Polypharmacy in the Mental Health Treatment of Patients with IDD

Jennifer McLaren, MD; Jarrett Barnhill MD, DFAPA, FAACAP; Steve Erickson PharmD; Angela Hassiotis, PhD

Overview

People with IDD are vulnerable to high-risk prescribing practices such as polypharmacy or the overuse of antipsychotics.1,2 Polypharmacy, often defined as the use of 5 to 10 or more medications in a person’s regimen, affects 11% to 60% of people with IDD.3-5  

Appropriate Versus Problematic Polypharmacy

Appropriate polypharmacy: “the use of multiple medications that are clinically indicated, optimized, and prescribed according to best evidence. They extend life expectancy and improve quality of life for the patient.”6

Problematic polypharmacy: the use of medicines that are no longer appropriate, overuse of high-risk medications (e.g. second-generation antipsychotics, or anti-epileptics in absence of a seizure disorder), the benefits do not outweigh harm, combinations cause or risk harm and usage become unmanageable or distressing.

  • Prescribing cascade: adding additional, potentially avoidable medications to drug regimens, often without dropping an existing medication or reducing a dose.7
  • This commonly occurs with psychotropic medications and people with IDD.8-9
  • Polypharmacy with psychotropic medication leads to an increase in adverse events and drug interactions that negatively affect quality of life.9-11

Factors Contributing to Polypharmacy 

There are many factors that can contribute to polypharmacy. It is important to understand these factors and how they relate to the patient you are caring for; Figure 1 illustrates these factors.

Figure 1: Contributing Factors to Polypharmacy12

alt text needed

Risks and Consequences of Polypharmacy 

Patients treated with polypharmacy are at increased risks that prescribers should consider. Health risks are summarized in Table 1, while additional risks are detailed in Tables 2 and 3.

Table 1: Health Risks Associated with Polypharmacy

Health RisksExamples of High Risks with These Medications or Combination of These MedicationsConsequences
Metabolic Side Effects
  • Second generation antipsychotics (e.g., clozapine, olanzapine, risperidone)
  • Anti-epileptics (e.g., valproic acid) and second-generation antipsychotics
Obesity, hyperlipidemia, and diabetes
Seizures
  • Antipsychotics (e.g., clozapine, olanzapine, chlorpromazine, haloperidol)
  • Antidepressants (e.g., bupropion, tricyclic antidepressants, and selective serotonin reuptake inhibitors)
  • Stimulants
  • Lithium
  • Antibiotics (e.g., penicillin, cephalosporins, quinolones)
  • Analgesics (e.g., tramadol)
Decrease in seizure threshold
Cardiac
  • Antipsychotics and SSRIs/TCAs (e.g., haloperidol and citalopram
  • Antipsychotics and macrolide antibiotics
  • Antipsychotics and methadone
QTC prolongation and arrhythmias
Clozapine and benzodiazepinesMyocarditis, hypotension, cardiac arrest
SSRIs and beta blockersBradycardia and hypotension
Antipsychotics and TCAsTachycardia, orthostatic hypotension, QT prolongation
Lithium and diuretics/NSAIDS/ACE InhibitorsBradycardia and T wave changes
Akathisia
  • Antipsychotics
  • SSRI/SNROs
  • Stimulants
  • Antiemetics
  • Lithium
  • Anticholinergics
Increased restlessness, irritability, or agitation
Extrapyramidal Symptoms
  • Antipsychotics + antipsychotic
  • Antipsychotic + SSRI/SNRI or lithium or valproate
  • Antipsychotic + cholinesterase inhibitors
  • Antipsychotics + metoclopramide or prochlorperazine
Parkinsonism, dystonia, tardive dyskinesia, or neuroleptic malignant syndrome
Liver Injury
  • Valproate + antipsychotic or lamotrigine or atomoxetine
  • Carbamazepine + antipsychotic or antidepressant
  • Phenobarbital + phenytoin + psychotropics
  • Nefazodone + psychotropics
Mild enzyme elevations, severe hepatoxicity, to acute liver failure
Constipation
  • Antipsychotics (e.g., clozapine)
  • TCA
  • Opioid
  • Anticholinergics
Constipation or decreased gastrointestinal
motility
Sedation
  • Antipsychotics
  • Benzodiazepines
  • Mood Stabilizers (e.g., valproate, carbamazepine)
  • Antidepressants (e.g., trazodone, mirtazapine)
  • Other sedative agents (e.g., melatonin, hydroxyzine)
In people with IDD, sedative effects may be more significant and increase risk of falls, cognitive impairment, and reduced functioning.

 

Table 2: Quality of Life Risks with Polypharmacy 

Quality of Life RisksConsequences
FinancialIncreased costs due to multiple medications or may limit access to needed medications.
TimeIncreased time picking up and managing medications and monitoring.
Physical HealthPotential decline in physical health. 
Daily Functioning and Cognitive FunctioningPotential decline in physical and cognitive functioning.

Table 3: Prescribing and Administration Risks with Polypharmacy 

Prescribing and Administration RisksConsequences
Prescribing ErrorsCan lead to inappropriate drugs being prescribed, increasing risk of side effects or adverse reactions.
Dosing ErrorsIncorrect dose can lead to ineffective treatment or toxicity.
Mistakes in Taking or Administering MedicationsComplex medication regimens increase the risk of patient or caregiver errors.
Potential Difficulties with MonitoringHarder to track benefits and side effects of medication when multiple medications are prescribed.

Appropriate Prescribing 

It is imperative that the prescribing of psychotropic medication to people with IDD is aligned with evidence-based prescribing practices and is guided by clinical practice guidelines. Guidelines help ensure that patients receive treatments that are most appropriate for their care. 

  • OPTIMA-ID (Optimizing pharmaco-therapy and improving medication for ageing with intellectual disability) is a guide to optimization of medication regimens for older adults with intellectual disability, developed by healthcare providers as well as persons with intellectual disability.13
  • Twenty-two of the 67 criteria in OPTIMA-ID focus on psychotropic medications. Incorporating education and training with implementation of guidelines is another approach to working to ensure appropriate prescribing of psychotropic medications.
  • STOMP initiative (Stopping over-medication of people with intellectual disability, autism, or both -STOMP), was developed as an intervention to improve the prescribing of psychotropic medications taken by persons with ID living in the United Kingdom.
  • Implementation of the STOMP initiative has led to increased awareness of prescribing practices of psychotropic medications for persons with ID in the UK.14

It is important for clinicians and caregivers to investigate physical, environmental, and social factors when challenging behaviors are present, which may respond to non-medication approaches such as cognitive behavior therapy and positive behavior support.15 Because of the adverse effect profile of psychotropics, and antipsychotics, the decision to use these medications as an intervention for challenging behavior should be carefully rationalized.16,17

Key Steps in Deprescribing Psychotropic Medications18

  • Obtain a complete list of all the medications that the patient is taking and the reason for each medication.
  • Understand the effect of the medication on the patient (e.g., if it was helpful or not, if it has caused side effects and what side effects).
  • Conduct a complete evaluation of the patient, including a thorough understanding of what is going well and what is not going well in their life.
    • Full review of systems
  • Obtain any indicated measurements: e.g., BMI, labs, rating scales, etc.
  • Develop a crisis/safety plan.
  • Understand why the patient was put on polypharmacy (coordinate with other prescribers and have an interdisciplinary approach).
  • Consider each medication’s potential benefits against its potential risks or burdens, both now and in the future.
  • Provide psychoeducation to patients and caregivers and/or guardians about polypharmacy, the potential benefits, and the potential risks. Consider deprescribing with patient and caregiver and/or guardian.
    • Discuss the pros and cons of deprescribing
  • Consider deprescribing the medication with the lowest benefit or lowest risk of withdrawal or medication that is causing side effects.
  • Slowly taper the medication and closely monitor.
  • Most medications should be slowly tapered in a systematic and stepwise approach (e.g.,
    10-25% of dose every 2-4 weeks until discontinuation).
  • Some medications (e.g., stimulants) can be discontinued without a taper).
  • Use rating scales to monitor the underlying condition the medication was intended to treat (e.g., aberrant behavior checklist for behaviors that challenge).
  • Consider more frequent visits to check on the patient for improvement or side effects.

Conclusion

Polypharmacy is a common and concerning practice for people with IDD. While some cases of polypharmacy are appropriate, many involve inappropriate prescribing practices that can lead to adverse outcomes. Thoughtful, evidence-based prescribing is important, and active deprescribing of unnecessary medications is also a particularly important intervention. 


References

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