Skip to main content
Clinical Practice and Epidemiology in Mental Health : CP & EMH logoLink to Clinical Practice and Epidemiology in Mental Health : CP & EMH
. 2006 Sep 22;2:25. doi: 10.1186/1745-0179-2-25

Predictive factors for polypharmacy among child and adolescent psychiatry inpatients

Paul SS Russell 1,, Christina George 1, Priya Mammen 1
PMCID: PMC1584231  PMID: 16995933

Abstract

Background

Aim was to determine the predictive factors for polypharmacy among inpatient children and adolescents with psychiatric disorders.

Methods

Blinded, case-note review of children and adolescents with ICD 10 diagnosis of psychiatric disorders on psychotropic medication was conducted. Data on demography, illness, and treatment was analyzed with univariate and multivariate techniques.

Results

Proscribing non-pharmacological interventions (OR = 4.7) and pro re nata medication (OR = 3.3), increased the risk of polypharmacy. Prescribing physical restraint reduced the risk of receiving multiple medications (OR = 0.3).

Conclusion

Proscribing non-pharmacological interventions, pro re nata medication and physical restraints increased polypharmacy.

Background

Despite the pitfalls of advocating polypharmacy to children and adolescents with psychiatric disorders [1], this practice is alarmingly escalating [2]. This trend is predicted to increase with pharmacological treatments targeting symptoms without a clinical diagnosis, and when a pursuit for treatment perfection with medication is attempted [3]. Polypharmacy lacks safety or efficacy [4], but increases the incidence of drug interactions [5]. There is a need for research on polypharmacy in this population [6]. This study aims to provide further information on the risk factors associated with polypharmacy in the child and adolescent, inpatient, psychiatry population.

Methods

Subjects included in the study (N = 268) were consecutive admissions to the Child and Adolescent Psychiatry Unit, Christian Medical College and Hospital (a tertiary care centre), Vellore, from January 1997 to September 2001. Children and adolescents below 18 years of age, with an ICD-10 diagnosis (Clinical Guidelines Diagnostic Criteria version) of psychiatric disorder and treated with at least one psychotropic (excluding the anti-parkinsonian medication) were identified from unit registry. Reversible anonymisation as well as restricted access and disclosure of the obtained data ensured the privacy of patients. The Institution's Ethics Committee approved this study. A psychiatrist not part of the treating team reviewed the case-notes for demographic, and illness details (independent variables) made by the treating team during the time of admission prior to the design of this retrospective study. Another psychiatrist blinded to the case note details collected the treatment details from the inpatient admission-discharge records (dependent variable). Only the last admission was considered for subjects who were admitted more than once during this period. There was no discernible change in the prescribing pattern of psychotropics in the unit because of any secular trend, change in institutional protocol or any multiple-drug trial that was underway during this period. Information from these sources was grouped as demographic variables (sex), illness variables (diagnoses, co-morbidity, psychotic symptoms) and treatment variables (pro re nata medication, nonpharmacological intervention, physical restraint, side effects). Pro re nata was operationalized as medication administered on an 'as and when needed' basis. Nonpharmacological intervention was defined in this study as the psychoeducation about the nature of the illness and supportive psychotherapy administered to the patient and family

Chi Square test, Mann-Whitney U test for comparison between groups and logistic regression (enter method) was used to assess the association of polypharmacy and the three groups of variables. P < 0.05 (two-tailed) was considered significant and data was analyzed with SPSS (version 10.0).

Results and discussion

103 subjects were included in the study and the rest (N = 165) were excluded, as their psychiatric condition did not require treatment with psychotropic medication (N = 152), or incomplete data set (N = 13). The sample mean (sd) age and number of days spent in the hospital was 14.4 (2.6) years and 34.7 (10.9) days respectively. The mean (sd) age difference in years between the monopharmacy and polypharmacy groups was not statistically significant [14.2(2.7) Vs. 14.7(2.6), Z = -1.05; P = 0.3]. The disorders noted were mood disorders (n = 58), psychoses (n = 33) and others (n = 12). About 49(47.6%) subjects had single medication and 54 (52.4%) had multiple medication where, 35(64.8%) had 2 psychotropic, 13(24.1%) had 3 psychotropic, 5(9.3%) had 4 psychotropic, and 1(1.8%) had 5 psychotropic medications. There was no statistically significant difference in the demographic, illness or treatment variables between groups.

Gender, diagnosis, comorbidity, psychotic symptoms, side effects were not statistically significant in the logistic regression models. Proscribing nonpharmacological treatments was the strongest predictor of risk, and not prescribing pro re nata medication also increased the risk for polypharmacy. However, prescribing physical restraint was protective in nature and reduced polpharmacy (Table 1).

Table 1.

Association between risk factors and polypharmacy

Mono Pharmacy (n = 49) Poly Pharmacy (n = 54) Unadjusted OR df P Value Adjusted ORa 95% CI for OR P Value
n % n %
Demographic
Gender
 Male 25 24.3 31 30.1 1.2 1 0.5 1.2 0.5 2.7 0.6
 Female 24 23.3 23 22.3
Illness
Diagnosis
 Psychosis 24 23.3 12 11.7 1.4 1 0.2 1.6 0.8 3.2 0.1
 Mood 20 19.4 35 34
 Others 5 4.9 7 6.8
Comorbidity
 Yes 29 28.2 35 34 1.2 1 0.5 1.3 0.6 3.0 0.4
 No 20 19.4 19 18.4
Psychotic symptom
 Yes 27 26.2 33 32 1.2 1 0.5 1.2 0.5 2.8 0.5
 No 22 21.4 21 20.4
Treatment
Nonpharmacological
 Yes 33 32 17 16.5 4.5 1 0.001 4.7 2.0 11.1 0.001
 No 16 15.5 37 35.9
PRN medication
 Yes 19 18.7 8 7.8 3.6 1 0.007 3.3 1.2 8.8 0.01
 No 30 29.1 46 44.7
Physical restraint
 Yes 39 37.9 32 31.1 0.4 1 0.02 0.3 0.1 0.8 0.02
 No 10 20.4 22 40.7
Side effect
 Yes 35 18.4 27 21.4 1.5 1 0.3 1.9 0.7 4.7 0.2
 No 19 34 22 26.2

a Adjusted for age, number of days as inpatient, amount of antipsychotic in chlorpromazine equivalent.

The prevalence of polypharmacy in 52% of the population in this study is less than the 60.3% reported previously [7] and proscription of non-pharmacological therapy and pro re nata medication were identified as risk factors for polypharmacy as their odds ratio was high. As the odds ratio was around 1 for most of the other factors, their contribution as a risk or protective factor could not be predicted. However, prescribing physical restraint had low odds ratio suggesting it being a protective factor.

Proscribing nonpharmacological therapies as a risk factor is not surprising as non-pharmacological interventions [8] like psycho education [9,10] when combined with medication have resulted in a more rational use of medication and reduction of polypharmacy in previous studies.

However, in contrast to previous finding, pro re nata medication has reduced polypharmacy. This is explained by the treatment policy adopted in the facility, to convert and add pro re nata doses (if required on more than two or three occasions) to the existing regular medication regime, resulting in reduced polypharmacy. However, predictive factors documented elsewhere and not included in this study could have affected the results [11].

Beneficial effects of physical restraint reflect the protocol followed in the unit to use physical restraint before chemical restraint because the time spent in restraint is lesser than the elimination half-lives of most of the psychotropics, reducing the risks associated with these medicines [12]. Also, despite the existing negative attitude, the advantages of physical restraint have to be considered in assaultive and destructive children and adolescents [13].

The retrospective nature of the study limited our ability to search for the presence of certain other risk factors of polypharmacy and also it is possible that the small sample size and only those with the most severe psychopathology were on polypharmacy as inpatients compromising the generalizability of the finding.

Conclusion

In conclusion these results suggest that proscribing non-pharmacological interventions, pro re nata medication and physical restraint increases the risk of polypharmacy among children and adolescents with psychiatric disorders. Therefore, prescribing non-pharmacological interventions, pro re nata medication and physical restraint might decrease the risk of polypharmacy. However, further studies are needed to validate these findings along with subgroup analysis of multi-class polypharmacy, same-class polypharmacy, adjunctive polypharmacy and augmentation strategies.

Abbreviations

ICD 10 = International Classification of Diseases, version 10.

PRN = pro re nata

Competing interests

The author(s) declare that they have no competing interests.

Authors' contributions

PSSR was involved in conception, designing, data analysis and interpretation, drafting and approving the final version. CG was involved in conception, drafting and revising the final draft. PM was involved in conception, drafting and revising the final draft. All authors read and approved the final manuscript.

Contributor Information

Paul SS Russell, Email: russell@cmcvellore.ac.in.

Christina George, Email: mukkath@yahoo.com.

Priya Mammen, Email: marym@cmcvellore.ac.in.

References

  1. Woolston JL. Combined pharmacotherapy: pitfalls of treatment. J Am Acad Child Adolesc Psychiatry. 1999;38:1455–1457. doi: 10.1097/00004583-199911000-00021. [DOI] [PubMed] [Google Scholar]
  2. Walkup JT. Increasing use of psychotropic medications in children and adolescents: what does it mean? J Child Adolesc Psychopharmacol. 2003;13:1–3. doi: 10.1089/104454603321666126. [DOI] [PubMed] [Google Scholar]
  3. Jellinek MS. Overzealous prescription of medication. J Am Acad Child Adolesc Psychiatry. 1998;37:900–901. doi: 10.1097/00004583-199809000-00004. [DOI] [PubMed] [Google Scholar]
  4. Jensen PS, Bhatara Vs, Vitiello B, Hoagwood K, Feil M, Burke LB. Psychoactive medication prescribing practices for US children: gaps between research and clinical practice. J Am Acad Child Adolesc Psychiatry. 1999;38:557–565. doi: 10.1097/00004583-199905000-00017. [DOI] [PubMed] [Google Scholar]
  5. Behr R. Overzealous prescription of medication. J Am Acad Child Adolesc Psychiatry. 1998;37:900. doi: 10.1097/00004583-199809000-00003. [DOI] [PubMed] [Google Scholar]
  6. Stubbe DE, Martin A. The use of psychotropic medications in young children: the facts, the controversy, and the practice. Conn Med. 2000;64:329–333. [PubMed] [Google Scholar]
  7. Conner DF, Ozbayrak KR, Kusiak KA, Caponi Ab, Melloni RH. Combined pharmacotherapy in children and adolescents in residential treatment. J Am Acad Child Adolesc Psychiatry. 1997;36:248–254. doi: 10.1097/00004583-199702000-00016. [DOI] [PubMed] [Google Scholar]
  8. Weisz JR, Jensen PS. Efficacy and effectiveness of child and adolescent psychotherapy and pharmacotherapy. Ment Health Serv Res. 1999;1:125–157. doi: 10.1023/A:1022321812352. [DOI] [PubMed] [Google Scholar]
  9. Colley CA, Lucas LM. Polypharmacy: the cure becomes the disease. J Gen Intern Med. 1993;8:278–283. doi: 10.1007/BF02600099. [DOI] [PubMed] [Google Scholar]
  10. Brambilla P, Monzani E, Alessandri M, Frova M, Barbui C, Erlicher A. The use of psychotropic drugs in an Italian psychiatric hospital: a two-year-long follow-up study. Epidemiol Psychiatr Soc. 1999;8:262–269. doi: 10.1017/s1121189x00008174. [DOI] [PubMed] [Google Scholar]
  11. Ito H, Koyama A, Higuchi T. Polypharmacy and excessive dosing: psychiatrists' perceptions of antipsychotic drug prescription. Br J Psychiatry. 2005;187:243–247. doi: 10.1192/bjp.187.3.243. [DOI] [PubMed] [Google Scholar]
  12. Royal College of Psychiatrists. Council Report (CR4) London, Royal College of Psychiatrists; 1995. Strategies for the Management of Disturbed and Violent Patients in Psychiatric Units. [Google Scholar]
  13. Masters KJ, Bellonci C, Bernet W, Arnold V, Beitchman J, Benson RS, Bukstein O, Kinlan J, McClellan J, Rue D, Shaw JA, Stock S. American Academy of Child and Adolescent Psychiatry. Practice parameter for the prevention and management of aggressive behavior in child and adolescent psychiatric institutions, with special reference to seclusion and restraint. J Am Acad Child Adolesc Psychiatry. 2002;41(suppl 2):4S–25S. doi: 10.1097/00004583-200202001-00002. [DOI] [PubMed] [Google Scholar]

Articles from Clinical Practice and Epidemiology in Mental Health : CP & EMH are provided here courtesy of Bentham Science Publishers

RESOURCES