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
| Admission | Indication | Discharge | Indication |
| Venlafaxine 75 mg: 3 by mouth in the morning and 2 by mouth at bedtime | Antidepressant | ||
| Lamotrigine 200 mg by mouth in the morning | Mood stabilizer | Lamotrigine 200 mg at bedtime | Mood stabilizer |
| Mirtazapine 30 mg by mouth at bedtime | Antidepressant | Mirtazapine 30 mg at bedtime | Antidepressant |
| Clonazepam 1 mg by mouth in the morning and at bedtime | Antianxiety | Hydroxyzine 25 mg every 8 h as needed | Antianxiety |
| Ziprasidone 80 mg by mouth in the morning and at bedtime | Antipsychotic | Ziprasidone 80 mg twice daily | Antipsychotic |
| Zolpidem 10 mg by mouth daily as needed for anxiety | Hypnotic | ||
| Metformin hydrochloride 1,000 mg by mouth twice daily | Diabetes | Metformin hydrochloride 1,000 mg in the morning and 500 mg at bedtime | Diabetes |
| Atorvastatin 40 mg by mouth at bedtime | High cholesterol | ||
| Esomeprazole 40 mg by mouth at bedtime | Gastroesophageal reflux disease | Esomeprazole 40 mg daily | Gastroesophageal reflux disease |
| Lithium carbonate 600 mg by mouth twice daily | Mood stabilizer | Lithium carbonate 600 mg twice daily | Mood stabilizer |
| Buspirone 7.5 mg by mouth twice daily | Antianxiety | Buspirone 7.5 mg twice daily | Antianxiety |
| Levothyroxine 50 mcg by mouth in the morning | Hypothyroid | Levothyroxine 100 mcg daily | Hypothyroid |
| Amphetamine/dextroamphetamine 25 mg by mouth in the morning and 20 mg at noon | Stimulant | ||
| Multivitamin: 1 by mouth daily | General health | ||
| Baby aspirin: 1 by mouth daily | Cardiovasular | ||
| Quinine sulfate: 2 tablets by mouth at bedtime | Leg cramps | ||
| Cetirizine 10 mg by mouth in the morning | Antihistamine | ||
| Atropine/diphenoxylate: 1 by mouth twice daily | Irritable bowel syndrome | ||
| Bismuth subsalicylate over-the-counter by mouth twice daily | Irritable bowel syndrome | ||
| Insulin glargine 45 IU subcutaneous twice daily | Diabetes | Insulin glargine 47 units subcutaneous in the morning and at bedtime | Diabetes |
| Insulin lispro sliding scale | Diabetes | Insulin lispro sliding scale | Diabetes |
| Ferrous sulfate 324 mg daily | Anemia | ||
| Pregabalin 50 mg twice daily | Paresthesia |
Full article at: http://goo.gl/ubG1uX
By: Alok Madan, PhD, MPH,
John M. Oldham, MD, Sylvia Gonzalez, MD, and J. Christopher Fowler, PhD
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 author: Alok Madan, PhD, MPH, The Menninger Clinic,
12301 S Main St, Houston, TX 77035 (Email: ude.regninnem@nadama).
More at: https://twitter.com/hiv_insight
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