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Clinical practice guidelines for the treatment of borderline personality disorder: a systematic review of best practice in anticipation of MAiD MD-SUMC
Borderline Personality Disorder and Emotion Dysregulation volume 12, Article number: 13 (2025)
Abstract
Background
Countries permitting assisted dying for mental disorder as the sole underlying condition (MD-SUMC) find that individuals with Borderline Personality Disorder (BPD) constitute a significant proportion of people requesting MAiD. In anticipation of forthcoming changes to Canadian MAiD legislation, clinical practise guidelines will be important in the decision-making process for eligibility to ensure that evidence-based treatments have been exhausted in making determinations of irremediability.
Aims
This is a systematic review of international, English-language treatment guidelines for BPD with two primary objectives: First, to identify areas of consensus and disagreement in best practise for the treatment of this disorder and second, to assess whether the guidelines offered insight into defining irremediable BPD and/or its management.
Methods
In accordance with PRISMA guidelines, we performed a systematic review of five databases and identified five clinical practise guidelines in the English language. Two authors independently performed data extraction on the core components of these treatment guidelines, which was synthesized into a narrative review.
Findings
Several conclusions may be drawn about the state of the evidence on BPD treatment. First, psychological therapies are broadly considered the preferred treatment modality for BPD but there is no consensus regarding whether any one intervention is preferable. Second, all guidelines suggest pharmacotherapy may have a role in the management of BPD, but the nature and extent of this is disputed. Third, there is no guidance alluding to, defining, or commenting on the management of irremediable BPD. Finally, there are no Canadian treatment guidelines for BPD. The implications of these findings for MAiD MD-SUMC are discussed.
Background
On March 17th 2027, Canada may join five countries in which assisted dying is available for mental disorder as the primary condition (Luxembourg, Belgium, The Netherlands, Switzerland, Spain; [1, 2]) when revisions to current Federal legislation are scheduled to come into effect [3]. In reviewing available data from countries where assisted dying for mental disorder is permissible, individuals with BPD have constituted a significant proportion of individuals requesting MAiD. In Belgium and The Netherlands, the primary psychiatric diagnoses for which MAiD is administered are mood or personality disorders (Hageman D, Van Assche K, De Hert M: Levensbeëindiging op verzoek op basis van een psychiatrische aandoening: descriptief onderzoek Nederland en België, submitted). These findings concur with another Belgian study that reported 50% of the participants requesting MAiD were diagnosed with a personality disorder and an additional 29% had both a treatment resistant mood disorder with comorbid personality disorder [4]. Of note, 54% of those with personality pathology were diagnosed with BPD. Findings from the Netherlands similarly report that most individuals receiving MAiD for psychiatric reasons had personality disorders [5]. Thus, the available data suggests that individuals with BPD will likely constitute a significant proportion of MAiD requests when this intervention becomes available in Canada, and elsewhere, as assisted-dying legislation expands. Therefore, guidance for clinicians in this regard is necessary and timely.
BPD is characterized by emotional instability, unstable self-image and interpersonal dysfunction [6] affecting approximately 2% of the general population, 10% of psychiatric outpatients, and 20% of psychiatric inpatients [7]. The term “borderline” originally meant a state that bordered on psychosis [8]. The historical psychoanalytic framework in which the term originated conceptualized psychoses as untreatable because these patients defied analysis [9] and this opinion of intractability endures. However, current data with longitudinal evidence supports that patients with BPD achieve remission [10] with up to 90% of patients recovering by age 50 [11].
There has been significant progress over recent decades in developing and evaluating psychotherapies for individuals with BPD. Currently established evidence-based interventions for BPD include Dialectical Behaviour Therapy [12] Transference-Focused Psychotherapy [13], Mentalized-Based Treatment [14], Schema-Focused Therapy [15] and Systems Training for Emotional Predictability and Problem Solving [16]. However, there are some areas of continuing debate in the management of BPD: specifically, whether all specialized evidence-based therapies perform comparably [17]; generalist versus specialist psychotherapy [18]; and the role of psychopharmacology in management [19].
BPD and irremediability
By very nature of the psychopathology, disordered beliefs and cognitions are likely to bear upon the patient’s own understanding of the irremediability of their illness [20]; that is, intolerability of suffering, especially when this intolerability is pathognomonic of the disease state, may be mistaken for evidence of irremediability rather than a reflection of disease severity or treatability. This judgment of irremediability is arguably more imprecise given that there is no consensus on what constitutes “treatment-resistant BPD”. This renders decision-making about eligibility for MAiD in the context of BPD immensely challenging, likely idiosyncratic, and entirely unsystematized. The risk of overestimating irremediability is especially elevated in this patient population given that BPD is a highly stigmatized disorder that has been historically regarded with limited prospects of improvement [21, 22]. There are also considerations regarding the general clinical course of BPD, with evidence that the majority of patients with BPD remit with time [23]. Given that remissions are possible later in the course of the disorder, this renders decision-making about irremediability challenging in the context of BPD, in particular.
The question of whether irremediability for mental disorders is fundamentally knowable is an immensely important debate on the ontologic and epistemic limitations of psychiatry, especially in the context of MAiD. Our position on irremediability in the context of MAiD evaluations is a functional definition rather than an ontological one, driven by the necessity of developing a framework for assessment rather than a statement about the existence of irremediability in mental disorder itself. One of the challenges in determining irremediability is that it is inherently a prospective notion that is assessed retrospectively [24]. For example, a recent study on Dutch Psychiatrists’ experiences of evaluating irremediability for the purpose of MAiD found that assessors frequently relied on failed past treatments in defining irremediable suffering. In addition, assessors also regarded treatment guidelines as valuable resources in making these determinations. One of the recommendations from the Expert Panel on MAiD and Mental Illness in Canada similarly suggests that assessors should reference past treatments and their outcomes in determining incurability [3]. However, there is a need for the development of some evidence-based, disorder-specific criteria derived from clinical consensus in advance of these changes to legislation or we risk relying entirely on individual opinion in the assessment of irremediability. Mehlum et al. [25] have asserted the need for adherence to clinical practise guidelines (CPGs) in the decision-making process for MAiD eligibility when assessing patients diagnosed with BPD to ensure that evidence-based treatments have been exhausted before making determinations of irremediability. CPGs are “systematically developed statements to assist practitioner and patient decisions about appropriate health care for specific clinical circumstances” [26].
Current study
The present study is a systematic review of international, English-language treatment guidelines for BPD to establish a starting point for updated North American guidelines and to facilitate the development of a decision-making framework for MAiD eligibility. First, we aim to identify areas of consensus in treatment approaches such that clinicians may evaluate whether requests are being made after having been exposed to appropriate interventions with suitable duration, frequency, and other relevant parameters as per best practise. We also intend to elucidate areas of conflict among treatment guidelines regarding BPD management. Second, we endeavour to qualify what constitutes “treatment-resistant” BPD according to available guidelines, how to assist in determining irremediability, and whether the existing guidelines offer any guidance on management of this population. We anticipate this research will be theoretically and practically significant in the treatment and management of BPD more generally, but especially in the context of anticipated changes to MAiD eligibility in Canada.
Methods
This review was completed in accordance with Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines [27]. MEDLINE, EMBASE, the Cochrane Library, Web of Science, Google Scholar, and PsycINFO databases were searched on May 5, 2022 by author HA. Search terms included the following for Borderline Personality Disorder: Borderline personality disorder, borderline states, borderline personality symptoms, borderline personality features, BPD, Emotionally unstable personality disorder, borderline Pattern, and borderline PD. Search terms for guidelines were guidelines, practise guidelines, standards, consensus, recommendat*, protocol, best practi*, and treatment guidelines. Search terms were intentionally broad to ensure capture of all relevant articles. The initial search yielded 6323 articles, which were imported to Covidence, a systematic review software. After removing duplicates (n = 2183), two authors (HA, PL) screened titles and abstracts for the remaining 4136 articles. Of these, 35 articles proceeded to full text review. Only five of these articles were determined to be appropriate for this review based on inclusion criteria through a consensus discussion after independent review (Fig. 1). Articles were excluded if they were narrative or systematic reviews, single-authored, or written in a non-English language. The guidelines yielded by this search were cross-referenced with a pre-existing list of known guidelines on the treatment of BPD, and no additional articles were identified or found to have been omitted by this bottom-up search strategy. Inclusion and exclusion criteria for this review were guided by the “PICAR” framework (Table 1).
The primary authors (HA and PL) performed independent data extraction on all guidelines using an adapted version of the Cochrane data collection template for intervention reviews [29]. Data extraction included intended population attributes, key recommendations, types of interventions, intervention duration and frequency (psychotherapy), and intervention class and dosage (pharmacotherapy). As per PRISMA guidelines, each guideline was assessed for risk of bias using the AGREE GRS tool. This tool provides a rating from 1 to 7, where a score of 1 denotes the lowest quality and a score of 7 indicates the highest quality in each of the following areas: Process of development, Presentation style, Completeness of reporting, Clinical validity, and Overall Assessment. Due to the small number of available CPGs, we did not exclude studies based on evidence ratings. Data were synthesized by the lead author (HA) using a narrative synthesis approach of extracted data from both independent reviewers, with emphasis on recent CPGs (i.e., published after 2000). A more structured or formalized approach such as thematic analysis was not deemed appropriate due to insufficient data to demonstrate trends [30].
Results
Study characteristics
Our systematic review resulted in five English-language CPGs; these were from the American Psychiatric Association (APA, [31]); World Federation of Societies of Biological Psychiatry (WFSBP, [32]); National Health and Medical Research Council (NHMRC, [33]); Project Air [34]; and, the National Institute for Health and Care Excellence (NICE; [35]). Of these, Project Air is classified as grey literature. However, the APA released a working draft of their updated guidelines during the preparation of this review (May 15, 2023), and because the new guidelines were not finalized until December 10, 2024 (see https://www.psychiatry.org/news-room/news-releases/updated-borderline-personality-disorder-guideline; [36]), we elected not to supplant the published recommendations with recommendations from the draft document, but have instead indicated where the updated recommendations diverge from the original published APA guidelines. NHMRC displays a warning that these guidelines have been rescinded but no further information is available.
Quality assessment (Agree Ratings)
Three resources (NHMRC, NICE, and Project Air) were given an overall rating of 5. One resource (APA) was not amenable to the AGREE rating system due to lack of data on which the score is predicated. One CPG (WFSBP) was provided an overall rating of 1.
Recommendations on pharmacotherapy
Summarized in Tables 2, 3, 4, 5 and 6. Most guidelines felt pharmacotherapy was not suitable as a primary treatment for BPD, but may be appropriate for affective symptoms, in crisis, and for the treatment of comorbid disorders. Polypharmacy was discouraged by all guidelines except the original APA guideline. Most guidelines cautioned against the use of monoamine oxidase inhibitors and tricyclic antidepressants due to concerns about intentional toxic ingestion.
Recommendations on psychotherapy
Summarized in Table 7. Psychological therapies were generally regarded as first-line treatments for BPD, with most guidelines emphasizing a longer treatment course. There was no consensus on whether any psychological intervention was superior.
Discussion
The objective of this review was to elucidate areas of agreement among existing guidelines regarding what constitutes evidence-based interventions for BPD in anticipation of forthcoming changes to MAiD legislation. Findings from our systematic review of CPGs in the English language for the treatment of BPD supported several conclusions. First, most guidelines felt that psychological therapy was the preferred treatment modality for BPD, and that short-term interventions were of limited use. However, there was no consensus regarding whether a single psychological intervention was more effective than others. For example, although both WFSBP and NICE reported good evidence for DBT for self-harm and suicidality, NHMRC indicates that most treatments (including treatment as usual) had a positive effect on this outcome measure, with data favouring the use of mentalization therapy. Project Air similarly felt that all psychosocial interventions were equally effective for BPD management but was less prescriptive in its recommendations overall. Regarding length of interventions, most guidelines recommended longer interventions, ranging from a minimum of three months to one year, with weekly sessions. These recommendations should be tempered by more recent research suggesting treatment duration of 3 to 6 months as noninferior to longer interventions in BPD [37, 38]. Both APA and NHMRC suggested combined group and individual therapy as more effective than either as a standalone intervention. However, the updated draft APA guidelines no longer comment on this.
Second, the nature and scope pharmacotherapy in the management of BPD was disputed. While most guidelines discouraged pharmacotherapy as primary treatment, there was acknowledgment that pharmacotherapy has some utility in highly circumscribed situations. There was some consensus that pharmacotherapy has utility for treating at least one of acute crises, comorbid disorders (e.g., depression), mood reactivity and affective disturbances. However, there was no guidance with respect to treatment resistance, complex multi-morbid presentations, family approaches, or approach to the management of acute crises in the Emergency Department. Except for APA, all other guidelines advised against the use of polypharmacy in this population. However, the updated APA draft guidelines clarified their stance on polypharmacy such that they are not only in keeping with other guidelines, but also incorporate deprescription planning and medication review as a component of the overall treatment strategy. Most guidelines also commented on the risk of overdose in this population, with specific concern for monoamine oxidase inhibitors and tricyclic antidepressants. Notably, there were conflicting recommendations regarding the use of psychological and pharmacotherapy as adjunctive treatments. For example, both NICE and NHMRC discouraged this, but APA recommended psychotropic interventions as important to combine with psychotherapy. The updated APA guidelines draft states that while psychotherapy is the gold standard for treatment for BPD, pharmacotherapy should only ever be used as an adjunct.
Third, and most pertinent to MAiD MD-SUMC, was the finding that there was no specific guidance alluding to, defining, or managing irremediable BPD in any CPG. However, there was reference to the importance of considering co-morbid psychiatric disorders that may be impacting the person’s prognosis or contributing to their suffering. NHMRC made reference to “complex and severe BPD” but made no recommendations due to lack of definitional consensus and evidence. When published, the updated APA guidelines will be the most up-to-date clinical recommendations on BPD management and should consider incorporating some approach to irremediability.
There are also general comments on the state of evidence for the management of BPD, especially as it pertains to the North American context. Based on our review, there are only five CPGs available in English for the treatment of BPD, and no Canadian guideline. Of these five, two guidelines (NHMRC and APA) have been either rescinded or display a warning that they are no longer current, although APA is in the process of developing new guidelines for which a preliminary draft has been made available and which we have incorporated into our review. We have retained these rescinded guidelines in this review in the interest of providing an accurate survey of the existing state of evidence for English-speaking contingents. Moreover, among this small number of CPGs, the recommendations regarding the management of BPD are conflicting and not infrequently contradicting. Certainly, some of this may be attributable to the evidence base consulted for the development of the CPG. For example, WFSBP guidelines are still considered to be current, but are based on literature from 1980 to 2007, and exclude severely ill patients with comorbid disorders or suicidal ideation. Given the exceedingly high rate of comorbidity in this population (i.e., [39, 40]) and that chronic suicidality is a feature of BPD [7, 41] we wonder how appropriate these recommendations are for the management of BPD in clinical settings in the real world. The preliminary draft of the APA guidelines, however, provides some grounds for optimism as the updated recommendations appear to be more consistent with other available CPGs, especially with respect to pharmacotherapy.
Recognizing the limitations of existing guidelines, irremediability in psychiatry is the subject of both ontological debate and considerable diagnostic challenge that is unlikely to be definitively addressed through CPGs. We acknowledge the latter concerns in our recent paper on assessing patients with BPD for MAiD regarding irremediability [42], including issues related to definition, prognosis, course, and lack of treatment response. We propose a functional approach to the assessment of irremediability in BPD which includes assessing severity of illness, and the use of retrospective information to determine treatment-resistance. Although the DSM-5’s categorical nosology does not have a severity criterion for BPD, the Alternative Model for Personality Disorders Criterion A and the ICD-11 model of personality disorders incorporate assessments of severity. However, research using these alternate models in BPD is proceeding but still limited, and there are challenges to implementation [43].
The literature on models of staging and profiling in mental disorders may also be relevant for assessments of irremediability in the context of MAiD MD-SUMC [44] but there is presently insufficient evidence for models of staging and stepped care approaches with BPD [37, 45]. There may also be other ways to characterize complexity (e.g., concept mapping; [46]) but there remains, at present, no clear method to evaluate or address irremediability in borderline patients. Moreover, while treatment-resistance in depression has often been invoked as a prototype of irremediability in the context of MAiD, there remains considerable debate about what irremediability means in this context (see [44]), as well as in psychiatry more generally [47]. Assessments of irremediability are certainly complicated by psychiatric comorbidity, physical comorbidities, substance use [42], and iatrogenic polypharmacy, particularly in BPD. More broadly, risk stratification in the context of suicidal ideation and behaviour will be critical in determining eligibility for MAiD MD-SUMC. While acute suicidality would likely impact eligibility, chronic suicidality is generally modifiable but may not be sufficient grounds for exclusion. If suicidality is not addressed, this may impact determinations of irremediability [44] but further guidance on chronic suicidal ideation in the context of MAiD is necessary.
The findings of this review must be tempered by several limitations. First, this review is constrained by a small sample size of only five guidelines. We acknowledge that there are additional international guidelines in non-English languages (e.g., Swiss, German; [48, 49]) for which there are no English translations. However, limiting this review to English-only CPGs was an intentional decision to both acknowledge and summarize the existing state of evidence for BPD management in English-speaking contingencies. Relatedly, we anticipate that the exclusive reliance on CPGs – as opposed to randomized controlled trials or other evidence – may be considered an additional limitation. However, CPGs are, by definition, recommendations based on a systematic review of existing evidence [50]. Given suggestions that CPGs should constitute an important part of determining MAiD eligibility [25], it is imperative to evaluate their quality and whether they facilitate (i.e., via consensus) or hinder (i.e., via contradiction) the decision-making process. Our review suggests that existing English-language CPGs for the treatment of BPD are inadequate for these purposes due to being either themselves outdated, based on evidence that is not contemporary, and/or stringent exclusion criteria that limits their utility in clinical settings. The poor consensus among these various publications is also concerning and poses challenges for clinicians who may look to these for decision-making in MAiD. Last, this review was based on English language guidelines given the focus on changing legislation in Canada, as well as authors’ native language. We are aware that there are additionally a small number of published guidelines in European countries, including Denmark [51], Finland and Germany. However, none of the English-language guidelines are from countries where MAiD for mental disorders is available.
Conclusions
Our review suggests that the current state of evidence on BPD treatment may hinder reliable decision-making about MAiD eligibility and contribute to inequities in access. Inequitable access includes both overly restrictive or overly permissive practises. The most significant concern lies in the risk of overestimating irremediability, especially in this patient population given that BPD is a highly stigmatized disorder that has been historically regarded with limited prospects of improvement. Future efforts must prioritize research on what constitutes irremediable BPD, as well as an approach to treating recalcitrant BPD symptomatology. In addition, there is a need to update existing CPGs on the management of BPD, and ensure that the evidence on which recommendations are based reflects the complexity of the disorder as encountered in the real world.
Data availability
No datasets were generated or analysed during the current study.
Abbreviations
- MAiD:
-
Medical Assistance in Dying
- CPG:
-
Clinical Practise Guidelines
- BPD:
-
Borderline Personality Disorder
- WFSBP:
-
World Federation of Societies of Biological Psychiatry
- APA:
-
American Psychiatric Association
- NHMRC:
-
National Health and Medical Research Council
- NICE:
-
National Institute for Health and Care Excellence
References
Ramos-Pozón S, Terribas-Sala N, Falcó-Pegueroles A, Román-Maestre B. Persons with mental disorders and assisted dying practices in Spain: an overview. Int J Law Psychiatry. 2023;87:101871.
De Hert M, Loos S, Sterckx S, Thys E, Van Assche K. Improving control over euthanasia of persons with psychiatric illness: lessons from the first Belgian criminal court case concerning euthanasia. Front Psychiatry. 2022;13. Available from: https://www.frontiersin.org/articles/10.3389/fpsyt.2022.933748.
Health Canada. Expert Panel on MAiD and Mental Illness. Final report on expert panel on MAiD and mental illness. Ottawa: Government of Canada; 2022. Available from: https://www.canada.ca/en/health-canada/corporate/about-health-canada/public-engagement/external-advisory-bodies/expert-panel-maid-mental-illness/final-report-expert-panel-maid-mental-illness.html.
Thienpont L, Verhofstadt M, Van Loon T, Distelmans W, Audenaert K, De Deyn PP. Euthanasia requests, procedures and outcomes for 100 Belgian patients suffering from psychiatric disorders: a retrospective, descriptive study. BMJ Open. 2015;5(7):e007454.
Kim SY, De Vries RG, Peteet JR. Euthanasia and assisted suicide of patients with psychiatric disorders in the Netherlands 2011 to 2014. JAMA Psychiatry. 2016;73(4):362–8.
American Psychiatric Association. Diagnostic and statistical manual of mental disorders. 5th ed. 2013.
Lieb K, Zanarini MC, Schmahl C, Linehan MM, Bohus M. Borderline personality disorder. Lancet. 2004;364(9432):453–61.
Paris J. Borderline personality disorder. CMAJ. 2005;172(12):1579–83.
Gunderson JG. Borderline personality disorder: ontogeny of a diagnosis. Am J Psychiatry. 2009;166(5):530–9.
Zanarini MC, Frankenburg FR, Hennen J, Silk KR. The longitudinal course of borderline psychopathology: 6-year prospective follow-up of the phenomenology of borderline personality disorder. Am J Psychiatry. 2003;160(2):274–83.
Paris J. Implications of long-term outcome research for the management of patients with borderline personality disorder. Harv Rev Psychiatry. 2002;10(6):315–23.
Linehan MM, Heard H, Clarkin J, Marziali E, Munroe-Blum H. Dialectical behavior therapy for borderline personality disorder. New York: Guilford; 1993.
Yeomans FE, Clarkin JF, Kernberg OF. Transference-focused psychotherapy for borderline personality disorder: a clinical guide. Washington (D.C.): American Psychiatric Pub; 2015.
Bateman AW, Fonagy P. Mentalization-based treatment of BPD. J Personal Disord. 2004;18(1):36–51.
Giesen-Bloo J, Van Dyck R, Spinhoven P, Van Tilburg W, Dirksen C, Van Asselt T, et al. Outpatient psychotherapy for borderline personality disorder: randomized trial of schema-focused therapy vs transference-focused psychotherapy. Arch Gen Psychiatry. 2006;63(6):649–58.
Blum N, St. John D, Pfohl B, Stuart S, McCormick B, Allen J, et al. Systems training for emotional predictability and problem solving (STEPPS) for outpatients with borderline personality disorder: a randomized controlled trial and 1-year follow-up. Am J Psychiatry. 2008;165(4):468–78.
Gabbard GO. Do all roads lead to Rome? New findings on borderline personality disorder. AJP. 2007;164(6):853–5.
Choi-Kain LW, Finch EF, Masland SR, Jenkins JA, Unruh BT. What works in the treatment of borderline personality disorder. Curr Behav Neurosci Rep. 2017;4(1):21–30.
Ingenhoven T. Pharmacotherapy for borderline patients: business as usual or by default? J Clin Psychiatry. 2015;76(4):e522–523.
Appelbaum PS. Physician-assisted death in psychiatry. World Psychiatry. 2018;17(2):145–6.
Kealy D, Ogrodniczuk JS. Marginalization of borderline personality disorder. J Psychiatr Pract. 2010;16(3):145–54.
Biskin RS. The lifetime course of borderline personality disorder. Can J Psychiatry. 2015;60(7):303–8.
Zanarini MC, Frankenburg FR, Hein KE, Glass IV, Fitzmaurice GM. Sustained symptomatic remission and recovery and their loss among patients with borderline personality disorder and patients with other types of personality disorders: a 24-year prospective follow-up study. J Clin Psychiatry. 2024;85(4):57387.
van Veen SMP, Ruissen AM, Beekman ATF, Evans N, Widdershoven GAM. Establishing irremediable psychiatric suffering in the context of medical assistance in dying in the Netherlands: a qualitative study. CMAJ. 2022;194(13):E485–91.
Mehlum L, Schmahl C, Berens A, Doering S, Hutsebaut J, Kaera A, et al. Euthanasia and assisted suicide in patients with personality disorders: a review of current practice and challenges. Borderline Personal Disord Emot Dysregul. 2020;7:15.
Field MJ, Lohr KN. Clinical practice guidelines. Directions for a new program. 1990.
Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ. 2021;372:n71.
Johnston A, Kelly SE, Hsieh SC, Skidmore B, Wells GA. Systematic reviews of clinical practice guidelines: a methodological guide. J Clin Epidemiol. 2019;108:64-76.
Cochrane. Data Collection Form. Available from: https://training.cochrane.org/sites/training.cochrane.org/files/public/uploads/resources/downloadable_resources/English/Collecting%20data%20-%20form%20for%20RCTs%20and%20non-RCTs.doc. Accessed 2 Feb 2023.
Fugard AJB, Potts HWW. Supporting thinking on sample sizes for thematic analyses: a quantitative tool. Int J Soc Res Methodol. 2015;18(6):669–84.
APA. Practice guideline for the treatment of patients with borderline personality disorder. Am J Psychiatry. 2001;158(Suppl10):1–52.
Herpertz SC, Zanarini M, Schulz CS, Siever L, Lieb K, Möller HJ, et al. World federation of societies of biological psychiatry (WFSBP) guidelines for biological treatment of personality disorders. World J Biol Psychiatry. 2007;8(4):212–44.
Australian Government. Clinical Practice Guideline - Borderline Personality Disorder | NHMRC. 2013. Available from: https://www.nhmrc.gov.au/about-us/publications/clinical-practice-guideline-borderline-personality-disorder. [cited 2023 Dec 9].
Grenyer B, Jenner B, Jarman H, Carter P, Bailey R, Lewis K. Project Air Strategy for Personality Disorders*(2015). Treatment Guidelines for Personality Disorders 2nd Ed. Wollongong: University of Wollongong, Illawarra Health and Medical Research Institute.* Guideline development team: Brin FS Grenyer, Bernadette Jenner, Heidi Jarman, Phoebe Carter. 2011.
National Collaborating Centre for Mental Health (UK). Borderline personality disorder: treatment and management. 2009.
APA. American Psychiatric Association publishes updated practice guideline on the treatment of borderline personality disorder. 2024. Available from: https://www.psychiatry.org/news-room/news-releases/updated-borderline-personality-disorder-guideline. [cited 2024 Dec 17].
Laporte L, Paris J, Bergevin T, Fraser R, Cardin J. Clinical outcomes of a stepped care program for borderline personality disorder. Personal Ment Health. 2018;12(3):252–64.
McMain SF, Chapman AL, Kuo JR, Dixon-Gordon KL, Guimond TH, Labrish C, et al. The effectiveness of 6 versus 12 months of dialectical behavior therapy for borderline personality disorder: A noninferiority randomized clinical trial. Psychother Psychosom. 2022;91(6):382–97.
Simonsen S, Bateman A, Bohus M, Dalewijk HJ, Doering S, Kaera A, et al. European guidelines for personality disorders: past, present and future. Borderline Personality Disorder Emot Dysregulation. 2019;6(1):1–10.
Oldham JM, Skodol AE, Kellman HD, Hyler SE, et al. Diagnosis of DSM-III—R personality disorders by two structured interviews: patterns of comorbidity. Am J Psychiatry. 1992;149(2):213–20.
Paris J. Chronic suicidality among patients with borderline personality disorder. PS. 2002;53(6):738–42.
Links PS, Aslam H, Brodeur J. Assessing and managing patients with borderline personality disorder requesting medical assistance in dying (MAiD). Front Psychiatry. 2024;15:1364621.
Zimmerman M. Why hierarchical dimensional approaches to classification will fail to transform diagnosis in psychiatry. World Psychiatry. 2021;20(1):70.
Nicolini ME, Jardas E, Zarate CA Jr, Gastmans C, Kim SY. Irremediability in psychiatric euthanasia: examining the objective standard. Psychol Med. 2023;53(12):5729–47.
Choi-Kain LW, Albert EB, Gunderson JG. Evidence-based treatments for borderline personality disorder: implementation, integration, and stepped care. Harv Rev Psychiatry. 2016;24(5):342–56.
Van Manen J, Kamphuis J, Goossensen A, Timman R, Busschbach J, Verheul R. In search of patient characteristics that May guide empirically based treatment selection for personality dIsorder patients—a concept map approach. J Personal Disord. 2012;26(4):481–97.
Van Veen SM, Evans N, Ruissen AM, Vandenberghe J, Beekman AT, Widdershoven GA. Irremediable psychiatric suffering in the context of medical assistance in dying: a Delphi-study. Can J Psychiatry. 2022;67(10):758–67.
Euler S, Dammann G, Endtner K, Leihener F, Perroud NA, Reisch T, et al. SGPP-Behandlungsempfehlungen Borderline-Persönlichkeitsstörung. Bern: Schweizerische Gesellschaft für Psychiatrie und Psychotherapie (SGPP); 2018.
Renneberg B, Schmitz B, Doering S, Herpertz S, Bohus M, Persönlichkeitsstörungen L. Behandlungsleitlinie persönlichkeitsstörungen. Psychotherapeut. 2010;4(55):339–54.
Committee on Standards for Developing Trustworthy Clinical Practice Guidelines, Board on Health Care Services, Institute of Medicine. Clinical practice guidelines we can trust. Graham R, Mancher M, Wolman DM, Greenfield S, Steinberg E, editors. Washington, D.C.: National Academies Press; 2011. Available from: https://www.nap.edu/catalog/13058. [cited 2023 Dec 9].
Vind AB, Jensen AM, Simonsen E, Axelgaard G, Bach Nielsen K, Grage KR et al. National klinisk retningslinje for behandling af emotionel ustabil personlighedsstruktur, borderline type. 2015.
Acknowledgements
We would like to thank Dr. Natasha Snelgrove for her input on earlier versions of this manuscript.
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This review has been primarily designed, analyzed, and authored by HA and PL. JB has been involved in editing and critical feedback at various stages, as well as approval of the submission in its final form. All authors read and approved the manuscript in its final form.
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Aslam, H.M., Brodeur, J. & Links, P.S. Clinical practice guidelines for the treatment of borderline personality disorder: a systematic review of best practice in anticipation of MAiD MD-SUMC. bord personal disord emot dysregul 12, 13 (2025). https://doiorg.publicaciones.saludcastillayleon.es/10.1186/s40479-025-00284-5
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DOI: https://doiorg.publicaciones.saludcastillayleon.es/10.1186/s40479-025-00284-5