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While the preceding two chapters focused on the physiological domains whose motions take place ‘by nature’, that is, involuntarily, this chapter looks at the activities of the physiological system responsible for the motion ‘by will’. Galen depends on Hellenistic anatomists, especially Herophilus, for much of what he knows about the nervous system, but this chapter looks at both inherited knowledge and polemic interaction. In a rare case of disagreement, Galen criticizes Herophilus regarding the claims about the inherent sensitivity of the nerve tissue. The fact that Galen does not accept Herophilus’ experiments and maintains that nerves only receive capacity from the brain shapes his understanding of this physiological domain. The activities of the nervous system encompass not only voluntary motion but also sense perception and pain, and this chapter argues that each of them has distinctive implications for the unity of the living body as a whole.
Pain is a complex experience that includes physical sensations and emotional responses. Research has shown that the central nervous system plays a significant role in how we experience pain. In this chapter, we review the current understanding of the neuroscience of pain, with a particular emphasis on pain processing in the brain. We cover early theories that emphasized the brain’s role in integrating and modulating pain, as well as modern approaches that view pain as distributed processing in the brain. We also introduce functional and computational frameworks for understanding the sensory and motivational aspects of pain and discuss various factors that contribute to the multidimensional nature of pain. The future direction of the study of pain neuroscience includes a deep sampling of subjective pain experience and the use of generative models.
Chapter 2 is concerned with research questions. We discuss the different processes through which research questions can be identified and developed in corpus-based research on health communication. Three case studies are considered. The first study involved the analysis of press representations of obesity. In this study, the researchers developed their own research questions in a variety of ways, including by drawing from the non-linguistic literature on obesity. The second study focused on the McGill Pain Questionnaire – a well-known language-based diagnostic tool for pain. A pain consultant asked the researchers if they could help understand why some patients find it difficult to respond to some sections of the questionnaire. In response, the researchers formulated a series of questions that could be answered using corpus linguistic tools, and identified some issues with the questionnaire that address the pain consultant’s concerns. The third study involved the analysis of patient feedback on the UK’s National Health Service. The researchers were approached by the NHS Feedback Team and given 12 questions that they were commissioned to answer by means of corpus linguistic methods.
In Tusculans 2 the interlocutors discuss the value of physical pain. They swiftly agree that it is not the greatest evil but take longer to consider whether it is bad or, as the Stoics think, merely indifferent. Enduring pain is taken to be an indication of courage and manliness (virtus) and this is undermined by the claim that physical pain is not bad. Therefore neither the Epicureans nor the Stoics provide a wholly satisfactory account of the value of physical pain and its relationship to virtue.
Cicero composed the Tusculan Disputations in the summer of 45 BC at a time of great personal and political turmoil. He was grieving for the death of his daughter Tullia earlier that year, while Caesar's defeat of Pompey's forces at Munda and return to Rome as dictator was causing him great fears and concerns for himself, his friends and the Republic itself. This collection of new essays offers a holistic critical commentary on this important work. World-leading experts consider its historical and philosophical context and the central arguments and themes of each of the five books, which include the treatment of the fear of death, the value of pain, the Stoic account of the emotions and the thesis that virtue is sufficient for happiness. Each chapter pays close attention to Cicero's own method of philosophy, and the role of rhetoric and persuasion in pursuing his inquiries.
The opioid overdose crisis has become a global public health emergency, claiming more than 100,000 lives each year. In North America, shifting opioid prescribing practices in response to the crisis have profoundly affected people living with chronic pain, who now face reduced access to prescription opioids. Against this backdrop, pain stakeholders have become increasingly active in policymaking arenas to shape how opioids and pain are understood. This study examines the Canadian Pain Task Force (CPTF) — a federal advisory body charged with creating a national pain strategy — by analyzing its reports, public and patient consultations, and internal documents. Through qualitative framing analysis, we find that stakeholders overwhelmingly depicted the overdose crisis as the result of illicit and irresponsible opioid use, while positioning stigma as both a driver and consequence of the crisis that compounded the challenges faced by people with chronic pain. From these problem definitions flowed policy proposals centered on expanding opioid access, reducing stigma, and advancing patient-centered care. These findings demonstrate how pain stakeholders shape, and are simultaneously shaped by, opioid policy debates — with consequences for both overdose prevention and chronic pain management.
Rural communities make up 19% of the US population, yet are underrepresented in clinical trials. Community engagement methods can facilitate collaboration and trust with local healthcare personnel to enhance enrollment. The purpose of this manuscript is to describe community engagement methods and their impact on enrollment in a pragmatic clinical trial.
Methods:
We describe a variety of methods used in the Fibromyalgia TENS in Physical Therapy Study (FM-TIPS) to enhance enrollment in rural communities and low-enrolling clinics. Community engagement methods were implemented partway through the trial for selected groups: Targeted Rural (TR) (n = 10), Targeted Low Enrolling (TLE) (n = 6), and compared to Untargeted Groups (UT) (n = 13). The impact of these methods on inquiries, screening, and enrollment were evaluated by comparing actual enrollment to projected enrollment.
Results:
We trained and employed community engagement coordinators to implement strategies in TR and TLE physical therapy clinics. These included, posting flyers, community events, physician outreach, social media ads, and direct mailing. These methods increased study inquiries, screening and enrollment in the study. Specifically, when compared to projected values there were increases in enrollment for both the TR and the TLE groups, but not the UT group. Of those that passed screening 99% of rural and 32% of urban residents enrolled in the study.
Conclusion:
A multi-pronged and individualized community engagement approach can increase enrollment of rural residents in clinical trials. Building strong relationships and partnering with community clinics and local communities is essential to success.
The plays of Sean O’Casey are filled with aches and pains, debilitating diseases, and traumatic wounds. He was himself a disabled writer. Furthermore, his presentation of disease and disability is inseparable from his critique of class, militarism, and masculinist ideology. This chapter shows how O’Casey’s depictions of disability are more nuanced than they may at first appear. He does demonstrate an essentialist tendency to see female resilience as a triumph over the failures of male impairment, yet, in plays such as Juno and the Paycock and The Silver Tassie, O’Casey allows space for contrary readings that speak with relevance to contemporary understandings of disability.
Edited by
Rebecca Leslie, Royal United Hospitals NHS Foundation Trust, Bath,Emily Johnson, Worcester Acute Hospitals NHS Trust, Worcester,Alex Goodwin, Royal United Hospitals NHS Foundation Trust, Bath,Samuel Nava, Severn Deanery, Bristol
In this chapter we discuss analgesic agents used in anaesthesia and peri-operative care. The main focus is upon opioid agents, different classes and preparations, their uses, effects and side-effects. We go on to explore non-steroid anti-inflammatory agents and paracetamol, with a section on paracetamol toxicity.
from
Section 4
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Walking the Walk (and Talking the Talk)
William Fawcett, Royal Surrey County Hospital, Guildford and University of Surrey,Olivia Dow, Guy's and St Thomas' NHS Foundation Trust, London,Judith Dinsmore, St George's Hospital, London
Chronic pain can be categorised as nociceptive, neuropathic or nociplastic based on the underlying pathophysiology. It is considered a disease in its own right and can be sub-classified to differentiate types of chronic pain syndromes. Chronic primary pain is defined as pain in one or more anatomical regions, persisting or recurring for more than 3 months, and associated with significant emotional distress or interference with activities of daily life e.g. fibromyalgia or complex regional pain syndrome. Chronic secondary pain includes six subgroups where pain has initially developed as a symptom of another disorder or disease process e.g. chronic cancer-related pain and chronic neuropathic pain.
The experience of pain is a consequence of a variety of biological, psychological, and social factors and a wide range of pharmacological and non-pharmacological interventions are available. Pharmacological management involves opioid agents and non-opioid medications including simple analgesics, topical lidocaine, and capsaicin, anti-epilepsy drugs and antidepressants. Tolerance to opioids can develop rapidly. Misuse and abuse are increasing concerns. Non-pharmacological interventions include psychological and physical therapies. Patient engagement in the process is key and an interdisciplinary approach is recommended which focusses on the individual patient and uses a shared-decision model.
Much research has assessed methods of pain control for cattle castration, but there remains a lack of consensus regarding best practice. We conducted a systematic review and meta-analysis of published research including both an untreated control (i.e. castrated without pain mitigation) and at least one unimodal or multimodal analgesia treatment (i.e. castrated with a local anaesthetic alone, or in combination with a non-steroidal anti-inflammatory drug) to summarise findings on castration pain management. Studies were included if they castrated by surgery, elastration or crushing, and reported at least one of the following outcomes: cortisol, change in bodyweight, foot stomping, wound licking, a subjective assessment of pain using a visual analogue scale, or stride length. Our search identified 383 publications, of which 17 were eligible for inclusion. Most publications focused on surgical castration (n = 14), and the most frequently reported outcome was blood cortisol (n = 13). None of the included studies were assessed as having a low risk of bias, mostly due to a lack of reporting blinding procedures and reasons for missing data. Using a three-level random effect model, we concluded that multimodal analgesia reduced blood cortisol concentrations in the first hour following surgical castration in comparison to the control group; this effect was diminished but still evident at 3 and 4 h, but not beyond at 6, 12 and 24 h. Too few data were available to meaningfully assess other outcomes and methods. Variability in methods and outcomes between studies, and risks of bias, hinder our capacity to provide science-based recommendations for best practice.
Galen’s most deeply held professional values included clarity of expression and the epistemological importance of clinical experience. Therefore, it is not surprising that he thought and wrote about communication with patients. His stories about patients show that he questioned them about their symptoms and history, and some stories explicitly teach the lesson that this type of questioning is important. His stories often quote patients indirectly or directly; they are often told partly from the patient’s perspective, and some contain constructions indicating that Galen paid attention to an individual patient’s exact words. In On the Affected Parts, his discussion of the vocabulary of pain – a problem in medical communication still important today – he privileges the common usage of patients over the technical vocabulary invented by Archigenes. He argues that only by listening to patients and their words can we construct a useful vocabulary of metaphors for pain that can bridge the gap in experience between physician and patient. He does not dismiss the words of women or enslaved patients; on the other hand, in a few stories where the patriarch of a family is present and the patient is female or enslaved, Galen’s dialogue tends to engage the head of the household rather than the patient. While some of his stories show off his ability to diagnose patients without talking to them, and others raise the problem of the lying patient, none of these stories would have meaning unless the patients’ words were normally crucial to clinical practice.
In this chapter of Complex Ethics Consultations: Cases that Haunt Us, the author encounters a 50-year-old woman who is requesting her arm be amputated to alleviate her complex regional pain syndrome. This is not a usual indication for an amputation, but a surgeon is willing to offer the procedure. The author attempts to bring about clarity even in the face of uncertainty. Moral distress played a substantial role in the consultation.
In this chapter of Complex Ethics Consultations: Cases that Haunt Us, the authors describe a 70-year-old man who is refusing all options available to him and expresses faith that his suffering must have some meaning since it was "God’s will." The team struggled with apparently inconsistent patient expressions of turning down surgery but insisting on attempted resuscitation. The case additionally highlights the uncertainty involved in medical decision making.
Cannabis has a long history as a medicine and was a part of medical practice until the late 19th century. The discovery of cannabidiol (CBD) and ∆9-tetrahydrocannabinol (THC) in the mid-20th century, and then the various components of the endocannabinoid system (ECS) over the following decades has again brought cannabis back into the public eye as a potential therapeutic agent. At present, cannabis is being used in the community across the world for both recreational and medical purposes. In the case of medical usage, it may be prescribed by a medical doctor or purchased either legally or illicitly for medical purposes such as symptom relief. Evidence for cannabis as a medicine is still an emerging field, and while potential mechanisms of action for a variety of conditions have been elucidated, including cancer, epilepsy, and chronic pain, high-quality randomized controlled trials in humans are still lacking. Despite popular beliefs, cannabis, like all other medicines, has potential benefits and harms, and long-term consumption of cannabis, even for medical reasons, may not be risk-free. In addition, consumption via modes of administration such as smoking or using a bong may increase the risk of negative health outcomes.
The chapter describes how forms of ill-treatment other than torture have been defined over the last 85 years since they were prohibited in the Universal Declaration of Human Rights. The core elements are described of cruel, inhuman, or degrading treatment or punishment are described in turn with the distinctions between these terms and the definition of torture highlighted. The distinct features of other ill-treatment under international humanitarian law are also described.
To date, the NIH Helping to End Addiction Long-term (HEAL) Initiative has funded over 1,000 projects that aim to identify new therapeutic targets for pain and substance use disorder (SUD), develop nonpharmacological strategies for pain management, and improve overdose and addiction treatment across settings. This study conducted a portfolio analysis of HEAL’s research to assess opportunities to advance translation and implementation.
Methods:
HEAL projects (FY 2018–2022) were classified into early (T0–T1) and later (T2–T4) translational stages. Eleven coders used a 54-item data collection tool based on the Consolidated Framework for Implementation Research (CFIR) to extract project characteristics (e.g., population, research setting) relevant to translation and implementation. Descriptive statistics and visualization techniques were employed to analyze and map aggregate characteristics onto CFIR’s domains (e.g., outer setting).
Results:
HEAL’s portfolio comprised 923 projects (33.7% T0–T1; 67.3% T2–T4), ranging from basic science (27.1%) and preclinical research (21.4%) to clinical (36.8%), implementation (27.1%), and dissemination research (13.1%). Most projects primarily addressed either addiction (46.3%) or pain (37.4%). Implementation-related gaps included the underrepresentation of certain populations (e.g., sexual/gender minorities: 0.5%). T0–T1 projects occurred primarily in laboratory settings (35.1%), while T2–T4 projects were concentrated in healthcare settings (e.g., hospitals: 21.6%) with limited transferability to other contexts (e.g., community: 12.9%).
Conclusion:
Opportunities to advance translational and implementation efforts include fostering interdisciplinary collaboration, prioritizing underserved populations, engaging with community leaders and policy stakeholders, and targeting evidence-based practices in nonclinical settings. Ongoing analyses can guide strategic investments to maximize HEAL’s impact on substance use and pain crises.
The Introduction provides an overview of the central questions raised in the book, the arguments presented, and the methodology employed. It frames key questions about the shifting meanings of childhood pain and its implications for the construction of adult worlds. Additionally, it highlights the interplay between the child as an object of clinical observation and as a symbolic figure within cultural and scientific narratives. Through this lens, it contributes to broader debates on the intersections of science, emotion, and society. The methodology used is one of interdisciplinary history, drawn largely from the history of medicine and cultural history, which assesses visual as well as written material.
Situated between the history of pain, history of childhood and history of emotions, this innovative work explores cultural understandings of children's pain, from the 1870s to the end of the Second World War. Focusing on British medical discourse, Leticia Fernández-Fontecha examines the relationship between the experience of pain and its social and medical perception, looking at how pain is felt, seen and performed in contexts such as the hospital, the war nursery and the asylum. By means of a comparative study of views in different disciplines – physiology, paediatrics, psychiatry, psychology and psychoanalysis – this work demonstrates the various ways in which the child in pain came to be perceived. This context is vital to understanding current practices and beliefs surrounding childhood pain, and the role that children play in the construction of adult worlds.