Prevention of Future Deaths reports · 2021

Vinnie Dodds

Regulation 28 report to prevent future deaths, reference 2021-0249, written 20 Jul 2021. A coroner writes one of these when an inquest reveals a risk that could cause further deaths unless something changes.

Date of report20 Jul 2021
Reference2021-0249
DeceasedVinnie Dodds
CoronerDerek Winter DL
Coroner areaCity of Sunderland
CategoryChild Death (from 2015)
Organisation namedSouth Tyneside and Sunderland NHS Foundation Trust
Sourcejudiciary.uk record · original PDF
Responses published1

The report

Text extracted from the PDF text layer. Reproduced verbatim, including the scan's own layout.

Derek Winter DL 
Senior Coroner for the City of Sunderland 

REGULATION 28 REPORT TO PREVENT FUTURE DEATHS 

THIS REPORT IS BEING SENT TO: 

Secretary of State for Health and Social Care 

1 

CORONER 

I am Derek Winter DL, Senior Coroner for the City of Sunderland 

2 

CORONER’S LEGAL POWERS 

I make this report under paragraph 7, Schedule 5, of the Coroners and Justice Act 2009 
and regulations 28 and 29 of the Coroners (Investigations) Regulations 2013. 
http://www.legislation.gov.uk/ukpga/2009/25/schedule/5/paragraph/7 
http://www.legislation.gov.uk/uksi/2013/1629/part/7/made 

3 

INVESTIGATION and INQUEST 

On 20th August 2020 I commenced an Investigation into the death of Master Vinnie 
William Ord Dodds (Vinnie), who was born on 14th April 2020 and died in Sunderland 
Royal Hospital on the same day. 
The Investigation concluded at the end of the Inquest on 1st July 2021. The medical 
cause of death was confirmed as: - 

Ia Hypoxic Ischaemic Encephalopathy 
Ib Shoulder Dystocia 

4 

CIRCUMSTANCES OF THE DEATH 

Vinnie William Ord Dodds died at Sunderland Royal Hospital on 14th April 2020 when a 
major shoulder dystocia was recognised following a forceps delivery of his head. Appropriate 
manoeuvres were undertaken, and the birth was completed, but Vinnie could not be 
successfully resuscitated. 
I recorded a narrative conclusion Complications of childbirth. 

5 

CORONER’S CONCERNS 

During the course of the Inquest the evidence revealed matters giving rise to concern. In 
my opinion there is a risk that future deaths will occur unless action is taken. In the 
circumstances it is my statutory duty to report to you. 
The MATTERS OF CONCERN are as follows: – 
Although shoulder dystocia is a medical emergency for which staff are trained, it was the 
elements of the mother’s antenatal care which gave rise to concerns notwithstanding the 
obvious impact of the pandemic. 
The Trust carried out and acted on a full review. However, there are concerns of wider 

Civic Centre, Burdon Road, Sunderland, SR2 7DN 

www.sunderlandcoroner.co.uk 

         DX 60729 Sunderland 

 
 
 
 
 
 
         
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 significance: - 
1.  There is no national guidance for the management of large babies in pregnancy, 

unless diabetes is present, so it may not be possible to produce a safety 
recommendation to advise mothers with a suspected large baby. 
a)  should counselling/management be based on 'macrosomia' (i.e. weight estimated 
>4500g for diabetes and >5000g for non-diabetic) or alternatively should it now 
be applied to all babies estimated to be >90th centile by scan >34 weeks? 
b)  in counselling women about risk of shoulder dystocia in LGA, should this 

include formal mention of the rare risk of foetal death and if women are to be 
fully informed should this be balanced by the rare risk of maternal death with an 
elective Caesarean section (the only other mode of delivery to be considered)? 

c)  in fact, point b is highly relevant to counselling ALL women about the risks 
associated with shoulder dystocia and would be very useful to rationalise. 
2.  NICE in 2015 indicated a glucose tolerance test at 24-28 weeks. Should the optimum 

be at 26 weeks? 

3.  The risk of death from shoulder dystocia was not discussed and is not included in the 

current RCOG shoulder dystocia patient information leaflet (RCOG 2013). 

6 

ACTION SHOULD BE TAKEN 

In my opinion action should be taken to prevent future deaths and I believe you have the 
power to take such action. 

7 

YOUR RESPONSE 

You are under a duty to respond to this report within 56 days of the date of this report, 
namely by 14th September 2021. I, the Coroner, may extend the period. 

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

8 

COPIES and PUBLICATION 

I have sent a copy of my report to the Chief Coroner and to the following Interested 
Persons: - 
•  Family 
•  Care Quality Commission (CQC) 
•  Healthcare Safety Investigation Branch (HSIB) 
•  South Tyneside and Sunderland NHS Foundation Trust and their Solicitors 
•  Risk and Inquest Manager, South Tyneside and Sunderland NHS Foundation Trust 

I am also under a duty to send the Chief Coroner a copy of your response. 

The Chief Coroner may publish either or both in a complete or redacted or summary 
form. He may send a copy of this report to any person who he believes may find it useful 
or of interest. You may make representations to me, the Coroner, at the time of your 
response, about the release or the publication of your response by the Chief Coroner. 

9 

Dated this 20th July 2021 

Signature
Senior Coroner for the City of Sunderland

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 Dept of Health and Social Care (PDF)
From Maria Caulfield MP 
Parliamentary Under Secretary of State for Primary Care and Patient Safety 

39 Victoria Street 
London 
SW1H 0EU 

Mr Derek Winter DL 
HM Senior Coroner, City of Sunderland 
HM Coroner's Office 
Civic Centre 
Burdon Road 
Sunderland SR2 7DN 

    24 September 2021 

Dear Mr Winter, 

Thank you for your letter of 20 July 2021 to Sajid Javid about the death of Vinnie William 
Ord Dodds.  I am replying as Minister with responsibility for maternity care and patient 
safety.  

I would like to start by saying how very sorry I was to read the circumstances of the death 
of baby Vinnie.  I can appreciate how devastating his loss must be to his parents and all 
who loved him.  It is vitally important that we take the learning from Vinnie’s death to 
prevent future tragedies.  

In preparing this response, my officials have taken advice from NHS England and NHS 
Improvement (NHSEI), the National Institute for Health and Care Excellence (NICE), as 
well as the Royal College of Obstetricians and Gynaecologists (RCOG).  

NHSEI advise that there is currently a lack of evidence on the management of large babies 
in pregnancy (unless diabetes is present), In particular, it is not clear whether the 
incidence of shoulder dystocia can be reduced through inducing labour in women with big 
babies or whether it is better to wait for labour to begin naturally.  Progress in this area of 
maternity care should be more clearly informed when the results of the Induction of labour 
for predicted macrosomia – The ‘Big Baby Trial’1 are published in 2022/23 by the 
University of Warwick.  The purpose of the Big Baby Trial is to find out if starting labour 
earlier than usual, at 38 weeks, makes it less likely that shoulder dystocia will happen in 
women whose babies appear to be bigger than expected.   

1 Big Baby (warwick.ac.uk) 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
  
 
 
 
 
 NHSEI further advise that the General Medical Council (GMC) guidance on informed 
consent (2020)2 and the Montgomery Lanarkshire ruling3, describe using the ‘material 
facts’ to facilitate informed decision making.  This means that doctors must provide 
information about all material risks including any to which it would be reasonable for them 
to think the individual patient would attach significance.  In its guidance, the GMC advises 
that doctors must try to find out what matters to patients so that they can share relevant 
information about the benefits and harms of proposed options and reasonable alternatives, 
including the option to take no action. The GMC guidance also advises that doctors should 
tailor the discussion about potential benefits and harms to each individual patient, being 
guided by what matters to the patient and sharing information in a way they can 
understand. 

Under the NHS Long Term Plan, the Maternity Transformation Programme4 led by NHSEI, 
is committed to ensuring that all women have a Personalised Care and Support Plan in 
place, where the principle of fully informed consent is central.  A Personalised Care and 
Support Plan is a series of facilitated conversations in which the person actively 
participates to explore the management of their health and well-being within the context of 
their whole life and family situation, so that all considerations that might impact on safe 
care are accounted for.  The agreed personalised care and support plan is a live document 
that should reflect the decisions the woman makes about the care and support she wants 
to receive as she moves through her maternity journey.  Those decisions should be 
informed by the discussions she has with her healthcare professional about the benefits 
and harms of the evidence-based options available at each step on that journey.  

In addition, NHSEI advises that clinicians should use the RCOG patient information leaflet 
for Shoulder Dystocia5 during conversations where appropriate, which provides 
information about the balance of risks associated with shoulder dystocia and its 
management.  You may wish to note that the RCOG has advised my officials that an 
updated RCOG Shoulder Dystocia patient information leaflet has been commissioned, 
which will refer to the extremely low risk of death after shoulder dystocia.  

Turning to the specific matters of concern in your report, I am able to advise the following.   

On the matter of national guidance for the management of large babies in pregnancy, you 
will wish to note that NICE has made recommendations on large for gestational age babies 
in its clinical guideline on Intrapartum care for women with existing medical conditions or 
obstetric complications and their babies [NG1216]. 

2 Decision making and consent - GMC (gmc-uk.org) 

3 montgomery.pdf (rcog.org.uk) 

4 NHS England » Maternity Transformation Programme 

5 pi-shoulder-dystocia.pdf (rcog.org.uk) 

6 Overview | Intrapartum care for women with existing medical conditions or obstetric complications and their 
babies | Guidance | NICE 

 
 
 
  
  
 
 
 
 
 
 
 
 
 
 In this guideline, NICE recommends that healthcare professionals should:  

1.17.1 Explain to women in labour whose babies are suspected to be large for 

gestational age that: 
• 

it is sometimes difficult to be certain the suspicion is correct until the baby is 
born 

•  when making decisions about mode of birth (for example, vaginal birth or 
caesarean section), this uncertainty needs to be taken into account. 

1.17.2 Discuss with women in labour whose babies are suspected to be large for 

gestational age the possible benefits and risks of vaginal birth and caesarean 
section, including:  
•  higher chance of maternal medical problems such as infection with 

emergency caesarean section 

•  a higher chance of shoulder dystocia and brachial plexus injury with vaginal 

birth 

•  a higher chance of instrumental birth and perineal trauma with vaginal birth. 

Explain to the woman and her birth companion(s) what it might mean for her and 
her baby if such problems did occur. 

1.17.3 Offer women in labour whose babies are suspected to be large for gestational 

age a choice between continuing labour, including augmented labour, and 
caesarean section. 

I am informed by NICE that during the development of this guideline, NG121, NICE’s 
committee acknowledged that there is no standardised definition of large for gestational 
age and so did not specify this in its recommendations. 

In addition, NICE advises that there was no convincing evidence for one mode of birth 
over another for women in labour whose babies are suspected to be large for gestational 
age. The committee discussed the difficulty of estimating a baby's size when a woman is in 
labour and acknowledged that ultrasound is difficult to perform in labour and is less 
accurate at estimating a baby's weight than in the antenatal period.  As such, they agreed 
that women should be told about this uncertainty. 

Evidence showed an increased risk of maternal infection when women in labour had an 
emergency caesarean section.  In the committee's experience, there was a risk of 
shoulder dystocia and perineal trauma with vaginal birth and the committee agreed that 
women should be provided with information so that they can make their own decisions 
about mode of birth when their baby may be large for gestational age. 

It is the opinion of NICE that the guideline adequately covers the options and counselling 
that should be discussed with mothers with a suspected large baby. 

 
 
 
 
 
 
 
 
 
 
 
 NICE is currently consulting on an update to Clinical Guideline 70: Inducing labour7, and 
the evidence review of the induction of labour for suspected fetal macrosomia8.  The 
Guideline defines fetal macrosomia as “a fetus that is believed to be large for its 
gestational age, defined for the purposes of this guideline as an estimated fetal weight 
above the 95th percentile, at or after 36 weeks of pregnancy.” 

The aim of the evidence review was to determine if Induction of Labour for suspected fetal 
macrosomia at, or after, 35 weeks gestation, has benefits and reduces the risk of adverse 
outcomes for the mother and the baby, compared to expectant management.  The review 
looked at all women apart from those with treated diabetes (pre-existing or gestational).  
The review looked at the following outcomes; third/fourth degree tears; shoulder dystocia; 
perinatal death; hypoxic ischaemic encephalopathy; maternal satisfaction; brachial plexus 
injury; and, caesarean birth.  

The evidence review concluded that “suspected large for gestational age babies (or babies 
with suspected macrosomia) are at an increased risk of having difficult births. Preventing 
babies from getting too large by having an earlier birth may mitigate the associated risks, 
however the available evidence was not sufficient to recommend inducing labour and 
having an early birth over managing the pregnancy expectantly and waiting until birth 
started spontaneously.” 

The draft update to Clinical Guideline 70 currently states: 

Suspected fetal macrosomia  
Offer women with suspected fetal macrosomia, and without diabetes, the choice of 
induction of labour or expectant management after a discussion of the benefits and 
risks of both options. Discuss that: 

• 

• 

there is limited evidence that induction of labour could reduce the risk of shoulder 
dystocia  
there is very limited evidence that induction of labour could increase the risk of 
third- or fourth-degree perineal tears  
there is evidence showing no difference in the risk of perinatal death, brachial 
plexus injuries in the baby, or the need for caesarean birth between the 2 options 
•  Base the choice of care on the woman’s circumstances and her preferences and 
support her decision. Support recruitment into clinical trials, if available. (2021). 

• 

In relation to glucose tolerance testing, I am advised by NICE that National Guideline NG3, 
Diabetes in pregnancy, published in 2015 and last updated in December 2020, 
recommends that women who have had gestational diabetes in a previous pregnancy 
should be offered: 

1.2.6  For women who have had gestational diabetes in a previous pregnancy,  
         offer: 

7 1 (nice.org.uk) 

8 NICE Guideline Template 

 
 
  
  
 
 
 
   
 
 
 
 
 
 •  early self-monitoring of blood glucose or 
•  a 75-g 2-hour oral glucose tolerance test (OGTT) as soon as possible after booking 
(whether in the first or second trimester), and a further 75-g 2-hour OGTT at 24 to 
28 weeks if the results of the first OGTT are normal. 

Healthcare professionals should offer women with any of the other risk factors for 
gestational diabetes (outlined in recommendation 1.2.2) a 75-g 2-hour OGTT at 24 to 
28 weeks (recommendation 1.2.7).  NICE advises that it does not consider that there is 
sufficient evidence to make a recommendation for OGTT at 26 weeks. 

I am further advised by NHSEI that in clinical practice, glucose tolerance tests are routinely 
arranged to be performed at around 26 weeks gestation and that the 24-28 week 
recommendation allows some flexibility should there be a problem with the woman 
attending at exactly 26 weeks.  

I hope this response is helpful.  

MARIA CAULFIELD 

Minister for Primary Care

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