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Receiving Valid Consent: It’s Better Received Than Taken

Receiving valid consent is a fundamental aspect of healthcare, including optometry and optics. It ensures that patients are fully informed and willing to participate in their care. Unconsented contact, such as touching an eyelid, may be considered assault in the eyes of the law, making it essential to receive valid consent to stay within legal bounds. The College of Optometrists even emphasises that failing to gain consent before a procedure can lead to serious repercussions.

When referring patients, receiving valid consent is crucial as it involves sharing personal details with other professionals. Procedures like using a non-contact tonometer or instilling drops can cause discomfort or temporarily affect vision, making consent even more important.

Patients must be fully aware and agree voluntarily. This helps maintain trust and uphold the integrity of the profession. Understanding and respecting the principles of valid consent, as outlined by the General Optical Council (GOC) standards, is vital for every optometrist. In this post, we’ll explore how to ensure consent is given willingly, appropriately, and remains valid throughout treatment.

What is Valid Consent and Why We Need to Receive It?

Receiving valid consent means obtaining permission from a patient before proceeding with any examination, treatment, or involvement in teaching or research activities. Valid consent is essential because it respects the patient’s autonomy and legal rights. The NHS guidelines, GOC Standards and other organisations involved in healthcare state that valid consent must be given voluntarily, by an appropriately informed person, and by someone with the capacity to consent.

Receiving valid consent ensures that patients are fully aware of what the procedure involves and any potential risks. This practice not only builds trust but also protects optometrists from legal repercussions. For instance, obtaining explicit consent before instilling eye drops ensures the patient understands the process and agrees to it, thus avoiding any misunderstandings or complaints.

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In addition to protecting legal rights, receiving valid consent helps in providing patient-centered care. Patients need to be informed about their options and have the right to make decisions regarding their care. By explaining procedures and potential outcomes, patients can make informed choices that align with their preferences and values.

Moreover, receiving valid consent fosters a collaborative relationship between optometrists and patients. It empowers patients to take an active role in their care and ensures that their wishes are respected. This approach enhances patient satisfaction and promotes better health outcomes.

In essence, receiving valid consent is about respecting the patient’s right to make informed decisions and ensuring they willingly participate in the process. It’s a fundamental aspect of ethical and legal practice in healthcare.

Explicit and Implicit Consent

There are two main types of consent: explicit and implicit consent. Both play important roles in optometry, depending on the procedure and its associated risks.

Explicit consent is when a patient gives clear and specific permission, either orally or in writing, for a particular action. For example, before instilling eye drops or performing contact lens fittings, you must explain the process and risks, ensuring the patient fully understands and agrees. Explicit consent is crucial for more invasive or higher-risk procedures.

Implicit consent, on the other hand, is assumed through a patient’s actions. For instance, when a patient places their chin on a rest after you’ve explained how an autorefractor works, this can be considered implied agreement. However, implicit consent is only valid if the patient understands the procedure.

You will encounter both forms of consent during your role as an optometrist.

The Importance of Receiving Valid Consent Voluntarily

Receiving valid consent means ensuring that the patient’s consent is given voluntarily. It’s vital to differentiate between “receiving” consent and “taking” consent. The former implies that consent is willingly provided by the patient, making it more likely to be valid. Valid consent must be given without any form of coercion or pressure. Thinking of “receiving” the consent as opposed to “taking” it, can help keep this in mind.

Voluntary consent ensures that patients are fully aware and agreeable to the procedure. For instance, when I explain a new treatment plan to a patient, I make sure they understand it thoroughly and feel comfortable with the decision. If a patient feels pressured or unsure, the consent may not be genuine, leading to a breakdown of trust – as well as the potential for legal issues to arise.

Consider a scenario where a patient is hesitant about having their eyes dilated. I take the time to explain the benefits of the procedure, the risks of not doing the procedure, possible side effects, and how I plan to instill them. The patient then has the ability to make an informed decision as to whether or not to accept the procedure from being carried out.

In cases involving vulnerable patients, such as children or those with cognitive impairments, it’s crucial to ensure that consent is obtained from someone authorised to act on their behalf. This approach aligns with the General Optical Council (GOC) standards and NHS guidelines, ensuring ethical and legal compliance.

Receiving valid consent voluntarily helps maintain a trusting and cooperative relationship between both you and the patient. It empowers patients to make informed choices and ensures they feel respected and understood throughout their care journey.

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Who Can Give Consent?

Receiving valid consent means understanding who is authorised to provide it. Typically, patients themselves give consent. However, there are instances where consent must come from an authorised individual, such as a parent, guardian, or legal representative. Valid consent must be given by a person with the capacity to understand and make informed decisions.

Capacity to consent involves the ability to comprehend information about the proposed treatment or examination and to consider the consequences of agreeing or refusing. Most adults are presumed to have the capacity to consent. However, certain factors, such as cognitive impairments, mental health conditions, or temporary states like shock or confusion, can affect a person’s capacity.

For example, I once had a patient with severe dementia whose decision-making capacity was impaired. In this case, I obtained consent from their daughter, who had power of attorney for the patient’s health and welfare. This ensured that the patient received appropriate care while respecting their legal rights. It’s crucial to assess each patient’s capacity individually and involve authorised individuals when necessary.

When working with children and young people, different legal considerations apply. The age of the patient and their ability to understand the information determine whether they can provide consent or if a parent or guardian must consent on their behalf.

Usually, patients aged 16 and over can make their own decisions about their care. However, children under 16 can consent to their treatment if they are deemed to have sufficient intelligence, competence, and understanding to fully grasp what the treatment entails. This is known as Gillick competence.

The Mental Capacity Act 2005

When assessing a patient’s capacity to consent, the Mental Capacity Act 2005 provides a clear framework. It outlines that individuals must be able to understand, retain, and weigh up information about a decision, and communicate their choice. This legal guidance is invaluable for ensuring ethical and compliant practices, particularly when caring for vulnerable patients, such as those with dementia or cognitive impairments.

Ensuring that consent is given by an appropriately informed and authorised person is a fundamental aspect of receiving valid consent. This practice aligns with ethical and legal standards, ensuring that patients receive care that respects their rights and autonomy.

Ensuring Patients are Appropriately Informed When Receiving Valid Consent

Receiving valid consent means making sure patients are appropriately informed about the procedure, its risks, and their options. Patients need clear, accurate information presented in a way they can understand. This helps them make informed decisions about their care, enhancing trust and collaboration between the optometrist and the patient.

It’s also important to provide information about patients’ rights, such as their ability to refuse treatment or request a chaperone or interpreter. When discussing treatment plans, I always inform patients of their options and respect their choices. This empowers them and reinforces their autonomy.

Additionally, using visual aids, written materials, and clear language can help patients better understand complex information. For example, I often use diagrams and leaflets to explain eye conditions and treatments. This makes the information more accessible and helps patients feel more confident in their decisions. College of Optometrist members have access to high-quality patient leaflets, of which I find invaluable when discussing ocular diseases and treatment plans.

Receiving valid consent involves ongoing communication and reassessment. I regularly check in with patients to ensure they still understand and agree with the proposed treatment. This helps maintain the validity of their consent throughout their care journey.

Ensuring patients are appropriately informed is a crucial part of receiving valid consent. It promotes patient autonomy, trust, and satisfaction, leading to better health outcomes.

Maintaining Valid Consent Throughout Treatment

Receiving valid consent is not a one-time event; it must be maintained throughout the entire treatment process. This involves regularly checking in with patients to ensure they continue to agree with the proposed treatment plan and fully understand any changes.

For example, during a patient’s eye examination, the situation may evolve. Initially, you may receive consent to dilate the patient’s pupils, but upon assessing their anterior chamber angles, you realise it isn’t safe to do so. In this case, it’s essential to explain the change in circumstances to the patient and obtain new consent for the revised plan. This ensures that consent remains valid and the patient is aware of any adjustments.

Additionally, when referring patients to other professionals, it’s important to receive valid consent again, especially if the referral pathway changes. This could happen if a referral centre rejects your referral or suggests a different pathway to send the patient. Clear communication about these changes and obtaining consent for the new referral ensures that the patient remains informed and agrees to the updated course of action.

Maintaining valid consent also means being attentive to any verbal or non-verbal signals indicating a patient’s discomfort or reluctance. If a patient expresses concerns or withdraws consent during a procedure, it’s crucial to stop immediately, address their concerns, and re-confirm their willingness to proceed.

By regularly re-confirming consent and adapting to changes in the treatment plan, optometrists can ensure that valid consent is maintained throughout the patient’s care journey.

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Recording Consent Adequately in Optometry

Recording consent adequately is vital. Proper documentation ensures a clear, contemporaneous record of the patient’s understanding and agreement, which can be essential for legal, ethical, and professional accountability.

Explicit consent, such as for instilling drops or performing a procedure, should be clearly recorded. For instance, you might document the patient’s verbal agreement or use a signed consent form for more complex or high-risk interventions (e.g. contact lens fitting and myopia management). Similarly, if a patient provides implied consent—for example, by cooperating with a technique, making a general note on their record is advisable.

Equally important is documenting any refusal or withdrawal of consent. Record the patient’s reasons, if provided, along with the discussions around their decision. Keeping accurate, legible notes about how you ensured the patient was informed can protect both the practitioner and the patient.

In addition to traditional methods, digital consent tools such as electronic signatures are increasingly being adopted in optometry, particularly for remote consultations. These tools offer efficiency and clarity in documenting patient agreements.

Remember; Recording that you have received valid consent is not only there for the benefit of the patient; but also there to protect you should things go wrong.

Conclusion: Why Receiving Valid Consent Matters

Receiving valid consent is essential in optometry, safeguarding both the patient’s rights and the practitioner’s professional integrity. It goes beyond a simple agreement—it ensures that the patient is informed, autonomous, and comfortable with every step of their care. From explaining procedures like tonometry or fundus imaging to handling more complex decisions such as referrals or treatment plans, receiving valid consent underpins ethical practice.

Taking time to assess capacity, provide clear information, and address patient concerns fosters trust and collaboration. It’s not just about meeting legal standards; it’s about creating an environment where patients feel respected and empowered. By maintaining consent throughout the treatment journey and adapting to changes in circumstances, optometrists can ensure that care remains patient-centred.

By embedding the principles of valid consent into daily practice, optometrists not only uphold legal and ethical standards but also cultivate an environment of trust and respect. Ensuring that consent is informed, ongoing, and well-documented strengthens the relationship between practitioner and patient, setting a high standard for care.

Thank you for taking the time to read this post about the topic of receiving valid consent. If you have colleagues, students or pre-registration optometrists that are looking to revise the topic of receiving valid consent, please consider sharing this guide with them. Furthermore, if you wish to be notified of the next post from The Eye Care Advocate is released, please subscribe to our mailing list below.

Further Reading on Receiving Valid Consent

The topic of receiving valid consent is continually being reviewed. It is also a far more complex subject than the scope of this article. The following sources were used in creating this article on receiving valid consent and should also be reviewed if you are learning about this area.

Ensure you keep up to date with your understanding and follow local policies and protocols for the area that you are working in.

Association of Optometrists: Obtaining Valid Consent

College of Optometrists – Guidance on Consent

GOC Standards: Number 3. Obtain Valid Consent

GOC Supplementary Guidance on Consent

Mental Capacity Act 2005

NHS England Letter – Avoidance of Doubt Letter Regarding GOS Sight Tests

NHS Guidance – Consent to Treatment (General)

NHS Guidance – Consent to Treatment (Children and Young People)

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