Administrative work may seem far removed from clinical care, but it is often the first line of defence in patient safety. The systems, decisions, and boundaries managed by non-clinical staff shape patient experience.
At Medical Protection, our ethos remains to help members avoid problems before they occur, and we regularly highlight areas of practice that can contribute to complaints, claims or regulatory matters. Often our focus is on the clinical, technical and communication aspects of medicine, but increasingly we are noting cases arising from what appear at first glance to be the most innocuous or simplest of administrative errors.
These “simple” errors can result in significant health consequences for patients, distress for doctors and financial and efficiency costs for the health provider. This may be due to increased hospital stays, increased staff workloads, large clinical negligence claim settlements and ultimately loss of patient trust in the healthcare professional and organisation.
The below case study explores how well intended help can overstretch into clinical support. I also highlight some of the common administration related errors seen in Medical Protection’s case files and provide suggestions to help avoid them.
A female patient visited her GP practice because she had recent-onset arm pain and felt nauseous. She told the receptionist her symptoms and asked for an urgent appointment. The receptionist advised there were no appointments left that day and reassured her that it did not appear to be anything serious. She was advised to go home and call again the next morning when more appointments would be available. No clinician was asked to assess her symptoms.
That night, the patient’s symptoms deteriorate and she was taken to hospital, where it was discovered she had suffered a heart attack. She later instructed solicitors and alleged that if she had been seen by a GP earlier, the GP might have recognised the signs and sent her to emergency care sooner, and hence might have had a better outcome and shorter hospital stay.
On the whole administrative colleagues reduce our administrative burden and often identify errors that assist both the clinician and the patient. However, they can play a role in communication, records and scheduling errors. For instance, one claim demonstrated the impact of a receptionist providing well-meaning guidance about waiting times to a patient attending the emergency department with a head injury. Due to the incorrect information provided by the receptionist, the patient made the decision to return home where their condition suddenly deteriorated resulting in permanent brain damage. The Court judgement advised that the receptionist had a duty of care to provide accurate information and hence the hospital could be held liable for the subsequent injury to the patient.
Medication errors are common, often preventable and can be due to human factors such as fatigue, distractions and high workload or from inadequate systems and processes. A 2024 WHO report states that globally at least 1 in 20 patients experience preventable medication related harm, with the cost of medication errors alone estimated at US$ 24 billion annually, so the issue is not insignificant. The most common errors from our case files arise from the following:
Although many clinicians now have the support of prescribing via electronic systems, errors still occur when clinicians override alerts for allergies or potential reactions with other medications. In addition, selecting a similar sounding medication from a drop-down box, such as Xalatan rather than Xalacom eye drops, or Daktarin rather than Daktacort is easily done in haste.
When transcribing medication, it is easy to see how errors occur in prescribing the wrong medication, dose, rate or administration route or even writing the medication on the wrong patients record. For clinicians writing prescriptions by hand, misinterpretation of illegible handwriting is not always picked up by the pharmacist or dispenser. Failure to adjust medications to patient specifics such as weight or renal function has also resulted in significant patient harm. For example, failing to recognise that the recorded weight for a paediatric patient was inconsistent with the child’s appearance, resulted in inadequate antibiotics being given for suspected meningitis and a poor outcome for the patient.
The prescription of repeat medications is commonplace and necessary to ensure efficiency for both patients and clinicians. Many cases arise from a failure to ensure regular medication reviews with the patient to check the medication is still required (particularly with opioids). Another common cause is a failure to monitor for adverse effects of the medication, particularly for drugs that require regular blood test monitoring such as ACE-inhibitors, digoxin, lithium, methotrexate, etc.
Administration and dispensing errors often arise from incorrect route of administration, giving the medication to the wrong patient, or at the incorrect frequency or rate, and many times this can be due to not following established protocols or due to human factors such as fatigue or stress.
Writing and receiving referrals, reports and results requires significant time and attention. The advent of AI in healthcare brings with it the promise to ease that burden, however the responsibility for any errors is still likely to remain with the clinician even when AI is used as an adjunct, so attention to detail remains critical.
Despite the clinicians’ best intentions, delayed or missed referrals following an accurate patient assessment remain common in alleged delay in diagnosis claims, particularly in relation to cancer diagnoses. In addition, failing to advise or action the speed at which a patient should be seen (routine or urgent) has been deemed pertinent in many cases where the resulting delay has caused poorer outcomes or more significant treatment.
One of the most common causes of cases in this area is the failure to act on significant results, or letters from other clinicians. Routine tests, such as cervical smears, that throw up abnormal results, can easily be missed leading to the receiving clinician failing to arrange repeat tests or make appropriate referrals. Reports from radiology and pathology also feature highly in this context, where typographical errors, abbreviations or lack of clarity regarding next steps can lead to incorrect actions by the recipient. AI could be a solution in screening results received; however, sometimes normal results need to be seen by a clinician as much as an abnormal result. Take for example a patient with haematuria and a negative urine culture, which should prompt further investigation. Increasingly, we are also seeing misinterpretation of results given verbally in urgent situations and then failure to compare with the subsequent written report which may differ in detail.
Despite technological advances such as barcode scanning and increased use of protocols, patient identification errors still occur, and the potential harms can range from minor to catastrophic. Some of the more serious consequences arise in the surgical arena, particularly in high volume specialties, where the wrong procedure is performed on a patient or the incorrect equipment or prosthesis used, for example, inserting the incorrect lens during a LASIK procedure due to confusion over which patient was next on the operating list.
Consider the below takeaways for each section discussed: