GUP v EUP & Anor

This is an application concerning EUP, a woman in her late eighties. Later in this judgment, I will consider what EUP’s views may have been regarding her medical treatment. To try to evaluate this it is necessary for me to consider something of her life and the code by which she has lived it. EUP has plainly experienced a full and interesting life. Like all her generation, she was a child of the Second World War. The partitioning of India led ultimately to her and her husband settling in the United Kingdom. The couple was obviously happy and there were five children. They are a Hindu family and the traditions and customs of that religion and culture percolate, in varying degrees, and to different effect, throughout the entire family, as one would expect. One of EUP’s sons has suffered from significant mental health problems and has lived all his life in the family home. He is now, as I understand it, in his sixties. Until latterly, EUP was his primary carer. The application has been brought by GUP, her youngest son. The family have plainly agreed that he should bring the application, which they all support, though with differing degrees of emphasis. EUP’s life has not been without sadness or disappointment. In his early 70’s, her husband developed dementia. EUP cared for him personally for as long as she could and even at the very end of his life took an active role in managing his condition. That illness and decline had a significant emotional impact on EUP and her son and, I strongly suspect, the whole family. From seeing their father as a strong and independent man, they saw him transform into somebody they did not recognise and who did not recognise them. By the end, he lost his ability to swallow. This is something I will return to because it highlights something of EUP’s approach to death and terminal illness.

Though EUP declined, physically, with age and loss of mobility, she remained strong, cognitively. GUP told me in his evidence that though she rarely left the house, in recent years, she remained active, engaged and interested in the world. She enjoyed cooking. She managed the housework and had been an active gardener, sometimes taking on tasks which GUP worried were too much for her. He once discovered her moving a number of quite large bricks around the garden. As he told me this, he communicated to me, not only his concern for his mother’s welfare, but an underlying delight with her energy and commitment. The recollection struck me as soothing to him. Happily, EUP lived at home with her eldest son and daughter throughout the pandemic.

EUP was hopeful for a grandchild. I sensed that with five children, she considered there to be a reasonable prospect of her becoming a grandmother. In her mid-eighties, however, EUP received the news that her daughter gave birth to a son. EUP’s delight was unconfined and, despite her present parlous condition, communicates itself, almost palpably, through GUP’s evidence. I am told that there is some confusion about EUP’s date of birth and that the birth certificate might be inaccurate. Accordingly, I am simply going to refer to her as being in her eighties.

EUP has a history of bilateral severe strokes because of bilateral internal carotid artery severe stenoses (narrowing of intracranial vessels). Prior to her first admission to hospital on 21^st October 2023, her “premorbid clinical frailty score” was between 5-6, meaning that she was “moderately frail”. She has a history of osteoarthritis of her knees which limited her mobility indoors (she required a frame to mobilise). She has a background of GCA (Giant Cell Arteritis) for which steroid therapy was given.

On admission on 21^st October 2023, following a left Middle Cerebral Artery (MCA) stroke, EUP had difficulty finding words, dysphagia and right arm weakness. These were investigated and she was discharged home on 27^th October 2023. Sadly, EUP was readmitted to the National Hospital for Neurology & Neurosurgery following an unwitnessed fall on 28^th October 2023. While admitted, she suffered from recurrent infarcts (ischaemic strokes due to lack of blood supply). She initially received dual antiplatelet therapy (blood thinners) but because of ongoing stroke events she later underwent stenting of the left internal carotid artery (ICA). This was explained to be a procedure that carried significant risk and to be associated with further strokes.

There has been poor neurological recovery since the stent was inserted on 17^th November 2023. I have not been able to identify a clear or consistent approach to EUP’s care since that date. There has been increasing divergence between the growing hope of the family for some meaningful recovery and the view of the clinicians that comfort and dignity ought to be the focus of EUP’s care, at what they assess to be the end of her life. Whilst these two perspectives of EUP’s medical needs have diverged, I am concerned that the treatment she has received reflects a convergence between the two. In other words, the treatment plan has an air of compromise about it, a negotiation between the family and the medical team. There may, sometimes, be a place for that, but not if the person at the centre of it becomes marginalised. P (the protected party) must always be afforded care, which is identifiably in her own best interests. The family’s views are relevant only insofar as they provide a conduit for P’s own wishes and feelings. Families, however loving and well-meaning gain no dominion over their dying and incapacitous relatives. The family’s role, which is crucial, is to promote and not subvert P’s autonomy.

From 15^th December 2023, it was impossible to deliver nutrition to EUP. She was, however, provided with hydration. It has been difficult to tease out the reasoning behind this approach. Ultimately, I have been unable to identify a cogent rationale. It reflects a compromise between the two different approaches identified above. Moreover, I do not consider it has been in the best interests of EUP. It is important, therefore, that I consider EUP’s clinical history. In doing so, I can draw heavily from the statement filed in this application by Dr Robert Simister, a Consultant/Neurologist and Clinical Director for Stroke and Acute Neurology at the National Hospital. It is important that I identify from the outset that I have found Dr Simister to be an extremely impressive witness. He has engaged with all the questions put to him, whether supportive or challenging. He has displayed, in my judgement, both kindness and empathy towards his patient and her family. Where he has, occasionally, advanced views expressed by a collection of other professionals and found those conclusions wanting, he has unhesitatingly withdrawn from them. I have been greatly impressed by his integrity, in circumstances where others perhaps might have been inclined to obfuscate.

EUP was admitted to the National Hospital for Neurology & Neurosurgery on 21^st October 2023 following a left Middle Cerebral Artery (MCA) stroke. Following her MCA stroke on 21^st October 2023, she was treated with high intensity antiplatelet therapy but had recurrent left MCA territory ischemic events. Through her period of admission she had the highest possible protective treatment strategy. This treatment strategy was discussed during several MDTs by multiple consultants. Prior to the stenting procedure the ward team noted that EUP was aphasic (unable to express or comprehend language) and had complete weakness in the right arm with weakness also noted in the left arm and both legs.

On 17^th November 2023, she underwent a left internal carotid artery stenting and was subsequently admitted to the ICU and was, at this time intubated and ventilated. This was a higher risk intervention which required a complex decision- making process. The family were, by Dr Simister’s recollection, informed that the stenting procedure itself carried a risk of stroke. This was estimated at a likelihood of approximately 15% for poor clinical outcome and an additional 3% for mortality. GUP’s recognition of these statistics differs slightly but not in any significant way. On the ICU the managing team recognised that EUP was not awakening following the procedure and accordingly, further brain imaging was requested and undertaken. This showed that there had unfortunately been further stroke events in both cerebral hemispheres following the stenting.

There was a clinic review on 27^th November by the Attending Stroke Consultant, Dr Fiona Humphries. What was observed was a persistent low level of alertness was noted despite withdrawal of sedation. Further meetings between the ICU team and Dr Humphries, resulted in the family agreeing to extubation and transfer to the ward. There was no other option. I am satisfied that it was understood, at least by GUP, that this transfer would not carry with it potential for recovery and carried with it a high risk for intercurrent infection. EUP was discharged from ICU to the stroke ward, on 30^th November 2023. When on the ICU, a nasogastric tube (NGT) had been inserted. It remained in place as it had been possible to insert it with direct vision and anaesthetic agents. Earlier attempts at direct insertion were unsuccessful. NG feeding and medication was continued until 15^th December 2023 when it was documented that approximately a length of 17cm of tubing was below the level of diaphragm, and there was bending of the tube within the stomach with its tip appearing to at the gastro-oesophageal junction. In the course of treatment, the use of that tube became impossible, hence on 15^th December 2023 the NGT was removed because it was displaced and no longer functional.

There were daily unsuccessful attempts at NGT insertions between 15^th December 2023 and 21^st December 2023, it was a distressing time for all concerned. For 7 days, every day, and sometimes twice per day, attempts were made at NGT insertion. There is clear documentation as to the extent to which these attempts were distressing, most particularly, for EUP. Not all, but some of the attempted insertions took place with the family in attendance. That must have been acutely distressing for them also. On 22^nd December 2023, Dr Turner, another Attending Stroke Unit Consultant reviewed EUP. He noted that there had been no change in the level of arousal or general function since the discharge from ICU. He records that the NGT insertions were unsuccessful and causing distress. Dr Turner was clear, as it must be stated, the entire clinical team are now clear, that EUP is in the final phase of life. Consideration of that review, on 22^nd December 2023, led to the conclusion that it was in EUP’s benefit, to stop the attempts to insert the NGT. It strikes me that no other humane conclusion could have been reached and I do not see, from the way the case has been presented by the family that they would take issue with this point. The focus of the plan became, to maintain EUP’s comfort and dignity, predicated on the recognition that there was no neurological improvement. That decision, I am satisfied, was communicated to the family in clear and sensitive terms.

On 3^rd January 2024, there was a clinical review by Dr Simister. He too identified no change in the level of arousal or function. There was no distress. Discussion on this date was held with the family in the presence of the Charge Nurse and Dr Jonathan Martin, Consultant in Palliative Care. The meeting updated the family on the level of function and then focussed on feeding. It was in this meeting, that the medical team explained, in clear terms, why it would not be possible for surgical treatments to be performed on EUP to introduce feeding via a tube through the abdominal wall or to insert tubes into the large veins. In consequence, focus returned to whether NGT insertion should be tried yet again. I am bound to say, I cannot see how, having regard to the history, this was thought to be in EUP’s interests. It strikes me that it was undertaken to console the family. In any event, ENT guided insertion was arranged and performed on 4^th January 2024. There has been an enormous range of specialists involved in EUP’s care. The ENT specialist, Mr I, struggled but eventually placed the NGT, with direct visualisation of the back of the throat. This was recorded to have been “a prolonged and distressing procedure”, to which I would add, as it had been on the many times it had been attempted before.Mr I noted that the NGT was persistently expelled from the oesophagus, despite initial correct placement. That presented a challenging clinical scenario and he drew from it, the conclusion, that there was some kind of “functional obstruction” that made the procedure very difficult. The NGT remained in position for 24 hours and then was spontaneously expelled into the mouth by EUP. No feeding was possible via this route thereafter.

Further meetings were held with the medical team and with the family. Following this failed final NGT insertion procedure, it was explained to the family that NGT insertion had been distressing, and that the NGT would not, in any event, change her prognosis. It was further explained that they could not secure a safe and reliable feeding route. Since that point, EUP has been based on the ward. She has received, what is manifestly, a very high level of nursing care. It is testimony to that care that there has been no ward based significant infections and no skin injury due to immobility. The team and the family are in agreement that there is no obvious distress in day-to-day nursing. Intravenous fluids have continued. These have led to some fluid overload, which has become manifest as swelling and oedema of the arms and legs.

There can be no doubt that EUP lacks capacity. It is recorded that from her admission on to the ward from 30^th November 2023 to today, a typical level of arousal is that EUP will have eyes closed and make no sound even with unpleasant stimulation. She has periods of spontaneous eye opening which are recorded by staff as “short lasting” and predominantly reported at night. There is no account of any observation that she will direct her gaze to a visual target or away from visual threat. I have listened carefully to her son’s evidence, and although he speculates more optimistically as to the potential to fix visual gaze, his description does not support his contention, nor am I satisfied that he believes that his mother can fix her gaze. There has been no observed episode of any directed limb movement. Prior to the stenting procedure, it was agreed that EUP was aphasic. This limited her ability to understand or verbally communicate her wishes on any question relating to her care. The bedside assessment, since the stenting, demonstrates that EUP has little or no interaction with her environment and is unable to non-verbally communicate her wishes.

The Trust has sought, rightly, second opinions from two Consultant Stroke Physicians. The first one was from Dr Maneesh Bhargava of North Middlesex University Hospital. Dr Bhargava is the Clinical Lead of the North Middlesex Stroke Service. A further second opinion was elicited, on 3^rd January 2024, from Dr Adam Webber, Clinical Lead of the Barnet General Hospital Stroke Service on 18^th January 2024. Dr Bhargava’s view was that feeding would be inappropriate and that EUP is in final weeks of life. It was his view that EUP should be kept as comfortable as possible.

Dr Webber was also of the view that there is no prospect of EUP making a meaningful neurological recovery. He too, thought it appeared as though she is nearing end of life. Dr Webber expressed the view that there is a high risk of her being in pain, discomfort and suffering. All the surrounding evidence that I have referred to, supports and corroborates that opinion. In view of that, the main motivation of any medical interventions should be directed at symptom support. He was clear that it would not be appropriate, in his opinion, to pursue enteral feeding either PEG, RIG or surgical gastrostomy, nor TPN. This, he was clear, would only serve to generate burdensome side effects without changing her prognosis. It is this that has been the central issue for the family. In line with the emerging philosophy of EUP’s care plan, she was reviewed on 17^th January 2024 by Dr Mike Young, Consultant in Elderly Care at UCLH. I have been taken by all, to Dr Young’s observations. Dr Young’s review of EUP took place in the presence of the family and spoke at length with the family following this assessment. However, what is striking about his report is that he was alarmed that the intravenous fluids were beginning to cause potential distress with respect to the limb swelling. He confirmed that feeding was not possible and recommended that care is to be focussed, palliatively, at the final stage of life. In the statement that he provided at short notice, Dr Simister emphasised Dr Young’s observations on this occasion. Dr Simister is emphasising that Dr Young, at the very least, was flagging up that the intraveneous fluids were likely to be of “dubious benefit”. Expressly, Dr Simister noted that the fluids were actively appearing to cause harm. I find this incredibly troubling. Dr Simister confronted the question with the integrity I have already found to be characteristic, as to why this was thought to be in EUP’s best interests at all. In my survey of this clinical picture, I must, for completeness, incorporate two further views. First from the nutrition team.

The Nutrition Team input has been provided on several occasions since January 2^nd 2024 and the decision made by the Nutrition Team that surgical insertion of a feeding tube into the stomach or insertion of a tube into the veins would not be appropriate was documented in the notes on 4 January 2024 and this judgement has been further confirmed on the MDT meeting of 23 January 2024.

There was a further review by Dr Magee, on 19 January 2024, which confirmed this position and also confirmed that further NGT placement would also not be appropriate given the ongoing status of EUP. His report sets out, in some detail, the explanation the unacceptable risks that would be associated with gastrostomy tube insertion. He also explained that parenteral nutrition (known as TPN) would be particularly hazardous generating, as it does, elevated risks for sepsis and vessel clotting. The statistical possibilities of this strike me as irrelevant to the evaluation as to whether this course should even be tried, given that it would not alter EUP’s prognosis. In simple terms, there would be burden without benefit and risk of a painful and difficult death. Due to the challenges of placing a central line and because of the expectation that EUP would need to move back to a high dependency environment for daily and sometimes multiple daily blood testing. Dr Magee noted that the typical indications for TPN in patients with limited life expectancy are covered by national guidelines and require either excellent performance status or expected life expectancy greater than 3 months, neither of which is the case for EUP. All feedback from these assessments has been shared on several occasions with the family.

Dr Simister, in his evidence, has told me that there is no clinical potential to restart provision of artificial nutrition in an ethical way. As I have emphasised, intravenous fluids have continued to be provided, whilst these have ensured some degree of hydration and alertness, they have also caused significant limb oedema and swelling. It is accepted that risks of further stroke acquiring infection or irreversible salt/electrolyte imbalance remain unchanged with or without nutritional support. It is anticipated that, inevitably, one of these risks will cause EUP’s death in the coming days.

In his witness statement, Dr Simister stated as follows:

As I have foreshadowed, the medical team is aware that ongoing intravenous hydration is causing limb swelling, increases the risk of skin break down and makes cannula resiting more difficult and distressing. The intravenous fluids are likely to be prolonging life but will not change final outcome. In his oral evidence, Dr Simister told me that having communicated more widely with his colleagues overnight, the only identifiable ‘benefit’ of the hydration is to maintain a level of alertness. It has no impact on symptom control, indeed, this can be done more effectively by alternative strategies such as moistening of the mouth and tongue. The swelling has caused stretching of the tissues, as well as tearing. It is difficult to insert the cannula which requires to be replaced regularly. GUP agrees that this is, at best, every two or three days, but sometimes more frequently. Resiting has become difficult and uncomfortable. One of the clinical team has noted crepitations in EUP’s chest, bilaterally. This, he suspected, to be caused by a leakage of fluid into the lungs, consequent upon the hydration related oedema. This was causing EUP to struggle and cough. Based on his working hypothesis, the doctor treated this with a diuretic. At risk of stating the obvious, the diuretic was intended to dispel the fluid, that is its job. It was successful. The fluid was expelled. In these circumstances, it is reasonable to conclude that the leakage into the lungs is related to the artificial hydration. In my judgement, GUP, who is an articulate and intelligent man, who has navigated these proceedings and the range of views within his family, regarding his mother’s treatment with skill and sensitivity, also recognises the force of this analysis. He told me that if driven to choose between the provision of nutrition or hydration, he would choose nutrition. He reasoned that the concomitant hydration involved in the provision of nutrition might reduce the risk of swelling and oedema. This struck me as an intelligent hypothesis and Dr Simister, when it was put to him, did not discount it. It is perhaps convenient to say at this point, that I have been enormously impressed with GUP’s integrity. I think his evidence on this point illustrates it. I heard from his twin sister, HUP. It was clear that she loves her mother greatly but I found her to be oppositional and angry towards the clinical team in a way that is unproductive for all concerned. Anger is a recognised facet of grief and sadly, the onset of grief does not await death itself. I emphasise that I do not condemn or criticise her, but I do strongly encourage her to make what I am satisfied are the last days or weeks of her mother’s life as comfortable as possible and free from conflict. I have no doubt that she has the capacity to do so.

GUP has struggled to accept the fact that Dr Simister and the Nutrition Team have been clear that there are no options for tube insertion in the stomach (a gastrostomy) because of extreme risks with insertion, risk of skin breakdown at the site, distress incurred during insertion and post insertion monitoring. These risks extend similarly to the provision of total parenteral nutrition (TPN). The Nutrition team and the expert assessors have all been clear that there are no options related to repeated NGT insertion. This is because of the clear evidence that repeated insertion would be unlikely to secure a meaningful feeding route and because of well documented evidence of the distress caused by insertion attempts.

EUP has a devastating series of strokes leaving her profoundly disabled with obvious injury to language and limb function, even before further stroke events post stent insertion in November 2023. The November stroke has been described as “massive” by Dr Simister, and given his obvious expertise and experience, it is not a phrase that he will use lightly and reflects the real extent of these catastrophic injuries. Whilst GUP and HUP and, I am told, a number of their friends, have seen eye movements which they believe were not observable a few months ago, the extent of the brain damage and the broad neurological clinical picture provides no foundation for any hope that EUP will survive or recover in any meaningful way. I accept what GUP says about the changes in his mother’s eye movements. He has questioned himself, properly, as to whether these can bear the significance that he wishes to attribute to them. This, he tells me, is why he has solicited the observations of friends. Dr Simister and the treating clinicians have not observed this change. Inevitably, they do not spend anything like the time that GUP and HUP do with their mother. Both stay with her regularly overnight at the hospital. Indeed, as I understand it, for the last two weeks, they have both stayed there every night. The nursing staff do not appear to have seen these changes either. They, of course, spend far more time with EUP than the Consultants do and so I attribute some significance to the fact that they have not seen these changes. Nonetheless, I am prepared to accept what GUP says but I do so on the basis that EUP’s opening of her eyes must be infrequent (otherwise, the nurses would have noticed it). Dr Simister was prepared to take the same approach.

The extent of the irreversible damage, over every hemisphere of the brain, comprehensively discounts the possibility of the kind of neurological recovery that the family would wish for. Such “improvements” as may theoretically be possible, at the margins of consciousness, cannot accurately be described as “meaningful” in the sense of engagement with the world. With real candour, GUP tells me that if something like her present condition is all that can be achieved, he does not think his mother would wish to live in this way. He does not accept the poverty of the prognosis and argues that some form of nutrition should be provided to his mother. As Mr Lawson puts it in his written closing submissions:

Dr Simister concludes:

It is also important to highlight the conclusions of Dr Adam Webber, Consultant Geriatrician and Stroke Physician at the Royal Free London NHS Foundation Trust:

The law in this sphere is settled and relatively easy to state. The application of it, however, is always intensely difficult involving, as it invariably does, the intersection of ethics, medicine, the law and, not infrequently, religious belief.

In Burke v General Medical Council  [2005] EWCA Civ 1003   [2006] QB 273  the Court of Appeal described the general position as follows:

Lord Stephens, in A Local Authority v JB  [2021] UKSC 52   [2022] AC 1322 , described the relationship between the MCA and the Court of Protection as follows (at [47]):

Baroness Hale, in Aintree v James  [2013] UKSC 67   [2014] AC 591 , described the questions for the court as follows:

There is no obligation on a patient with decision-making capacity to accept life-saving treatment, and doctors are neither entitled nor obliged to give it. As set out by Lord Brandon in Re F (Mental Patient: Sterilisation) [ 1990] 2 AC 1 :

In Aintree v James  [2014] AC 591  at §§35 - 6 Baroness Hale stated as follows:

In North West London Clinical Commissioning Group v GU (Rev1)  [2021] EWCOP 59 , I made the following observations:

Where a person is unable to decide for himself, there is an obligation to act in their best interests: s.1(5) MCA 2005.

Where a decision relates to life-sustaining treatment, the person making the decision must not be motivated by a desire to bring about death: s.4(5) MCA 2005.

When determining what is in a person’s best interests, consideration must be given to all relevant circumstances, to the person’s past and present wishes and feelings, to the beliefs and values that would be likely to influence their decision if they had capacity, and to the other factors that they would be likely to consider if they were able to do so: s.4(6) MCA 2005.

Account must be taken of the views of anyone engaged in caring for the person or interested in their welfare: s.4(7) MCA 2005.

Carers, including health professionals, are permitted to carry out acts in connection with personal care, health care, or treatment of a person who lacks capacity to consent: s.5 of MCA 2005. It provides a significant degree of protection from liability, provided that the act is done in the reasonable belief that capacity is lacking and that the act is in the person’s best interests.

The provisions of ss.15 to 17 MCA 2005 give the court power to make decisions about personal welfare and to make declarations and orders in respect of a person who lacks capacity. Section 15 deals with declarations, including declarations as to the lawfulness or otherwise of any act which has been or is to be done. Section 16 enables the court, by making an order, to make personal welfare decisions for a person without capacity, and, by section 17, the court’s power in this regard extends to giving or refusing consent to the carrying out or continuation of a treatment by a person providing health care.

Section 16(3) MCA 2005 makes it clear that the court’s powers under section 16 are subject to the provisions of MCA 2005 and, in particular, to section 1 and to section 4. What governs the court’s decision about any matter concerning personal welfare is therefore the person’s best interests.

The MCA 2005 Code of Practice (‘the Code’) issued under s.42 MCA 2005 came into effect in April 2007. Chapter 5 of the Code titled ‘How should someone’s best interests be worked out when making decisions about life-sustaining treatment?’ includes the following guidance:

I think it is important to this family that I confront the fact that somewhere within the fabric of this case is an instinctive recoil from a treatment regime that deprives their mother of the very basics of life, nutrition and hydration. It is not difficult to see how they might react in that way. She was, for them, a dutiful and devoted mother. She was plainly strong minded. She was uncompromising on her daughter’s divorce, which she volubly disapproved of. Her approach, I suspect, was probably wrong, but undoubtedly well-meaning. She provided an upbringing for her family, which manifestly allowed their potential to flourish and find expression in their interesting and varied careers. GUP told me that he was a “fussy eater” and his mother would prepare dishes for him which were “lamb and chicken based”, as he preferred. It is an instinct for mothers to provide their children with food, the first of which comes, for most children, from the maternal breast. Co-operation with a regime which requires the withdrawal from a mother of that with which she has provided for them throughout their lives is intensely painful to contemplate.

When EUP’s husband was at the very end of his life, unable to swallow, in consequence of his advanced dementia, she was dogged in her determination that he should be provided with artificial nutrition. GUP, though himself traumatised, took another view. Insofar as this casts light on what EUP would have wanted, in her present predicament, it points to her being prepared to go to any length to hold on to life. However, GUP has also told me that if her present circumstances were all that was open to her, or something very like them, he did not think that his mother would want such a situation. GUP identified nothing in anything his mother had said to support this. I have more than a suspicion that it reflects his objective view of her circumstances and is not, strictly speaking, a reflection of his mother’s views. I recognise the strain he faces. Ultimately, the evidence does not provide any clear indication of what EUP would have wanted other than every opportunity to see more of her children and grandchild. However, the providing of nutrition is not a medically ethical option nor, in my judgement of the available evidence, has it been for some time. It cannot be achieved without further burden and there is no prospect of it changing the prognosis. In any event, even if I were unpersuaded by the medical evidence, I certainly could not compel the doctors to undertake treatment contrary to their own medical ethics: R (Burke) v GMC [2005] EWCA Civ 1003, [2006] QB 273.

In relation to the question of hydration, Ms Dolan KC, on behalf of the Official Solicitor, makes the following submission:

For the reasons succinctly set out in this submission and following my evaluation of the evidence above, I have come to the clear conclusion that neither provision of nutrition nor hydration is in EUP’s best interests. In his evidence, Dr Simister was at pains to draw a distinction between artificial provision of nutrition and consuming food by eating. He told me that patients sometimes get to a stage when the desire for nutrition goes altogether. It is not experienced any longer as pain or starvation. He considers this likely to be EUP’s situation and does not think that this will cause her pain. Furthermore, he points to the availability of an experienced palliative care team who will be able to ensure her comfort.

At this point, and I emphasise only at this point, I note that the evidence of each of the specialists instructed and those consulted in relation to the question of hydration is unanimous. Both the Trust and the Official Solicitor on behalf of EUP invite me to make declarations reflecting this analysis of EUP’s best interests. I do so. I have appended the declarations to this judgment.

I know that this lengthy ex-tempore judgment is painful for the family to hear. Though I do not wish to protract it unnecessarily, it is important that I say something relating to the issues concerning the procedure that has been pursued in this case. The Official Solicitor expressly deprecates the fact that GUP was required to bring this application before the court himself. The consequence has been some procedural confusion which has generated delay and led to this case being listed in the urgent applications list. Inevitably, as a litigant in person, GUP had not identified in advance or in clear terms the relief he sought. The Trust had also failed to give sufficient thought to their obligations to their patient in relation to the hydration that she was receiving and which had been identified as delivering burden without benefit. The hearing, therefore, has been to some degree dynamic, however, as is clear from the above, GUP has advanced his case clearly and cogently and made it perfectly plain what he would wish to happen. I have found many of his questions to be insightful and well-constructed, as I have commented upon during the evidence.

In this case, the hospital had put in place a regime focused on palliative care. As I have identified above, this is undoubtedly in EUP’s best interests, at least at the stage at which I am hearing the case. However, it was also clear that GUP and his family were never fully on board with that plan. It is certainly the case that there was a broadly co-operative relationship with GUP but I think it was equally clear that he had not accepted the medical consensus. The same applies to his sister, HUP. Who has expressed strenuous resistance to the hospital’s plans at this hearing. GUP has told me that the hospital had indicated to him that they were to make an application to court to seek endorsement of their approach. I do not think this is in dispute. However, on 16^th January 2024, the Trust confirmed to the family that they had been advised by their lawyers that it was not necessary for them to issue an application. The likely reasoning behind this is that the Trust considered that there was no ethical route to provide nutrition to EUP. The family disagreed and saw this as passivity, with profound consequences. They perceived an important decision having been taken, even though the decision was to take no action. They considered that the Court ought to be able to review that decision making process and identify its own evaluation of where EUP’s best interests lay. I agree with the family. A decision not to provide nutrition is every bit as serious as a decision to withdraw nutrition. Where there is conflict, these cases must be resolved by the court.

The preceding day, 15^th January 2024 (Monday), GUP had made attempt to contact the out of hours duty High Court Judge. I am not clear what occurred on that occasion but I note that by the 18^th January 2024, GUP had prepared a full application which was emailed to the court. On the Friday evening, 19^th January 2024, GUP made a further out of hours application to Theis J who asked the Official Solicitor to speak to him. A representative of the Official Solicitor’s office also provided him with details of solicitors specialising in this area of law. On 22^nd January 2024, in the afternoon, GUP appeared before me in the urgent applications list. I ensured that the documents were sent to the Trust and listed the case for the following day. On the 23^rd January 2024, as the application was plainly urgent, I began to hear it.

Ms Dolan submits that the practice guidance, which I issued in January 2020, then as Vice President of the Court of Protection, indicates that the Trust, in circumstances such as these, should bring the case to court promptly. Whilst that document is expressly stated to be by way of guidance only, it is rarely departed from in cases of this gravity. Had the Trust followed it, and at an earlier stage, it would have greatly alleviated the stress to the family. Ms Dolan goes further in her written submissions but I do not. Neither can I imagine that the lawyers advising this Trust were unfamiliar with the guidance. It has been widely promulgated, see also [2020] EWCOP 2 . Where there is conflict in these serious medical treatment cases, it is in everybody’s best interests, but most importantly P’s, to bring an application to court. That will be most efficiently achieved where it is driven by the Trust’s application. There are many and obvious reasons why it is also to the Trust’s advantage to have their treatment plans, in cases such as this, scrutinised by the court.