“(1) As a Critical Care Physician I am specifically focused on interventions provided in the intensive care unit. Based on Mr Barnor’s current condition and irreversible injuries I expect stepwise deterioration will occur. In my opinion a return to invasive ventilation by endotracheal tube or tracheostomy, circulatory support with vasopressors, or continuous renal replacement therapy (if intermittent dialysis is not tolerated) would be futile, as they would not work to achieve the therapeutic goal of recovery from critical illness, but at best would restabilise Mr Barnor’s condition in the same or a worse state. (2) I am also of the opinion that endotracheal intubation or a tracheostomy to facilitate deep endobronchial suction would be invasive interventions that can only be experienced as noxious stimuli. I understand that the family recognise the potential for pain and distress with these interventions and perceive them as invasive. While I recognise the concept of best interests can extend beyond individual’s ability to perceive quality of life to that of a wider family group - I can’t see it being in anyone’s interests to inflict invasive interventions on a loved one with no prospect of sustained benefit. (3) Furthermore, I would also support a decision to not provide further haemodialysis but to focus care on comfort and dignity of Mr Barnor and his family. In my opinion dialysis is an intermittent intervention that is objectively only drawing out a prolonged dying process.”
“The team at King’s would not offer kidney replacement therapy of any sort in these circumstances. We do not believe it would be right to offer a treatment to support someone where deterioration and complications are inevitable, starting from a very low level of consciousness. In practice, Mr Barnor is dependent on high intensity nursing care in a hospital environment to remain well. Any move out of that setting will result in deterioration. Dialysis treatment, even if it were technically and logistically possible, would serve only to prolong inevitable deterioration, without benefit. Can I extend my sympathies to Mr Barnor’s family. Having met him sitting out in the intensive care unit I feel I can begin to imagine the kind of person he was and so can begin to imagine how awful the situation must be for them.”
“The clinical team on the ICU is in agreement that further treatment is futile and clinically inappropriate to offer. However, despite multiple detailed discussions, his family has not accepted the irreversible nature of his brain injury and prognosis, and continue to demand ongoing treatment, including dialysis. You have asked me for advice regarding the clinical decision-making process for withdrawal of treatment in line with the National Clinical Guidelines.”
“First of all, on a clinical level, I confirm that sadly RB will not regain consciousness. He is clearly dying and would not survive for more than a few days/weeks without the ongoing life-sustaining treatments that you are giving him, which include dialysis and clinically assisted nutrition and hydration (CANH). He could not live outside of the hospital environment and I agree with your team’s view that any further active medical treatment at this point is futile and clinically inappropriate.”
“I would recommend that your records should be amended to replace any references to ‘PDOC’ ‘and ‘Minimally conscious state (MCS)’ with ‘TDOC’.”
“Key points that I would highlight are as follows: 1. It is the giving, (and not the withdrawing) of treatment that needs to be justified. Just because you can give a treatment does not mean to say that you should. 2. It is first up to the clinical team to decide which treatments are on offer. A clinician may decide that a given treatment would be futile or clinically inappropriate within the particular context of a patient’s presentation, in which case they are under no obligation to offer it, and such decisions are made routinely as part of everyday clinical practice. 3. If a treatment is not on offer, the family must be informed of the decision and the reasons for it, but it is not a best interests decision, and neither the patient nor their family can demand it. 4. If the family disputes the decision, the treating team should seek a second opinion and do due diligence to determine whether another provider would offer it. Importantly, the question to the second opinion is not whether they agree with and support the approach taken by the current treating team, but whether they would take a different view and be prepared to take over the patient’s management and offer the treatment themselves. 5. If they would, then the team should take the necessary steps to transfer the patient to their care (if that is agreed to be in the patient’s best interests). 6. If a treatment is on offer, then there needs to be a ‘best interests decision’ to determine whether it is in the patients best interests to receive it. 7. If there is a dispute about whether or not it is in the patient’s best interests, the matter should be referred to the Court of Protection to decide and the treating organisation is responsible for making that application. 8. However, the Court of Protection can only decide whether or not a treatment that is on offer is in the patient’s best interests (or on which treatment, if more than one alternative is available). The Court of Protection cannot compel a clinician or a Trust to deliver a treatment that they believe to be clinically inappropriate. 9. If there is continued dispute about a decision not to offer treatment, then the family may make an application to the courts, but such disputes are normally dealt with by the Administrative Court by way of a judicial review. The treating organisation should inform the family of their legal rights, but is not under any obligation to brings the case itself. I note that you are seeking legal advice in this case which is entirely appropriate. However, when seeking legal advice, it is extremely important that you, as a clinical team, are absolutely clear about whether you are making: a) a clinical decision not to offer treatment because you consider it to be clinically inappropriate, or b) a best interests decision because you do not believe it to be in the patient’s best interests. This is important because disputes are dealt with by different legal frameworks as described above. However, it is often my experience that clinicians muddle the language and write in the notes that a treatment “is not on offer because it is not in the patient’s best interests”
“The consensus is that further escalation of care would not be in his best interest”
“a. Irreversible terminal neurological condition (TDOC): Mr Barnor’s brain injury is severe, widespread, and longstanding. There has been no meaningful recovery over many months. In TDOC there is no realistic potential for improvement, and continuing burdensome life-sustaining treatments cannot achieve the intended goals of intensive care (recovery or restoration of an acceptable level of awareness and function). b. Dialysis cannot deliver a meaningful benefit for Mr Barnor: Dialysis cannot improve or reverse [his] neurological condition. In this context it serves only to prolong the process of dying, without the prospect of recovery or a quality of life Mr Barnor could experience. c. Increasing burdens and harms: Continued dialysis requires ongoing invasive line access. Mr Barnor’s long-term tunnelled dialysis catheter has now failed. The usual life-expectancy of tunnelled dialysis catheters is approximately six months, and almost all fail eventually due to a build-up of biofilm and clots. On occasion, these clots can be removed by administering ‘clot busting drugs’, but these were unsuccessful, despite repeated administration. Between the time of tunneled dialysis catheter failure on30 January 2026 and his last dialysis session on11 February 2026 , Mr Barnor was dialysing via a temporary groin catheter (a “Vascath”), which carried significant risks. Vascaths are intended only for short-term use. Repeated line insertions and replacements would expose Mr Barnor to avoidable harm (notably infection, bleeding, thrombosis, and procedural complications) with no counterbalancing prospect of clinical recovery. d. No pathway to discharge or outpatient dialysis: Because of his profound and irreversible impairment of consciousness and high dependency needs, Mr Barnor cannot safely receive outpatient dialysis or live outside an acute hospital environment. Local and independent renal expert opinion confirms that long-term dialysis (haemodialysis or peritoneal dialysis) would not be offered in these circumstances, as he is not medically suitable for outpatient dialysis and would not survive in an environment outside of the acute hospital setting. e. For these reasons, the consensus of Mr Barnor’s treating teams (Intensive Care, Renal, Neurology) and three independent external experts is that continued dialysis is futile, clinically inappropriate and is prolonging the process of dying rather than providing therapeutic benefit. The clinical plan is therefore to focus on comfort, dignity, and symptom control, with palliative care support, recognising that Mr Barnor is nearing the end of life.”
“The Trust has made a clinical decision not to provide further and long-term dialysis to this patient beyond a final dialysis session which will take place on Wednesday11 February 2026 if the current temporary line is still working at that time. There are no other treatment options and without dialysis it is anticipated that Mr Barnor will die within a matter of days. He will of course be provided with palliative care by way of symptom management to the extent that his clinical condition requires it.”
“The Trust has made a clinical decision that it is not appropriate to provide Mr Barnor with further dialysis. We acknowledge that there may have been some confusion caused with the use of language previously and we apologise for this. Having explored this today with the Trust and Counsel, we can confirm that there is no best interests decision available to be determined by the Court, but that a clinical decision has been made, and it is that dialysis will not continue to be provided by this Trust…. We reiterate that there is no best interests decision for the Court to make. As per the case law detailed above, it would therefore be inappropriate for the Trust to make an application to the Court of Protection and so the Trust will not be making an application.”
“(a) I acknowledge and have raised during hearing that there has been confusion in language used with the family, but the evidential reality is that the medical decision making process has concluded that dialysis will no longer be offered by the clinical treating team; (b) Secondly, if Mr Barnor had capacity, save for issuing proceedings for Judicial Review, getting leave for that and seeking orders, a person of capacity would not be able to compel a medical clinician for that treatment to be provided. The Court of Protection in its position acting as proxy for somebody who lacks capacity is in no different position when faced with the decision that has been made in this case as a person with capacity would have. (c) There is no option for the Court of Protection to consider and as a result the application in my judgment has no real prospects of success and in those circumstances leave should not be given under s.50 MCA.”
“- the existence in domestic law and practice of a regulatory framework compatible with the requirements of art.2; - whether account had been taken of the applicant’s previously expressed wishes and those of the persons close to him, as well as the opinions of other medical personnel; and - the possibility to approach the courts in the event of doubts as to the best decision to take in the patient’s interests.”
“(1) In determining for the purposes of this Act what is in a person’s best interests, the person making the determination must not make it merely on the basis of (a) the person’s age or appearance or (b) a condition of his, or an aspect of his behaviour, which might lead others to make unjustified assumptions about what might be in his best interests. (2) The person making the determination must consider all the relevant circumstances and, in particular, take the following steps. (3) He must consider (a) whether it is likely that the person will at some time have the capacity in relation to the mater in question, and (b) if it appears likely that he will, when that is likely to be. (4) He must, so far as reasonably practicable, permit and encourage the person to participate, or improve his ability to participate, as fully as possible in any act done for him and any decision affecting him. (5) Where the determination relates to life-sustaining treatment he must not, in considering whether the treatment is in the best interests of the person concerned, be motivated by a desire to bring about his death. (6) He must consider, so far as is reasonably ascertainable, (a) the person’s past and present wishes and feelings (and, in particular, any relevant written statement made by him when he had capacity); (b) the beliefs and values that would be likely to influence his decision if he had capacity, and (c) the other factors that he would be likely to consider if he were able to do so. (7) He must take into account, if it is practicable and appropriate to consult them, the views of (a) anyone named by the person as someone to be consulted on the matter in question or on matters of that kind; (b) anyone engaged in caring for the person or interested in his welfare; (c) any donee of a lasting power of attorney granted by the person, and (d) any deputy appointed by the court. … (10) “Life-sustaining treatment” means treatment which in the view of a person providing health care for the person concerned is necessary to sustain life. (11) “Relevant circumstances” are those— (a) of which the person making the determination is aware, and (b) which it would be reasonable to regard as relevant.”
“One of the key principles of the Act is that any act done for, or any decision made on behalf of a person who lacks capacity must be done, or made, in that person’s best interests. That is the same whether the person making the decision or acting is a family carer, a paid care worker, an attorney, a court-appointed deputy, or a healthcare professional, and whether the decision is a minor issue – like what to wear – or a major issue, like whether to provide particular healthcare”
“5.31 All reasonable steps which are in the person’s best interests should be taken to prolong their life. There will be a limited number of cases where treatment is futile, overly burdensome to the patient or where there is no prospect of recovery. In circumstances such as these, it may be that an assessment of best interests leads to the conclusion that it would be in the best interests of the patient to withdraw or withhold life-sustaining treatment, even if this may result in the person’s death. The decision-maker must make a decision based on the best interests of the person who lacks capacity. They must not be motivated by a desire to bring about the person’s death for whatever reason, even if this is from a sense of compassion. Healthcare and social care staff should also refer to relevant professional guidance when making decisions regarding life-sustaining treatment. 5.32 As with all decisions, before deciding to withdraw or withhold life-sustaining treatment, the decision-maker must consider the range of treatment options available to work out what would be in the person’s best interests. All the factors in the best interests checklist should be considered, and in particular, the decision-maker should consider any statements that the person has previously made about their wishes and feelings about life-sustaining treatment. 5.33 Importantly, section 4(5) cannot be interpreted to mean that doctors are under an obligation to provide, or to continue to provide, life-sustaining treatment where that treatment is not in the best interests of the person, even where the person’s death is foreseen. Doctors must apply the best interests’ checklist and use their professional skills to decide whether life-sustaining treatment is in the person’s best interests. If the doctor’s assessment is disputed, and there is no other way of resolving the dispute, ultimately the Court of Protection may be asked to decide what is in the person’s best interests. … 5.36 As mentioned in paragraph 5.33 above, where there is any doubt about the patient’s best interests, an application should be made to the Court of Protection for a decision as to whether withholding or withdrawing life-sustaining treatment is in the patient’s best interests.”
“Procedurally I can see no present alternative to an application to the court such as that made in the present case. This view is reinforced for me when I reflect, against the background of your Lordships' conclusions of law, that, in the absence of an application, the doctor who proposes the cessation of life-supporting care and treatment on the ground that their continuance would not be in the patient's best interests will have reached that conclusion himself and will be judge in his own cause unless and until his chosen course of action is challenged in criminal or civil proceedings.”
“where a patient is unable to consent to treatment it is lawful to give her treatment which is necessary in her best interests.Section 5 of the Mental Capacity Act 2005 now provides a general defence for acts done in connection with the care or treatment of a person, provided that the actor has first taken reasonable steps to establish whether the person concerned lacks capacity in relation to the matter in question and reasonably believes both that the person lacks capacity and that it will be in his best interests for the act to be done. However, section 5 does not expressly refer both to acts and to omissions, the giving or withholding of treatment. The reason for this, in my view, is that the fundamental question is whether it is lawful to give the treatment, not whether it is lawful to withhold it.”
“Hence the focus is on whether it is in the patient’s best interests to give the treatment, rather than on whether it is in his best interests to withhold or withdraw it. If the treatment is not in his best interests, the court will not be able to give its consent on his behalf and it will follow that it will be lawful to withhold or withdraw it. Indeed, it will follow that it will not be lawful to give it. It also follows that (provided of course that they have acted reasonably and without negligence) the clinical team will not be in breach of any duty towards the patient if they withhold or withdraw it.”
“As paragraph 5.33 makes clear, doctors have to decide whether the life-sustaining treatment is in the best interests of the patient.”
“The most that can be said, therefore, is that in considering the best interests of this particular patient at this particular time, decision-makers must look at his welfare in the widest sense, not just medical but social and psychological; they must consider the nature of the medical treatment in question, what it involves and its prospects of success; they must consider what the outcome of that treatment for the patient is likely to be; they must try and put themselves in the place of the individual patient and ask what his attitude to the treatment is or would be likely to be; and they must consult others who are looking after him or interested in his welfare, in particular for their view of what his attitude would be.”
“The purpose of the best interests test is to consider matters from the patient's point of view. That is not to say that his wishes must prevail, any more than those of a fully capable patient must prevail. We cannot always have what we want. Nor will it always be possible to ascertain what an incapable patient's wishes are. Even if it is possible to determine what his views were in the past, they might well have changed in the light of the stresses and strains of his current predicament …. But insofar as it is possible to ascertain the patient's wishes and feelings, his beliefs and values or the things which were important to him, it is those which should be taken into account because they are a component in making the choice which is right for him as an individual human being.”
“what is the decision-maker to do if he has reached the conclusion that a particular course of action is in the best interests of P but the body who will be required to provide or fund that course of action refuses to do so? Specifically, what is the role of the Court of Protection where there is a dispute between the providers or funders of health or social care services for a person who lacks the capacity to make the decision for himself and members of his family about what should be provided for him?”
“So how is the court’s duty to decide what is in the best interests of P to be reconciled with the fact that the court only has power to take a decision that P himself could have taken? It has no greater power to oblige others to do what is best than P would have himself. This must mean that, just like P, the court can only choose between the “available options”.”
“38. … It is perhaps unfortunate that the issue was described in the Court of Protection as one of “jurisdiction” and that term was used in the statement of facts and issues before this Court. The issue is not one of jurisdiction in the usual sense of whether the court has jurisdiction to hear the case. After all, the Court of Protection made the orders which it was asked to make in this case and no-one has suggested that it had no jurisdiction to do so. It was seized of an application properly made by the authorities responsible for providing services for MN. The context was a care order giving the local authority parental responsibility for him which was about to come to an end. No doubt if there had been no dispute with the family about his care, there would have been no need to make an application. Section 5 of the 2005 Act gives a general authority, to act in relation to the care or treatment of P, to those caring for him who reasonably believe both that P lacks capacity in relation to the matter and that it will be in P’s best interests for the act to be done. This will usually suffice, unless the decision is so serious that the court itself has said it must be taken to court. But if there is a dispute …. the court clearly has jurisdiction to make any of the orders or declarations provided for in the Act. The question is not strictly one of jurisdiction but of how the case should be handled in the light of the limited powers of the court. 39. What may often follow such an application will be a process of independent investigation, as also happened in this case, coupled with negotiation and sometimes mediation, in which modifications are made to the care plan and areas of dispute are narrowed, again as happened in this case. But it does not follow that the court is obliged to hold a hearing to resolve every dispute where it will serve no useful purpose to do so.”
“41. The court is clearly entitled to take the view that no useful purpose will be served by holding a hearing to resolve a particular issue. In reaching such a decision, many factors might be relevant. In a case such as this, for example: the nature of the issues; their importance for MN; the cogency of the parents’ demands; the reasons why the CCG opposed those demands and their cogency; any relevant and indisputable fact in the history; the views of MN’s litigation friend; the consequence of further investigation in terms of costs and court time; the likelihood that it might bring about further modifications to the care plan or consensus between the parties; and generally whether further investigation would serve any useful purpose.”
“43. Case management along these lines does not mean that a care provider or funder can pre-empt the court’s proceedings by refusing to contemplate changes to the care plan. The court can always ask itself what useful purpose continuing the proceedings, or taking a particular step in them, will serve but that is for the court, not the parties, to decide.”
“124. …. The survival of patients such as Anthony Bland, then so unprecedented, is now a well-established feature of medical practice. The documentation supplied to us shows that the difficulty that there is in assessing the patient and in evaluating his or her best interests is well recognised. The process is the subject of proper professional guidance, covering vitally important matters such as the involvement in the decision-making process of a doctor with specialist knowledge of prolonged disorders of consciousness, and the obtaining of a second opinion from a senior independent clinician with no prior involvement in the patient’s care. The second opinion, as contemplated in the guidance (see paras 79 and 80 above, for example), is, in my view, a crucial part of the scrutiny that is essential for decisions of this sort, and the guidance sets parameters which should ensure that it is an effective check, in that the clinician who provides the second opinion must (so far as reasonably practical in the circumstances of the case) be external to the organisation caring for the patient, and is expected to carry out his or her own examination of the patient, consider and evaluate the medical records, review information about the patient’s best interests, and make his or her own judgement as to whether the decision to withdraw (or not to start) CANH is in the best interests of the patient. Thus the interests of patients and their families are safeguarded, as far as possible, against errors in diagnosis and evaluation, premature decisions, and local variations in practice. 125. If, at the end of the medical process, it is apparent that the way forward is finely balanced, or there is a difference of medical opinion, or a lack of agreement to a proposed course of action from those with an interest in the patient’s welfare, a court application can and should be made. As the decisions of the ECtHR underline, this possibility of approaching a court in the event of doubts as to the best interests of the patient is an essential part of the protection of human rights. The assessments, evaluations and opinions assembled as part of the medical process will then form the core of the material available to the judge, together with such further expert and other evidence as may need to be placed before the court at that stage.”
“8. If, at the conclusion of the medical decision-making process, there remain concerns that the way forward in any case is: (a) finely balanced, or (b) there is a difference of medical opinion, or (c) a lack of agreement as to a proposed course of action from those with an interest in the person's welfare, or (d) there is a potential conflict of interest on the part of those involved in the decision-making process (not an exhaustive list) then it is highly probable that an application to the Court of Protection is appropriate. In such an event consideration must always be given as to whether an application to the Court of Protection is required. 9. Where any of the matters at paragraph 8 above arise and the decision relates to the provision of life-sustaining treatment an application to the Court of Protection must be made. This is to be regarded as an inalienable facet of the individual’s rights, guaranteed by the European Convention for the Protection of Human Rights and Fundamental Freedoms (“ECHR”). For the avoidance of any doubt, this specifically includes the withdrawal or withholding of clinically assisted nutrition and hydration.”
“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, on16th 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.”
“This case is stark. There is only one available option before this court. The reality is that this court has no choice to make. Accordingly, I have concluded that there is no best interest decision to make here, and I do not do so.”
“It appears to me that the declaration is really being sought to protect the clinicians and medical staff now and in the future from potential legal action given AA's parents fundamental disagreement with the PCP. I have considered whether I should grant the declaration sought in such circumstances. If I thought that on the ground that the declaration would make any difference to the outcome for AA then I may have been persuaded to make it. But the reality here is that the declaration will not alter anything. The clinicians will continue to treat in accordance with their clinical judgment whether or not I make the declaration. AA's parents' views, whether reasonable or not, are deeply held. In my view, granting the declaration sought will not change his parents' views nor actually how they are likely to behave to staff implementing the plan. It is purposeless.”
“The stark reality of his case is that AA is too fragile to be moved to another hospital and that those at the RHRU are clear that the only treatment plan clinically viable for AA and which they are prepared to implement is the PCP. The court has no choice and I have asked myself whether in circumstances such as these, when the court has no choice at all, it should rubber stamp the decision of others. I have decided that I should not. In coming to that decision, I should emphasize that I have the greatest respect for the clinicians in this case and the difficult decisions that they have had to take and will have to take until AAs death. They do so in accordance with their hypocritic oath and to the highest of professional standards. I do not criticise them or the judgment they have made. However, the reality of this case is that the treatment decision in this case is purely a clinical decision not the court's decision. The court's approval is not required to implement it. The court is not needed to sanction the plan and the court has no further role to play in what treatment AA does or does not receive.”
“Where there is disagreement about whether a course of action is in the best interests of the patient, or the decision is ‘finely balanced’ (i.e., there is ongoing uncertainty), the Court of Protection remains the ultimate decision-maker, and can and should be asked to decide.”
“Clinicians should be aware that … if they decide that a given treatment would be clinically inappropriate within the particular context of a patient’s presentation, they are under no obligation to offer it, and this is not a matter to be considered with reference to the Mental Capacity Act.” (2) Recommendation 4.4, headed “Decisions regarding treatment and care”, includes: “Unless the decision is already covered by a valid and applicable advance decision to refuse treatment (ADRT), all decisions should be undertaken on the basis of best interests, under the terms of theMental Capacity Act 2005 .” (3) Recommendation 4.11, entitled “Applications to the court”: “1. If the provisions of the MCA 2005, the Code of Practice and the relevant guidance have been observed, with respect to best interests decision-making, and if all parties (including family members, treating team and second opinion) are in agreement that it is not in the patient’s best interests to continue CANH, then this can be withdrawn without application to the court. … 4. If, at the end of the clinical decision-making process, [emphasis added] there is disagreement between any of the parties that cannot be resolved by discussion and/or mediation, then the matter should be referred to the Court of Protection. Similarly, an application should be made if the decision is ultimately one that is finely balanced due to residual uncertainty about best interests. 5. Family members should not be in the position of having to make an application to the court in relation to serious medical treatment decisions. (a) If a court application is required, the NHS commissioning body with overall responsibility for the patient should bring an application to the court and should fund that application. (b) Every effort should be made to ensure that applications are made as soon as practicable and are processed in a timely and efficient manner.”