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July 1, 2024

Navigating the Two-Way Street: Obtaining Informed Consent in 2024

AlteaPlus Essential

By Will Marshall, Head of Legal and Risk Management, Dr. Harriet Lewis and Rachel Phillips

Navigating the Two-Way Street: Obtaining Informed Consent in 2024

This article provides an overview and outlines the responsibilities of healthcare professionals in ensuring well-informed consent to avoid liability.

Obtaining informed consent is a fundamental process in healthcare where a clinician and a patient agree on future treatment. Despite its importance, this process has become increasingly complex over the past decade, posing challenges for professionals and patients. This article provides an overview of the legal framework. It outlines the responsibilities of healthcare professionals in ensuring well-informed consent to avoid liability.

The Legal Framework

The legal framework for obtaining informed consent in England is based on two key Supreme Court decisions: Montgomery v Lanarkshire Health Board (2015) and McCulloch v Forth Valley Health Board (2023).

Montgomery

The Montgomery case is crucial for practitioners and their insurers due to its significant legal test:

“When obtaining informed consent, a doctor must take reasonable care to ensure that the patient is aware of any material risks involved in any recommended treatment, and of any reasonable alternative treatments.”

This test has two components: ensuring the patient is informed of material risks in the recommended treatment and informing them of reasonable alternative treatments. Montgomery clarified that a doctor cannot evade liability solely by demonstrating that their view as to what constitutes a material risk aligns with a responsible body of medical opinion, as was the case under the ‘Bolam Test’ that is used to determine the standard of care.

Instead, the determination of ‘reasonableness’ is based on the patient's individual circumstances, a matter for the Court rather than the medical professional to decide.

McCulloch

The McCulloch case (2023) focused on the second aspect of the Montgomery test: the obligation to inform patients about reasonable alternative treatments. Mrs McCulloch’s legal team argued that, like the duty to disclose material risks, the duty to inform about ‘reasonable alternative treatments’ should not be bound by the Bolam test but should be determined based on the individual patient’s circumstances, goals and values.

However, the Supreme Court agreed with the hospital's legal representatives, supported by the General Medical Council (GMC) and British Medical Association (BMA), that determining the ‘reasonableness of alternative’ treatments should remain a matter of professional judgment, assessed through the Bolam test. Consequently, a healthcare provider will not be considered negligent for not disclosing a treatment option if their professional judgment that it is not a reasonable alternative is supported by a responsible body of medical opinion.

A departure from Montgomery?

Many lawyers viewed the McCulloch ruling as a departure from the patient-centric approach championed in Montgomery, seeing it as a return to paternalistic medicine. However, the general legal consensus is that, rather than marking a substantive departure from Montgomery, the McCulloch judgment simply clarified that a ‘reasonable alternative’ is one that is clinically significant and consistent with professional judgment. A balanced assessment suggests that McCulloch underscores the interactive and collaborative nature of obtaining informed consent, requiring dialogue between healthcare professionals and patients. In this light, the impact of these key cases can be summarised as follows:

Montgomery: Mandates professionals to customise advice regarding material risks associated with those identified options for the patient.

McCulloch: Requires professionals to present options/alternatives recognised as reasonable by peers rather than an exhaustive list of every possible treatment.

How far are practitioners expected to go in advising of reasonable alternatives?

The McCulloch judgment has raised significant questions about the practitioner’s duty to inform patients about alternative treatments.

1. How detailed must the discussion of alternatives be? Clinicians operate within significant resource and time limitations, with brief appointments ranging from 10 to 15 minutes. With this constrained time frame, they must efficiently gather a full medical history, conduct thorough examinations, and communicate results and diagnoses. Introducing a comprehensive discussion on all ‘reasonable’ alternatives would inevitably affect the depth and quality of the information provided. This poses the risk of patients not achieving informed consent. Would highlighting headline points on the alternatives be sufficient?

2. What is meant by ‘treatment’? Must a hip surgeon discuss all surgical approaches with their varying benefits and risks? Do they need to advise on the benefits and risks of different implants or bearing surfaces? This additional information might place the burden of responsibility on the patient and lead to decision paralysis.

3. What is meant by ‘clinically appropriate’? Must a surgeon discuss alternative treatments with lower success rates, higher risks, or longer recovery times? Does this include treatments not provided by the practitioner/clinic but available elsewhere in a more specialised setting?

The courts will likely test these questions and limits in the coming months and years.

Achieving the aim of shared decision-making

Nadine Montgomery’s case undeniably influenced both professionals and patients. While some patients still prefer professionals to dictate treatment decisions, many are now empowered by the law and online resources to be more informed and autonomous in their choices. Thanks to legal frameworks, extensive guidance and training from regulators and professional bodies, clinicians are better equipped to engage with patients, fostering shared decision-making. To achieve this healthcare professionals should:

  • Communicate with the patient. Understand their perspectives, concerns, and goals. Many factors important to the patient can only emerge through conversation.
  • Discuss clinically appropriate treatment options. Include the choice of no treatment (‘first do no harm’).
  • Explain material risks. Tailor the explanation to the patient.
  • Stress the collaborative nature of the decision-making process. Provide detailed information in clinic letters, leaflets, and website directions to empower patients while maintaining their responsibility and autonomy.

It's all about the evidence

Given the litigious climate, focusing on steps to protect healthcare providers against allegations of a failure to obtain informed consent may seem defensive. However, allegations stemming from resource constraints, poor record keeping, factual disputes, and communication deficits are thriving in our claims culture. Recent judicial decisions offer reassurance to practitioners that patients who litigate after adverse outcomes but cannot prove lack of informed consent will not receive compensation.

Therefore, it is important to provide evidence of the consent process, highlighting its interactive and collaborative nature. All conversations between the practitioner and the patient should be recorded in the clinic notes and included in follow-up clinic letters. This should include the risks and benefits of operative and non-operative treatments, leaflets provided and directions to websites. This approach not only aids the patient's memory of the information discussed but is also invaluable for defence lawyers in consent claims, particularly when it includes the advice given and the rationale behind it. Ideally, the consent process should not be conducted on the day of the procedure although clinicians should always check with their patient whether anything has changed since the consent discussion. Providers should offer dedicated consent clinics to allow sufficient time for a thorough discussion.

Obtaining informed consent is a complex but essential process in healthcare. The legal framework, shaped by the Montgomery and McCulloch cases, provides a structure for practitioners to follow. Achieving shared decision-making requires effective communication, understanding patient perspectives and providing tailored information. By thoroughly documenting the consent process, healthcare professionals can protect themselves against allegations while ensuring patients are well-informed and autonomous in their treatment choices.

"The information contained in this article does not represent a complete analysis of the topics presented and is provided for information purposes only. It is not intended as legal advice and no responsibility can be accepted by Altea Insurance or WTW for any reliance placed upon it. Legal advice should always be obtained before applying any information to particular circumstances."

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