Practice Policies & Patient Information
Accessible Information Standard
The Accessible Information Standard aims to ensure that patients (or their carers) who have a disability or sensory loss receive information they can access and understand, for example in large print, braille or via email, and professional communication support if they need it, for example from a British Sign Language interpreter.
This applies to patients and their carers who have information and / or communication needs relating to a disability, impairment or sensory loss. It also applies to parents and carers of patients/service users who have such information and/or communication needs, where appropriate.
Individuals most likely to be affected by the Standard include people who are blind or deaf, who have some hearing and/or visual loss, people who are deaf, blind and people with a learning disability. However, this list is not exhaustive.
If you feel that this applies to you or someone in your care please send us an e-consult or speak to reception. If you are sending an e-consult, you may want to consider:
- Do you have communication needs?
- Do you need a format other than standard print?
- Do you have any special communication requirements?
- How do you prefer to be contacted?
- What is your preferred method of communication?
- How would you like us to communicate with you?
- Can you explain what support would be helpful?
- What is the best way to send you information?
- What communication support could we provide for you?
- If you have a carer do they need communication assistance?
- If ‘Yes’ what is your Main Carer’s name?
- Do you consent to the practice contacting your main carer regarding your care?
- What is the best way to contact them?
Chaperones
If you require a chaperone for an intimate examination please see the receptionist. If at the time it is not possible, we will arrange a new appointment so that a member of staff is free to accompany you.
This applies to male and female patients.
Complaints & comments
We make every effort to give the best service possible to everyone who attends our practice.
However, we are aware that things can go wrong resulting in a patient feeling that they have a genuine cause for complaint. If this is so, we would wish for the matter to be settled as quickly, and as amicably, as possible.
To pursue a complaint please contact the practice manager who will deal with your concerns appropriately. Further written information is available regarding the complaints procedure from reception.
Complaints & comments are most welcome and would no doubt help to improve communication and services.
Would you like to have your say about the services provided at the Lyndhurst surgery? The Practice Patient Participation Group would like to hear from you. If you would like to give and receive feedback about your views and experiences, please enquire to join our Patient participation group via reception team.
Our Practice Manager or Dr Johal would be more than glad to try to deal with or resolve any differences/complaints as effectively as possible within 56 days. Complaints can be made in writing, in person or via the complaint box situated in reception.
Complaint Email – Wfccg.prglyndhurst@nhs.net
Confidentiality
The practice is committed to strict confidentiality to patient information among the patient, staff & clinicians.
Disclosure to the third party is subject to written consent.
Ascertaining identity may be warranted in certain circumstances.
Did Not Attend Policy (DNA)
Due to the number of patients failing to attend for their appointments with appropriate notice, a policy has been developed to try and resolve this.
If you fail to attend appointments without informing us at least two hours prior to your appointment, we will contact you.
Where a third DNA has occurred, a final warning correspondence will be sent and the practice will review the individual case and a decision will be taken with regard to addressing the patient’s future ability to pre-book advanced appointments. The practice will consider whether consistent failure to adhere to our practice policy constitutes a breakdown between the patient and the GP (where the GP practice has given clear instruction on policy and service provision and the patient has chosen to disregard this on several occasions in spite of due warning). With the decision made the patient will be contacted in writing.
You may be removed from the practice list and have to find an alternative GP practice. If there are any specific problems preventing you from attending please let us know. Mistakes do happen and the practice understands that appointments can be forgotten or overlooked. In such cases, the practice will take into account the reason given by patients. The practice regularly advises patients to keep contact details up to date to avoid text message reminders being undelivered.
How to avoid a DNA
If the patient cannot attend or no longer needs an appointment they can contact the surgery at least 2 hours before the appointment either by;
- Calling: 0208 539 1663
- Text messaging: Replying to text message reminders sent automatically by the practice
- Through patient access
- In person at reception
(The practice does not recommend cancellations in writing as delay could occur in receiving).
Fair Processing
NHS Data Sharing in East London
In East London we can improve the quality of care you receive by sharing the right information about you between our local NHS and social care organisations who are providing you with your direct care. We call this sharing of information Data Sharing and the people sharing this data your Direct Care Team who will be people you will at some point be involved directly in your care be it your GP, or the A&E team when you visit for an emergency, or the social care team looking after you in your home. The sharing of information has always happened (to a lesser degree) with paper processes but systems are allowing us to share more relevant information about you amongst your Direct Care Team helping them to be more efficient and support theirs and your decision making on your care.
This work is being led by your local clinicians who want to help support you receiving the best quality care possible. They want to be as transparent as possible so that you can feel assured that data is being shared with your best interests at heart and they want you to be involved in this as best you see fit.
All of the people accessing and sharing your information (your Direct Care Team) will have some form of direct interaction with you otherwise they will not be accessing your information (in other words the A&E team would only ever access information if you had an emergency and actually attended A&E). The reason they want to access your information is that this can improve the quality of care that you receive from them. Imagine the information or data that is held about you are pieces of a jigsaw and these pieces are held on different systems by the providers of your care. If one of your Direct Care Team wants to make a decision on the best course of action for you, the more pieces of the jigsaw they have, the more they can know about you and your history of care and therefore they can make the most appropriate decision based on you and your needs.
The set of rules we use locally about sharing your information (or data) form our “Fair Processing” arrangements and this site will give you all the information you need to understand how this all works (or places you can go to find out more information).
Data Sharing and the law
The new General Data Protection Regulation (GDPR) is in application from 25 May 2018, and supersedes the UK Data Protection Act 1998 (DPA). With the onset of GDPR the professionals involved in your individual care (or direct care) will be using implied consent from you to see your shared medical records. In order for the sharing of Personal Data to comply with Article 5 of the General Data Protection Regulation it must be fair and lawful and one of the Article 6 conditions must be met. Article 9 conditions must also be met if Sensitive Personal Data or special category data is being shared. The following articles are the ones that apply for sharing of data for the professionals involved in your care:
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- A) Article 6 condition – The sharing of Personal Data is permitted under Article 6 paragraph (c) (processing for legal obligation); paragraph (d) (processing for vital interests of data subject); and/or paragraph (e) (public interest or in the exercise of official authority).
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- B) Article 9 condition – The sharing of Sensitive Personal Data or Special Category Data is permitted under Article 9 (h) (processing for medical purposes); and/or paragraph (i) (public interest in the area of public health). For the vast majority of sharing we will be relying on article (h) with an implied consent model for direct individual care (more detail below where we talk about the Common Law Duty of Confidentiality). In certain instances, however, we may also rely on paragraph (a) (explicit consent) or paragraph (c) (vital interests) but these will be specified in any sharing agreements or data processing contracts related to those special cases.
Common Law Duty of Confidentiality
Common law is not written out in one document like an Act of Parliament (like the Data Protection Act). It is a form of law based on previous court cases decided by judges; hence, it is also referred to as ‘judge-made’ or case law. The law is applied by reference to those previous cases, so common law is also said to be based on precedent. This duty of confidence means that professionals should not disclose a patient’s personal information to anyone outside the team providing care for them without the explicit consent of the patient. For those providing care for the patient there is an implied consent in place. There are three circumstances where your information can be shared to someone outside of the team involved in your direct care. These are:
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- where you have consented to have this information shared
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- where disclosure is necessary to safeguard you, or others, or is in the public interest
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- where there is a legal duty to do so, for example a court order
Audit, service evaluation and research
We do also use de-identified data to help us to audit our services, do re-evaluation of their outcomes (to help continually improve your care) and for research purposes. This de-identifying process is also called pseudonomisation whereby your distinct personal details (name, date of birth) are either removed or scrambled in such a way as to stop you being identified. This data mainly falls outside of GDPR and the national opt out, as this only applies for identifiable data for secondary use.
Healthcare cannot stand still and we need to constantly strive to improve the services and care you receive and this can only be done by looking at the totality of data to look at outcomes and any trends in those outcomes.
The Organisations involved in your Direct Care Team
The local organisations involved in your Direct Care Team include:
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- Barts Health NHS Trust
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- Homerton University Hospital
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- Barking, Havering and Redbridge University Hospitals NHS Trust
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- East London Foundation Trust
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- North East London Foundation Trust
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- GP Provider Federations
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- General Practices
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- Community Health Services (on their own or through the organisations they are hosted in)
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- City of London Corporation
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- London Borough of Hackney
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- London Borough of Newham
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- London Borough of Tower Hamlets
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- London Borough of Waltham Forest
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- London Borough of Barking & Dagenham
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- London Borough of Havering
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- London Borough of Redbridge
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- St Joseph’s Hospice
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- City and Hackney Urgent Healthcare Social Enterprise
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- London Ambulance Service
How it works
Data sharing securely connects different medical and care computer systems together. When a patient’s records are requested, it collects the information from the different system and shows the information to the requestor. None of the information it collects is stored and none of it can be changed. Because it collects the information only when it is needed, the information is always accurate and as up to date as possible.
Before any information is collected or displayed to a care professional, they must be involved in your individual or direct care. Not everyone can see your shared data, nor should they. It will only be accessed by the people involved in looking after you directly. The Fair Processing Programme uses the secure NHS network to retrieve the information that has been approved to be shared with that care setting and displays a read only view for the care professional to use to support the delivery of care at that specific point in time.
No information is stored or saved within the or the care setting from where it is accessed so there is no need to worry about what could happen to your information without your knowledge or permission. There are two major ways that Data Sharing is taking place in East London.
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- The Summary Care Record – The Summary Care Record contains information about your allergies, medications and reactions you have to medications, so that in an emergency or when your GP practice is closed this information is available so that you can be cared for. This is a national programme for sharing your information. For more information please go to www.nhscarerecords.nhs.uk
- East London Patient Record (eLPR) – This is a local programme which shares more information about you than the Summary Care Record to better support your Direct Care Team and your care. Currently this is sharing between the following organisations:
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- Barts Health NHS Trust
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- Homerton University Hospital
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- East London Foundation Trust
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- All General Practices in City & Hackney CCG, Newham CCG, Tower Hamlets CCG, Waltham Forest CCG, Barking CCG, Havering CCG and Redbridge CCG
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- St Joseph’s Hospice
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- North East London Foundation Trust
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- GP Provider Federations
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- Community Health Services (on their own or through the organisations they are hosted in)
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- London Borough of Hackney
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- London Borough of Newham
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- City and Hackney Urgent Healthcare Social Enterprise
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- London Ambulance Service
The East London Patient Record (eLPR) will be adding more organisations and this site will be update with those details in due course.
What does it mean to you?
Joined up safer care + More time spent on your care + All of your information in one place = Safer and better care for you! The following sites contain some useful information and videos to help you understand data sharing better:
Discovery Data Service
The Discovery Data Service is a brand new service in development in east London. Primarily the aim of Discovery is to link up all of the local data held about you to improve direct patient care. The secondary aim to produce a de-identified (or pseudonymised) linked database for service evaluation, audit, and research.
This service will see all of the data come directly from the local providers (GP Practices, Barts and the Homerton and so on) and will mean that those providers are in control of that data and how it should be best used for your care and to improve the way we operate to deliver your care. There will be stringent Information Governance controls around the usage but these will be managed by us locally (including by you the patients who ultimately own the data) and will mean we can better use our data the ways we know will improve healthcare here locally in east London. This service has been shaped with these main aims:
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- To improve direct care for patients by using the totality of their health record from all the
local providers in real time
- To improve direct care for patients by using the totality of their health record from all the
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- To use the data to research and improve the quality of services we supply locally
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- To support east London in other population health research
This Service is under development so we hope to come back to you and update you when the
service starts producing its first outputs.
- To support east London in other population health research
FAQs
Why do you need to share my information?
Data sharing will provide health and social care professionals directly involved in your care access to the most up-to-date information about you. This allows the professionals caring for you to more fully understand your needs. Information is already shared by phone and paper records, data sharing simply allows this to happen more efficiently. It does this by sharing appropriate information from your medical and care records between health and social care services involved in your care.
Can anybody see my records?
Definitely not. Only care professionals directly involved in your care will see your personal care information through data sharing.
How do I know my records are secure?
By law, everyone working in, or for, the NHS and adults’ and children’s social care must respect your privacy and keep your information safe. Your information is stored on secure computer systems connected on a private health and social care network.
Can I access my records?
Yes. Under the GDPR you can request access to all information that organisations hold about you. Please contact the organisations directly to request the information.
Can I object to my records being shared?
You can object to your information being shared by talking to your providers of care. For direct care the people viewing your records are the people directly looking after you and are doing so to give you the best quality care they can. If you do however still want to object please contact the organisation who holds the records you do not want to be shared. It is worth noting that not sharing vital information about you with other organisations involved in your care could affect the quality of care that you receive and there may be circumstances where you objection may not be upheld. For example:
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- If it is in the public interest for data to still be shared. For example if there is a
safeguarding issue, or in the case of a mental health patient who might be at risk from harming themselves or a member of the public.
- If it is in the public interest for data to still be shared. For example if there is a
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- If clinical care cannot be provided. For example in referring a patient to hospital and data needs to be shared for the hospital clinician to do their job properly. In this instance obviously the patient can then choose not to have the treatment and therefore not have their data shared.
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- If systems are not well enough developed enough to not share the information. For
example GP Systems are relatively well developed and can handle objections a lot more easily than other providers but they still may be asked not to share something which the system cannot do. In this instance points 1 and 2 above would apply.
- If systems are not well enough developed enough to not share the information. For
What information will be shared?
Your shared record will contain a summary of your most up-to-date, relevant health information which includes things such as:
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- Your recent diagnosis and test results;
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- What allergies you have;
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- What medications and treatment you currently receive.
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- Any Current or Past (and significant) Illnesses
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- Encounters and Referrals
Can everybody see everything on my medical and care records?
No. We are working very carefully, supported by health and social care professionals, to make sure only relevant information is shared into specific care settings.
Can my records be accessed by health and social care professionals outside of my borough?
Yes they can, but only with other professionals who are caring for you directly. On top of the programmes mentioned above there is also the Summary Care Record is a national programme and as such means that it is available to care organisations outside of these boroughs (but again only for direct care purposes). The Summary Care Record contains important health information such as:
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- Any prescription medication a patient is taking
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- Any allergies a patient may have
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- Any bad reaction to any medication a patient may have previously had
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- More information about the Summary Care Record can be found at www.nhscarerecords.nhs.uk
If you have any queries or want to know more about data sharing or our fair processing please contact your local provider that holds the information you wish to discuss.
GDPR & Information Sharing
The Lyndhurst Surgery has taken measures to comply with the New General Data Protection Regulations (GDPR) which has come into effect on the 25th May 2018.
Summary Care Records (SCR)
Your Summary Care Record is a short summary of your GP medical records. It tells other health and care staff who care for you about the medicines you take and your allergies. This will enable health and care professionals to have better medical information about you when they are treating you at the point of care.
All patients registered with a GP have a Summary Care Record, unless they have chosen not to have one. The information held in your Summary Care Record gives health and care professionals, away from your usual GP practice, access to information to provide you with safer care, reduce the risk of prescribing errors and improve your patient experience.
Your Summary Care Record contains basic information about allergies and medications and any reactions that you have had to medication in the past.
Some patients, including many with long term health conditions, have previously agreed to have Additional Information shared as part of their Summary Care Record. This Additional Information includes information about significant medical history (past and present), reasons for medications, care plan information and immunisations.
During the coronavirus pandemic period, your Summary Care Record will automatically have Additional Information included from your GP record unless you have previously told the NHS that you did not want this information to be shared.
There will also be a temporary change to include COVID-19 specific codes in relation to suspected, confirmed, Shielded Patient List and other COVID-19 related information within the Additional Information.
By including this Additional Information in your SCR, health and care staff can give you better care if you need health care away from your usual GP practice:
- in an emergency
- when you’re on holiday
- when your surgery is closed
- at out-patient clinics
- when you visit a pharmacy
Opting out
The purpose of SCR is to improve the care that you receive, however, if you don’t want to have an SCR you have the option to opt out. If this is your preference please inform your GP or fill in an SCR opt-out form and return it to your GP practice.
Please visit the NHS Digital website for more information.
GP Earnings
NHS England require that the net earnings of Doctors engaged in the Practice is publicised, and the required disclosure is shown below. However it should be noted that the prescribed method for calculating earnings is potentially misleading because it takes no account of how much time Doctors spend working in the Practice, and should not be used to form any judgment about GP earnings, nor to make any comparison with any other Practice.
All GP Practices are required to declare the mean earnings (e.g. average pay) for GPs working to deliver NHS services to patients at each Practice. The average pay for GPs working in The Lyndhurst Surgery in the last financial year was £62,374 before tax and national insurance. This is for two full-time GPs and two locums who worked in the Practice for more than 6 month
Named GP
You may be aware that from April 2015 all practices are required to provide all their patients with a named GP who will have overall responsibility for the care and support that our surgery provides to them.
Patients aged 75 years and over were allocated named GP last year which will remain the same.
Dr P Goel will be the named GP for all female patients under 75 years and Dr H Johal will be the named GP for all male patients under 75 years.
If you wish to change your allocated named GP please contact reception staff.
Having an allocated GP does not prevent you from seeing any GP in the practice
National Data Opt-Out
The Lyndhurst Surgery is one of many organisations working in the health and care system to improve health care for patients. Whenever you use a health or care service, such as attending Surgery for a consultation, Accident & Emergency or Community Care services, important information about you is collected in a patient record for that service. Collecting this information helps to ensure you get the best possible care and treatment. The information collected about you when you use these services can also be used and provided to other organisations for purposes beyond your individual care, for instance to help with: This may only take place when there is a clear legal basis to use this information. All these uses help to provide better health and care for you, your family and future generations. Confidential patient information about your health and care is only used like this where allowed by law. Most of the time, anonymised data is used for research and planning so that you cannot be identified in which case your confidential patient information isn’t needed. You have a choice about whether you want your confidential patient information to be used in this way. If you are happy with this use of information you do not need to do anything. If you do choose to opt out your confidential patient information will still be used to support your individual care. To find out more or to register your choice to opt out, please visit www.nhs.uk/your-nhs-data-matters. On this web page you will: You can also find out more about how patient information is used at: You can select your opt-out by visiting: https://www.nhs.uk/your-nhs-data-matters/ You can change your mind about your choice at any time. Data being used or shared for purposes beyond individual care does not include your data being shared with insurance companies or used for marketing purposes and data would only be used in this way with your specific agreement. Health and care organisations have until 2020 to put systems and processes in place so they can be compliant with the national data opt-out and apply your choice to any confidential patient information they use or share for purposes beyond your individual care. Our organisation is currently compliant with the national data opt-out policy. If you do not want your identifiable patient data to be shared outside of your GP practice for purposes except for your own care, you can register an opt-out with your GP practice. This is known as a Type 1 Opt-out. Type 1 Opt-outs were introduced in 2013 for data sharing from GP practices, but may be discontinued in the future as a new opt-out has since been introduced to cover the broader health and care system, called the National Data Opt-out. If this happens people who have registered a Type 1 Opt-out will be informed. NHS Digital will not collect any patient data for patients who have already registered a Type 1 Opt-out in line with current policy. If this changes patients who have registered a Type 1 Opt-out will be informed. If you do not want your patient data shared with NHS Digital, you can register a Type 1 Opt-out with your GP practice. You can register a Type 1 Opt-out at any time. You can also change your mind at any time and withdraw a Type 1 Opt-out. If you have already registered a Type 1 Opt-out with your GP practice your data will not be shared with NHS Digital. If you have previously registered a Type 1 Opt-out and you would like to withdraw this, you can contact your practice to ask for a revision form. You can send the form by post or email to your GP practice or call 0300 3035678 for a form to be sent out to you. If you register a Type 1 Opt-out after your patient data has already been shared with NHS Digital, no more of your data will be shared with NHS Digital. NHS Digital will however still hold the patient data which was shared with us before you registered the Type 1 Opt-out. If you do not want NHS Digital to share your identifiable patient data with anyone else for purposes beyond your own care, then you can also register a National Data Opt-out. There is more about National Data Opt-outs and when they apply in the National Data Opt-out section above. Your confidential patient information is important to us. Your information can also be called your data. There are strict rules about how your confidential patient information can be used. Confidential patient information says who you are and has things like your name and information about your health and care in it. This information is about the choices you have about how we use your confidential patient information. We promise to keep your information safe and always be clear about how it is used. You can find out more about this on: nhs.uk/your-nhs-data-matters Information about your health and care helps us: You can choose if your confidential patient information can be used to help with new treatments and planning services. When we can we try not to use your name on information used for things like planning. We will still use your name and address and your NHS number so we can tell you about any changes to your services for example changes with your GP. Sometimes we do need to use your details and information about your health, care or treatment. Your patient confidential information can be used by: You can choose if you want your confidential patient information to be used for planning and looking into new treatments. If you decide not to share your confidential patient information that will not change your care at all. We will still send you invites for things like screening for bowel cancer. If you are happy about how your confidential patient information is used you do not have to do anything else. If you do not want your confidential patient information to be used for planning and looking into new treatments you can: Choose to opt out safely online: nhs.uk/your-nhs-data-matters Or you can use our telephone service, call: 0300 303 5678 Ask a friend or carer if you need help. You can change your choice at any time.How the NHS and care services use your information
Opting out of NHS Digital collecting your data (Type 1 Opt-out)
Your information matters to the NHS
How your data is used
Including your information
Who can use your confidential patient information for planning and looking into new treatments?
Choosing if you want your confidential patient information to be used for planning and looking into new treatments
What to do
Patient Responsibilities & Rights
Practice observes a zero tolerance policy to abusive & violent behaviour.
Abusive and violent behaviour towards practice team leads to deregistration of the patient at the practice.
- To use appointments appropriately
- Inform surgery of cancellation of appointments well in time at least 2 hours in advance. Please see Did not attend policy.
- Order repeat prescriptions in good time and order all items together.
- To cooperate in health promotion & screening programmes:
Immunisations – For children & adult at risk
Cervical Smears (screening)
Breast Screening
Bowel Cancer Screening
Medical Reviews