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Medical Student Essay Prizes 2012

Prizes are useful additions to your CV, demonstrating both a commitment to a surgical career and achievement of excellence. Winning is not necessary for inclusion – being short-listed or getting any kind of placing will still be a CV boost. 

The Annual Professor Harold Ellis Medical Student Prize For Surgery

This prestigious national award is open to all UK medical students and the winner receives a prize of £500. The surgical society at the universities of the three prize winners will also receive £100 each. We are not currently accepting entries for this prize.

The 2015 guidance and regulations are available for information. Please send any queries to research@rcseng.ac.uk. 

The topic for the 2015 essay competition was: 'Is public health a surgical concern? The role of the surgeon in promoting healthy lifestyles'. Short-listed candidates were invited to give a five minute presentation on "The Role of Social Media for Modern Surgeons".

2016 winners

  1. Owen Davis of University of Keele - Owen's presentation
  2. Molly Nielsen of University of Newcastle - Molly's presentation
  3. Richard Bartlett of University College London - Richard's presentation

2015 winners

  1. Jacob King of Peninsula - Jacob's presentation
  2. Michael Bath of Leicester - Michael's presentation
  3. John Eraifej of Birmingham - John's presentation

2014 winners

  1. Elizabeth Redman of UCL - Elizabeth's presentation
  2. Wei Cheang of Dundee University - Wei's presentation (joint)
  3. James Baggott of Kings College London - James' presentation (joint)

Read a report of the 2014 prize day written by the joint second prize winners.

2013 winners

  1. David Ferguson of University of Leicester
  2. Ibrahim Sheriff of Kings College London
  3. James Glasbey of Cardiff University 

2012 winners

  1. Maral Rouhani of Cambridge University - Presentation | Notes
  2. Mueez Waqar of Liverpool University - Presentation | Notes
  3. Emma Keohane of Barts and the London - Emma's presentation | Notes (joint)
  4. Jason Yuen of Oxford University - Presentation | Notes (joint)

Other prizes

Many medical schools and surgical societies also run competitions for students. If you run a prize for students and you would like us to include it in this list please email us. 

What to read next

Careers Medical student

Abstract

This article examines the 1957 trial for murder of Dr John Bodkin Adams in the context of medical care of the dying in postwar Britain. R v Adams is significant because it is understood to have rendered lawful the medical administration of pain-relieving drugs to the dying even when it is known they will hasten death. I argue the legal sanction of this practice in the 1950s reflected and reinforced the rising authority and faith invested in physicians as specialists in terminal care. Specifically, the case highlights the role of the administration of potent narcotics in the establishment of care of the dying as a branch of medicine requiring specialised knowledge and skills. Finally, I argue that by drawing attention to a medical intervention intent on eliminating pain, the Adams case enables exploration of an aspect of the medicalisation of dying in the twentieth century that is rarely examined.

history of dying, palliative care, R v Adams, postwar Britain, medico-legal history, pain

On the morning of 18 March 1957, John Bodkin Adams, a successful and prosperous middle-aged general practitioner from the picturesque English seaside town of Eastbourne, appeared in London's Old Bailey charged with murdering an elderly patient, Mrs Edith Alice Morrell, with doses of heroin and morphine in the hope of pecuniary gain. So began a long and sensational trial: it ran for three weeks and, as one reporter put it, kept ‘the eyes of the whole newspaper-reading world focused in fascination’ until Dr Adams' acquittal on 9 April.1

The Adams case has disappeared from the headlines, but it lives on in a less sensational manner in medico-legal literature dealing with end-of-life matters. Here it is understood to have rendered lawful the administration of pain-relieving drugs to the dying even when it is known they will accelerate death.2 Legal sanction of this practice is traced back to a passage of Justice, later Lord, Devlin's directions to the jury in R v Adams.3 Devlin directed that a doctor was entitled to relieve the pain and suffering of a dying patient even if the measures he took precipitated death.

Most scholarly discussion of this case has taken place in medico-legal and bioethical circles. Here scholars have sought to explain Devlin's directions to the jury in terms of ethical and/or legal principles that obscure the historical context of the case.4 Meanwhile, other commentators appear unaware or uninterested in the novelty of Devlin's direction and its implications for end-of-life care. Instead, they are engaged in what Kieran Dolin has described as an ‘historical contest over Adams's guilt or innocence’; a debate over whether Adams was in fact a doctor who got away with serial murder.5 In the most sympathetic of these, by journalist Percy Hoskins, Adams emerges as the victim, albeit a roguish and avaricious one, of a scurrilous trial-by-newspaper.6 Pamela Cullen, the first writer to be granted official access to the police files, sees him as a more sinister figure.7 She argues that Dr Adams was a murderer who probably had more victims than Dr Harold Shipman, Britain's most prolific serial killer.8

This article approaches the Adams case from a different historical perspective, examining the case and trial in the context of a history of dying. It follows legal historian A. W. Simpson's suggestion that Devlin's comments to the jury might best be seen as a deferral to ‘current conventions in medical treatment’, bearing in mind that ‘practices in the care of the dying differ over time and between cultures’.9 My argument is also informed by Shai Lavi's work on the history of dying in the United States, which has highlighted life-shortening palliative care and its legal sanction as historical (and not simply medico-legal or ethical) phenomena. Lavi points to these developments as indicative of the medicalisation of dying. The rise of this form of care reflects the transformation of dying from an experience governed by religion to one increasingly governed by modern medicine and the law. This is inextricably entwined with changing cultural conceptions of the ‘good death’—in particular the modern understanding that to die well one should be free of pain and suffering.10

The analysis that follows draws on medical literature and the police files and trial transcript of the Adams case to offer a close reading of R v Adams in the context of medical care for the dying in postwar Britain.11 I argue that the medical evidence presented during the course of the Adams trial and Devlin's unprecedented sanctioning of life-shortening terminal care should be understood as reflecting and reinforcing the rising authority and faith invested in physicians as scientific specialists in dying and its care, or ‘treatment’. In particular the case highlights the role of the administration of potent narcotics in the establishment of care for the dying as an exclusive medical activity requiring specialist knowledge and skills. This nascent specialisation is evident in the pivotal role medical experts played in the trial of Dr Adams. Specifically, it is evident in medical accounts of the care of the dying that were bound to arcane technical language and techniques that appeared beyond the assessment or judgment of the court.

This recasting of R v Adams builds on two bodies of scholarship. First, it engages with work on the history of the relationship between medicine and the law.12 As Catherine Crawford observes, influenced by Foucault, much modern scholarship in this area has illuminated the way ‘“juridical power” (that of a sovereign) has, during the past few centuries, been overtaken in significance by “biopower” (the power of the norm), a process that has tended to enhance the power and importance of medicine’.13 A substantial body of literature has explored aspects of this shifting balance of power through the changing conception, role and importance of medical experts and expertise in the Anglo-American legal enterprise.14 This is an evolution often examined in relation to the spectacular rise of forensic medicine and science in the nineteenth and twentieth centuries—a development heralded by the emergence of, and courts' increasing dependence on, expert medical witnesses in two areas that began to appear ‘most difficult for the non-expert to penetrate: insanity and poisoning’.15

This work demonstrates that the increasing value and authority accorded to expert medical testimony in the English courtroom corresponds with dramatic improvements in the efficacy of medical science and technology but also with processes of professionalization, specialisation and medicalisation through which, writes Ian Burney, ‘social understandings and responses to such basic human experiences as pain, illness and death’ were ‘displaced by arrangements that produce and legitimate a narrower set of expert interventions’.16 As Joel Eigen points out, the very public nature of the courtroom provides historians with a particularly fruitful arena in which to examine wider acceptance of these emerging expert medical interventions, for here the budding medical expert has to assert their opinion not just before colleagues but the lay (and legal) public.17

Through the figure of the expert witness, R v Adams offers a rich as well as rare opportunity to study the expansion of medical expertise and authority into the realm of dying. In an era when the medical management of those close to death was rarely publically discussed, even within medical circles, physicians were required to testify as to the ethics and practice of terminal care in the midst of a sensational trial. The evident lay and legal deference to this medical testimony is indicative and constitutive of the extent to which dying was becoming an area of expert medical intervention by the 1950s. The following analysis draws attention to the enormous discretion thus afforded the medical profession at the deathbed, where the decision of whether, and in what circumstances, hastening death with pain-killers was justifiable was devolved to individual practitioners. In this way it seeks to underline the historical contingency of an aspect of contemporary medical ethics, reminding that ‘like “nature,” the “ethical” is what society and culture attribute to it at any particular historical moment’.18R v Adams offers insight into the way modern notions of what might constitute ethical medical care of the terminally ill have evolved and, thus, this analysis also aims to contribute to the literature on the history of dying.

As Julie-Marie Strange observes, while in the wake of Philippe Ariès's seminal scholarship death has become a major area of academic inquiry, investigation into the history of attitudes and practices specifically surrounding dying, as opposed to death and its aftermath (funeral rites, grief and mourning), is relatively new.19 This is particularly true of the early to mid-twentieth century where research into dying and its care remains limited, due at least in part to a scarcity of relevant sources.20 The inter-and-early postwar years are largely bereft of the rich religious, fictional, personal and, in the nineteenth century, medical literature that historians such as Pat Jalland and Ralph Houlbrooke have employed to illuminate the attitudes and practices that shaped dying in England in earlier eras.21 This is also a time prior to the rise of a professional literature on dying and terminal care (in England associated with the pioneering work of Cicely Saunders) that historians and sociologists have drawn on to examine the rise of the modern hospice movement and, more broadly, what Tony Walter has described as the ‘revival’ of death from the 1960s.22

However, while the picture of terminal care in early twentieth-century Britain remains sketchy, a broad outline of the history of dying in the modern Western world has become widely accepted. Most scholarship addressing the subject emphasises that dying, like many aspects of life, became increasingly medicalised in the twentieth century—a process often associated with the steady rise in the number of deaths taking place in hospitals from the 1930s.23 Strange notes that much of the relevant literature has focused on the way that in a climate where medicine had developed unprecedented means to cure the sick, death was often seen as a medical ‘failure’ in the twentieth century and dying patients were increasingly either subject to aggressive treatments intended to prolong life, or ignored and neglected by the medical profession.24 Milton Lewis argues that prior to the 1960s, in advanced Western societies such as Britain, twentieth-century medicine put the cure of the body before its care and that too often ‘medicine's great concern with advancing scientific knowledge’ subordinated ‘the relief of suffering of the dying’.25 Caroline Murphy has documented how in the twentieth century cancer hospitals (established in the nineteenth century to care for the sick with little expectation of cure) shifted their focus towards research and ‘patients admitted for aggressive treatment aimed at cure’ replaced those who were dying.26 David Clark and Jalland have detailed the way in the postwar years a National Health Service intent on cure and rehabilitation failed to provide guidance on terminal care or systematic provision for the dying, condemning the poor and disadvantaged to inadequate, sometimes tragic, living conditions at home or under-resourced and under-staffed institutions.27

This study aims to further the discussion of the medicalisation of dying in the twentieth century by exploring an aspect of this history that remains less well examined. The two major postwar reports into terminal care in the United Kingdom, which provide central historical sources for this period, are, understandably, most concerned to document and detail the inadequate provision made for the poor and otherwise disadvantaged in the community.28 The Adams case, however, offers a rare glimpse of what dying might have looked like in the homes of England's more comfortable classes. And it enables exploration of quite a different medical discourse on dying in postwar Britain, one that assumed physicians had a duty to provide care for those in the last stages of life and to relieve the pain associated with dying. Over a decade ago Clark looked at the emergence in postwar Britain of a medical discourse on dying that expressed active interest in terminal care and in which can be glimpsed the foundations of modern palliative medicine.29 More recently he has examined health professionals' use of analgesics in institutions for the dying from the 1930s.30 This paper draws on Clark's work to explore this aspect of the medicalisation of dying further, seeking to foreground the evolution and accommodation of a specialist form of medical treatment for terminal patients that was more intent on eliminating pain than staving-off death.

Easing the Passing in Postwar Britain

In her study of death in Victorian Britain, Jalland has documented the changing attitudes towards death and suffering in middle- and upper-class families.31 For much of the nineteenth century the pain associated with dying, like death itself, was a matter of divine providence and to be faced with faith and fortitude. For relatives and friends attending the dying, the focus was on the spiritual rather than the physical state of those close to death, and hope was invested above all in the prospect of salvation rather than the restoration of health or the elimination of pain.

However, in the latter part of the century, fear of death, which had once centred on the post-mortem horrors of eternal physical punishment, came to focus on the dying process itself. As fear of hell dimmed, even amongst the devout, there were ‘more accounts of deathbed scenes which described dreadful physical or mental suffering with little or no reference to spiritual and devotional consolation, and none at all to the state of the soul in the final hours’.32

This increasing anxiety about the physical suffering that might precede death was fostered in part by the rising prominence of the doctor at the bedside of the dying in middle- and upper-class families. Once attended by family and clergy, those near the end of their life became the subjects of medical care and attention, a fact reflected in the emergence of medical literature on the subject. Victorian doctors such as William Munk advised on the importance of spiritual reflection as well as the physical management of the death chamber (proper ventilation, bedding, nutrition). These medical practitioners also advocated the cautious use of opiates to treat pain.33 Caution was paramount. Concerned that pain-relief that precipitated death was illegal, violated the medical duty to preserve life and risked eroding the trust of patients and families, nineteenth-century physicians warned against the administration of such drugs in any situation where death might be hastened even accidently.34

While in the first half of the following century there is a relative dearth of medical literature dedicated to detailing appropriate care for the terminally ill, it seems clear physicians did not desert the deathbed. In a major postwar report on terminal care in the United Kingdom prepared for the Calouste Gulbenkian Foundation, H. L. Hughes noted patients' ‘touching’ reliance on their family doctor, observing that whether in hospital or at home, the patient ‘always felt better for a daily visit, and he often finds it easier to talk to his doctor than his relatives or a priest’.35 What is less clear is what medical management of the dying actually involved. Jalland observes that a lack of contemporaneous documentation means little has been written ‘about the actual care of the dying’ in England in the immediate postwar years.36 It is particularly difficult to discern what terminal care consisted of in the significant proportion of situations where death took place in the privacy of the home and the dying were attended by their general practitioner and professional nursing staff.37 As Irvine Loudon and Mark Drury write, ‘we know very little about the care of the dying in general practice before the 1960s, except that it was shrouded in silence. Few talked about it, wrote about it, or were taught anything about it as students’.38

Clark has begun to shed light on this period by pointing to the emergence from the 1930s of a medical discourse that not only cautioned against the heroic prolongation of life, but also expressed an active interest in terminal care. It is evident in the limited and fragmentary material that emanated from terminal care homes and associated charities as well as interested clinicians. This is a literature that drew on physicians' personal experience and observations and lay the foundations for the development, under the auspices of Cicely Saunders, of the modern palliative care movement in the coming decades—a movement which would make dying and the relief of associated pain the subject of systematic scientific observation, research and clinical techniques.39 This published medical commentary on terminal care did not signal a new interest in the medical management of those at the end of life, so much as a new type of interest. This is a period that marks a transition in the history of the medicalisation of dying, not its emergence. It is a point where, as Clark observes, terminal care, ‘which had previously belonged to the realm of medical folklore’ was beginning to be seen as a branch of medicine that involved—and could be promoted as involving—specialist knowledge and skills.40 These would not begin to be consolidated into a professional literature until the 1960s, but the assumptions and priorities that underpinned this new medical specialisation are clearly evident in earlier medical writings and practices.

By the postwar years the most prominent aspect of specifically medical care for those at the end of their life (as opposed to more prosaic nursing and the provision of comfort and consolation) was the treatment of the pain associated with dying using the powerful narcotics that had become the exclusive province of medicine. Chief among these was opium and its derivatives. As Virginia Berridge and others have shown, for much of the nineteenth century opiates were widely available and used for recreational purposes as well as self-administered, or prescribed, as remedies for numerous common complaints (toothache, diarrhoea, chilblains). However, the emergence of medicine and pharmacy as powerful scientific specialities, coupled with growing medical and lay concerns about the dangers associated with consumption (addiction and poisoning but also deviance) led to the increasing regulation and restriction of such drugs in the twentieth century. The introduction of numerous milder forms of pain relief further curtailed the need for opiates and they were used increasingly conservatively within medicine.41 Marcia Meldrum suggests that by the 1920s one of the very few situations in which the prolonged medical administration of opiates was considered legitimate was in the context of the care of those deemed in the last stages of life.42

In a 1948 article discussing care of the dying that appeared in The Practitioner, W. N. Leak observed that ‘purely medical treatment’ for the dying could ‘almost be written in one word—morphine’.43 At a meeting of the British Medical Association, Dr Ian Grant counselled that, while morphine should be withheld from terminal patients as long as possible to avoid problems of tolerance, it could sometimes be administered to ‘curative and euphoric effect’. And in cases of desperate misery he advised his colleagues that it should not be spared, as ‘our first duty is to relieve pain and to induce merciful oblivion’.44 While acknowledging ‘the smoke of battle’ lingered over its use, another medical practitioner observed that regular injections of heroin, rather than morphine, were most effective ‘for bringing analgesia and peace of mind to those who have not long to live’.45

Opiates were also administered to the dying orally, often in the form of what one physician described as ‘that famous Brompton requiem’.46 There was no standard composition of this mixture but, as formulas or recipes endorsed by clinicians and textbooks at the time indicate, it almost invariably included morphine or heroin and cocaine mixed with a sweetener (maybe honey) and alcohol (which might be adjusted to suit the individual taste of the patient). The doses of opiates recommended by physicians writing on the subject varied and were clearly intended as guides to be adjusted by individual doctors as they saw fit—presumably based on the assumption that the doctor at the bedside was best qualified to make judgements as to what sort of dosage was in the best interests of his patient. Authorities advised, for example, that Brompton cocktails be given ‘as often as required’ or that in the last stages of illness the dose of opiates would need to be increased ‘fairly rapidly’ at the discretion of the doctor.47

The administration of opiates to the dying was not just advocated by individual physicians but as part of terminal care in the, albeit few, institutions that accommodated the dying in the first half of the twentieth century. Between the 1930s and 1950s ‘Brompton mixtures’, which were to become a central component in the work of the modern hospice movement, were widely prescribed to those deemed terminal in religious and charitable homes as well as in hospitals.48 Norman Sprott, Medical Superintendent at St Columba's hospital in London, advised that these potent analgesic cocktails could be given freely to the dying and described the effect this way: ‘Large doses of narcotics will sometimes shorten a life—a result for which the patient might be profoundly thankful—but just as often, by bringing rest and sleep and comfort, they seem to prolong life, though even then the suffering is greatly lessened.’49

Sprott's observations, as well as those of the other physicians quoted here, draw attention to the way powerful narcotics were administered to the dying, but also to the ambiguous clinical purpose and effect of the medical administration of such drugs. As Clark writes of the administration of the Brompton to the dying in various institutions: ‘Was it intended to induce euphoria? Did it potentiate moribundity? Most intriguing of all, was it originally intended to bring about an “easeful” death or even to hasten death?’50

At the time what might constitute ‘proper’ medical treatment—as opposed to an unjustifiable hastening of death—for the terminally ill was not simply a matter of clinical propriety. In a very frank and widely circulated lecture, Clifford Hoyle, physician at King's College Hospital, made it clear that any knowing ‘acceleration of death in the dying’ was illegal—from a conventional legal standpoint a doctor who deliberately hastened the death of a terminally ill patient opened himself/herself to a charge of homicide.51 Yet in Hoyle's view the physician attending the deathbed was best placed to decide how far pain-relief for the dying should go—and in some instances this meant violating the law by hastening the death of a patient. Moreover, he assured colleagues, ‘the law forbids in theory but ignores in practice’. In practice, he advised, it was tacitly accepted that doctors ‘here, as in other spheres, should be protected from the consequences of steps honestly taken in the interests of patients’.52

There is no suggestion in Hoyle's article—or, indeed, in any of the medical literature on care of the dying—that such decisions should be discussed with the patient, the patient's family or even colleagues: quite the opposite. ‘If there are occasions when hastening death seems the most sensible and humane procedure the proper course then becomes a matter for one's own conscience,’ instructed Hoyle, ‘the first essential on these occasions is to keep one's own counsel’. He went on to suggest that one of the best ways to effect ‘such treatment’ was by administering quickly cumulative doses of morphine.53

It was this ambiguous aspect of terminal care that Justice Devlin unexpectedly found himself navigating during the trial of Dr Adams in 1957. As he reflected some decades later, it became clear that he needed to clarify for the jury ‘how far the law allowed the orthodox doctor to go in easing the passing’.54 However, when the Adams story broke in 1956 quite different issues appeared at stake.

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