| Literature DB >> 28824467 |
Untara Shaikh1, Iqra Qamar2, Farhana Jafry3, Mudasar Hassan4, Shanila Shagufta5, Yassar Islamail Odhejo1, Saeed Ahmed6.
Abstract
Borderline personality disorder (BPD) patients, when in crisis, are frequent visitors of emergency departments (EDs). When these patients exhibit symptoms such as aggressiveness, impulsivity, intense anxiety, severe depression, self-harm, and suicidal attempts or gestures, diagnosis, and treatment of the BPD becomes challenging for ED doctors. This review will, therefore, outline advice to physicians and health-care providers who face this challenging patient population in the EDs. Crisis intervention should be the first objective of clinicians when dealing with BPD in the emergency. For the patients with agitation, symptom-specific pharmacotherapy is usually recommended, while for non-agitated patients, short but intensive psychotherapy especially dialectical behavior therapy (DBT) has a positive effect. Although various psychotherapies, either alone or integrated, are preferred modes of treatment for this group of patients, the effects of psychotherapies on BPD outcomes are small to medium. Proper risk management along with developing a positive attitude and empathy toward these patients will help them in normalizing in an emergency setting after which treatment course can be decided.Entities:
Keywords: aggression; borderline personality disorder; cluster B personality disorders; emergency psychiatry; impulsivity; psychosocial issues; psychotherapy; suicidality
Year: 2017 PMID: 28824467 PMCID: PMC5543278 DOI: 10.3389/fpsyt.2017.00136
Source DB: PubMed Journal: Front Psychiatry ISSN: 1664-0640 Impact factor: 4.157
Studies that investigated immediate crisis intervention in BPD patients.
| Study | Study design | Number of patients | Treatment strategy | Results/treatment response |
|---|---|---|---|---|
| Philipsen et al. ( | An open label study | 14 females with acute states of strong aversive inner tension and urge to commit self-injurious behavior | 75 and 150 μg of oral clonidine | After administration of clonidine in both doses, aversive inner tension, dissociative symptoms, urge to commit self-injurious behavior, and suicidal ideations significantly decreased. The peak effect was after 30–60 min |
| Damsa et al. ( | Observational study | 25 patients with acute agitation | Olanzapine 10 mg IM single injection | Significant improvement of agitation with good tolerance noticed 2 h after the first injection. 60% of patients required a second injection |
| Linehan et al. ( | A double-blind, placebo-controlled pilot study | 24 female patients with BPD | Patients received DBT for 6 months, then olanzapine or placebo | Olanzapine may promote more rapid reduction of irritability and aggression than placebo for highly irritable women with PBD |
| Berrino et al. ( | A prospective cohort study | 200 BPD patients; 100 received crisis intervention and 100 received treatment as usual | Crisis intervention vs. treatment as usual 1–10 days and followed up for 3 months | The results suggested that short-term intensive care at the general hospital may contribute to BPD emergency although this treatment is not considered as an alternative to structured psychiatric acute treatment |
| Bertsch et al. ( | A randomized placebo-controlled double-blind group design | 40 patients and 41 controls | 26 IU of oxytocin or placebo as single dose | Oxytocin may decrease social threat hypersensitivity and thus reduce anger and aggressive behavior in PBD with enhanced threat-driven reactive aggression |
| Carvalho Fernando et al. ( | A crossover placebo-controlled double group design | 32 females with BPD and 32 healthy females | A single administration of 10 mg hydrocortisone or placebo | Acute hydrocortisone administration enhances response inhibition of face stimuli in BPD patients and healthy controls, regardless of their emotional valence |
| Brune ( | A double-blind placebo-controlled study | 15 PBD patients and 15 controls | Intranasal oxytocin single dose | Oxytocin was associated with less fight behavior in both groups |
Studies that investigate follow-up and treatment of patients with BPD.
| Study | Study design | Number of patients | Treatment strategy | Results/treatment response |
|---|---|---|---|---|
| Hollander et al. ( | A preliminary double-blind, placebo-controlled trial | 16 | Divalproex sodium vs. placebo for 10 weeks | Divalproex sodium was more effective than placebo for global symptomatology, aggression, and depression |
| Zanarini and Frankenburg ( | A double-blind, placebo-controlled study | 28 females | Olanzapine vs. placebo for 6 months | Olanzapine had greater effect than placebo in all symptoms except depression |
| Rinne et al. ( | A randomized, placebo-controlled clinical trial | 38 BPD female patients | The SSRI fluvoxamine for 6 weeks followed by a blind half-crossover for 6 weeks and an open follow-up for another 12 weeks | Fluvoxamine significantly improved rapid mood shifts in female borderline patients, but not impulsivity and aggression |
| Rocca et al. ( | An open-label study | 13 patients | Risperidone at low-to-moderate doses | There was a significant reduction in aggression based on Aggression Questionnaire scores |
| Zanarini et al. ( | A randomized double-blind study | 45 patients | Fluoxetine, olanzapine, or olanzapine–fluoxetine combination for 8 weeks | The three groups showed significant improvement of symptoms. Olanzapine monotherapy and fluoxetine–olanzapine combination were superior to fluoxetine alone |
| Bogenschutz and George Nurnberg et al. ( | A randomized double group, placebo-controlled trial | 40 BPD patients | Olanzapine 2.5–20 mg/day or placebo for 12 weeks | Olanzapine was found to be significantly ( |
| Simpson et al. ( | A randomized, double-blind, placebo-controlled study | 20 patients with BPD | All subjects received individual and group DBT followed by 40 mg/day of fluoxetine or placebo for 12 weeks | Adding fluoxetine to an efficacious psychosocial treatment does not provide any additional benefits |
| Villeneuve and Lemelin ( | An open-label study | 23 | Quetiapine 175–400 mg/day for 12 weeks | A low dose of quetiapine was associated with a strong positive clinical impact, including improvement of impulsivity |
| Bellino et al. ( | An open-label pilot study | 17 | Oxcarbazepine 1,200–1,500 mg/day for 12 weeks | A statistically significant response to oxcarbazepine was observed according to CGI-S and BPRS mean score No cases of significant hyponatremia or severe adverse effects were reported |
| Soler et al. ( | A double-blind, placebo-controlled study | 60 patients with BPD | Dialectical behavior therapy followed by olanzapine or placebo for 12 weeks | Olanzapine was associated with a statistically significant improvement over placebo in depression, anxiety, and impulsivity/aggressive behavior |
| Hollander et al. ( | A double blind, placebo-controlled trial | 52 BPD patients | Divalproex or placebo for 12 weeks | Divalproex was superior to placebo in reducing impulsive aggression in patients with borderline personality disorder |
| Tritt et al. ( | A randomized, double-blind, placebo-controlled study | 24 females with BPD | Lamotrigine or placebo for 8 weeks | Highly significant ( |
| Loew et al. ( | A double-blind, placebo-controlled study | 56 patients | Topiramate titrated from 25–200 mg/day or placebo for 10 weeks | Significant changes on the somatization, interpersonal sensitivity, anxiety, hostility, phobic anxiety, and Global Severity Index scales of the Symptom Checklist were observed in the topiramate-treated subjects after 10 weeks |
| Nickel et al. ( | A double-blind, placebo-controlled study | 29 female patients | Topiramate or placebo for 8 weeks | Significant improvements on four subscales of the STAXI (state-anger, trait-anger, anger-out, anger-control) were observed in the topiramate-treated subjects after 8 weeks, in comparison with the placebo group |
| Linehan et al. ( | A randomized controlled trial | 100 women with recent suicidal attempts or self-injuring behavior | One year of DBT or 1 year of community treatment by experts | Dialectical behavior therapy was associated with better outcomes in the intent-to-treat analysis than community treatment by experts in most target areas during the 2-year treatment and follow-up period |
| Giesen-Bloo et al. ( | A multicenter, randomized, two-group design trial | 88 patients | Three years of either SFT or TFP with sessions twice a week | Statistically and clinically significant improvements were found for both treatments. More patients in SFT group showed significant recovery and clinical improvement |
| Nickel et al. ( | A double-blind, placebo-controlled study | 42 patients | 15 mg/day of aripiprazole for 8 weeks | Significant changes in scores on most scales were observed in the subjects treated with aripiprazole after 8 weeks |
| Bellino et al. ( | An open-label pilot study | 14 | Quetiapine at the dose of 200–400 mg/day for 12 weeks | Data suggested that quetiapine is effective in BPD patients specially with impulsiveness/aggressiveness-related symptoms |
| Clarkin et al. ( | A multi-wave study | 90 patients | Transference-focused psychotherapy, dialectical behavior therapy, or supportive treatment | Both transference-focused psychotherapy and dialectical behavior therapy were significantly associated with improvement in suicidality |
| Silva et al. ( | An open label study | 59 patients | Flexible doses of fluoxetine for 12 weeks | LL carriers had a better response than S carriers in the reduction of total OAS-M scores and on the aggressiveness and irritability components of the OAS-M |
| Bateman and Fonagy ( | A follow-up study after randomized, controlled trial was complete by 8 years | 41 patients | Mentalization-based treatment or treatment as usual for 18 months | Mentalization-based treatment showed superior results in suicidality, service use, use of medication, and global function above 60 than treatment as usual group |
| Adityanjee et al. ( | An open-label pilot trial | 16 | Quetiapine for 8 weeks | Significant reductions in symptoms were observed in this pilot study |
| Blum et al. ( | A randomized controlled trial and 1-year follow-up | 124 | STEPPS plus treatment as usual or treatment as usual alone | STEPPS an adjunctive group treatment, can deliver clinically meaningful improvements in borderline personality disorder-related symptoms and behaviors, enhance global functioning, and relieve depression |
| Clivaz et al. ( | A case report | A 17-year-old woman with BPD, administrated to ER with panic attacks | Topiramate (TPM) at 25 mg daily for a month | Panic attacks intensity increased and disappeared after discontinuation of TPM |
| Pascual et al. ( | A double-blind, placebo-controlled study | 60 | Ziprasidone 84.1 mg/day vs. placebo for 2 weeks | There was no statistically significant difference between ziprasidone and placebo |
| Van den Eynde et al. ( | An open-label study | 41 | Quetiapine 100–800 mg/day for 12 weeks | The results showed that quetiapine may be effective in the treatment of impulsivity and affective symptoms in BPD. |
| Bellino et al. ( | An open-label study | 21 patients with BPD resistant to sertraline therapy | Aripiprazole 100–200 mg/day for 12 weeks | Aripiprazole is an efficacious and well-tolerated add-on treatment for sertraline-resistant BPD patients |
| McMain et al. ( | A single blind randomized controlled study | 180 patients | Dialectical behavior therapy or general psychiatric management for 1 year | Patients benefited equally from both types of treatment |
| Farrell et al. ( | A randomized controlled trial | 32 | A group received schema-based therapy plus as usual treatment. The other received treatment as usual only | Schema-based therapy had more significant improvements that led to recovery and improved overall functioning |
| Reich et al. ( | A double-blind, placebo-controlled study | 28 patients | Lamotrigine or placebo for 12 weeks | Patients in the lamotrigine group had significantly greater reductions in the total Affective Lability Scale scores. Lamotrigine is an effective treatment for affective instability and for the general impulsivity characteristic of BPD |
| Ziegenhorn et al. ( | A randomized, double-blind, placebo-controlled, crossover study trial | 18 patients with BPD, with or without comorbid PTSD, and with a prominent hyperarousal syndrome | Clonidine or placebo | Clonidine might be a useful adjunct to pharmacotherapy in patients with BPD who have marked hyperarousal and/or sleep problems |
| Shafti and Shahveisi ( | A randomized double-blind trial | 28 female patients | Olanzapine or haloperidol for 8 weeks | Both groups showed significant improvement but no inter-group difference was found |
| Bellino et al. ( | A pilot study | 18 patients | Open-label duloxetine, 60 mg/day, for 12 weeks | A notable change was found for: BPRS, HAM-D, SOFAS, BPDSI total score, and items “impulsivity,” “outbursts of anger,” and “affective instability” and HSCL-90 SOM |
| Doering et al. ( | A randomized controlled trial | 104 females with BPD | Transference-focused psychotherapy or by an experienced community psychotherapist for 1 year | Transference-focused psychotherapy is more efficacious than treatment by experienced community psychotherapists in the domains of borderline symptomatology, psychosocial functioning, and personality organization. Self-harming behavior did not change in either group |
| Harned et al. ( | An open label study | 51 women with suicidal or self-injuring behavior | Dialectical behavior therapy for 1 year | BPD clients with and without PTSD were equally likely to eliminate the exclusionary behaviors during 1 year of DBT |
| Bellino et al. ( | A randomized double group design | 55 patients with BPD | Two groups: fluoxetine 20–40 mg/day plus clinical management, or fluoxetine 20–40 mg/day plus interpersonal psychotherapy adapted to BPD | Combined therapy with adapted IPT was superior to fluoxetine alone in BPD patients, concerning a few core symptoms of the disorder, anxiety, and quality of life |
| Zanarini et al. ( | A randomized, double-blind, placebo-controlled study | 451 | Olanzapine 2.5 mg/day, olanzapine 5–10 mg/day, or placebo | Olanzapine 5–10 mg/day showed a clinically modest advantage over placebo in the treatment of overall borderline psychopathology |
| Zanarini et al. ( | An open label study | 472 | Patients received open-label olanzapine for 12 weeks after 12 weeks of double-blind olanzapine or placebo | The results suggest that continued therapy with olanzapine may sustain and build upon improvements seen with acute olanzapine treatment of patients with BPD |
| Moen et al. ( | A placebo-controlled study | 17 | All patients received dialectical behavior therapy for 4 weeks, then assigned into two groups; one received placebo and the other received divalproex ER for 12 weeks | There was a significant improvement in both groups from baseline. However, there was no advantage observed for divalproex ER and DBT over placebo and DBT |
| Schmahl et al. ( | Two double-blind placebo-controlled randomized trials | 25 | Patients received both 3 weeks of naltrexone (50 or 200 mg/day) and 3 weeks of placebo in a randomized order | The dissociative symptoms were numerically not statistically significant lower under naloxone than placebo |
| Carrasco et al. ( | A preliminary open-label study | 49 patients with refractory BPD | The initial dose of 37.5 mg IM injection of LA risperidone repeated every 2 weeks, which could be raised to 50 mg for 6 months | IM risperidone may be effective and safe in patients with refractory BPD |
| Kröger et al. ( | An open label study | 1,423 patients with BPD | Dialectical behavior therapy | The response rate was 45%, 31% remained unchanged, and 11% deteriorated. Approximately 15% showed a symptom level equivalent to that of the general population |
| Jørgensen et al. ( | A randomized controlled study | 85 patients with BPD | 2 years of intensive (twice weekly) combined (individual and group), mentalization-based psychotherapy or 2 years of less-intensive (biweekly) supportive group therapy | Significant changes in both treatment groups were identified for several outcome measures |
| Reneses et al. ( | A randomized and controlled trial | 44 patients | Psychic representation, focused psychotherapy, or treatment as usual | Results showed significantly better outcomes for the experimental group in all the main variables measured and in most of the secondary ones |
| Gratz et al. ( | A randomized controlled trial and uncontrolled 9-month follow-up | 61 patients | Adjunctive emotion regulation group therapy for 14 weeks | Results revealed significant improvements from pre- to posttreatment on all outcomes |
| Black et al. ( | A randomized, double-blind, placebo-controlled trial | 95 patients with BPD | 150 mg/day of quetiapine (the low-dosage group), 300 mg/day of quetiapine (the moderate-dosage group), or placebo | Participants treated with 150 mg/day of quetiapine had a significant reduction in the severity of borderline personality disorder symptoms compared with those who received placebo. Adverse events were more likely in participants taking 300 mg/day of quetiapine |
| Harned et al. ( | A pilot randomized controlled trial | 26 with recent and recurrent intentional self-injury | DBT or DBT with the DBT Prolonged exposure | Patients who completed the DBT PE protocol were 2.4 times less likely to attempt suicide and 1.5 times less likely to self-injure than those in DBT |
| Linehan et al. ( | A single blind randomized clinical trial and component analysis | 99 women who had at least two suicide attempts and/or non-suicidal self-injury (NSSI) acts in the last 5 years, an NSSI act or suicide attempt in the 8 weeks before screening, and a suicide attempt in the past year | The study compared standard DBT, DBT-S, and DBT-I for 1 year and follow-up for another year | All treatment conditions resulted in similar improvements in the frequency and severity of suicide attempts, suicide ideation, use of crisis services due to suicidality, and reasons for living |
| Leichsenring et al. ( | A randomized controlled efficacy-effectiveness study | 179 patients | Manual-guided psychoanalytic-interactional therapy or non-manualized psychodynamic therapy by experts in personality disorders or placebo | Both PIT and E-PDT achieved significant improvements in all outcome measures and were superior to the control condition |