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Research Article

Use of Clozapine in Older Asian Patients with Schizophrenia between 2001 and 2009

  • Yu-Tao Xiang equal contributor mail,

    equal contributor Contributed equally to this work with: Yu-Tao Xiang, You-Hong Li

    xyutly@gmail.com (YTX); si.tian-mei@163.com (TMS)

    Affiliations: Department of Psychiatry, Chinese University of Hong Kong, Hong Kong, China, Beijing Anding Hospital, Capital Medical University, Beijing, China

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  • Robert W. Buchanan,

    Affiliation: Maryland Psychiatric Research Center, Department of Psychiatry, University of Maryland School of Medicine, Baltimore, Maryland, United States of America

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  • Gabor S. Ungvari,

    Affiliations: School of Psychiatry and Clinical Neurosciences, University of Western Australia, Perth, Australia, The University of Notre Dame Australia/Marian Centre, Perth, Australia

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  • Helen F. K. Chiu,

    Affiliation: Department of Psychiatry, Chinese University of Hong Kong, Hong Kong, China

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  • Kelly Y. C. Lai,

    Affiliation: Department of Psychiatry, Chinese University of Hong Kong, Hong Kong, China

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  • You-Hong Li equal contributor,

    equal contributor Contributed equally to this work with: Yu-Tao Xiang, You-Hong Li

    Affiliation: The Key Laboratory of Mental Health, Ministry of Mental Health & Peking University Institute of Mental Health, Beijing, China

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  • Tian-Mei Si mail,

    xyutly@gmail.com (YTX); si.tian-mei@163.com (TMS)

    Affiliation: The Key Laboratory of Mental Health, Ministry of Mental Health & Peking University Institute of Mental Health, Beijing, China

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  • Chuan-Yue Wang,

    Affiliation: Beijing Anding Hospital, Capital Medical University, Beijing, China

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  • Edwin H. M. Lee,

    Affiliation: Department of Psychiatry, University of Hong Kong, Hong Kong, China

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  • Yan-Ling He,

    Affiliation: Department of Psychiatric Epidemiology, Shanghai Mental Health Center, Shanghai, China

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  • Shu-Yu Yang,

    Affiliation: Department of Pharmacy, Taipei City Hospital, Taipei, Taiwan

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  • Mian-Yoon Chong,

    Affiliation: Kaohsiung Chang Gung Memorial Hospital and Chang Gung University School of Medicine, Kaohsiung, Taiwan

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  • Ee-Heok Kua,

    Affiliation: Department of Psychological Medicine, National University of Singapore, Singapore, Singapore

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  • Senta Fujii,

    Affiliation: Hyogo Institute for Traumatic Stress (HITS), Kobe, Japan,

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  • Kang Sim,

    Affiliation: Department of General Psychiatry, Institute of Mental Health, Buangkok View, Singapore, Singapore

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  • Michael K. H. Yong,

    Affiliation: Department of Medicine, Alexandra Hospital/Jurong Health Services, Singapore, Singapore

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  • Jitendra K. Trivedi,

    Affiliation: Department of Psychiatry, C.S.M. Medical University UP, Lucknow, Uttar Pradesh, India

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  • Eun-Kee Chung,

    Affiliation: Department of Psychiatry, National Seoul Hospital, Seoul, Korea

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  • Pichet Udomratn,

    Affiliation: Department of Psychiatry, Faculty of Medicine, Prince of Songkla University, Songkhla, Thailand

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  • Kok-Yoon Chee,

    Affiliation: Department of Psychiatry and Mental Health, Tunku Abdul Rahman Institute of Neuroscience, Kuala Lumpur Hospital, Kuala Lumpur, Malaysia

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  • Norman Sartorius,

    Affiliation: Association for the Improvement of Mental Health Programs, Geneva, Switzerland

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  • Chay-Hoon Tan,

    Affiliation: Department of Pharmacology, National University of Singapore, Singapore, Singapore

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  • Naotaka Shinfuku

    Affiliation: Department of Social Welfare, School of Human Sciences, Seinan Gakuin University, Fukuoka, Japan

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  • Published: June 10, 2013
  • DOI: 10.1371/journal.pone.0066154

Abstract

Background

To date there has been no large-scale international study that examined the use of clozapine in older patients with schizophrenia. This study examined the use of clozapine and its demographic and clinical correlates in older patients with schizophrenia in East Asia during the period between 2001 and 2009.

Method

Information on 1,157 hospitalized patients with schizophrenia aged 50 or older in five East Asian countries and territories (China, Hong Kong, Korea, Singapore and Taiwan) was extracted from the database of the Research on Asian Psychotropic Prescription Patterns (REAP) project. Socio-demographic and clinical characteristics and prescription of psychotropic medications were recorded.

Results

Clozapine was prescribed for 20.6% of the pooled sample; 19.0% in 2001, 19.4% in 2004 and 22.9% in 2009. Multiple logistic regression analysis of the whole sample revealed that patients taking clozapine had a longer duration of illness, more negative symptoms and were less likely to receive first generation antipsychotic and anticholinergic drugs, but more likely to report weight gain compared to those not receiving clozapine. Compared to those in other sites, older patients in China were more likely to receive clozapine.

Conclusions

The prescription of clozapine for older Asian schizophrenia inpatients has remained at a stable level during the past decade. The appropriateness of use of clozapine in China needs to be further explored.

Introduction

In the past two decades a number of second-generation antipsychotic medications (SGAs) have been developed. To date there is no clear evidence that SGAs are more effective than FGAs in treating schizophrenia [1] apart from clozapine which is still the most effective antipsychotic drug for treatment-resistant schizophrenia [2]. In the past decades, prescribing patterns of clozapine have been extensively reported in patients with adult schizophrenia. In addition to its efficacy and side effects, different socio-economic situations, health care policies, prescribing traditions and clinicians' and patients' attitudes towards clozapine have influenced its prescription patterns across countries [3]. For example, clozapine was not available in Japan until the end of 2009, while in China it was one of the most commonly used antipsychotics in the past two decades (42.2% and 34.9% of schizophrenia inpatients and outpatients, respectively) [4].

Although their life expectancy is still significantly worse than that of the general population [5], nowadays, with the general improvement of psychiatric and medical care, many patients with schizophrenia live into older adulthood. In contrast to younger adults, psychotropic drug prescription for older patients must consider age-related changes in drug absorption, metabolism, and excretion and medical comorbidity. Thus, prescription patterns of clozapine observed in younger adult patients may not reflect the situation in patients with advanced age. We could not find a large-scale international study that examined the use of clozapine in older patients with schizophrenia. In order to rationalize clozapine use, it is important to understand its prescription patterns in clinical practice.

In most East Asian countries, community-based psychiatric care is not well developed and hospital-based services still dominate psychiatric care [6]. Initiated in 1999, the Research on Asian Psychotropic Prescription Pattern (REAP) project is an ongoing pharmaco-epidemiological survey on prescription trends of psychotropic drugs in schizophrenia inpatients in Asia [7], [8]. This report is based on a secondary analysis of the data of the REAP project, which was designed to: (1) examine the prescribing pattern of clozapine in Asian schizophrenia patients aged 50 years and above during the period between 2001 and 2009; and (2) explore its demographic and clinical correlates. Considering the poorer general health status of older patients, their increased vulnerability to side effects [9], [10] and the 10–15% of schizophrenia patients who are not fully responsive to FGAs [11], we hypothesized that the proportion of older Asian schizophrenia patients receiving clozapine would be less than 15%. For the purpose of this study, we defined ‘common use of clozapine’ as a figure of more than 15% in a schizophrenia patient population.

Methods

Settings, study design, and subjects

The first two surveys of the REAP project were conducted in July 2001 and July 2004, while the data for the third one were collected between October 2008 and March 2009. The participating countries and territories included mainland China (China hereafter), Hong Kong, Japan, Korea, Singapore and Taiwan; centres in India, Malaysia, and Thailand joined the surveys in 2009. Hospitals were selected according to convenience in the participating countries/regions. Details of the REAP project have been described elsewhere [6]. In this study, data of patients who met the following criteria in the REAP projects were analyzed: (1) a diagnosis of ICD-10 or DSM-IV schizophrenia, (2) being 50 years or older [12], (3) receiving antipsychotic treatment, and (4) having the ability to understand the study, and being willing and able to provide written or oral consent according to the requirements of the clinical research ethics committees in the respective study sites. Patients with major medical conditions were excluded.

In the REAP surveys, eligible patients were enrolled consecutively at each site. Socio-demographic and clinical information including age, gender, ethnicity, the type and dose of antipsychotic medications, benzodiazepine (BZD) and anticholinergic (ACM) drugs, length of illness, psychopathology (positive symptoms: hallucinations, delusions and thought disorder; negative symptoms: affective flattening, alogia and avolition) in the past month, extrapyramidal symptoms (EPS; including rigidity, akinesia, tremor, akathisia and dystonia) and weight gain within the past three months were collected by a review of medical records in 2001, and by either the same method or patient interviews in both 2004 and 2009 using a form designed for the study. Tardive dyskinesia (TD) is treated separately from the other forms of EPS because of its treatment characteristics. The data were collected by the patients' attending psychiatrists or by members of the research team with the agreement of the patients' treating psychiatrists.

A total of 6,761 schizophrenia inpatients were recruited in the three surveys; 2,399 from 31 psychiatric institutions, 2,136 from 25, and 2,226 patients from 50 in the 2001, 2004, and 2009 surveys, respectively. Altogether 2,236 patients fulfilled the above criteria for this report. There were only 15 patients in India, 14 in Malaysia and 8 in Thailand; in addition, in Japan clozapine was not available during the survey period. Therefore these four sites were excluded and thus 1,157 patients were included in the analyses; 405 in 2001, 319 in 2004 and 433 in 2009. In order to compare clozapine use between the current sample and younger adult patients (i.e., those under the age of 50 years) in the REAP project, figures of clozapine prescription in younger adult patients are also presented.

The study protocol was approved by the clinical research ethics committees of Chinese University of Hong Kong, Hong Kong; Peking University Institute of Mental Health, China; Taipei City Hospital, Taiwan; Chang Gung University, Taiwan; National University of Singapore, Singapore; Institute of Mental Health, Singapore; C.S.M. Medical University UP, India; National Seoul Hospital, Korea; Prince of Songkla University, Thailand; Kuala Lumpur Hospital, Malaysia; Seinan Gakuin University, Japan. Given the anonymous nature of this observational study and the minimal risk to patients, informed consent was deemed unnecessary in some study sites in line with the requirements of the local clinical research ethics committee if only a review of case notes was used. All patients receiving the interview provided written or oral consent according to the requirements of the Clinical Research Ethics Committee in the respective study sites.

Statistical analysis

The data were analyzed using SPSS 19.0 for Windows. Comparisons of clozapine use between the three surveys were performed with chi-square test. Multiple logistic regression analysis with the “Enter” method was used to determine the demographic and clinical variables independently influencing clozapine use. Cross sectional use of clozapine was the dependent variable, while independent variables included study sites and time, age, gender, psychopathology, length of illness, use of FGAs, BZD and ACM, EPS and TD. The level of significance was set at 0.05 (two-tailed).

Results

Of the 1,157 older adult patients who met study criteria, 238 (20.6%) received clozapine: 77 (19.0%) in 2001, 62 (19.4%) in 2004 and 99 (22.9%) in 2009. There was no difference between the three surveys (χ2 = 2.2, df = 2, p = 0.33). In contrast, 21.6% (747/3,461) of younger adult patients in the REAP project received clozapine: 20.2% (271/1,343) in 2001, 23.0% (278/1,209) in 2004 and 21.8% (198/909) in 2009. There was no significant difference in terms of prescription patterns of clozapine between the two age groups in general (χ2 = 0.5, df = 1, p = 0.47), or at each survey (in 2001: χ2 = 0.3, df = 1, p = 0.61; in 2004: : χ2 = 1.8, df = 1, p = 0.17; in 2009: : χ2 = 0.2, df = 1, p = 0.66). Figure 1 depicts the use of clozapine in older schizophrenia patients. Table 1 shows the socio-demographic and clinical characteristics and the use of clozapine in the whole sample and separately for patients by study sites.

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Figure 1. Percentage of older patients with schizophrenia receiving clozapine.

doi:10.1371/journal.pone.0066154.g001
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Table 1. Socio-demographic and clinical characteristics of older Asian patients with schizophrenia in REAP surveys 2001–2009.

doi:10.1371/journal.pone.0066154.t001

Table 2 presents independent demographic and clinical correlates of clozapine prescription in older schizophrenia patients. Patients taking clozapine had longer length of illness, more negative symptoms and were less likely to receive FGAs and ACM, but more likely to report weight gain compared to those not receiving clozapine.

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Table 2. and clinical correlates independently associated with clozapine in the combined sample (n = 1,157).

doi:10.1371/journal.pone.0066154.t002

Discussion

In this study, prescription patterns of FGAs and SGAs varied greatly across participating countries/regions (for details see Xiang et al. [13]). Our hypothesis that the proportion of older Asian schizophrenia patients receiving clozapine would be less than 15% was not confirmed. The frequency of clozapine use in the pooled sample of older patients was 20.6%, varying from 19.0% to 22.9% across surveys; the results are similar to the corresponding figures in patients under the age of 50 years in the REAP project (21.6% in the pooled sample, varying from 20.2% to 23.0% across surveys). It is noteworthy that there were great variations in clozapine use between the participating sites. The frequency of clozapine prescription was 40.7% in China and ranged between 2.5–19.6% in the other sites. The high frequency of clozapine prescription in older Chinese patients could be explained by the following reasons: (1) clozapine has continuously been used in China since its introduction in 1976 with regular blood monitoring and it has become one of the most frequently used antipsychotic drugs in China, even as the first-line treatment in some areas [14], yielding extensive clinical and research experience [3]; (2) clozapine is cheap in China costing approximately US$0.08 for 300 mg; and (3) only clozapine and risperidone were covered by basic public health insurance in most areas of China before 2005. The gradually decreasing trend of clozapine use in China (44.8% in 2001, 40.2% in 2004 and 37.2% in 2009; χ2 = 1.8, df = 2, p = 0.42), could be due to the introduction of strict guidelines for clozapine use and the increasing use of other SGAs. The reasons for the increased use of clozapine in 2009 in Singapore and Taiwan are unknown.

Clozapine should be used in patients unresponsive to other antipsychotic drugs [3], [15], which could explain the association of clozapine use and longer duration of illness. As negative symptoms are far more difficult to treat, they tend to occur more frequently in treatment-resistant schizophrenia. The recommended use of clozapine in this population [16] may explain the association between clozapine and negative symptoms.

In this study, adjunctive FGAs were used less frequently in the clozapine group, which is in line with current recommendations [17], [18]. There is no compelling evidence suggesting the superiority of such combinations [19]; furthermore, polypharmacy could increase the risk of adverse effects and makes it difficult to gauge which drug really works [20], [21]. People on clozapine were less likely to receive concurrent ACMs compared to non-clozapine users. This represents rational practice due to the doubtful effectiveness and elevated risk of adverse effects accompanying such co-prescription [19]. As expected, clozapine was associated with more weight gain in this study, which supports the findings of previous studies [22].

The results of this survey should be interpreted with caution due to several limitations. First, the REAP project only focuses on inpatients in selected East Asian countries and regions. The restriction of the study sample to hospitals selected according to convenience where patients were consecutively examined limits generalizability of the findings. In addition, the number of patients on clozapine was very small in some participating countries/regions, which hinders within-group comparisons between the three surveys in each site. Second, the severity of psychopathology and the drug-induced side effects were not assessed by standardized instruments. Third, the data were collected by a review of medical records in 2001 and by either a review of medical records or patient interviews in 2004 and 2009, which might have potentially led to observational bias. Fourth, some important factors likely to influence appropriate clozapine use, such as age of onset, use of prior antipsychotics, local prescription guidelines, reimbursement policies and the type of psychiatric facilities were not evaluated. There are differences in healthcare schemes, prescribing traditions and treatment guidelines between institutions even within one country, and within one institution between different study times. The confounding effects of these differences and the potential multiple interactions between them could not be explored. More advanced analyses are needed using a sophisticated design in future REAP surveys. Finally, the appropriateness of clozapine use could not be explored.

In conclusion, one fifth of older Asian schizophrenia inpatients received clozapine over the period between 2001 and 2009. Clozapine was particularly commonly prescribed in China (40.7%). Given that most treatment guidelines for schizophrenia suggests clozapine only in treatment-resistant patients [3], [16] and considering the poorer general health status of older patients and their increased vulnerability to psychotropic-induced side effects, the reasons for common use of clozapine in older patients in China warrant further investigations.

Acknowledgments

The authors are grateful to the following clinicians involved in the data collection: Hong Deng and Wei Hao in China; Ajit Avasthi, Dipesh Bhagabati, Roy Abraham Kallivayalil, Shubhangi R. Parkar, and YC Janardhan Reddy in India; Tateno Masaru, Masamune Yayoi, Akiyama Tsuyoshi, Sato Soichirou, Nakagome Kazuyuki, Nakamura Jun, and Kuroki Toshihide in Japan; Tae-Yeon Hwang, Seok Hyeon Kim, Yo Wang Lee, and Jong- Il Lee in Korea; Tung-ping Su, Shih-ku Lin,Tzu-ting Chen, Chieh-hsin Chang, Hong-chieh Hsu, Chi-Fa Hung, and Cheng-chung Chen in Taiwan; Krisakorn Sukavatvibul, Jittima Kleawtanong, Tantawan Suradechasakul, Manote Lotrakul, Usaree Srisutudsanavong in Thailand; and Norharlina Bahar in Malaysia. The authors also thank clinicians who helped to organize the study in each study site.

Author Contributions

Conceived and designed the experiments: NS CHT MYC EHK GSU NS. Performed the experiments: YTX CYW YHL TMS EHML YLH GSU HFKC SYY MYC NS CHT EHK SF KS MKHY JKT EKC PU KYC. Analyzed the data: YTX CYW TMS GSU. Wrote the paper: YTX RWB CYW TMS EHML YLH GSU HFKC KYCL SYY MYC NS CHT EHK SF KS MKHY JKT EKC PU KYC NS. Contributed to and approved the final manuscript: YTX RWB GSU HFKC KYCL YHL TMS CYW EHML YLH SYY MYC EHK SF KS MKHY JKT EKC PU KYC NS CHT NS.

References

  1. 1. Geddes J, Freemantle N, Harrison P, Bebbington P (2000) Atypical antipsychotics in the treatment of schizophrenia: systematic overview and meta-regression analysis. BMJ 321: 1371–1376.
  2. 2. Suzuki T, Uchida H, Watanabe K, Kashima H (2011) Factors associated with response to clozapine in schizophrenia: a review. Psychopharmacol Bull 44: 32–60.
  3. 3. Xiang YT, Weng YZ, Leung CM, Tang WK, Ungvari GS (2007) Clinical correlates of clozapine prescription for schizophrenia in China. Hum Psychopharmacol 22: 17–25.
  4. 4. Si TM, Shu L, Yu X, Ma C, Wang GH, et al. (2004) Antipsychotic drug patterns of schizophrenia in China: a cross-sectional study (in Chinese). Chinese Journal of Psychiatry 37: 152–155.
  5. 5. Xiang YT, Weng YZ, Leung CM, Tang WK, Ungvari GS (2008) Socio-demographic and clinical correlates of lifetime suicide attempts and their impact on quality of life in Chinese schizophrenia patients. J Psychiatr Res 42: 495–502.
  6. 6. Shinfuku N, Tan CH (2008) Pharmacotherapy for schizophrenic inpatients in East Asia–changes and challenges. Int Rev Psychiatry 20: 460–468.
  7. 7. Chong MY, Tan CH, Fujii S, Yang SY, Ungvari GS, et al. (2004) Antipsychotic drug prescription for schizophrenia in East Asia: rationale for change. Psychiatry Clin Neurosci 58: 61–67.
  8. 8. Sim K, Su A, Fujii S, Yang SY, Chong MY, et al. (2004) Antipsychotic polypharmacy in patients with schizophrenia: a multicentre comparative study in East Asia. Br J Clin Pharmacol 58: 178–183.
  9. 9. Meyers BS, Jeste DV (2010) Geriatric psychopharmacology: evolution of a discipline. J Clin Psychiatry 71: 1416–1424.
  10. 10. Uchida H, Pollock BG, Bies RR, Mamo DC (2009) Predicting age-specific dosing of antipsychotics. Clin Pharmacol Ther 86: 360–362.
  11. 11. Carpenter WT Jr, Conley RR, Buchanan RW, Breier A, Tamminga CA (1995) Patient response and resource management: another view of clozapine treatment of schizophrenia. Am J Psychiatry 152: 827–832.
  12. 12. Dassori AM, Copeland LA, Zeber JE, Miller AL (2011) Factors in second-generation antipsychotic switching patterns in a national sample of older veterans with schizophrenia. Psychiatr Serv 62: 47–53.
  13. 13. Xiang YT, Kreyenbuhl J, Dickerson FB, Ungvari GS, Wang CY, et al. (2012) Use of first- and second-generation antipsychotic medications in older patients with schizophrenia in Asia (2001–2009). Aust N Z J Psychiatry 46: 1159–1164.
  14. 14. Liu TL, Li CY (2003) The comparison of use of antipsychotics in first-episode patients with schizophrenia (in Chinese). Medical journal of Chinese people Health 15: 289–290.
  15. 15. Iqbal MM, Rahman A, Husain Z, Mahmud SZ, Ryan WG, et al. (2003) Clozapine: a clinical review of adverse effects and management. Ann Clin Psychiatry 15: 33–48.
  16. 16. Buchanan RW, Kreyenbuhl J, Kelly DL, Noel JM, Boggs DL, et al. (2010) The 2009 schizophrenia PORT psychopharmacological treatment recommendations and summary statements. Schizophr Bull 36: 71–93.
  17. 17. Chinese Medical Association. Guideline for the Prevention and Treatment of Schizophrenia in China. Beijing, Chinese Medical Association, 2003
  18. 18. Segovia J, Bartlett RF, Edwards AC (1989) The association between self-assessed health status and individual health practices. Can J Public Health 80: 32–37.
  19. 19. Remington G, Saha A, Chong SA, Shammi C (2005) Augmentation strategies in clozapine-resistant schizophrenia. CNS Drugs 19: 843–872.
  20. 20. Henderson DC, Goff DC (1996) Risperidone as an adjunct to clozapine therapy in chronic schizophrenics. J Clin Psychiatry 57: 395–397.
  21. 21. Kapur S, Roy P, Daskalakis J, Remington G, Zipursky R (2001) Increased dopamine d(2) receptor occupancy and elevated prolactin level associated with addition of haloperidol to clozapine. Am J Psychiatry 158: 311–314.
  22. 22. Wetterling T (2001) Bodyweight gain with atypical antipsychotics. A comparative review. Drug Saf 24: 59–73.