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Royal College of

Obstetricians and

Gynaecologists

•Setting standards to improve women’s health









•Risk Management and Medico-Legal Issues In Women’s Health

•Joint RCOG/ENTER Meeting









•Please turn off all mobile phones and pagers

How can we reduce stillbirth rates

in diabetic pregnancies?





Jo Modder

CEMACH Clinical Director (Obstetrics)

Consultant Obstetrician UCLH NHS Trust

What is a diabetic pregnancy?



• Pregnancy in a woman with pre-existing

diabetes



• Either type 1 or type 2 diabetes that had

been diagnosed at least 1 year before the

woman’s estimated delivery date (EDD)

CEMACH 2005

What is the stillbirth rate in diabetic

pregnancies?

Type 1 diabetes



Type 2 diabetes

35 31.7 32.3

30 29.2 England, Wales &

25.

Northern Ireland

25 8 (2002)

20

15

8.5 9.6 9.5

10

5.7

5 3.6

0



Stillbirth rate* PNMR* Neonatal death

rate**

*per 1000 total births **per 1000 live births

† Source: Confidential Enquiry into Maternal and Child Health: Pregnancy in women with type 1

and type 2 diabetes in 2002-03, England, Wales and Northern Ireland. CEMACH: London; 2005.

Possible mechanisms for stillbirth





↑ maternal ↑ fetal

↑ fetal insulin

blood glucose blood glucose









↓ O2 release ↑O2 ↑ fetal basal

from RBC Consumption metabolic rate







Fetal hypoxia

Fetal Fetal

polycythaemia thrombosis









↑ maternal

↑ lactate

blood glucose







↓fetal pO2 ↓fetal pH

Current interventions to

reduce stillbirth rate



• Good glycaemic control

– Early booking

– Frequent antenatal visits

– Multidisciplinary team

• Fetal surveillance

– Frequent ultrasound scans

• Delivery between 38 – 40 weeks

The CEMACH national enquiry

• National survey of diabetes maternity services

• Descriptive study of 3808 pregnancies to women

with diabetes

• Panel enquiry into 442 + 79 additional type 2

pregnancies

– Audit of care

– What factors associated with poor

pregnancy outcome?

– Comparison of type 1 and type 2 diabetes

Causes of stillbirth and neonatal death

Extended Enquiry General p-value

Wigglesworth classification (N=98) maternity

(N=5756)

Congenital defect 18% 19% 0.68



Unexplained antepartum death 59% 44% 0.002



Death from intrapartum causes 10% 8% 0.30



Immaturity 4% 18% 90th centile

Issues underlying suboptimal fetal

monitoring for big babies (n=58)



• Lack of timely follow-up

• Poor interpretation of ultrasound scans

• Incorrect actions taken as a response to

tests

Maternity care factors associated

with death from 20 weeks



Cases Controls ORa [95% CI]





No discussion of mode 12% 2% 5.9 (1.7 – 20.7)

and timing of delivery†

Suboptimal maternity 76% 44% 4.2 (2.3 – 7.4)

care during the

antenatal period

a Adjusted for maternal age and social deprivation

† for women who delivered from 24+0 weeks only

Issues identified by panels underlying

suboptimal maternity care in the antenatal

period



• Suboptimal fetal surveillance

• Poor management of maternal risks

• Problems with the multidisciplinary team

• Need for more senior obstetrician input

• Poor communication between health

professionals

• Inappropriate mode and/or timing of delivery

Discussion of mode and

timing of delivery



• Median 35 weeks (range 5 – 40 weeks)



• Women who did not have a discussion

delivered earlier than those who had a

discussion (median gestation at delivery 35

versus 37 weeks).

Current interventions to

reduce stillbirth rate



• Good glycaemic control

– Early booking

– Frequent antenatal visits

– Multidisciplinary team

• Fetal surveillance

– Frequent ultrasound scans

• Delivery between 38 – 40 weeks

Could we reduce the

stillbirth rate further by:



• Consistent provision of consistent

preconception care?

– Folic acid

– Contraception

– Glycaemic control

– Education of health professionals

Could we reduce the

stillbirth rate further by:



• Consistent provision of maternity care?

– Careful antenatal fetal surveillance

– Identification and management of maternal

risk factors

– Senior obstetrician input into management

– Effective diabetes antenatal multidisciplinary

team

– Good communication?

Questions to be answered



• How can we improve the provision and

uptake of preconception care in the UK?

• What test/s can be used to predict the

fetus of a woman with diabetes who is at

risk of intrauterine death?

• At what gestation should babies of diabetic

mothers be delivered?

• CEMACH recommendations

• NICE Diabetes in Pregnancy guideline

Thank you

www.cemach.org.uk

Royal College of

Obstetricians and

Gynaecologists

•Setting standards to improve women’s health









•Risk Management and Medico-Legal Issues In Women’s Health

•Joint RCOG/ENTER Meeting









•Please turn off all mobile phones and pagers

A DOUBLE BLIND RANDOMISED CONTROLLED TRIAL COMPARING THE

EFFICACY OF INTRAMUSCULAR SYNTOMETRINE AND INTRAVENOUS

SYNTOCINON, IN PREVENTING POST PARTUM HAEMORRHAGE



Mohammed Rashid, Medical Student, Imperial College

Dr Mumtaz, Consultant O&G, James Paget Hospital, Norfolk









Abstract Presentation

Risk Management Conference April 2008

Introduction

• Post partum haemorrhage (PPH) remains the leading

cause of maternal death in the developing world,

accounting for 25-33% of all maternal deaths1

• The most common cause of PPH is uterine atony2

• Prevention of PPH is of great importance in the

pursuit of improved health care for women, even

more so in developing countries where parity, and

therefore the risk of uterine atony, is higher

Existing Knowledge

• Routine prophylactic administration of an oxytocic

during the third stage of labour reduces the risk of

PPH by 40%3

• In the UK and Ireland, intramuscular syntometrine is

most commonly used, while in the rest of Europe,

the USA and Canada, syntocinon is most commonly

used4

• But which is better?

• This study is the first randomised controlled trial

comparing intramuscular syntometrine and

intravenous syntocinon in a population group that

included high risk women.

Method

• Study done in a high risk population in the Gulf

• Patients who were seen in the obstetric clinic at 36

weeks of gestation were invited to participate in the

trial

• Strict inclusion/exclusion criteria

• 686 patients were randomly allocated to receive

either one vial of intramuscular syntometrine or 10

units of intravenous syntocinon

• Each patient received their allocated drug with the

delivery of the anterior shoulder of the baby

Outcome measures

• The primary outcome measure was the amount of

blood loss during delivery

• Secondary outcome measures included other

indicators of blood loss and possible side effects

Quick look at demographics

• 340 women received intramuscular syntometrine

and 346 women received intravenous syntocinon

• 37% of maternities were para four or above, 27%

were para five or above, 16% were para six or above

and the highest parity was thirteen.

Results

Primary outcome measure





Syntometrine Syntocinon Size of estimated 95% CI

n = 340 n = 346 difference*

Average 245.74 (135.86) 248.41 (124.03) 2.68 (-16.82,22.17)

Blood loss p = 0.7877

during

delivery (ml)

Postpartum 8 (2.35) 9 (2.60) 0.90 (0.35,2.32)

haemorrhages p = 0.834

(> 500 ml)

Post partum 6 (1.76) 8 (2.31) 0.76 (0.27,2.18)

haemorrhages p = 0.612

(> 1000 ml)

* The size of the estimated difference is the difference in means for the continuous outcomes and the

relative risk for the binary outcomes

Results

Secondary outcome measures



• There was an increase in the incidence of having a

diastolic blood pressure of between 90 and 100,

thirty minutes after the delivery (p=0.004), with

intramuscular syntometrine

Discussion

• In higher parity women, the myometrium is gradually

replaced by more and more fibrous tissue.

Syntocinon contracts the myometrium, but has little

effect on fibrous tissue thus theoretically making it

less effective in such women, however this was not

supported by our study

• The superior effect of intravenous syntocinon

compared its intramuscular counterpart may be

related to the earlier onset of action expected when

using an intravenous administration

Discussion continued

• The increased incidence of having diastolic

hypertension was demonstrated (>90 mm Hg thirty

minutes after delivery) in the syntometrine group,

was supported by findings in other studies5,6 and is

thought to be due to the vasoconstriction effect of

syntometrine

Strengths and Weaknesses

+ The researchers, the patients and the midwives were

blinded

+ Midwives were carefully instructed on how to

properly measure blood loss

+ Every measurement was repeated

- Visual estimation of blood loss is known to be

inaccurate

Conclusion

• Intramuscular syntometrine and intravenous

syntocinon are equally effective in preventing

postpartum haemorrhage, in a high risk population.

There is an increased risk of diastolic hypertension

after the delivery with intramuscular syntometrine.

References

1. Duffy S. Global perspective Obstetric haemorrhage in Gimbie, Ethiopia. TOG 2007;9:121-

126.

2. Lewis, G. The Confidential Enquiry into Maternal and Child Health (CEMACH) ‘Saving

mother’s lives: Reviewing maternal deaths to make motherhood safer’-2003-2005. The

seventh report on Confidential Enquiry into Maternal Deaths in the United Kingdom.

2007, London. CEMACH.

3. Prendiville WJ, Elbourne D, McDonald S. Active versus expectant management in the third

stage of labour. Cochrane Database Syst Rev 2003:CD000007.

4. Winter C, Macfarlane A, Deneux-Tharaux C, Zhang WH, Alexander S, Brocklehurst P,

Bouvier-Colle MH, Prendiville W, Cararach V, van Roosmalen J, Berbik I, Klein M, Ayres-

de-Campos D, Erkkola R, Chiechi LM, Langhoff-Roos J, Stray-Pedersen B, Troeger C.

Variations in policies for management of the third stage of labour and the immediate

management of postpartum haemorrhage in Europe. BJOG 2007;114(7) :845-54.

5. Choy CMY, Lau WC, Tam WH, Yuen PM. A Randomised controlled trial of intramuscular

syntometrine and intravenous oxytocin in the management of the third stage of labour.

BJOG 2002;109 (2):173-177.

6. Khan G Q, John I S, Chan T, Wani S, Hughes A O, Stirrat G M. Abu Dhabi third stage

trial: oxytocin versus Syntometrine in the active management of the third stage of labour.

Eur J Obstet Gynecol Reprod Biol 1995; 58(2):147-51.

Questions & Answers



Thank you for listening

Flowchart

Recruitment Statistics

Total number of deliveries in 6950

the hospital

Number of women delivered 686

within the trial

Number of women delivered 5095

not in the trial

Number not fulfilling the 2021

criteria

Number who refused 870



Language barrier 2104

Characteristics of the study population

Syntometrine Syntocinon

n = 340 n = 346

Age in years 29.43 (5.64) 29.17 (6.41)

Gestation at delivery (weeks) 39.25 (1.14) 39.43 (1.08)



Nulliparity 56 (16.47) 59 (17.05)

Average parity 3.03 (2.40) 3.03 (2.47)

Parity of 4 or more 91 (26.77) 97 (28.52)

Previous Caesarean Section (1 missing) 28 (8.26) 30 (8.67)



Previous manual removal of placenta 7 (2.06) 7 (2.02)





Spontaneous onset of labour 280 (82.35) 296 (85.55)





Augmentation with Syntocinon 198 (58.24) 189 (54.62)





Spontaneous vaginal delivery 319 (93.82) 322 (93.06)





Episiotomy 39 (11.47) 47 (13.58)

Genital tract trauma 189 (55.59) 192 (55.49)

Instumental Delivery 319 (93.82) 322 (93.06)

Birthweight (g) 3230.33 (445.33) 3247.56 (442.25)





Values are shown as mean (standard deviation) or n (%)

Primary outcome measures



Syntometrine Syntocinon Size of estimated 95% CI

n = 340 n = 346 difference*



Average Blood 245.74 (135.86) 248.41 (124.03) 2.68 (-16.82,22.17)

loss during p = 0.7877

delivery (ml)







Postpartum 8 (2.35) 9 (2.60) 0.90 (0.35,2.32)

haemorrhages p = 0.834

(> 500 ml)





Post partum 6 (1.76) 8 (2.31) 0.76 (0.27,2.18)

haemorrhages p = 0.612

(> 1000 ml)





* The size of the estimated difference is the difference in means for the continuous outcomes and the

relative risk for the binary outcomes

Sub-group analysis of blood loss during

delivery by parity



Syntometrine Syntocinon

n = 340 n = 346

Parity p = 0.0074



0–1 287.48 250.27 (112.72) p = 0.0478

(160.74)

2 -5 233.66 246.44 p = 0.3318

(118.57) (126.78)

>5 200.88 250.847 p = 0.0329

(109.99) (137.24)

Other indicators of blood loss

Syntometrine Syntocinon Relative risk 95% CI

n = 340 n = 346

Duration of third 5.90 (4.75) 6.14 (8.24) -0.24 (-0.78,1.24)

stage p = 0.651

Prolonged third 4 (1.18) 3 (0.87) 1.36 (0.31,6.02)

stage p = 0.249

(greater than

30 minutes)

Repeated 35 (10.29) 34 (9.83) 1.05 (0.67,1.64)

syntocinon p = 0.839

Post delivery 10.86 (1.32) 10.86 (1.38) -0.01 (-0.21,0.20)

haemoglobin p = 0.9490

Blood transfusion 6 (1.76) 2 (0.58) 3.05 (0.62, 15.02)

needed p = 0.148

Secondary PPH 0 1 - 1.000

Blood pressure

Syntometrine Syntocinon Relative risk 95% CI

n = 340 n = 346

Immediately after delivery



SBP > 140 24 (7.06) 30 (8.67) 0.81 p = 0.433

(0.49,1.36)

SBP > 150 2 (0.59) 4 (1.16) 0.51 p = 0.425

(0.09,2.76)

DBP > 90 7 (2.06) 10 (2.89) 0.71 p = 0.484

(0.27,1.85)

DBP > 100 0 0 - -

30 minutes after delivery



SBP > 140 9 (2.65) 12 (3.47) 0.76 p = 0.532

(0.33,1.79)

SBP > 150 4 (1.18) 3 (0.87) 1.36 p =0.687

(0.31,6.02)

DBP > 90 15 (4.41) 3 (0.87) 5.09 p = 0.004

(1.49,17.42)

DBP > 100 0 0 - -

Other side effects

Syntometrine Syntocinon Relative risk 95% CI

n = 340 n = 346

Headache 2 (0.59) 2 (0.58) 1.02 p = 1.000

(0.14, 7.18)

Nausea 12 (3.53) 10 (2.89) 1.22 p = 0.670

(0.53,2.79)

Vomiting 4 (1.18) 1 (0.29) 4.07 (0.46,36.23( p = 0.213



Chest pain 2 (0.59) 3 (0.87) 0.68 p = 1.000

(0.11,4.03)

Shortness 0 0 - -

of

breath

Manual 0 1 (0.29) - p = 1.000

removal

of

placenta

Royal College of

Obstetricians and

Gynaecologists

Setting standards to improve women’s health









Risk Management and Medico-Legal Issues In Women’s Health

Joint RCOG/ENTER Meeting









Please turn off all mobile phones and pagers

Audit of decision to delivery interval for

emergency caesarean sections in 2007







Michelle Judd

Consultant Obstetrician

rural location

Bury St Edmunds

market town

2500 deliveries per year

25% CS rate

Aims and objectives

 To ensure that the urgency of an emergency CS is

documented in a standardised way



 To use timing standards which have been agreed

between obstetric and anaesthetic staff



 To review decision to delivery interval for all

emergency CS



 Required audit for the unit’s CNST Level 3

assessment

Audit standards

CS Indication Decision to delivery

grade interval (minutes)

1 Immediate threat to life of 30

woman or fetus



2 Maternal or fetal compromise, 60

not immediately life threatening



3 Needing early delivery but no To be delivered within

maternal or fetal compromise an acceptable time



4 Elective cases Booked on elective CS

lists

Audit method

 Review decision to delivery interval for all emergency

CS

 Data collected monthly using emergency CS diary

 Diary recorded

– Reason for CS

– Grade of CS

– Decision time for CS

– Time of delivery

 Results presented at monthly Clinical Governance

meetings

Emergency CS decision to delivery interval

% standard achieved in 2007





100

90

80

70

60

50 grade 1 CS

40 grade 2 CS

30

20

10

0

J F M A M J J A S O N D

Audit results -Standards achieved for 2007





Grade 1 CS – target achieved 98%

Grade 2 CS – target achieved 78%

Grade 3 CS – target achieved 100%

Results: reason for delay

Reason for delay No. %

Anaesthetic difficulty 12 24

Surgical difficulty 3 6

Delay in transfer to theatre 15 28

Another obstetric case in theatre 12 24

Lack of staff/awaiting arrival staff 6 11

Patient needed time to make decision 2 4

Unknown (notes missing) 1 2

Results: length of delay

Delay Anaesthetic Delay in Other obstetric Other

(min) problem transfer to case in theatre causes

theatre

1-10 4 11 4 6



11-20 5 2 - 2



21-30 2 - 1 2



>3060 - - 4 -

Results: length of delay

Delay (minutes) Number %

1-10 25 49

11-20 9 18

21-30 5 10

>3060 4 7

Summary of delays

 Anaesthetic difficulties

– Unavoidable delay

– Most related to maternal obesity

– Use of regional anaesthesia is safest option

 Delay in transfer to theatre

– Avoidable delay

– CDS Coordinator to be responsible for timely transfer to

theatre

 Lack of obstetric theatre

– Avoidable delay

– Feasibility of providing another theatre when there is a

second obstetric emergency

BMI at booking appointment

BMI Midwifery-led care Consultant-led care



18.5-24.9 56% 40%



25-29.9 30% 20%



30-34.9 7% 20%



35 or greater - 10%



Not recorded 7% 10%

Summary of delays

 Anaesthetic difficulties

– Unavoidable delay

– Most related to maternal obesity

– Use of regional anaesthesia is safest option

 Delay in transfer to theatre

– Avoidable delay

– CDS Coordinator to be responsible for timely transfer to

theatre

 Lack of obstetric theatre

– Avoidable delay

– Feasibility of providing another theatre when there is a

second obstetric emergency

….and finally



 Level 1 CNST in March 2004



 Level 2 CNST in March 2006



 Level 3 CNST in January 2008

Royal College of

Obstetricians and

Gynaecologists

Setting standards to improve women’s health









Risk Management and Medico-Legal Issues In Women’s Health

Joint RCOG/ENTER Meeting









Please turn off all mobile phones and pagers

National Maternity Hospital Dublin









Postpartum Urinary Retention

R.C.O.G. Risk Management & Medico Legal

Issues in Woman’s Health

30th April 2008



M. Jacob MSc BSc RGN RCN RM FFNMRCSI

Midwife Prescriber



29 November 2011 71

Definition of Postpartum Urinary Retention





 No uniform definition exists

 Has been classified into ‘overt’ or ‘covert’

categories

Rane and Frazer, (1999) 0bs &Gynae 1 (4): 311-313









29 November 2011 72

Overt Retention



Is the inability to pass urine within six hours

after delivery requiring catheterisation with

removal of a volume equal to or greater than

normal bladder capacity



Rane and Frazer (1999) 0bs &Gynae 1 (4): 311-313









29 November 2011 73

Covert Retention



 More difficult to define



 Clinically can be described as failure of the bladder

to empty properly where a catheter yields at least

50% of normal bladder capacity or a post void

residual bladder volume of 150 ml

Yip et al., (1998) Effect of duration of labour on postpartum post void residual

bladder volume (Gynaecol Obstet Invest 45, 3: 177-180)









29 November 2011 74

Consequences of Postpartum Urinary

Retention







 In short term, may lead to atonic bladder

and infection if not identified and relieved

Page (2005)









29 November 2011 75

Consequences of Postpartum Urinary

Retention



Single episode of bladder over-distension

(Not diagnosed and treated early may cause

persistent postpartum urinary retention and

irreversible damage to the detrusor muscle

with recurrent urinary tract infections and

permanent voiding difficulties

Hinman, 1976; Versi, 1987; Mills, 1998)







29 November 2011 76

Pathophysiology



 Poorly understood

 Nervousness, modesty & similar factors causing

inhibition by the CNS.

 Unnatural posture

 Lack of elasticity of bladder

 Injury, swelling of vulva, urethra and bladder trigone.

 Reflex spasm of external urethral sphincter from

tears & incisions in perineum.

 An unspecified temporary derangement of the

neuromuscular mechanism of bladder & urethra

Francis, W.J. J. Obstet Gynaecol Br. Emp (1960) 67: 353-366.

29 November 2011 77

Pathophysiology



 Hormones and contractile responses of bladder –

hormone-responsive organ & functions may be

subjected to fluctuations of hormones during

pregnancy & postpartum period.

 Injured bladder innervation – urinary retention

occurs when neurological lesions occur below the

spinal reflex arc, at or below the level of the outlet of

sacral nerves – hypotonic or acontractile bladder.

 Pudendal nerve, with afferent nerve branches (S2-4)

supplying the bladder is damaged during pelvic

surgery & vaginal delivery – 1st pregnancy

significant pelvic floor tissue stretching & pudendal

nerve damage.

29 November 2011 78

Yip et al. (2004) Acta Obstet Gynecol Scand 83: 881-891

Literature Review





 Dearth of studies



 Limited urodynamic studies in women

following postpartum urinary retention



 Bladder remains a largely neglected organ





29 November 2011 79

Literature Review



 Voiding dysfunction after delivery 10-15% (Bennets,

1941)







 Positive correlation between epidural

anaesthesia and postpartum urinary retention

irrespective of the mode of delivery (Weil et al., 1983;

Tapp et al., 1987; Yip et al., 1997)









29 November 2011 80

Literature Review

 Urinary retention occurred in about 0.05% of pts.

could last as long as 30 – 40 days (Watson, 1991)

2 pts had prolonged urinary retention 10-15

days. 1 pt had persistent urgency, frequency and

strenuous voiding 9 months postpartum

(Watson,1991).







 43% women abnormal postpartum voiding (Ramsay

& Tarbet, 1993)









29 November 2011 81

Literature Review



 Voiding difficulties during labour and in

immediate postpartum period could be

associated with epidurals.

 Early resort to ultrasound scan & supra pubic

catheter to estimate the residual volume

Kulkarni R, Bradford WP, Forster SJ, James ED (1994) Aust N Z J Ostet Gynaecol

34 (1): 107-8









29 November 2011 82

Literature Review



 4 patients with prolonged postpartum urinary

retention who had U.D.S. 1 month after the

symptoms of retention ceased, 1 pt had S.U.I.

and 1 pt had urgency & urge incontinence (Groutz et

al. 2001)





 Increased use of epidural analgesia and

instrumental deliveries (Ching Chung et al. 2002; Carey, 2002)







29 November 2011 83

National Survey for Intrapartum &

Postpartum Bladder Care U.K.



 189 maternity units in England and Wales hospitals

 Findings: Majority of units were non-compliant with

limited RCOG recommendations.

 All units should be timing & measuring the voided

volume and ideally checking first post-void residual

volume.

 Further research needed to develop evidence-

based guidelines.

Zaki M., Pandit M., Jackson S. (2004) British Journal Obst & Gynae 111 (8):

874-6.

29 November 2011 84

Use of epidural anesthesia and risk of acute

postpartum urinary retention

 Sample – 2,000 women delivered at 3 primary

hospitals.

 Findings: APUR may lead to serious short term and

long term problems – changes in detrusor

contractility and increased incidence of lower or

upper U.T.I.s.

 Increased risk for APUR - prolonged 2nd stage

labour, instrumental delivery, perineal damage or

use of narcotics during delivery.

 Risk of developing APUR after epidural analgesia

during labour may increase by up to 3-fold

29 November 2011 85

Musselwhite et al., 2007 Am J Obstet Gynaecol)

Acute Postpartum Urinary Retention in Calgary

Health Region’s Policy & Procedures





 Need for at least 1 catheterisation within first 24

hours postpartum



 Patient did not void within 6 hours postpartum.



 Voiding frequently in small amounts.



 Urge to void but unable to do so

Musselwhite et al., 2007 Am J Obstet Gynaecol)



29 November 2011 86

Background







 Large numbers of clinical incident report

forms relating to urinary retention



 Add to the body of knowledge already

existing on the subject of urinary retention



29 November 2011 87

Definition of Clinical Audit





 A quality improvement process that seeks

to improve patient care and outcomes

through systematic review of care against

explicit criteria and the implementation of

change



National Institute for Clinical Excellence (2002) Principles for Best Practice in Clinical

Audit.



29 November 2011 88

Results of NMH audit of patients with postpartum

urinary retention (volumes >1,000ml)







Action research cycle methodology

Retrospective medical records review of women

March 2006 – April 2007

Data recorded

Parity, birth weight, type of delivery, epidural,

bladder scan, Foley catheter, residuals,

supra pubic catheter, time post delivery,

intermittent self catheterisation.



29 November 2011 89

Action Research Cycle

Coughlan, D. & Brannick, T. (2001) Doing Action Research in Your Own Organisation.

Sage pg 17







Diagnosing









Evaluation Planning Action









Taking Action







29 November 2011 90

NMH audit of patients with postpartum

urinary retention





 Total sample 91 – 3 pts without epidural

 11 patients had second Foley Catheter

 3 patients had Supra Pubic Catheter

 1 patient required intermittent self

catheterisation







29 November 2011 91

Birth Weight Range



Drop Page Fields Here

Total









Count of BW Range (g)

45





40





35





30





25 Drop Series Fields Here



Total

20





15





10





5





0

2500 - 2999 3000 - 3499 3500 - 3999 4000 - 4449 4500 - 4999 Unknow n (blank)

Number





BW Range (g)







29 November 2011 92

Parity



Drop Page Fields Here

Total









Count of Parity

60







50







40





Drop Series Fields Here

30

Total







20







10







0

1+0 1+1 1+2 1+3 2+0 2+1 2+2 2+3 3+0 3+1 3+2 (blank)





Parity







29 November 2011 93

Primips





 Number in cohort 62/91: 68.1%



 Number of primips 2006 3579/7986: 44.8%



 Chi squared test for proportions 18.8

(p2.5lts :6

• ITU admissions : 2 (+3 PPH)

• Eclampsia :1

• Rupture uterus :1

• CVA (Cerebellar bleed) :1

(not delivered)







RCOG 131

MOH (APH+PPH) – TT

MOH (APH+PPH) – BF

Judged Appropriate









RCOG 132

PPH – CJ

PPH – SL

Judged Appropriate









RCOG 133

PPH - SJ

Judged substandard - Minor









RCOG 134

PPH- NM

Judged Substandard - Incidental









RCOG 135

ITU – Ruptured Cornual

Pregnancy-SL

Judged Substandard Minor









RCOG 136

ITU – Sepsis /Abruption-EL

Judged Appropriate









RCOG 137

Rupture uterus - CH

Judged Substandard Major









RCOG 138

Eclampsia + HELLP -NS

Judged Appropriate









RCOG 139

RSH

• Total number of LW deliveries : 3660

• Incidence of 1:332 deliveries

• Total number of maternal deaths : 2

• One maternal death - RTA

• Total number of near-misses : 11

• Near-miss: death ratio of 11:1







RCOG 140

Quality of Care



• Appropriate :6

• Substandard – Incidental :1

• Substandard – Minor :2

• Substandard – Major :1









RCOG 141

Lessons learnt…

• Documentation

• Electronic database

• System errors

– Referral pathway from peripheral units

– Busy shifts

– Treating coagulopathy secondary to abruption

– Treating liver rupture





RCOG 142

Thank you









143

Royal College of

Obstetricians and

Gynaecologists

Setting standards to improve women’s health









Risk Management and Medico-Legal Issues In Women’s Health

Joint RCOG/ENTER Meeting









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