A clinical "near miss" highlights risk management issues surrounding ultrasound-guided and wire-localised breast resections
© Leff et al.; licensee BioMed Central Ltd. 2012
Received: 27 March 2012
Accepted: 16 July 2012
Published: 16 July 2012
The introduction of the National Health Service (NHS) Breast Screening Programme has led to a considerable increase in the detection of impalpable breast cancer. Patients with impalpable breast cancer typically undergo oncological resection facilitated either by the insertion of guide wires placed stereo-tactically or through ultra-sound guided skin markings to delineate the extent of a lesion. The need for radiological interventions on the day of surgery adds complexity and introduces the risk that a patient may accidentally transferred to the operating room directly without the image guidance procedure.
A case is described of a patient who required a pre-operative ultrasound scan in order to localise an impalpable breast cancer but who was accidentally taken directly to the operating theatre (OR) and anaesthetised without pre-operative intervention. The radiologist was called to the OR and an on-table ultrasound was performed without further consequence.
It is evident that breast cancer patients undergoing image-guided resection are exposed to an additional layer of clinical risks. These risks are not offset by the World Health Organisation surgical safety checklist in its present guise. Here, we review a number of simple and inexpensive changes to the system that may improve the safety of the breast cancer patient undergoing surgery.
The National Health Service (NHS) Breast Screening Programme led to the detection of over 17,000 new breast cancers between 2009–2010 . Approximately 50 % of surgically treated screen detected cancers had an invasive tumour diameter of less than 15 mm1. Impalpable breast cancers require radiological localisation to guide the surgeon as to the approximate location of the lesion within the breast and to help determine the extent of the oncological resection. Localisation is commonly achieved through the use of either guide wires placed stereo-tactically or skin markings under ultrasound guidance. The necessity for pre-operative image-guided interventions introduces additional challenges for the patient (e.g. anxiety, additional psychological morbidity, physical pain associate with wire insertion, etc); the surgeon (i.e. planning, scheduling) and surgical teams (e.g. confirmation that all the necessary pre-operative procedures have been conducted).
Surgeons and surgical teams have of course always been safety conscious. However, systematic studies of error and harm in healthcare have revealed high levels of adverse events, many of which concern surgery [2–4]. In recent years studies of process failures, communication, teamwork, interruptions and distractions have now identified multiple vulnerabilities implicit within systems of surgical care [5–8]. We consider that the case discussed here exposes a number of important weaknesses in the process of care of breast cancer patients undergoing surgery .
She arrived on the morning of her operation and as per hospital protocol was taken to the admissions area for routine checks and observations by the nursing staff as well as to facilitate the consenting process by the surgical team. She was the first patient on the afternoon operating list. The surgical registrar went to see the patient, confirmed the clinical history, imaging findings, histopathological results and MDT recommendations. The patient was informed of the risks and benefits of the proposed procedure as well as the need for image-guided skin marking to assist resectional surgery and it was explained that this would occur prior to her being transferred to the operating theatre. The patient appeared to understand the process, the risks and benefits and duly signed the consent form. The registrar went to the breast imaging department to ensure that the radiologists were expecting the patient for an ultrasound scan. Prior to leaving for the imaging department the registrar explained to the sister in charge of the ‘admissions unit’ that the patient needed to have a pre-operative ultrasound scan and she was not to be transferred to the anaesthetic room until the image guided-skin marking had been conducted. The responsible consultant surgeon, who was otherwise engaged in clinic communicating a new diagnosis of breast cancer to another patient, received a telephone call from the theatre staff informing him that the patient was anaesthetised and enquiring as to his likely arrival time in the operating theatre. No ultrasound skin marking had been conducted. No-one had contacted the surgical team to ask them if it was acceptable to transfer the patient to the anaesthetic room. The patient herself had not queried being transferred to the operating theatre without a pre-operative procedure that only a few minutes beforehand she was informed was an absolute necessity.
The consultant radiologist due to perform the pre-operative ultrasound scan was called to the operating theatre, and thankfully was able to perform the image-guided localisation ‘on-table’ without further insult. The patient subsequently underwent the planned procedure and histopathological assessment confirmed a completely excised 5.2 mm IDC (closest margin 5.5 mm).
The “near-miss” described here raises several important clinical risk issues surrounding breast cancer patients who require pre-operative procedures prior to cancer surgery. These patients follow a complex pathway with a number of different decision points (Figure 2). The pathways constrain a number of mandatory checks, such as the World Health Organisation (WHO) surgical safety checklist , that are integral to the safety of the breast cancer patient undergoing surgery. However, the ‘near miss’ highlights a number of intrinsic vulnerabilities in the system with respect to the flow of the breast cancer patient through the perioperative process. The weaknesses inherent in the system can be summarised as follows:
Asymmetry in safety checks between the pre-operative and operative phase of care. As the current case and Figure 2 illustrate, there is a comparative asymmetry in terms of safety checks, with a greater emphasis placed prior to, rather than during the operative phase of care. The WHO surgical safety checklist  would not have detected nor prevented the current “near miss” as typically the checklist is conducted after the induction of general anaesthesia. There is a clear necessity to formalise the safety briefing prior to induction of general anaesthesia. This is essential, not only to ensure that image-guidance has been performed (if required) but that other mandatory pre-operative manoeuvres have been conducted (e.g. radioisotope injection for sentinel lymph node biopsy). Formalised pre-operative safety checks would also act as a vehicle to confirm the surgery side, accuracy of skin markings and to check the availability of allied equipment (e.g. breast prosthesis for post-mastectomy reconstruction).
Issues pertaining to patient proximity and preoperative location. The current case highlights the potential dangers involved if all patients (whether image guidance procedures are required or not) are observed pre-operatively in the same location. Clearly the flow of patient transport in this situation will vary. Some patient will move directly from the admissions area to theatre and some will be transported to the radiology department first and then subsequently back to the admissions area prior to being taken to the anaesthetic room. This is akin to travellers all arriving at an given airport gate ‘x’ with some people departing for destination ‘z’ and others destined for ‘z’ via another location ‘y’. In such a circumstance there would be a significant chance of boarding the wrong flight. Finally, the proximity of the admission lounge to the operating theatre, which in the case of our NHS Trust is only a few yards, may compound the problem as it may prevent a clear distinction between the two departments in the minds of the healthcare staff. There is therefore always a risk of a patient entering an incorrect pathway. The only factors preventing a patient being incorrectly taken straight to the operating theatre are a member of the surgical team staying with the patient (often impractical); communication between surgeon and admissions / theatre team (failed in the current case); the theatre ‘scrub team’ interpreting the theatre list (should state ‘wire guidance’ or ‘ultrasound skin mark’ as was clearly documented in the current case) and /or the astuteness of the patient who queries being taken straight to theatre, bypassing the radiology department.
Procedural risks specific to the breast cancer patient. It is valuable to reflect more broadly on the specific risks to breast cancer patients that are illuminated by the current case. Evidently, not all breast cancer patients are the same and nor are all breast cancer surgeries. Some patients require pre-operative image guidance interventions, some require pre-operative isotope and/or patent blue V injections, others undergoing reconstruction require the availability of a specific breast prosthesis or specialist lipomodelling equipment, whilst certain patients requiring nothing but ‘standard’ operating equipment universal to most operating theatres in the Western world. Those that require pre-operative interventions or specific operative equipment are potentially exposed to another layer of risks that are inherent in the system. The current case highlights the need to make these distinctions, a process that may be aided by changing the emphasis towards safety checks conducted in the pre-operative phase of care (prior to induction) for breast cancer patients.
The importance of pre-operative safety briefing. Communication between surgical teams is critical to patient safety. In particular, prior to starting an operating theatre list it is the duty of the surgeon to communicate with the anaesthetist and theatre teams to ensure that all members are aware of the patients being operated on and so that any unique or specific steps can be addressed. Regarding the current case, the briefing was succinct and focused (i.e. list order, patients to be operated on and operation type) and may have dealt better with broader issue surrounding the importance of image guidance, medical past history, and in which patient lesions were deemed to be impalpable. Broader preoperative safety briefings such as this have been shown to improve communication and reduce adverse events [11, 12]. In addition to the preoperative briefing, the theatre staff typically inform the surgeon that the patient is about to be transferred to the operating theatre. This is commonly referred to as ‘sending’ for the patient. The theatre staff did not inform the operating surgeon that they were ‘sending’ for the patient. One may argue that the theatre co-ordinator and anaesthetic team should have informed the surgical team that they had summoned the patient to operating theatre. This may have revealed that image-guidance had not yet taken place, thereby circumventing the “near-miss”.
Inability to rely on the patient to prevent errors in flow. Surgery is extremely stressful for the patient and they are likely to be anxious, nervous and prone to forgetting information given to them on the day of surgery. While patients should of course be encouraged to speak up if they notice any inconsistencies in their care it is not ultimately their responsibility to monitor the safety of the process. As highlighted here, patients’ may not challenge healthcare staff as to the appropriateness of the procedures they are undergoing. Had the patient informed the theatre staff that she was due to have an ultrasound scan then this “near miss” may not have occurred. Clearly, one cannot rely on the patient to prevent such an incident, and a new process of safety checks for breast cancer patients may be required. Of great concern is that a breast patient can currently arrive in the operating without a series of systematic safety checks being performed prior to the induction of general anaesthesia.
Breast cancer patients requiring pre-operative localisation should not enter the operating theatre space or admissions area until the wire-insertion and / or image-guided skin marking have been conducted. These patients should go directly to the radiology department on the morning of surgery.
Patients should not be consented by the surgical team until the necessary localisation procedures have occurred. This may be complicated by the fact that pre-operative consent for wire-guided excision is, in effect used as consent for the wire-localisation procedure as well as the subsequent wide local excision. Nevertheless, the absence of a signed consent form typically acts a barrier to proceeding with induction of general anaesthesia and would have circumvented the current adverse event.
Proposed variation on the WHO surgical safety checklist to augment the pre-operative safety briefing and enhance the safety of the breast cancer patient undergoing surgery
Read aloud before administering general anaesthesia
Has the patient confirmed their name / site of surgery / procedure and consent?
Is the anaesthetic machine / medications complete?
Does the patient have an allergy (especially to blue dye)?
YES (if yes – details)
Which breast / axilla is being operated on?
Is the surgical site marked?
NO (If ‘NO’ - do not administer GA, consult with surgeon / surgical team)
Is a pre-operative localisation procedure required?
If a pre-operative localisation procedure is required, has it been performed?
NO (If ‘NO’ - do not administer GA, consult surgeon / surgical team)
Is a SLNB procedure being conducted?
If a SLNB procedure is being conducted has radioisotope injection been administered and is patent blue V / gamma probe available?
NO (If ‘NO’ - do not administer GA, consult surgeon / surgical team)
Is the patient having a breast prosthesis inserted?
If a breast prosthesis is required has it been ordered / available in theatre?
NO (If ‘NO’ - do not administer GA, consult surgeon / surgical team)
Thankfully, the current patient came to no actual harm as a result of the “near miss” but should this adverse event have occurred in a patient requiring stereotaxic guidance for wire positioning, reversal of the general anaesthetic and transfer to the x-ray department would have been mandated. In light of this case we are exploring the pre-operative patient pathway for breast cancer surgery in our own Trust and are lobbying the WHO surgical safety team to develop a more specific checklist to maximise the safety of the breast cancer patient undergoing surgical interventions within the National Health Service.
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