578), and a National Center of Neurology and Psychiatry Intramural Research Grant for Neurological and Psychiatric Disorders (29-1). KM has also received a collaborative research fund from the WPI-International Institute for Integrative Sleep Medicine, University of Tsukuba, and Taisho Pharmaceutical Co., Ltd. KM has received speaker’s honoraria from Eisai Co., Ltd., MSD Inc., Takeda Pharmaceutical Co., Ltd., Astellas Pharma Inc., Pfizer Inc., Otsuka Pharmaceutical Co., Ltd., Mochida Pharmaceutical Co., Ltd., Mitsubishi Tanabe Pharma Corporation (Yoshitomiyakuhin Corporation), and Janssen Pharmaceutical along with research grants from Eisai Co., Ltd., Nobelpharma Co., Ltd., Otsuka Pharmaceutical Co., Ltd., and Takeda Pharmaceutical Co., Ltd. GS has received research support from the Japanese Ministry of Education, Sports, Science and Technology (18K07597). The remaining authors declare no competing interests. Additional information Supplementary Information Rights and permissions Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit .

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