Coronial
VICother

Finding into death of Cherie Virginia Pearl Guest

Deceased

Cherie Virginia Pearl Guest

Demographics

61y, female

Coroner

Coroner Katherine Lorenz

Date of death

2018-08-18

Finding date

2023-06-22

Cause of death

Diffuse alveolar damage in a woman with restrictive lung disease following cataract surgery

AI-generated summary

A 61-year-old woman with severe restrictive lung disease, obesity, cardiac failure, and diabetes underwent cataract surgery at a private day surgery centre on 13 August 2018. She was unable to lie flat and became hypoxic (oxygen 60%) during the first part of the procedure. Despite this decompensation, the second part proceeded, requiring intubation for acute pulmonary oedema. She died five days later from diffuse alveolar damage. The coroner found the surgery was inappropriate at a day centre without critical care facilities for an ASA-4 (high-risk) patient. The surgeon failed to properly assess her fitness, the anaesthetist did not clearly refuse consent, and the hospital CEO failed to enforce admission criteria. Poor communication, inadequate monitoring, and lack of informed consent contributed to a preventable death.

AI-generated summary and tagging — may contain inaccuracies; refer to original finding for legal purposes. Report an inaccuracy.

Specialties

ophthalmologyanaesthesiarespiratory medicinecardiologyintensive care

Error types

diagnosticcommunicationsystemprocedural

Drugs involved

lidocaineinotropic medicationssedation agents

Clinical conditions

severe restrictive lung diseaseobesitykyphoscoliosiscongestive cardiac failurehypertensive heart diseasetype 2 diabetes mellitusnocturnal hypoventilation syndromeacute pulmonary oedemadiffuse alveolar damageacute respiratory distress syndromecommunity-acquired pneumoniacataractelevated intraocular pressure

Procedures

cataract surgeryfemtosecond laser cataract surgerycypass shunt insertionintubationarterial line insertion

Contributing factors

  • Patient not medically fit for surgery due to severe restrictive lung disease, obesity, kyphoscoliosis, cardiac failure, and diabetes
  • Failure to perform proper pre-operative multi-disciplinary assessment and optimisation
  • Surgery performed at inappropriate facility (private day surgery centre without critical care services) for ASA-4 patient
  • Surgeon failed to undertake own fitness assessment and ignored concerns from anaesthetist
  • Anaesthetist failed to clearly decline services and communicate risks to patient
  • Hospital CEO failed to enforce patient selection criteria policy excluding ASA-4 patients
  • Inadequate monitoring during procedure (no pulse oximeter provided by hospital)
  • Inadequate communication about decompensation during first stage of procedure
  • Failure to obtain informed consent regarding identified risks and option to stop second stage
  • Administration of medication (Xylocaine) against patient's expressed allergy concerns
  • Choice of femtosecond laser for first stage inappropriate for this patient

Coroner's recommendations

  1. The Royal Australian and New Zealand College of Ophthalmologists should review and strengthen guidance requiring ophthalmologists to undertake their own assessment of patient fitness for surgery, particularly regarding ability to lie flat and tolerance of general anaesthesia, and to properly consult with anaesthetists when concerns are raised.
  2. Ophthalmologists should not rely on employee-conducted 'trial runs' without proper medical supervision as adequate assessment tools for surgical fitness.
  3. Day surgery centres should rigorously enforce patient selection criteria policies and not admit patients outside accepted parameters regardless of pressure from surgeons.
  4. Anaesthetists in elective procedures should clearly communicate fitness concerns to both surgeon and patient, and should not make themselves available as 'back up' when they have determined a patient is not fit for the procedure; instead they should withdraw services.
  5. All surgical teams should ensure clear communication and monitoring during procedures, particularly regarding patient deterioration, and establish unambiguous roles and responsibilities for all participants.
  6. Informed consent processes must include discussion of material risks identified by any member of the treating team, options to proceed or decline, and potential consequences of deterioration.
  7. Hospitals should ensure appropriate monitoring equipment is available and used during procedures for at-risk patients.
  8. Root cause analyses and sentinel event reviews should be transparent, factually accurate, and include family involvement to improve understanding of adverse events and prevent recurrence.
Full text

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