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The welfare issues associated with water-bath stunning, particularly inversion and shackling, are widely recognised. This study aimed to develop, optimise and evaluate a prototype upright restraint system for broilers that avoids inversion and shackling of conscious birds. The device consisted of a horizontal conveyor with paired vertical side-belts fitted with rubber fingers to conform to the bird’s body, restraining the bird and preventing flapping. Fifty slaughter-weight broilers (1.7–3.6 kg) underwent up to five restraint runs each while behavioural indicators of distress, discomfort, trauma and positioning outcomes were assessed. Iterative design changes improved presentation, moving the side-belts closer, increased the odds of normal-like rhythmic breathing and removing the top finger row reduced head withdrawal. There were no overt signs of severe distress or trauma; however, vocalisations increased with run number. Repeated exposure may have influenced responses through habituation or sensitisation. However, in commercial use, birds would enter the device only once to be stunned and bled, so multi-run observations should not be over-generalised to slaughter conditions. These findings support the proof of concept for upright restraint as an improved welfare alternative compared to inversion-based systems for broilers.
The majority of small- to medium-scale and Halal poultry processors still rely on electrical water-bath stunning, despite recognised concerns regarding its humaneness and effectiveness. The aim of this study was to evaluate a mechanical system that restrains and stuns broilers in an upright posture using head-only constant current electrical stunning. Two experiments were performed on slaughter-weight broilers. Experiment A (n = 37) assessed behavioural indices, carcase quality during restraint, and time to recovery following head-only electrical stunning at 400 (n = 15), 600 (n = 12) or 800 (n = 10) mA at 50 Hz (2.5-s exposure). Experiment B (n = 15) assessed electroencephalographic (EEG) and behavioural indices of brain function after constant current 600 mA head-only electrical stunning (50 Hz, 2.5-s exposure period) to determine the time to recovery of brain function. In Experiment A, all birds were rendered unconscious with all three current levels. However, time to return of neck tension, rhythmic breathing and balance was variable and longer for birds stunned at 400 mA, while 800 mA resulted in more wing flapping leading to carcase damage. In Experiment B, all birds recovered normal-like EEG activity. The mean time to return of rhythmic breathing was 37 (± 2) s; range: 24–50 s, with a trend towards a moderate correlation with return of normal-like EEG activity. In conclusion, this project demonstrated the proof of concept of upright restraint for head-only electrical stunning of broilers and the recoverability of the method, in line with Halal requirements.
The use of restrictive care practices, such as physical restraint, seclusion and chemical restraint, is complex and controversial, posing ethical and legal dilemmas for healthcare professionals. These challenges often lead to reliance on subjective judgments, resulting in inconsistent clinical practices. This umbrella review synthesized findings from systematic reviews to identify and summarize key factors influencing healthcare practitioners’ decision-making regarding restrictive care practices in adult mental health inpatient settings. A comprehensive search of electronic databases and manual reference list reviews was conducted. Studies were screened using Covidence software, and eligible reviews underwent quality assessment with the JBI Critical Appraisal Checklist for Systematic Reviews. Only reviews reporting qualitative data on factors and contexts influencing clinician’s decision-making to implement restrictive care practices were included. The data were synthesized using inductive content analysis. The findings, presented in accordance with the PRIOR checklist, are based on 21 qualitative reviews. This review identified a wide range of contexts and actors influencing decision-making. Factors were grouped into five themes: healthcare professionals’ characteristics, service user-related factors, organizational and contextual factors, the involvement of other people and external elements such as international conventions, policies and cultural norms. Decision-making is shaped by the interplay of these factors, leading to variability in the application of restrictive care practices across healthcare settings. The findings emphasize the need for standardized frameworks to promote consistency in clinical practice. Addressing external pressures, such as organizational policies, staffing shortages, limited resources, time constraints and safety concerns, while providing healthcare professionals with appropriate tools and evidence-based guidelines, will support ethical, consistent and informed decision-making that aligns with best practices.
Global initiatives to reduce restrictive practices in mental health settings have gained increasing attention. However, discrepancies in restrictive practice rates create uncertainties about whether these variations reflect true differences in clinical practices or arise from inconsistent classification and reporting methods.
Aims
This study investigated how healthcare professionals classify and report potential restrictive practice scenarios, and examined variations in classification and documentation across diverse facilities.
Method
This was an international survey conducted using an online questionnaire via the Qualtrics platform. Healthcare professionals working in adult mental health in-patient settings were recruited through multiple media platforms and snowball sampling. The questionnaire included 44 potential restrictive practice case scenarios. Participants rated each scenario as follows: (a) whether it should be classified as a restrictive practice; (b) whether it should be recorded as such; (c) whether it would be classified as a restrictive practice within their facility; and (d) whether it would be reported as a restrictive practice in their facility. Survey development was guided by systematic reviews and co-design work with stakeholders. Data were analysed using ordered regression models, with clustering by participant identity and country. Robust standard errors were applied to ensure accurate estimation of variability.
Results
A total of 491 healthcare professionals from 41 countries participated. Results indicated substantial inconsistencies in clinicians’ perspectives regarding what constitutes restrictive practices and whether a given action should be reported as a restrictive practice. Although participants frequently identified scenarios as restrictive practices, their intention to report them was considerably lower. Additional discrepancies were observed between clinicians’ individual perspectives and their expectations of how these practices were actually being classified and reported as restrictive practices within the in-patient facilities where they work.
Conclusions
Discrepancies between healthcare professionals’ classification of restrictive practices and their reporting intentions, as well as between their perspectives and actual institutional practices, highlight potential errors in current reporting systems. These findings underscore the need for standardised definitions, enhanced reporting frameworks and structured training programmes and monitoring mechanisms to improve consistency in the management of restrictive practices across mental health settings.
The use of restraint in hospital settings is divisive, and internationally there are calls for its elimination. However, this is at odds with the experience of many hospital staff, who consider restraint, at times, a “necessary evil”. In this paper, we explore the definition of restraint and potential ethical justifications for its use. We argue that the current ethical literature employs two definitions of restraint — outcome-oriented and intent-oriented — neither of which successfully captures all ethically relevant features of the practice. We propose a new conceptualization of restraint which centers on the number of individuals impacted by an act of patient restraint — a continuum between therapeutic restraint and public-safety restraint. Understood in this way, neither the principlist nor human rights frameworks that dominate the current literature are appropriate for assessing the ethical legitimacy of restraint. We suggest that, given the similarities between restraint and public health interventions, the use of public health ethics principles to consider the ethical justifiability of restraint in hospitals is a potentially productive way forward in this controversial area.
In the last decade, UN bodies and the WHO call for the abolition of coercion in psychiatry. Studies provide some evidence for interventions to reduce the use of coercion, but it is unclear whether the use of coercion is decreasing in real-world practice. The aim of this study was to gather longitudinal ecologic data on the use of coercive interventions in European countries and to depict trends over time.
Methods
For each country, inclusion required access to ecologic datasets spanning a minimum of four years, pertain to a defined population (country or federal state level), and allowing the necessary elements to calculate both the proportion of psychiatric admissions affected by involuntary admissions (IAs) and coercive measures (CMs) and the rate per 100,000 inhabitants. Country experts were accessed via a European network of experts (FOSTREN group).
Results
Data were obtained from Austria, England, Germany, Norway, Sweden, and Switzerland, and covered periods between 4 and 10 years. In no country, an absolute decrease in IA and the use of CM could be observed. Rates of IA per 100,000 inhabitants changed between −5.4% (Sweden) and +37% (Germany). Rates of admissions exposed to any kind of CM changed between +11% (Austria) and +86% (Norway).
Conclusions
The findings suggest a persistence or rise in coercive practices despite national and international policy commitments. An increase in involuntary admissions suggests reasons outside psychiatric hospitals, whereas a disproportionate increase in coercive measures may indicate a change of practice in in-patient psychiatry. Further research is needed to explore the reasons from clinical and societal perspectives.
In this article, we maintain that the anticipated integration of artificial intelligence (AI)-enabled systems into state-level decision making over whether and when to wage war will be accompanied by a hitherto neglected risk. Namely, the incorporation of such systems will engender subtle but significant changes to the state’s deliberative and organisational structures, its culture, and its capacities – and in ways that could undermine its adherence to international norms of restraint. In offering this provocation, we argue that the gradual proliferation and embeddedness of AI-enabled decision-support systems within the state – what we call the ‘phenomenon of “Borgs in the org”’ – will lead to four significant changes that, together, threaten to diminish the state’s crucial capacity for ‘institutional learning’. Specifically, the state’s reliance on AI-enabled decision-support systems in deliberations over war initiation will invite: (i) disrupted deliberative structures and chains of command; (ii) the occlusion of crucial steps in decision-making processes; (iii) institutionalised deference to computer-generated outputs; and (iv) future plans and trajectories that are overdetermined by past policies and actions. The resulting ‘institutional atrophy’ could, in turn, weaken the state’s responsiveness to external social cues and censure, thereby making the state less likely to engage with, internalise, and adhere to evolving international norms of restraint. As a collateral effect, this weakening could contribute to the decay of these norms themselves if such institutional atrophy were to become widespread within the society of states.
How can ethics consultants weigh and balance patients’ physical and psychological needs when they are appear mutually exclusive? How might a disability-aware lens impact the way we address risk? A disconcerting clinical ethics consultation regarding "Jimmy" prompts reflection of these questions and our own complicity with ableism as consultants and providers. Jimmy, who was previously incarcerated, houseless, and facing mental status changes, spent months fighting four-point restraints to maintain a cervical collar meant to prevent disability and death.
The predominant paradigm of acute medical care has not integrated trauma-informed or disability aware lenses despite trauma prevalence among patients and the presence of disability for 25% of adults. The lack of these perspectives has hazardous ramifications in clinical decision making and beside care. The prevailing norm prioritizes physical and functional outcomes over identity and emotional well-being. There is a false assumption that people with disabilities have a worse quality of life than people without disability. This disability illiteracy undermines patient autonomy and the disability community. Medical professionals’ personal experience and relationship to disability can perhaps shift this perspective to a more inclusive and nuanced approach to ethical decision making A broader transformative approach to ethics consultation is needed to avoid complicity in moral harms.
Action at scale on climate change is urgent. It is unavoidable that such action must for a period of some decades include restraint, because we do not have time to construct enough emissions-free substitutes for all today’s emitting activities. Leaders in politics and businesses cannot promote restraint without losing their jobs, so leadership must come from us, individually and collectively, making decisions to live differently. We can all act, at home and at work or in other teams. We can prioritise our most emitting activities, make changes where possible and, where it is for now beyond our reach, we can promote change through raising awareness of what matters and what help we need. These choices and actions are virtuous. Not ‘virtuous’ in the sense we parodied in the opening, of something admirable but prim and outdated, but a joyful, life-enhancing virtue that expresses the best of what we hope to be. The virtue of restraint in climate action is an act of leadership, an expression of faith and charity, and above all, an act of love.
Seductive messaging about ‘convenient’ technological solutions have prevented us recognising and acting on the need for restraint as a core component of climate action, yet restraint has in the past led to faster change than technological innovation. The actions that allow us to deliver a safe climate are specified in the chapter and are highly specific. At home, we should aim to switch from gas boilers to electric heat pumps, from petrol to electric cars, to phase out our use of fossil aeroplanes and certain key foods, and we can also reduce our total requirement for energy. In teams, at work or in other contexts, we can pursue the same goals, while also aiming to reduce the construction of new large objects (buildings, vehicles, infrastructure or large equipment) and to support suppliers and customers on the same journey. As lobbyists, individually or in groups, we can influence politicians and business leaders to make it easier for us to follow the key actions that lead to zero emissions.
Efforts to reduce restrictive practices (RPs) in mental health care are growing internationally. Yet, inconsistent definitions and perspectives often challenge the consistent implementation and evaluation of reduction strategies. This study explored which scenarios different mental health stakeholders classify as RPs, examined the contextual factors influencing these classifications and compared classification patterns across clinicians, researchers, service users and family caregivers.
Methods
An international cross-sectional survey was conducted using a multilingual online questionnaire hosted on the Qualtrics platform. A total of 851 stakeholders participated, including clinicians (n = 517), service users (n = 80), family caregivers (n = 89) and researchers (n = 165). Participants were presented with 44 potential RP case scenarios and asked to rate whether each scenario should be classified as an RP using a four-point Likert scale (Definitely yes, Probably yes, Probably no, Definitely no). The scenarios were organized into 22 paired comparisons, each sharing the same core context but differing in specific details. Paired comparisons were analyzed one pair at a time, allowing us to identify classification patterns between the scenarios and isolate the effects of particular contextual factors using ordered logistic regression. Interaction analyses were then conducted to assess how classification patterns varied across stakeholder groups.
Results
Substantial discrepancies exist both within and between stakeholder groups regarding whether a given action should be considered an RP or not. Physically visible actions were often identified as RPs across all groups, while less visible forms often went unrecognized. Contextual differences, such as the healthcare professional’s intention, duration of the action, methods used, presence or absence of consent, door-locking status, and the severity of anticipated harm to be prevented influenced whether a given action was classified as an RP. Service users classified more scenarios as RPs than other groups; however, their decisions were more context-sensitive, shifting notably even with minor changes in scenario details. Among the 22 paired scenarios compared, 13 (59.09%) showed significant differences (p < 0.01) within at least one stakeholder group and eight demonstrated differences between groups.
Conclusions
Mental health stakeholders’ interpretations of RPs were often shaped not only by the inherent coercive nature of actions but also by the context in which they occurred and the professional role of the assessors. This underscores the need for harmonized definitions and classification frameworks for RPs, co-designed with diverse stakeholders. Addressing less visible forms of RPs in policy and clinical practice is also essential.
Iceland and the United Kingdom experienced a series of crises that follow a similar pattern. Iceland extended its maritime limits – to preserve more fish for Icelandic vessels and conserve fish stocks. Britain resisted the extension. Both sides escalated their behavior (e.g., issuing threats and coercively harassing each another’s vessels), and Britain ultimately conceded. This chapter covers the 1971–1973 Cod War. It follows the above pattern, but with a somewhat unique twist. In the 1971–1973 episode, domestic politics within both democratic states encourage escalation. Iceland, moreover, threatens to leave the North Atlantic Treaty Organization (NATO) and to evict United States (US) forces from the Keflavik air base. Because of these threats, as well as escalating coercion, NATO mediates, and NATO and the US pressure Britain to concede. Ultimately, this crisis does not escalate to a major-state war because the disputed issue (i.e., maritime limits) lacks sufficient salience and past, similar episodes demonstrate that a nonwar solution exists.
More than 116 million people in Africa live with mental health conditions. However, many African countries lack the infrastructure, training and workforce to effectively manage psychiatric emergencies. This has led to overuse of controversial practices such as physical and chemical restraint and involuntary seclusion, often violating patient rights. We conducted a scoping review of restraint and seclusion practices and their impacts in African clinical settings using the PubMed, Embase, CINAHL, PsycInfo and ProQuest databases. Titles/abstracts and full texts were reviewed for inclusion using the Covidence platform, and 29 studies were included in the final extraction. Restraint and/or seclusion were employed to manage aggression, enable involuntary treatment or prevent self-harm. Patients found restraint and seclusion to be dehumanizing, a cause of posttraumatic stress and a barrier to future help-seeking. Healthcare workers described inadequate training, overuse of restraint and seclusion, injuries and emotional distress after employing these treatments. Further research, intervention development and policy reform are urgently needed to promote humane and patient-centered psychiatric care, including verbal de-escalation training, in underresourced healthcare systems.
At a fairly early age Lucy was admitted to a psychiatric hospital and then spent years in low-security psychiatric units. After an episode of neuroleptic malignant syndrome, she became physically unwell and stopped eating. When her life appeared to be danger, ECT was suggested. Lucy refused to have it and the first sessions were given under restraint. After eight sessions ECT hadn’t worked, and the team stopped it. A second course was started later, this time with Lucy’s agreement, and it worked. She gradually improved, had psychological treatment, engaged in rehabilitation and eventually was discharged home. She continued with maintenance ECT as an outpatient. She got married and started work as an Expert by Experience for the local hospital.
Edited by
James Ip, Great Ormond Street Hospital for Children, London,Grant Stuart, Great Ormond Street Hospital for Children, London,Isabeau Walker, Great Ormond Street Hospital for Children, London,Ian James, Great Ormond Street Hospital for Children, London
This chapter explains the law surrounding consent for the medical treatment of children, when children can give consent themselves, who can give consent of their behalf and when a refusal of consent should be respected. It also considers guidelines relevant for the practice of restraint in paediatric anaesthesia. Finally, it discusses the unique features of the ethics of research involving children, including the levels of risk that are deemed acceptable.
Chapter 10 As the French Revolution became increasingly violent, there was an growing backlash in Britain against the celebration of liberty as independence. One response, popular among a number of conservative churchman, took the form of reviving the claim that all subjects have a duty of non-resistance and passive obedience. But a different although no less hostile response came from a number of self-styled ‘liberal’ legal and political writers who saw themselves as equally opposed to conservatives and revolutionaries. This group has been little studied, but the aim of this chapter is to show that they were of central importance in discrediting the ideal of liberty as independence. They accepted the Hobbesian view that most of our natural rights must be given up in the name of peace, and that the rights remaining to us as subjects of states must basically take the form of the silence of the law. Although the ideal of liberty as independence continued to be celebrated by early British socialists, the liberal writers paved the way for the explicitly Hobbesian commitments of the early utilitarians, who finally succeeded in turning the claim that liberty cannot mean anything other than exemption from restraint into a new orthodoxy.
Chapter 8 focuses on how the strand of legal argument traced in Chapter 7 was deployed by a number of pro-imperialist writers in England in reply to Price, Paine and the American colonists in 1776. The first to take up the claim that liberty is nothing other than absence of restraint were the lawyers John Lind and Richard Hey, and they were soon followed by a large number of other critics of Price, among whom the most prominent were Adam Ferguson, John Welsey and later William Paley. The chapter focuses in particular on three objections generally raised against Price’s account of liberty. The first was that his definition confuses the state of being unfree with that of merely lacking security for the liberty you possess. The second was that he connects liberty with an unviable concept of inalienable natural rights. The third was that, by defining liberty as absence of dependence, and then equating dependence with slavery, he commits himself to a morally indefensible definition of slavery. He forgets that slaves are not merely subject to the will of their masters, but that the chief horror of slavery is that they are also regarded as being their master’s property.
Chapter 7 begins with the reaction that followed from Price and Paine’s defence of the colonial cause. They agreed with the colonists that to live in dependence on the arbitrary will of someone else is what it means to be a slave, and consequently agreed that the colonists must have a natural right to free themselves from their servitude, if necessary by force. This was the moment when a large number of pro-imperial spokesmen came forward to claim that the colonists and their supporters were failing to understand what it means to speak of possessing or losing one’s liberty. They objected that we are not rendered unfree if we are merely subject to someone else’s will; we are only rendered unfree if we are restrained from acting in some particular way. Generally this definition of liberty has been seen as an invention of the late eighteenth century. But as this chapter shows, it arose out of a long tradition of legal and political argument that originated with Hobbes, Pufendorf and their followers. We already find it present in England in the early eighteenth century, and the pro-imperialist writers now brought it to the forefront of debate.
Conclusion: a reckoning. Liberty used to be defined as absence of dependence. Nowadays it is usually defined as absence of restraint. But the underlying aim of this book has been to establish that there are several reasons for thinking that the ideal of liberty as independence is to be preferred. We gain from it a better sense of how the mere fact of living in subjection -- whether or not we are restrained -- takes away our liberty. We also gain from it a more helpful way of thinking about fundamental rights. Rather than conceiving of them as universal moral claims, there may be good reasons for preferring to think of them as the creation of specific independent communities. Above all, the ideal of liberty as independence helps us to see the importance of cherishing the value of autonomy in relationships between states as well as individual citizens. It is difficult to see how the requirements of justice can be met in the absence of a commitment to the ideal of liberty as independence.
INTRODUCTION. When and why did it come about that one prevailing way of understanding what it means to be free was replaced by a strongly contrasting account that came to be no less widely accepted, and still remains dominant? The argument of the book is that, in Anglophone political theory, the change happened quite suddenly in the closing decades of the eighteenth century. Before that time it was generally agreed that what it means to be free is that you are not subject to, or dependent on, the arbitrary will and power of anyone else. Liberty was equated with independence. But by the early nineteenth century it had come to be generally accepted that liberty simply consists in not being restrained from acting as you choose. What prompted the change, the book argues, was not the imperatives of commercial society, as has often been argued. Rather it was a growing anxiety, in the face of the American and French Revolutions, about the democratic potential of the ideal of liberty as independence.