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Health

  • Report no:
    202100979
  • Date:
    June 2024
  • Body:
    Lanarkshire NHS Board
  • Sector:
    Health

The complainant (C) complained to my office about the treatment provided to their late spouse (A) by Lanarkshire NHS Board (the Board).

Following a period of ill health, A attended University Hospital Wishaw’s (UHW) Emergency Department (ED).  A was diagnosed with primary biliary cirrhosis (PBC) by the gastroenterology department.  A continued to be seen by the gastroenterology department as an outpatient over a period of months.  It was noted that A’s liver function had deteriorated over this period.

A then presented to UHW’s ED where they were reviewed and noted to have worsening liver failure.  A was subsequently admitted to the Emergency Care Unit (ECU).  A was transferred to a specialist liver unit in another NHS Board’s area four days later and sadly died there.

C complained that the Board had failed to adequately investigate and treat A’s condition; that they provided A with inadequate in-patient care and treatment in UHW; and that they failed to treat A with dignity when transferring them to the ECU. 

The Board reviewed A’s care by undertaking a Significant Adverse Event Review (SAER). In their SAER, and their written response to C’s complaint, the Board identified service failures. These were failures to timeously refer A to a specialist liver unit, in waiting times, the organisation of A’s care, in the medication prescribed to A, and in staff attitude for which they apologised and identified learning.  However, they found no failures in the in-patient care and treatment provided to A in UHW.

During my investigation I sought independent advice from a consultant hepatologist and gastroenterologist.  Having considered and accepted the advice I received, I found that:

  • A presented with clinical symptoms that were not typical of PBC, and that A had clear indicators of another underlying liver condition. 
  • Given A’s clinical symptoms the Board have arranged urgent tests and / or a referral to a specialist liver centre / transplant hepatologist within a few weeks of their presentation, and definitely by the time their condition deteriorated several months later. 
  • In terms of A’s treatment for PBC it is clear that there was a failure to have adequate regard to relevant guidelines. This had significant consequences to As’ health. Six of the seven service standard measures of the PBC guidelines were not met.
  • The symptoms that A presented with were also not in keeping with the additional condition that was considered of autoimmune hepatitis (AIH). 
  • A biopsy should have been offered to A much earlier. When this was subsequently offered, the Board should have done more to actively facilitate A’s attendance for a biopsy.  Other appropriate tests to diagnose AIH were not carried out.
  • In terms of A’s treatment for AIH, there was a failure to follow the relevant guidelines. In particular in relation to the use of contraindicated steroid medication and a failure to carry out regular blood checks.  
  • A’s steroid medication was continued, although they were exhibiting side effects, without considering either referral to a specialist, or a liver biopsy or other treatment. There was also a failure to consider if the side effects of the medication were a sign of deterioration of A’s liver disease. 
  • Although an additional condition of primary sclerosing cholangitis appears to have been suspected and an Magnetic Resonance Cholangiopancreatography (a medical imaging technique) was considered, this was not carried out early enough to exclude or confirm such a diagnosis. Nor were other important tests to differentiate between liver conditions carried out.
  • As A’s condition deteriorated acute severe AIH should have been considered and this should have triggered frequent clotting tests and a referral to a transplant unit. This was not done. The clinical team should have recognised that A’s presentation was not in keeping with PBC nor standard AIH.
  • If standard treatment guidelines for PBC and AIH had been followed then the outcome for A would have been significantly different and it is possible, if not likely, that A would still be alive.
  • There were failures in communication and to adequately take into account A’s personal circumstances.
  • There was a failure to provide A with an appropriate level of dignity and person centred care following their admittance to UHW.
  • There were significant failings in A’s in-patient care and treatment in UHW. There were failures in the management of A’s ascitic drain, steroid medication, and constipation. There was a failure to trigger a medical review in light of a fall A experienced on a ward. 
  • Despite significant signs of deterioration and infection during their in-patient admittance at UHW, A’s condition was not given sufficient priority and there was a lack of urgency in making a diagnosis and ensuring that A was provided the correct treatment. 
  • The Board’s SAER did not adequately address and identify the failings in A’s care and treatment that occurred from their initial presentation. 
  • There had been a failure to meet the requirements of the Duty of Candour process.

Taking all of the above into account, I upheld all of C’s complaint.

In investigating this case it is of significant concern to me that that I issued an earlier critical public report into the gastroenterology service at UHW on 22 June 2022 (case reference 202001373).  In that report I was critical of the care and treatment the patient received from the gastroenterology service for PBC and other clinical issues.  In particular I found serious failings in identifying and treating the patient’s deteriorating liver disease between 2017 and 2018.  I am concerned that I have found similar failings over a similar timescale in this case.     

 

Recommendations 

The Ombudsman's recommendations are set out below:

What are we asking the Board to do for C:

Rec number What we found Outcome needed What we need to see
1

 

Under complaint point a) I found that there was a failure to investigate and/ or diagnose A’s condition. In particular I found that:

  1. there was a failure to make an appropriate and timely diagnosis;
  2. there was a failure to appropriately refer A to a specialist liver service/ transplant hepatologist at an early stage in their treatment;
  3. there were significant and sustained failures in the consideration, management and treatment of A’s deteriorating condition including a failure to take into account relevant guidance; and
  4. there were failures in communication and to adequately take into account A’s personal circumstances.

Under complaint point (b) I found that the  Board failed to provide A with adequate care and treatment as a patient in University Hospital Wishaw between 4 August 2019 and 8 August 2019. Specifically:

  1. there were failures in the management of A’s ascitic drain, steroid medication and constipation; and 
  2. there was a failure to trigger a medical review in light of A’s fall and a failure to follow relevant guidelines in the management of patients with decompensated liver disease. 

I also found that there were failures in the Board’s handling of C’s complaint and the subsequent Significant Adverse Event Review.

Apologise to C for the failings identified in this investigation and inform C of what and how actions will be taken to stop a future reoccurrence. 

The apology should meet the standards set out in the SPSO guidelines on apology available at www.spso.org.uk/information-leaflets

 

A copy or record of the apology.

 

 

We are asking the Board to improve the way they do things:

Rec number What we found Outcome needed What we need to see

2

 

complaint point a) I found that the there was a failure to investigate and/ or diagnose A’s condition. In particular I found that:

  1. there was a failure to make an appropriate and timely diagnosis;
  2. there was a failure to appropriately refer A to a specialist liver service/ transplant hepatologist at an early stage in their treatment; 
  3. there were significant and sustained failures in the consideration, management and treatment of A’s deteriorating condition including a failure to take into account relevant guidance; and  
  4. there were failures in communication and to adequately take into account A’s personal circumstances
  5.  

Patients showing signs of advanced liver disease should receive appropriate and timely care and treatment that is in line with relevant guidance

 

Evidence that the Board have arranged, as a matter of urgency, independent external audit of the treatment of patients by the gastroenterology outpatient service at UHW with PBC/ AIH or an overlap syndrome  from 2018 to date to ensure there is no systemic or individual issue which may have affected other patients

The audit should be completed independently by individual(s) with the appropriate experience and expertise

My office should be provided with an update on the progress of the audit. 

My office and the complainant should be informed of the results of the audit including all learning points and any required action plan to implement and share findings

Evidence that the findings of my investigation have been shared with relevant staff in a supportive manner for reflection and learning

Evidence that learning from these events and the external audit is reflected in policy guidance and staff training

 

3

Under complaint point b) I found that the Board failed to provide A with adequate care and treatment as a patient in University Hospital Wishaw between 4 August 2019 and 8 August 2019. 

Specifically there were failures in the management of A’s ascitic drain, steroid medication, and constipation. We also found that there was a failure to trigger a medical review in light of A’s fall and a failure to follow relevant guidelines in the management of patients with decompensated liver disease.   

Patients admitted to hospital showing signs of advanced liver disease should receive appropriate and timely care and treatment that is in line with relevant guidance

Evidence that:

My findings have been shared with staff in a supportive way for reflection and learning and to ensure similar mistakes are not made again; and

That the learning from these events and the external audit is reflected in policy/ guidance and staff training 

 

 

We are asking the Board to improve their complaints handling:

Rec number What we found Outcome needed What we need to see
4

 

I found that the Board’s complaint handling was unreasonable. Specifically:

  1. there was a failure to meet the requirements of the Duty of Candour process; and
  2. a failure to undertake a reasonable Significant Adverse Event Review that identified key learning and improvements

 

When an incident occurs that falls within the Duty of Candour legislation, the Board’s Duty of Candour processes should be activated without delay. 

Local and Significant adverse event reviews should be reflective and learning processes that ensure failings are identified and any appropriate learning and improvement taken forward.  Adverse event reviews should be held in line with relevant guidance.

 

Evidence that the Board have reviewed their Duty of Candour processes, including timescales for activating the process and;

Evidence that the Board have reviewed their process for carrying out adverse event reviews to ensure these reviews properly investigate, identify learnings and develop system improvements to prevent similar incidents occurring 

 

 

We are asking the Board for evidence of action already taken 

Rec number What we found Outcome needed What we need to see

5

 

Under complaint point c) I found that there was a failure to provide A with an appropriate level of dignity and person centred care on 4 August 2019. 

The Board said that they had reminded staff of the professional and caring manner they would expect from them at all times.

Evidence of the action taken. 

 

 

Feedback 

Points to note

As noted at paragraph 81, A should have been referred to a tertiary liver service/ transplant hepatologist within a few weeks of presentation. The failure to do so raises the question in my mind as to whether there is a sufficiently open and transparent culture that encourages clinical staff at all levels to identify when they may require internal or external specialist support in treating complex cases and that enables them to request this. I urge the Board to consider how they can support clinicians to identify and raise when they may require internal or external specialist support when providing care and treatment.

This report will be as difficult for staff to read, as it no doubt is for the family.  It is incumbent on the Board to ensure staff are supported and that it is clear to them that my findings reflect failures in systems that should have been there to support them.

 

  • Case ref:
    202204908
  • Date:
    May 2024
  • Body:
    Tayside NHS Board
  • Sector:
    Health
  • Outcome:
    Upheld, recommendations
  • Subject:
    Clinical treatment / diagnosis

Summary

C complained about the care and treatment provided to their parent (A) during an admission to hospital. At the time of admission, A was taking medication for atrial fibrillation (a heart condition affecting the rhythm and rate of the heart). The medication included a blood-thinner to reduce the risk of blood clots. While A’s condition was being assessed, a decision was made to withhold this medication. A developed pain and discolouration in their leg and was unable to weight bear. C complained that there was a delay of 12 hours before medical staff acted upon this. A required a transfer to another hospital by ambulance, where they underwent emergency surgery for clots in the leg. A has been left with deep incisions in the lower leg and their mobility has been significantly reduced.

The board discussed the case at a Morbidity and Mortality meeting, and following review of the circumstances did not think that there was anything from a system perspective that should be changed.

We took independent advice from a consultant physician and geriatrician (specialist in medicine of the elderly). We found failings in record keeping and examination. We found that the board ought to have been alert to the risk of A developing blood clots after the blood-thinning medication was withheld, and should have acted more promptly when A started to deteriorate. We considered that A suffered pain for a longer period because their deterioration was not recognised in a timely manner. Their situation might not have been so serious had their condition been recognised sooner. We also found that the board did not carry out a suitably rigorous analysis of what happened, including review by staff who were not involved in A’s care. The board’s review failed to identify appropriate learning. Therefore, we upheld C’s complaint.

Recommendations

What we asked the organisation to do in this case:

  • Apologise to C and their family for the failings our investigation has identified. The apology should meet the standards set out in the SPSO guidelines on apology available at www.spso.org.uk/information-leaflets.

What we said should change to put things right in future:

  • Before reaching a decision to stop anticoagulant medication in patients with atrial fibrillation, full consideration should be given to the risks and benefits of doing so. Clear records of patient care should be maintained, with all patient examinations documented. Deterioration in patients should be escalated appropriately including clinical examination where merited. Staff are confident in identifying adverse events and conducting appropriate reviews.

We have asked the organisation to provide us with evidence that they have implemented the recommendations we have made on this case by the deadline we set.

  • Case ref:
    202206802
  • Date:
    May 2024
  • Body:
    Scottish Ambulance Service
  • Sector:
    Health
  • Outcome:
    Not upheld, no recommendations
  • Subject:
    Failure to send ambulance / delay in sending ambulance

Summary

C complained about delays in ambulance response time after their elderly parent (A) had a fall at their care home. Care home staff called 999 and, following triage, the call generated an emergency but non-life-threatening response. A clinical triage call took place shortly after followed by another 999 call by care home staff. A paramedic response unit arrived at A’s location, followed by an ambulance. A arrived at hospital around 5 and a half hours after the first 999 call.

Scottish Ambulance Service (SAS) acknowledged that the wait for an ambulance was unreasonable and apologised to C for this. They explained that the delay was due to limited resource and very high demand at that time. C was unhappy with this response and brought their complaint to us. C felt that A was not prioritised fairly following the 999 and clinical triage calls. C considered this to be partly due to A’s age. Although SAS had already acknowledged that there was an unreasonable delay, we carried out an investigation to determine whether the assessment and prioritisation of the calls also contributed to that delay.

We took independent advice from a paramedic. We found that the non-clinical call handling was appropriate. We also considered that there was no indication that A was treated differently or unreasonably as a result of their age. Therefore, we did not uphold C’s complaint. However, we did provide feedback to SAS regarding an aspect of the clinical triage call which did not cause or contribute to the delay in an ambulance being provided, but was not in line with relevant national guidance.

  • Case ref:
    202207139
  • Date:
    May 2024
  • Body:
    Lothian NHS Board - Acute Division
  • Sector:
    Health
  • Outcome:
    Upheld, recommendations
  • Subject:
    Clinical treatment / diagnosis

Summary

C complained about the ear, nose and throat surgery (ENT) that they received from the board. C was referred for surgery for biopsy of a nasal ulcer that would not heal, and for treatment of a nasal drip. C complained that the biopsy had not been taken as expected, which they were not aware of until making a complaint. C also complained that they had been left worse off due to a perforation being caused during the procedure. This has caused them to have an audible whistling sound when they breathe. C said that, while the risk of perforation had been mentioned at the outpatient appointment, they were led to believe it was not something they had to worry about. Furthermore, they were not told that if it happened, it wouldn’t heal naturally, and surgery to fix it often fails.

The board explained that the biopsy had not been taken as the ulcer had healed by the time C attended for surgery. The board apologised for the perforation. They noted that the surgeon was not aware of one occurring before in their career but had since changed their practice to ensure it was discussed when obtaining consent.

We took independent advice from an ENT adviser. We found that C had not been reasonably consented for surgery at the outpatient clinic or on the day of surgery. We noted that the documentation did not support the reported discussions which took place about the surgery or the associated risks, or the implications should C have decided not to proceed with the procedure. We also found that the written information provided to C was unreasonable. The patient information leaflet did not provide information about the short and/or long-term implications of a perforation or that it may occur after the surgery has taken place. It did not note that it was unlikely to heal on its own, that surgery to correct it may not be an option or, if attempted, successful.

We considered that C had received reasonable post-operative care and follow-up from the board. It was reasonable to plan to see them back at 3 – 6 months, and for this to be expedited at the point of C reporting their concerns about the whistling noise that had developed. On balance, we upheld C’s complaint.

Recommendations

What we asked the organisation to do in this case:

  • Apologise to C for the failures identified in relation to the consent process for surgery. The apology should meet the standards set out in the SPSO guidelines on apology available at www.spso.org.uk/information-leaflets.

What we said should change to put things right in future:

  • Patients should be reasonably consented for surgery and this should be documented in the patient’s medical record and on the consent form for the planned procedure.
  • Patients undergoing septoplasty surgery should be given appropriate verbal and written information about the procedure. Risks and complications should be fully explained to allow patients to make an informed decision.

We have asked the organisation to provide us with evidence that they have implemented the recommendations we have made on this case by the deadline we set.

  • Case ref:
    202204112
  • Date:
    May 2024
  • Body:
    Lothian NHS Board - Acute Division
  • Sector:
    Health
  • Outcome:
    Not upheld, no recommendations
  • Subject:
    Clinical treatment / diagnosis

Summary

C complained about the care and treatment provided to their parent (A) on two separate admissions to hospital. A was detained on both occasions under the Mental Health (Care and treatment) (Scotland) Act 2003. C had concerns about A being sedated and that staff had restrained A in an inappropriate manner.

In their response to the complaint, the board explained the care provided to A, the reasons for the administration of medication, how this was overseen and adjusted to address A’s levels of sedation, and the process and performance of restraints when they were required. C was dissatisfied with the board’s response and brought their complaint to us.

We took independent advice from a consultant psychiatrist and a mental health nurse. We found that on both admissions, there was appropriate oversight of A’s medication and care was taken to consider sedative effects and find a balanced approach. We found that medications were administered appropriately to manage A’s distress and aggression. Therefore, we did not uphold this part of C’s complaint.

In relation to the use of restraints, we found that these had been performed reasonably and that A’s concerns about pain to their ribs was appropriately assessed. Therefore, we did not uphold this part of C’s complaint. However, we did provide the board with some feedback on the requirements for accurate record keeping.

  • Case ref:
    202108871
  • Date:
    May 2024
  • Body:
    Lanarkshire NHS Board
  • Sector:
    Health
  • Outcome:
    Upheld, recommendations
  • Subject:
    Clinical treatment / diagnosis

Summary

C complained about the care and treatment that their late parent (A) received whilst in hospital following a stroke. C said that the board failed to provide appropriate nutrition for A when they lost the ability to swallow. A required a percutaneous endoscopic gastrostomy (PEG) feeding tube to be fitted (a tube passed into the stomach through the abdomen to provide a means of feeding). However, there were delays with this and A died shortly after the procedure was carried out. C was concerned that other types of feeding were not considered by the board and that staff were not appropriately qualified to deliver alternative feeding.

The board said as soon as it became apparent that a PEG feeding tube would be appropriate, a referral was made to have this done. A dietician identified another method of feeding called TPN (a type of nutritional fluid administered to a patient intravenously) however, ward staff were concerned that they were not trained on how to deliver this method of feeding. As such, a decision was taken to expedite the referral to have the PEG tube fitted instead.

Before surgery could take place, A had to be tested for COVID-19. The results of the test were not back in time for surgery to be carried out on the day it was initially scheduled. The board apologised for the delay that this caused.

We took independent clinical advice from a consultant geriatrician (specialist in medicine of the elderly). We found that the clinical decisions made in the management of A’s nutrition were reasonable. TPN feeding is not typically used in cases like this one. The standard of care was in keeping with guidance and was of reasonable quality. However, the delay in receiving the results of the COVID-19 test, and the failure to expedite this, was unreasonable. This led to the delay in treatment. On balance, we upheld C’s complaint.

Recommendations

What we asked the organisation to do in this case:

  • Apologise to C for the delay in receiving the results of the COVID-19 test that led to a delay in A having a PEG tube fitted. The apology should meet the standards set out in the SPSO guidelines on apology available at www.spso.org.uk/information-leaflets.

What we said should change to put things right in future:

  • Obtaining the results of tests required before surgery should not be delayed. In cases where surgery is urgent, tests should be expedited where required to ensure that they are received timeously in order to avoid delays in the patient receiving surgery. When delays are experienced, the reasons for this should be noted in the medical records.

We have asked the organisation to provide us with evidence that they have implemented the recommendations we have made on this case by the deadline we set.

  • Case ref:
    202203466
  • Date:
    May 2024
  • Body:
    Highland NHS Board
  • Sector:
    Health
  • Outcome:
    Some upheld, recommendations
  • Subject:
    Clinical treatment / diagnosis

Summary

C complained about the care and treatment provided to their adult child (A) in relation to A’s pregnancy. A attended hospital on two occasions over a weekend with no fetal movement. The baby (B)’s heartbeat was considered normal on both occasions and A left the hospital with a plan to return on the Monday. On A’s return to hospital, an intrauterine death (when a child dies in the womb) was diagnosed. A requested to have their waters broken to relieve the pressure that they were experiencing. A ‘s labour was very quick and they delivered B in the toilet of the labour suite at the hospital. They called for a midwife to attend and assist them.

C complained that the hospital did not listen to their concerns for B to be delivered as an emergency. C and A believed that there was too much focus on B’s heartrate and that further investigations, including ultrasound, should have been undertaken. C also complained about the difficult circumstances of B being born in the toilet, and the care provided in the run up to, and following, labour.

In response to the complaint, and following the completion of a Significant Adverse Event Review (SAER), the board found no specific failings of care which led to B’s death. Monitoring of A and B was appropriate, and ultrasound scanning was not available over the weekend. The board noted that A had chosen to return home, rather than be admitted over the weekend which was against medical advice. The board explained that early delivery by caesarean section was not indicated given the clinical picture was reassuring. C and A met with representatives from the board following the complaints response where issues relating to the delivery of B were discussed. The board acknowledged that a midwife should have responded to A’s calls that they were delivering B in the toilet, and acknowledged that A should not have been in a labour ward where they could hear other mothers and healthy babies.

C was dissatisfied with this response and brought their complaint to us. They disputed the accounts of doctors that A was advised about the risks of going home during the weekend and remained of the view that more should have been done for A and B over the weekend.

We took independent advice from a GP who worked as an obstetric and gynaecology registrar (a specialist in pregnancy, childbirth and the female reproductive system) and a registered midwife. We found that appropriate advice was offered to A about the risks of returning home over the weekend, that the level of monitoring and assessment was reasonable and that the assessments were reassuring with respect to the health of A and B. Therefore, we did not uphold this part of C’s complaint.

In relation to the treatment provided to A during labour, we found that care in preparation for delivery of B was reasonable, with appropriate monitoring and pain relief provided. When A rushed to the toilet, given the recent examinations checking the progress of A’s labour, it was reasonable for midwifery staff not to consider A was about to give birth. However, there was a lack of documentation and records at the time of delivery and the immediate period before and after this which prevented our office from drawing conclusions about the level of care provided. Given the board’s acknowledgements that a midwife should have attended immediately to A when they called for help, together with the lack of appropriate record keeping during labour, and the accommodation in the labour suite being inadequately soundproofed, we upheld this part of C’s complaint.

Recommendations

What we asked the organisation to do in this case:

  • Apologise to A for the failures identified. The apology should meet the standards set out in the SPSO guidelines on apology available at www.spso.org.uk/information-leaflets.

What we said should change to put things right in future:

  • Clinical and midwifery staff should keep clear and accurate records, relevant to their practice, in line with the Nursing and Midwifery Council code.

We have asked the organisation to provide us with evidence that they have implemented the recommendations we have made on this case by the deadline we set.

  • Case ref:
    202203142
  • Date:
    May 2024
  • Body:
    Highland NHS Board
  • Sector:
    Health
  • Outcome:
    Not upheld, no recommendations
  • Subject:
    Clinical treatment / diagnosis

Summary

C complained about the care and treatment provided to their late spouse (A). A was admitted to hospital with a suspected small bowel incarcerated in the hernia (a part of the intestine that becomes trapped in the sac of a hernia). Following a CT scan and assessment by a surgeon, it was decided to treat A’s condition conservatively and transfer them to a larger hospital in the area. However, there was a delay in the transfer taking place due to a lack of ambulance resource and A’s condition deteriorated further during their admission. A died shortly after admission. C complained about the delay in transferring A to another hospital or operating on them sooner. In C’s view, A did not receive a reasonable standard of treatment or end of life care following their admission to hospital. In addition to this, C complained about the board’s communication with the family during A’s time in hospital.

We took independent advice from an emergency medicine consultant and a general and colorectal surgeon (specialist in conditions of the colon, rectum or anus). We found that the treatment provided by the board was reasonable. In light of A’s presentation, and without the benefit of hindsight, it was reasonable to treat A conservatively and arrange for a transfer to a better resourced centre. We also found that the end-of-life care provided to A was reasonable, given A’s rapid deterioration and the circumstances within the hospital at that time. Therefore, we did not uphold this part of C’s complaint.

In relation to the standard of communication with the family, taking into account A’s rapid deterioration and the circumstances within the hospital at the time, we concluded that communication was reasonable. Therefore, we did not uphold this part of C’s complaint.

  • Case ref:
    202110511
  • Date:
    May 2024
  • Body:
    Greater Glasgow and Clyde NHS Board - Acute Services Division
  • Sector:
    Health
  • Outcome:
    Not upheld, no recommendations
  • Subject:
    Appointments / Admissions (delay / cancellation / waiting lists)

Summary

C suffers from chronic pain and had been receiving pain management and musculoskeletal physiotherapy treatment from the board for many years. Changes were made in the board’s approach to pain management which coincided with some experienced consultants retiring. C’s care and treatment was reassessed and a number of treatments previously provided to C were said to no longer be available and an emphasis was placed on self-management. C complained that withdrawing treatments harmed their health and wellbeing, the local pain management service was now limited requiring patients to travel for certain treatments, effective interventions were removed, the board prioritised cost over patient needs, and the transition to self-management relied too heavily on online resources.

The board stated that the changes were evidence based and in line with clinical guidelines.

We took independent advice from an experienced pain management consultant. We found that the board were correct in stating that the current guidance for the management of chronic pain does not support the long-term use of massage, acupuncture or trigger point injections. We noted that the transition away from this approach towards self-management can be very challenging for patients. We considered that C had been offered a person-centred management plan. We also found that it was reasonable for the board to have explained to C that previous therapies offered in an ongoing sense were likely provided because of discretion and goodwill on the part of a now retired physiotherapist. We noted that this is not uncommon for practitioners, however, approaches to treatment change over time. We did not uphold C’s complaint. However we provided feedback about the need to reflect on cases such as this to inform how best to manage similar situations in the future.

  • Case ref:
    202206729
  • Date:
    May 2024
  • Body:
    Grampian NHS Board
  • Sector:
    Health
  • Outcome:
    Upheld, recommendations
  • Subject:
    Clinical treatment / diagnosis

Summary

C, a support and advocacy worker, complained on behalf of their client (A) about the care and treatment that A received from the board in relation to a planned gynaecology (relating to the female reproductive system) surgical procedure. Following a discussion with the operating consultant on the day of the surgery, A said that the planned procedure was changed from a keyhole subtotal hysterectomy (removing the main body of the womb and leaving the cervix in place) to a keyhole total hysterectomy (removing the womb and the cervix). A said that they felt they had been put under pressure to accept the operation, and did not understand the consequences of losing their ovaries.

A’s surgery was carried out at a private sector hospital by the board’s surgical team due to the board experiencing issues with theatre capacity at that time. During the operation, a complication occurred which caused A to bleed and the procedure was converted to an open procedure to manage the bleeding. Having complained about the matter, the board explained to A that an issue with equipment during the surgery meant that the correct equipment had not been available during the procedure. A complained to the board on two further occasions in order to gain more understanding about the complication and the issue with the equipment which had occurred during the operation. A felt that the board’s responses were contradictory and asked C to complain to this office on their behalf.

We took independent advice from a consultant gynaecologist. We found that there were failings in relation to the process of consent at both the pre-operative clinic and on the day of surgery. We also found failings in relation to the documentation of the operation, including the complication and the way this had been managed during the procedure, and in the equipment log of the surgical instruments used during the procedure. To manage the bleeding, we found that the choice of equipment used had been unreasonable, noting it was likely this would have caused further tearing and bleeding, as appeared to have happened in this case. We found that the post-operative communication with A had been unreasonable in relation to the explanation given regarding the complication, and in relation to the change of procedure and the implications of this on A’s future health. Therefore, we upheld C’s complaint.

Recommendations

What we asked the organisation to do in this case:

  • Apologise to A for the failings identified. The apology should meet the standards set out in the SPSO guidelines on apology available at www.spso.org.uk/information-leaflets.

What we said should change to put things right in future:

  • Operations should be carried out to a reasonable standard. Operation notes should provide a clear record of the procedure carried out and include relevant information about technique, and of significant findings and incidents and on the management of same.
  • Patients should be given complete and accurate information during the consent process for surgery to enable them to make informed decisions about the planned procedure. Discussions with patients should be fully documented in the medical record and include key areas of discussion in relation to the pros/cons of the procedure; the risks associated with the procedure generally; and with reference to any specific risks for the individual patient.
  • Post-operative communication with patients should be informative and transparent. The discussion should be documented in the medical record.
  • When significant failings become apparent via the complaint process, the board should commence an internal risk management review process, appropriate to the circumstances of the case.

In relation to complaints handling, we recommended:

  • Complaint responses should be clear and fully respond to the issues raised. This should include a full explanation of what occurred and a description of what happened and/or what should have happened at the time.

We have asked the organisation to provide us with evidence that they have implemented the recommendations we have made on this case by the deadline we set.