Abstract

Twelve steps to safer patient care
A systematic review of studies on in-hospital adverse events, covering nearly 75,000 patients found an overall rate of 9.2% with nearly half adjudged preventable. While half of patients suffered little or no harm, 7.4% died. The majority of problems were related to operations or medication, so the authors recommend concentrating on these areas within hospital safety programmes.
Recognized evidence-based interventions are listed. For surgery, these include:
localizing care in high-volume centres; setting up a medical emergency team; providing training in laparoscopic procedures; ultrasound guidance for central vein catheterization; reducing postoperative infection with antibiotic prophylaxis, supplemental oxygen and periopertaive normothermia; glucose control in diabetics; perioperative beta blocker prescribing (but see below for caveats). having a clinical pharmacist consultation service; using barcode technology in pharmacies; using computerized physician order entry (CPOE) and clinical decision support system (CDSS); patient self-management of anticoagulation.
Medication-related errors can be reduced by:
Barely two cheers for perioperative beta blockers
The systematic review detailed above suggested perioperative beta blocker use was backed by strong evidence. While this is true, over the years some study results were less persuasive than others and many clinicians remain unconvinced. Recently, the Lancet published the results of the POISE trial, a large multinational randomized placebo-controlled trial of this group of drugs with over 8000 patients being randomized. That study found that for every 1000 patients undergoing non-cardiac surgery who are given perioperative beta blockers, 15 will be spared a myocardial infarction, 3 from needing coronary revascularization and 7 from developing atrial fibrillation – but an extra 8 will die and 5 have a stroke.
This month, a group of authors who collected data for the POISE study summarize their personal take home messages in a leading anaesthetic journal.
Patients already on these drugs before operation should stay on them; High-risk patients may need a larger dose and so require monitoring in a high dependency unit; All patients at high risk of coronary disease should be treated anyway, regardless of their need for surgery. However, if their heart disease is first discovered when admitted for operation, starting treatment may be inappropriate unless surgery is delayed; Perioperative beta blockers should be prescribed for individual patients after due consideration to the risks and benefits.
Ambulance services litigation risk quantified
From 1995–2005, the NHSLA handled 272 cases of litigation against UK ambulance services. The annual rate has increased fivefold over the period. In 75 cases the allegation was of lack of assistance or care and in 36 and 34, respectively, failure or delay in treatment and in diagnosis. Seventeen claims, mostly ongoing, were for over £1 million.
Assistance problems related in many cases to adverse incidents, such as falls during the transfer, including from wheelchairs and stretchers. There were 34 allegations of failing to immobilize (or incorrectly immobilizing) the spine, allegedly resulting in one death and 19 patients suffering neurological deficits. Delay was alleged in 42 cases, with meningitis being a notable component.
By February 2005, 187 cases had settled, 70 without a payment (with one patient held responsible for costs). Of the 17 large claims, eight were still open and 9 ‘on hold’. The 13 obstetric cases included four where lack of equipment to handle a premature baby or failure to recognize and treat neonatal hypoxia was a factor.
The findings suggest key training areas for paramedics and other ambulance personnel include obstetric care, how to recognize spinal cord injury and greater attention to decisions on not transferring patients to hospital. Joint Royal College Ambulance Liaison Committee guidelines have addressed the first two of these (see
Supporting clinicians after a patient disaster
We tend to forget that clinicians involved in a serious adverse event may need help and support at a stressful time in their lives. A paper from Virginia, published in the Patient Safety section of Anesthesia & Analgesia, reminds us that most anaesthetists will experience a ‘death on the table’ at least once in their career – handling the aftermath of which may not have been part of their training. Surveys have shown that death of a patient may have a major emotional impact on healthcare practitioners involved, regardless of whether the death was unexpected or the patient well-known to the practitioner. Those in the early part of their training are worst affected. Given that anaesthetists are at disproportionate risk of suicide and substance abuse, the authors suggest they may be a group particularly susceptible to stress-related disorders. Unsurprisingly, therefore, surveys have shown that a patient's death may lead to prolonged psychological distress with recovery hampered by lack of emotional and professional support.
The authors recommend putting into practice guidelines for support such as those issued by the Association of Anaesthetists of Great Britain and Ireland (see
Reducing the risk of Erb's palsy
A common reason for litigation in neonatal medicine is because of Erb's palsy, partial paralysis of a newborn baby's arm following traction injury to nerves of the brachial plexus running through the axilla. It is a particular problem with large babies where there is difficulty in delivering the shoulders (shoulder dystocia). Specific training in avoidance is mandated by the Clinical Negligence Scheme for Trusts in the UK (and recommended by the organization which accredits healthcare organizations in the US) but, until now, there has been no evidence of any associated improvement in outcome post-training.
A study from Bristol has compared the management and outcome of shoulder dystocia from 1996–1999 (before training was introduced) and 2001–2004 when staff received appropriate training during a multidisciplinary one-day course, including a 30-minute individual practical session on a mannequin. The dystocia rate (about 2% of all vaginal births) was similar in both periods, during which there were over 29,000 eligible deliveries.
Before training, the obstetric notes disclosed that in 50% of cases none of the manoeuvres recommended for handling shoulder dystocia were used (McRoberts' position, suprapubic pressure, internal rotation, delivery of the posterior arm, All-Fours-manoeuvre). Post-training, at least one of these was used in 90%. There was also marked reduction in descriptions suggesting excessive traction might have been used.
Brachial plexus injury at birth was reduced from 7.4% of babies with shoulder dystocia to 2.3%. Persistent brachial plexus injury at 6 and 12 months were fewer but the number did not reach statistical significance, possibly because of small numbers – with only 9 and 6 babies, respectively, pre-training and 2 and 2 post-training. The authors point out that studies published from three other UK hospitals have shown increases in brachial plexus injuries over the period in question. They believe they may have had greater success by mandating training for all staff and carrying it out in a labour suite, which is where the emergency usually occurs.
Call for papers
One of my aims for Clinical Risk is that our readers should aspire to be our contributors. If you are a clinician you will have encountered areas of practice which carry risks for patients – as well as the risk of complaints or litigation against Trusts, independent hospitals and clinics or individuals. Why not tell us about them, pointing out the pitfalls and the solutions? Readers who are managers may take pride in systems they have put in place to cut down on errors and otherwise enhance patient safety. Perhaps these have been subject to surveys or an audit process which could be generalized to other settings. If so, readers may value learning about them, so let us know. Claimant and Defendant lawyers will have encountered individual cases containing lessons for their colleagues and cautionary advice for clinicians. Such cases may eventually find their way into the AVMA Medical & Legal Journal or the Healthcare & Law Digest, which are such valued components of Clinical Risk. But many do not, especially now that such a large proportion of cases opened do not proceed to judgment. Please write them up for submission to the journal.
Articles for publication should be sent, according to our guidelines for authors, by email to CRproductionrsm.ac.uk. But if you would like to discuss a proposed topic in advance of submission, please contact me at h.marcovitch@btinternet.com with your contact telephone numbers.
