Wednesday, December 16, 2015

Reducing Adverse Polypharmacy in Patients with Borderline Personality Disorder: An Empirical Case Study

Objective:
Polypharmacy is common and especially challenging in the context of borderline personality disorder in light of impulsivity and self-harm associated with the disorder, risk of adverse drug-drug interactions, and financial burden. Reduction in polypharmacy could be conceptualized as a high priority in the treatment of borderline personality disorder. This case aims to demonstrate that potential.

Method:
This case report presents outcomes data for an individual with borderline personality disorder during the course of an extended psychiatric hospitalization. Symptomatic change is based on the Patient Health Questionnaire Somatic, Anxiety, and Depression Symptoms scales and World Health Organization 5-Item Well-Being Index. Change in polypharmacy is presented both in terms of absolute number and complexity of the medication regimen. Clinical outcomes data are provided at 2, 12, and 24 weeks postdischarge.

Results:
During a 56-day hospitalization, the patient demonstrated clinical improvement across clinical domains—all occurred within the context of reduced number (43%) and complexity (40%) of her medication regimen. Symptomatic improvement was sustained up to 6 months postdischarge.

Conclusions:
Despite good intentions, polypharmacy can be associated with iatrogenic harm and contribute to functional impairment, especially in the context of borderline personality disorder, in which symptomatic fluctuations are part of the illness itself. A reduction in the patient’s high-risk polypharmacy during treatment represents a noteworthy treatment outcome in and of itself. Additional measures of medication risk and liability have the potential to become markers of clinical effectiveness.

Clinical Points
  • Despite good intentions, polypharmacy is common and especially challenging in the context of borderline personality disorder in light of impulsivity and self-harm associated with the disorder, risk of adverse drug-drug interactions, and financial burden.
  • A reduction in patients’ high-risk polypharmacy during treatment represents a noteworthy treatment outcome in and of itself and might be conceptualized as a marker of clinical effectiveness.

Table 1.

Ms A’s Medications at Admission and Discharge
AdmissionIndicationDischargeIndication
Venlafaxine 75 mg: 3 by mouth in the morning and 2 by mouth at bedtimeAntidepressant
Lamotrigine 200 mg by mouth in the morningMood stabilizerLamotrigine 200 mg at bedtimeMood stabilizer
Mirtazapine 30 mg by mouth at bedtimeAntidepressantMirtazapine 30 mg at bedtimeAntidepressant
Clonazepam 1 mg by mouth in the morning and at bedtimeAntianxietyHydroxyzine 25 mg every 8 h as neededAntianxiety
Ziprasidone 80 mg by mouth in the morning and at bedtimeAntipsychoticZiprasidone 80 mg twice dailyAntipsychotic
Zolpidem 10 mg by mouth daily as needed for anxietyHypnotic
Metformin hydrochloride 1,000 mg by mouth twice dailyDiabetesMetformin hydrochloride 1,000 mg in the morning and 500 mg at bedtimeDiabetes
Atorvastatin 40 mg by mouth at bedtimeHigh cholesterol
Esomeprazole 40 mg by mouth at bedtimeGastroesophageal reflux diseaseEsomeprazole 40 mg dailyGastroesophageal reflux disease
Lithium carbonate 600 mg by mouth twice dailyMood stabilizerLithium carbonate 600 mg twice dailyMood stabilizer
Buspirone 7.5 mg by mouth twice dailyAntianxietyBuspirone 7.5 mg twice dailyAntianxiety
Levothyroxine 50 mcg by mouth in the morningHypothyroidLevothyroxine 100 mcg dailyHypothyroid
Amphetamine/dextroamphetamine 25 mg by mouth in the morning and 20 mg at noonStimulant
Multivitamin: 1 by mouth dailyGeneral health
Baby aspirin: 1 by mouth dailyCardiovasular
Quinine sulfate: 2 tablets by mouth at bedtimeLeg cramps
Cetirizine 10 mg by mouth in the morningAntihistamine
Atropine/diphenoxylate: 1 by mouth twice dailyIrritable bowel syndrome
Bismuth subsalicylate over-the-counter by mouth twice dailyIrritable bowel syndrome
Insulin glargine 45 IU subcutaneous twice dailyDiabetesInsulin glargine 47 units subcutaneous in the morning and at bedtimeDiabetes
Insulin lispro sliding scaleDiabetesInsulin lispro sliding scaleDiabetes
Ferrous sulfate 324 mg dailyAnemia
Pregabalin 50 mg twice dailyParesthesia

Full article at: http://goo.gl/ubG1uX

By:   Alok Madan, PhD, MPH,corresponding author John M. Oldham, MD, Sylvia Gonzalez, MD, and J. Christopher Fowler, PhD
The Menninger Clinic and Menninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, Texas.
corresponding authorCorresponding author.
Corresponding author: Alok Madan, PhD, MPH, The Menninger Clinic, 12301 S Main St, Houston, TX 77035 ( ude.regninnem@nadama).
 

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