Outcomes Study: Decreasing the Impact of Impaction in a Forensic Psychiatric Facility: Implementation of a Pharmacy Derived Clozapine-Induced Constipation Monitoring Protocol

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Outcomes Study: Decreasing the Impact of Impaction in a Forensic Psychiatric Facility: Implementation of a Pharmacy Derived Clozapine-Induced Constipation Monitoring Protocol

Background

  • Clozapine has uniquely complex binding properties allowing it to bind to a variety of receptors including histamine, muscarinic, dopaminergic, and serotonergic receptors which contribute to its diverse side effect profile.
  • Recommendations for routine evaluation and management of rare but serious side effects have been developed for: agranulocytosis (frequency <1%), myocarditis (frequency <1%), and seizures (frequency ~3).
  • Constipation is reported in 14%-25% of patients taking clozapine; however, no standard protocol for routine evaluation has been developed.

The purpose of this study is to evaluate the impact of a clozapine-induced constipation monitoring protocol at Fulton State Hospital, along-term forensic psychiatric setting.



Objectives

  • To determine if the implementation of a clozapine-induced constipation monitoring protocol affects:
    • Number of constipation related referrals made to an external academic medical facility
    • Number of referrals to Fulton State Hospital’s internal medical clinics
  • Establish a correlation between anticholinergic burden and severity of constipation
  • Survey employee understanding and reception of a clozapine-induced constipation monitoring protocol

 

Read the Outcomes Study by submitting the form below.

 

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