What makes good clinical records?
Content
Good clinical records will contain all the information one clinician needs to take over where another left off – or, to put it another way, to allow a clinician to reconstruct a consultation or patient contact without relying on memory. This will include:
- History – relevant to the condition including any positive and negative answers to direct questions
- Examination of the patient
- All systems examined
- All important findings, both positive and negative, with details of any objective measurement such as blood pressure, peak flow, etc
- Differential diagnosis
- Investigations – details of any investigations arranged
- Referral – details of any referral made
- Information – information given to the patient concerning risks and benefits of proposed treatments
- Consent – details of consent given to proposed investigations, treatments or procedures
- Treatment – details of the main doses of drugs, total amount prescribed, any other treatment organised with batch number and expiry date of any medications personally administered
- Follow-up – arrangements for follow-up tests, future appointments and referrals made
- Progress – any further consultations, the patient’s current condition, side effects, complications, etc.
Many follow-up consultations will be with different members of the team, who will be totally reliant on the clinical records and therefore will need as much information as possible
That may seem like a daunting list, but it is all important information that someone would have to remember if it is not recorded – and both doctors’ and patients’ memories are fallible. Many follow-up consultations will be with different members of the team, who will be totally reliant on the clinical records and therefore will need as much information as possible. The mnemonic SOAP is a useful reminder of the essential content you should include.
Box 1: Essential content (SOAP)
- Subjective – what the patient says
- Objective – what you detect – examination and test results
- Assessment – your conclusions – often the differential diagnosis
- Problem list & Plan – management and follow up.
Case 2
A 26-year-old single woman went to see her GP complaining of blackouts. He referred her to a neurologist, giving a detailed account of the blackouts but not disclosing the medication she was on, which included the oral contraceptive pill. The neurologist started the patient on anticonvulsants. Three months later she conceived. Her claim against both doctors succeeded.
He referred her to a neurologist, giving a detailed account of the blackouts but not disclosing the medication she was on
As the GP had failed to alert the neurologist to the fact the patient was taking the oral contraceptive pill, and the neurologist had not asked about medication, both had been in breach of their duty of care, leading to the unwanted pregnancy.
Presentation
Content is important, but so is presentation. If the records are unclear, inaccurate or written in such a way that they’re difficult to follow, the content might as well not be there; worse than that, it could cause errors and misunderstandings. Good notes therefore have the following attributes:
- Clear – both legible and understandable when handwritten. Each entry should be legibly signed with the date and time.
- Objective – clinical records should be factual and free from subjective comments about patients or their relatives. Always assume that patients will read their clinical records at some stage.
- Contemporaneous – clinical records should be written up at the time of, or as soon as possible after, an event to ensure accuracy. Retrospective entries should be clearly dated, timed and signed, together with an explanation of why it is being written retrospectively.
- Attributable – if information has been given to you by someone other than the patient, then you should record who provided the information as well as what they said.
- Original – sometimes it is necessary to amend or alter medical records, for example if a factual error has been made. Any correction must be clearly shown as an alteration, complete with the date the amendment was made and the name of the person who made it so there can be no allegation that the alteration was an attempt to deceive anyone into thinking that it is part of the original record. (See Box 2.)
Box 2: HSE guidelines on correcting medical records
3.3.11 Deletions or alterations are made by scoring out with a single line followed by:
a. signature (plus name in capitals) and counter-signature, if appropriate.
b. date and time of correct entry.
c. reason for amendment.
3.3.12 Corrections are made as close to the original recording as possible.
National Hospitals Office, Standards and Recommended Practices for Healthcare Records Management (2011).
Abbreviations
Abbreviations are commonly used in clinical records but can be misinterpreted and lead to mistakes in diagnosis or management. So the rule is, when in doubt, write it out – in full. (See Box 3 for the rules on abbreviations that apply in national hospitals.)
The rule is, when in doubt, write it out – in full
Sarcastic and derogatory abbreviations have no place in clinical records – they are gratuitously offensive and sure to destroy any therapeutic relationship once found out.
Case 3
A 38-year-old woman phoned her GP surgery complaining of back pain and difficulty passing urine.
The GP checked her notes and saw a reference to PID, which he interpreted as pelvic inflammatory disease. He concluded that she had another urinary tract infection and wrote a prescription for antibiotics for the patient to collect.
In fact PID referred to her recurring problems with a prolapsed intervertebral disc which had now given rise to a cauda equina syndrome and associated pain and urinary symptoms
In fact PID referred to her recurring problems with a prolapsed intervertebral disc which had now given rise to a cauda equina syndrome
Box 3: Use of abbreviations in national hospitals
3.4.28 Abbreviations should be avoided if at all possible, but in the event of abbreviations being utilised, only those approved by the National Quality &
Patient Safety Directorate and contained within the HSE approved abbreviations document are permitted.
3.4.29 If an abbreviation is used that is not contained within the HSE abbreviations document the full term used, followed by the abbreviation in brackets, should be written on each side of each page where the abbreviation is used.
3.4.30 Abbreviations should not be used on:
a. documentation that is used for transfer or discharge.
b. communication sent from the healthcare organisation, e.g. external
referral letters.
c. consent forms.
d. death certificates.
e. medication sheets.
National Hospitals Office, Standards and Recommended Practices for Healthcare Records Management (2011).