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Lithium is the only true mood stabiliser as it is able to both treat and prevent mania and depression. In practice, its popularity has declined despite discovering it has anti-suicidal and neuroprotective properties. Here, we argue for recognition of its benefits and advocate for its clinical use more widely.
This chapter provides multiple-choice questions designed to reinforce and expand your knowledge of anxiety and stress-related disorders, including symptom presentation and assessment, neurobiology, treatment mechanisms, clinical characteristics of treatments, treatment strategies, and considerations for special populations.
This chapter provides multiple-choice questions designed to reinforce and expand your knowledge of attention deficit hyperactivity disorder, including symptom presentation and assessment, neurobiology, treatment mechanisms, clinical characteristics of treatments, treatment strategies, and considerations for special populations.
This fully updated fifth edition offers over 150 case-based multiple-choice questions across ten core areas of psychiatry and psychopharmacology. An essential learning resource for psychiatrists, primary care physicians, nurse practitioners, psychologists, and pharmacists, it helps identify knowledge gaps and guide further study. Each question includes detailed explanations and references, enabling users to diagnose psychiatric symptoms, implement evidence-based treatments, and integrate recent advances into clinical practice. Aligned with Stahl's Essential Psychopharmacology, the content spans neurobiology to psychopharmacologic strategies and reflects current best practices and clinical dilemmas. Cross-references to key Stahl titles enhance integrated study, while peer benchmarking allows users to assess their proficiency. Ideal for trainees and experienced professionals alike, this book transforms exam preparation into a deeper, clinically relevant learning experience.
Misophonia is a condition characterised by intense emotional reactions to sounds that would not bother most people. Currently, there is no widely accepted and effective treatment for misophonia. Most published studies on treatment have used behavioural therapy, cognitive interventions, or audiological treatments; however, there is no comparison of the effectiveness of these approaches. This 6-week study aimed to compare the effects of brief, self-administered versions of exposure and tinnitus retraining therapy (TRT) in 58 adults with misophonia. The participants, randomly assigned to the two treatment groups and a wait-list group, were assessed at three time points (baseline, week 3, and week 6). The exposure group was given self-exposure homework assignments, where the patient was expected to self-expose to the live or recorded misophonic sound that was agreed upon during the week 0 assessment, for 20–40 minutes, three times a week. The patients in the TRT group were given a set of pre-recorded music pieces and asked to listen to any piece of their choosing for 20–40 minutes a day, three times a week. Self-report measures of misophonia severity (Misophonia Checklist), and interference due to symptoms were rated at each time point by the patients. The assessor also rated improvement at each time point. The study is registered in ClinicalTrials.gov (registration no. NCT05993286). The Intention to Treat (ITT) analyses revealed no difference between the three groups in terms of self-rated misophonia severity at week 6. The assessor-rated percentage of improvement favoured exposure, although the response rate was very low; only six out of 39 participants were rated as moderately or much improved, five of whom were in the exposure therapy group. The results underscore the need for finding ways to increase treatment response in misophonia.
Key learning aims
(1) To become familiar with the concept of misophonia; i.e. hatred of sounds.
(2) To evaluate the potential effectiveness of existing interventions for the treatment of misophonia.
(3) To gain insight into adapting established therapy methods to novel settings.
Edited by
Liz McDonald, East London NHS Foundation Trust,Roch Cantwell, Perinatal Mental Health Service and West of Scotland Mother & Baby Unit,Ian Jones, Cardiff University
Personality disorder (PD) is a complex condition, which has been the subject of both debate and research. However, maternal PD has only been the focus of research in the last two decades. In this chapter I discuss that research in the context of what is known generally about PD, as a disorder with a predictable presentation of signs and symptoms; an aetiology, and indications for effective treatment. There has been more research on maternal PD in the last 15 years, which shows that mothers with PD may struggle to care for their children, especially in the postnatal period, and their mental health may also deteriorate during pregnancy. In this chapter I describe the issues described above and discuss how clinicians approach the management of mothers with PD. I place special emphasis on the impact of maternal PD on mother-child relationships and attachment, and the implications for child health.
The notion that people with psychopathy traits do not respond positively to treatment efforts may sound intuitive. If people are inflexible, uncaring towards others, manipulative, and just generally difficult to get along with, it follows that treatment might be ineffective. However, what is intuitive and what is accurate do not always overlap perfectly. The analyses in this chapter contribute to a growing body of literature indicating that individuals with psychopathy traits can change and respond in expected ways to intervention strategies (Bernstein et al., 2021; Wong et al., 2015). The analyses in this chapter identified that people with psychopathy traits who spent more time incarcerated, thereby increasing access to rehabilitative services, experienced a subsequent decline in offending. It is possible that these findings reflect the efficacy of the risk-need-responsivity model, wherein intensive intervention strategies reduce criminal behaviour for high-risk persons. Treatment modalities for people with psychopathy traits are discussed.
I wrote this book to help readers entering into the psychopathy literature come away with an understanding of psychopathy that is not watered down. As a professor, I regularly encountered students who sought to learn more about psychopathy but found that peer-reviewed papers were overly technical and assumed a certain level of background knowledge on the part of the reader. Books are not always a viable alternative, as they can be informal and make statements about psychopathy in the absence of empirical evidence. Edited books feature multiple authors, which is a strength; however, they often present contrasting opinions, and no explanation is provided for the differences in opinion. Popular culture sources like True Crime podcasts are regularly factually inaccurate when it comes to discussing psychopathy. In this chapter, I reflect on the limitations of my analyses, describe key take-home messages from each chapter, and integrate these messages to identify overarching themes from the book.
Vasovagal syncope is the most common cause of syncope in children, and there is no satisfactory treatment currently. We evaluated the response to midodrine treatment in patients with vasovagal syncope who failed to benefit from conventional, non-pharmacologic treatments.
Materials and methods:
The study was a single-centre retrospective study. The data of 44 children between the ages of 6 and 18 years, who were diagnosed with recurrent vasovagal syncope, did not benefit from non- pharmacological treatments, and received midodrine treatment from 2015 to 2022 were enrolled in the study.
Results:
In total, 44 patients, 38 (86.4%) were girls, and 6 (13.6%) were boys. The primary outcome measure was the change in frequency of vasovagal syncope episodes from baseline to 6 months after treatment with midodrine. Patients received a midodrine treatment at an average of 2.5–5 mg/day and were followed for a median of 23.07 (8–72) months. The median number of syncope was 4.2 (3–9.8)/year prior to treatment and 1.2 (1–5)/year (p = 0.01) following the treatment. There was a significant improvement in syncope episodes in all patients.
Conclusion:
Vasovagal syncope is the common cause of syncope in children, and its treatment has not yet been found satisfactory. Midodrine treatment was found to be effective and safe in paediatric patients with recurrent vasovagal syncope. However, further research is needed to determine the most effective treatment for this condition.
Parenting is related to the development of callous-unemotional (CU) traits (i.e. low empathy and restricted guilt), making it an important target of interventions for childhood conduct problems (CPs). However, the relative importance of different parenting features in relation to the development of CU traits remains unclear. This study used machine learning to examine multiple parenting features assessed across infancy and early childhood as predictors of CU traits and CPs in early adolescence.
Methods
Data were from the Family Life Project (N = 1,292; 49% female, 41% Black, and 28% below the poverty line). Seventy-four parenting predictors were assessed at eight time points between children aged 6–90 months using parent-reported questionnaires and observer ratings of videotaped interactions and home visits. CU traits and CPs were assessed via parent-reported questionnaires in preadolescence (12–14 years).
Results
Parenting features explained 8.2% of CU traits variability in preadolescence, with top predictors including early sensitive parenting and later behavior management and scaffolding practices. Prediction of CPs was weaker, with parenting explaining 4.5% of the variability.
Conclusions
Results highlight that disruption in close and sensitive early parent–child relationships is relevant to the development of CU traits. Results from the prediction of CPs indicate a more heterogeneous etiology. Findings support targeting parental sensitivity and behavior management within preventative interventions for CU traits and CPs.
Lactate, generated through glycolysis, plays a dual role as both a metabolic substrate and a signalling molecule, influencing cellular functions in pathophysiological scenarios. Protein lactylation, a recently identified form of post-translational modification mediated by lactate, has garnered significant and increasing attention. Globally, hepatic disorders pose a significant public health burden, frequently involving disruptions in glucose metabolism and consequent lactate buildup.
Methods
This comprehensive review examines the discovery, regulatory mechanisms and pathogenic roles of lactylation in diverse liver disorders, while critically evaluating emerging lactylation-targeted therapeutics to guide future translational research.
Results
Lactylation modifications play a pivotal role in various pathophysiological processes, including hepatic inflammation, liver fibrosis, ischaemic injury, tumour growth and metastasis.
Conclusions
Modulation of lactylation pathways, coupled with pharmacological control of lactate synthesis and shuttling, emerges as a strategic approach to liver disease therapeutics.
Because of advances in technology and the provision of critical care, an increasing number of patients are surviving critical illness; this growing population of survivors of critical illness is characterized by heightened vulnerability to a host of adverse health outcomes and by the development of multidimensional impairments that significantly impact their quality of life and societal participation. Post-intensive care syndrome (PICS) is defined as new or worsening impairments in physical, cognitive, or mental health status arising after a critical illness and persisting beyond acute care hospitalization. PICS-Family describes the psychological and social impairments that family members, loved ones, and caregivers can develop as a consequence of their loved one’s critical illness. Survivors of critical illness are a heterogeneous patient population, and considerable variation exists with respect to the breadth, depth, duration, and mutability of their symptoms and impairments. This chapter explores the clinical manifestations of PICS, its incidence and prevalence, the co-occurrence of impairments in multiple domains, duration and severity of impairments, risk factors for its development, prediction tools, prevention strategies, screening and diagnosis, and treatment options. Additional topics include the biophysical model of disability, functional trajectories following critical illness, and the lack of communication about post-ICU problems.
As discussed in Chapter 1, the primary focus of this book is on the potential of neurotechnology to support the rehabilitation of convicted persons by improving risk assessment and risk management – rather than on its potential for diagnosing and treating mental or brain disorders. Still, in some cases, neurorehabilitation might well become conducive or even crucial to the improvement of mental health in forensic populations. Brain stimulation to attenuate aggressive impulses might serve to reduce the mental distress experienced by some persons subject to these impulses. Furthermore, aggression can be a symptom of a recognised mental illness, such as a psychotic disorder, or may be a core feature of a disorder, as in intermittent explosive disorder. Diminishing aggression using neurotechnology could in such cases be relevant to the person’s mental health, which appears to be an interest protected by human rights law. For example, Article 12 of the International Covenant on Economic, Social and Cultural Rights (ICESCR) recognises a “right to the highest attainable standard of physical and mental health”.
Delirium, which is an important risk factor for post-intensive care syndrome (PICS), is common during critical illness, affecting between 20% and 80% of patients. It is associated with numerous adverse outcomes, including longer time on mechanical ventilation, longer time in the intensive care unit (ICU) and hospital, death, and long-term cognitive impairment. Delirium in the ICU can be reliably detected using multiple tools, including the Confusion Assessment Method in the ICU (CAM-ICU) and the Intensive Care Delirium Screening Checklist (ICDSC). The exact cause of delirium, however, remains elusive even though there are many purported mechanisms, including neuroinflammation, metabolic insufficiency, neuronal dysfunction, and neurotransmitter disturbances. Due to knowledge gaps regarding the mechanism(s) of delirium, effective medical treatments for delirium also remains elusive. Current practice involves the prevention of delirium through the recognition and management of modifiable risk factors. The well-studied ABCDEF bundle is one such strategy, which is primarily non-pharmacologic, to prevent or mitigate delirium and thus limit its adverse outcomes. Unfortunately, delirium still occurs at a high rate, and the work to understand the underlying mechanism and its varied manifestations and to develop an effective treatment continues.
Catatonia can be associated with a diverse range of conditions, including autoimmune encephalitis. Although rare, autoimmune encephalitis accounts for a significant proportion of catatonia cases with autoimmune aetiologies. In instances where autoimmune mechanisms are suspected, autoantibody testing is a key component of the diagnostic evaluation. However, test results should always be interpreted in conjunction with clinical findings. This article highlights the diagnostic challenges involved, advocating for structured diagnostic algorithms and timely initiation of immune therapy in carefully selected cases – particularly when antibody confirmation is absent. It revisits the paper, ‘Retrospective chart review of cases with steroid-responsive catatonia: exploring a potential autoimmune etiology’.
Specific phobia of vomiting (SPOV) is a persistent, excessive fear of vomiting that is more prevalent in females, often begins in childhood and typically lasts 25 years before treatment is sought. It is a relatively neglected area of research, with most evidence consisting of single case studies. There are implications for the perinatal period, in particular the experience of pregnancy which for many involves symptoms of nausea and vomiting. However, there is a paucity of research on the experience of SPOV during pregnancy and currently no published treatment research. This study aimed to extend the existing literature by applying Veale’s (2009) protocol for SPOV to a pregnant client in her twenties. The intervention consisted of 12 one-hour face-to-face sessions and was effective in significantly reducing anxiety (GAD-7 reduced from 7 to 0), depression (PHQ-9 reduced from 6 to 1), impaired functioning (WSAS reduced from 20 to 4) and vomiting phobia (SPOVI reduced from 40 to 0).
Key learning aims
(1) To understand the impact of SPOV during pregnancy.
(2) To understand how to adapt Veale’s (2009) SPOV treatment protocol for a pregnant client.
(3) To learn how to carry out behavioural experiments and imagery rescripting related to SPOV during pregnancy.
Although theories of specific language impairment grounded in Universal Grammar (UG) have advanced the description of SLI considerably, they provide limited utility as far as treatment is concerned. Because UG assumes deficits in language principles and parameter setting, remediation of the difficulty is not possible; rather, reliance on compensatory mechanisms is recommended. Compensatory mechanisms rely on the same learning principles as are adopted by theorists that adopt a more Emergentist view. Thus, we agree with Ambridge, Pine, and Lieven that a UG-based approach is redundant and recommend focusing efforts on identifying and strengthening treatment strategies associated with general learning principles instead.
Cognitive problems represent one of the most common symptom dimensions in functional neurological disorder (FND; >80% of patients) and are frequently associated with distress, disability, and difficulties engaging in evidence-based treatments such as psychotherapy. Cognitive difficulties occur across the FND subtypes (eg, seizures, movement disorders, dizziness) but are largely underrecognized and undertreated by healthcare providers. That is, although a variety of interventions are available for primary functional symptoms and mental health comorbidities, there have not been any systematic efforts to date to specifically target cognitive functioning in FND, leaving an important gap in the literature.
Cognitive rehabilitation is a flexible approach utilizing diverse techniques aimed at improving cognition and enhancing functional independence in people with neuropsychiatric disorders. Cognitive rehabilitation can have positive impacts (moderate effect sizes) on cognition and everyday functioning across a variety of conditions, including traumatic brain injury, mild cognitive impairment, long COVID, PTSD, and others. Given the transdiagnostic clinical utility of cognitive rehabilitation, it has potential for benefit in many patients with FND if adapted and applied appropriately.
In this review, we highlight the utility of cognitive rehabilitation for FND, with a focus on clinically actionable advice and guidance. We describe fundamental principles of cognitive rehabilitation, evidence for its efficacy and effectiveness across neuropsychiatric disorders, and methods for avoiding potential pitfalls when applying it in FND. We then discuss a Case Vignette in order to emphasize the application of cognitive rehabilitation principles in an individual patient. We conclude with future directions for research and clinical care.
This chapter provides an overview of chronic traumatic encephalopathy (CTE), a neurodegenerative disease associated with repetitive head trauma. It discusses the historical background of CTE, its neuropathology, clinical features, and epidemiology. The chapter also explores the current understanding of CTE staging and common co-pathologies. It highlights the challenges in diagnosing and monitoring CTE in living patients and the ongoing research efforts to develop biomarkers for early detection. The chapter concludes by discussing the prevention, treatment, and future directions in CTE research. It is important to recognize the risks of head trauma and implement measures to reduce the incidence of CTE and other neurodegenerative diseases associated with head trauma.