Prevention of Future Deaths reports · 2018

Kathleen Bamforth

Regulation 28 report to prevent future deaths, reference 2018-0247, written 20 Jul 2018. A coroner writes one of these when an inquest reveals a risk that could cause further deaths unless something changes.

Date of report20 Jul 2018
Reference2018-0247
DeceasedKathleen Bamforth
CoronerMartin Fleming
Coroner areaWest Yorkshire (West)
CategoryCommunity health care and emergency services related deaths
Organisation namedSouth West Yorkshire Partnership Teaching NHS Foundation Trust
Sourcejudiciary.uk record · original PDF
Responses published1

The report

Text recovered by OCR from a scanned PDF. OCR is imperfect: check anything you rely on against the source PDF. Reproduced verbatim, including the scan's own layout.

IN THE WEST YORKSHIRE WESTERN CORONER’S COURT
IN THE MATTER OF:

The Inquests Touching the Death of Kathleen Gabrielle Bamforth
A Regulation Report - Action to Prevent Future Deaths

THIS REPORT IS BEING SENT TO:
Secretary of State for Health and Social Care

CORONER
Martin Fleming HM Senior Coroner for West Yorkshire Western

CORONER’S LEGAL POWERS
I make this report under paragraph 7, Schedule 5, of the coroners and
Justice Act 2009 and regulations 28 and 20 of the Coroners
(Investigations) Regulations 2013

INVESTIGATION and INQUEST

On 24/8/17 I opened an inquest into the death of Kathleen Gabrielle
Bamforth who, at the date of her death was aged 59 years old. The
inquest was resumed and concluded on 12/6/18

I found that the cause of death to be: -

la. The effects of clomipramine Toxicity

I concluded with a narrative conclusion as follows:

On 28/5/17, Kathleen Gabrielle Bamforth, who had a history of
depression and alcohol misuse, was found to have died at her home
address. At post mortem her blood was found to contain fatal quantities
of her prescribed medication clomipramine (3.1 ug/ml) along with
therapeutic amounts of her prescribed naproxen (21.2ug/ml), tramadol
(0.87 ug/ml) and pregabalin (2.3 ug/ml. Although there is no evidence
to suggest that she took an overdose deliberately or inadvertently, the
reason for the toxicity of the clomipramine toxicity remains unclear

RT3589 1

4 | CIRCUMSTANCES OF THE DEATH

At approximately 5.40am 28/5/17, Kathleen Bamforth was found
unresponsive in the living room of her home address. Immediate
attempts were made to resuscitate her, but upon the arrival of the
paramedics she was confirmed to have passed away. She had been
prescribed clomipramine for several years by her GP which was being
properly monitored although the GP had no clinical cause to check the
levels by way of a blood test. During the inquest the
toxicologist gave evidence and he was unable to confirm whether the
toxicity was acute or chronic and that the circumstances of how she
developed the toxicity remained unclear.

5 | CORONER’S CONCERNS
The MATTER OF CONCERN is as follows. -—

e To review current practice guidelines with respect to the
prescription of clomipramine

e To consider the merits of routine blood screens in patients
prescribed with long term use of clomipramine.

6 | ACTION SHOULD BE TAKEN

In my opinion action should be taken to prevent future deaths and I
believe that Secretary of State for Health has the powers to do this.

7 | YOUR RESPONSE
You are under a duty to respond to this report within 56 days of its date; I
may extend that period on request.

Your response must contain details of action taken or proposed to be
taken, setting out the timetable for such action. Otherwise you must
explain why no action is proposed.

8. | COPIES
Ihave sent a copy of this report to:
South West Yorkshire Partnership NHS Foundation Trust

RT3589 2

8 | COPIES

Thave sent a copy of this report to:
— Husband
e Daughter
e Chief Coroner

e NHS England

9 | DATED this 20/7/18 HM Senior Coroner

(2 i Z C SS M.D. Fleming

RT3589 3

Responses

1 response published against this report on judiciary.uk. A response is a body's written reply to the coroner's concerns; publication is at the discretion of the Chief Coroner's office, so an absent response does not mean nobody replied.

Response from Department of Health (PDF)
From the Lord O'Shaughnessy
Parliamentary Under Secretary of State for Health (Lords)

. ~~ Department of Health
epartment 39 Victoria Street
of Health rondon
SW1H 0EU

Tel: 020 7210 4850

Mr Martin Fleming 13 SEP 2018
HM Senior Coroner, West Yorkshire (Western)

City Courts

The Tyrls

Bradford

BD1 1LA

Your reference: MDF-HK/1505-2017
Our reference: PFD 1143536

Thank you for your letter of 27 July to the Secretary of State for Health and
Social Care about the death of Ms Kathleen Gabrielle Bamforth. I am
responding as Minister with portfolio responsibility for medicines.

I was very saddened to read of the circumstances surrounding Ms Bamforth’s
death and have noted carefully the matters of concern raised in your report.

My officials have taken advice from the Medicines and Healthcare Products
Regulatory Agency (MHRA) and the National Institute for Health and Care
Excellence (NICE) on these matters.

On the matter of clinical guidelines, NICE has advised that its guidelines set out
the expectation that prescribers will use a drug's Summary of Product
Characteristics (SmPC), as well as the "British National Formulary’ (BNF) to
inform decisions made with individual patients.

Regarding the prescribing of clomipramine, the NICE guideline, ‘Depression in
adults: recognition and management’ (CG90), includes recommendations on
monitoring in relation to people taking tricyclic antidepressants (TCAs). The
guideline is available at: https://www.nice.org.uk/guidance/cg90.

Recommendation 1.5.2.4 discusses the need for healthcare professionals to
consider the specific cautions, contraindications and monitoring requirements
for drugs (including TCAs), and recommendation 1.5.2.9 states that people who
start on low-dose TCAs and who have a clear clinical response can be
maintained on that dose with careful monitoring.

Where a patient has other health conditions or other medications they are taking,
recommendation 1.5.2 states that healthcare professionals should discuss
antidepressant treatment options with the patient, covering the choice of
antidepressant, including any anticipated adverse events, such as side effects
and discontinuation symptoms, and potential interactions with other medications
they are taking for physical health problems.

This guideline is currently in the process of being updated by NICE and final
recommendations have not yet been confirmed. Draft recommendations went
out for second consultation earlier this year and are available from the NICE
website at: https://www.nice.org.uk/guidance/indevelopment/gid-
cgwave0725/documents. The draft includes updated recommendations
regarding monitoring (and evaluating) treatment adherences, and harms, with
regard to pharmacological treatment. For example, recommendation 1.4.6
states:

‘1.4.6 For interventions for people with depression:
e review how well the treatment is working with the person
e monitor and evaluate treatment adherence
e monitor for harms of pharmacological and psychological treatment
e consider routinely using validated sessional outcome measures. [2018] '

The draft recommendations may be subject to change following the
consultation. I am advised that the expected publication date for the final
guidance is yet to be confirmed.

I am also advised by the MHRA that clomipramine is known to be toxic in
overdose, particularly in relation to its cardiovascular effects (hypotension,
tachycardia, QTc prolongation and arrhythmia including Torsade de Pointes,
conduction disorders, shock, heart failure; in very rare cases cardiac arrest); and
neurological effects (somnolence, stupor, coma, ataxia, restlessness, agitation,
hyperreflexia, muscle rigidity, choreoathetosis, convulsions, serotonin
syndrome).

The SmPC for clomipramine includes warnings for prescribers about the
possible risk of QTc prolongation and Torsade de Pointes, particularly at supra-
therapeutic doses or supra-therapeutic plasma concentrations of clomipramine,

| ee

Department
of Health

as well as warnings about the risks of serotonergic toxicity and convulsions.
The SmPC also provides advice on drug interactions and other conditions which
may increase the risk of toxicity with clomipramine and advises measures to
take to reduce the risk of toxicity, including adherence to the recommended
doses of clomipramine and not exceeding the recommended daily dose.

In relation to the additional prescribed medication detailed in your report, the
clomipramine SmPC advises that concurrent use of clomipramine with drugs
that are substrates or inhibitors of cytochrome P450 2D6 is not recommended as
these drugs may increase the plasma concentration of clomipramine; opiates
(such as tramadol) are included in the list of examples of such drugs provided in
the SmPC. The SmPC for tramadol advises that tramadol can increase the
potential for TCAs to cause convulsions, and that concomitant use of tramadol
and TCAs may cause serotonin syndrome. Clomipramine is not recognised to
interact with the other prescribed medication in your report (pregabalin and
naproxen).

With regard to the long-term use of clomipramine, the SmPC recommends
monitoring cardiac and hepatic function during long-term therapy. Routine
blood screens to check clomipramine levels in these patients are not currently
recommended.

The SmPC and Patient Leaflet for clomipramine and tramadol are available in

full on the MHRA website at: http:/Avww.mbhra. gov.uk/spce-pil/.

The MHRA has confirmed that it is seeking advice from its independent
experts, who advise the Commission on Human Medicines, on the merits of
routine blood screens during long term use of clomipramine.

The MHRA aim to provide an update in October 2018. To assist with
consideration of this issue, it would be helpful to the MHRA if you could
provide a full redacted copy of your report into this case. This can be directed
to Jose Miyar, Vigilance and Risk Management of Medicines Division, MHRA,
10 South Colonnade, Canary Wharfe, London E14 4PU.

Please note that the MHRA has added this case to its adverse drug reaction
database under the Yellow Card reference number ADR 24338113.

fe ite enenian aegis oa, .
i$ TT SEP 2018

‘am

I hope this information is helpfui. Thank you for bringing your concerns to our
attention.

2 Sy

JAMES O’SHAUGHNES

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