Nelson-PiercyTable 9.1. Indirect <strong>maternal</strong> <strong>deaths</strong> from congenital and acquired cardiac disease and rates per million maternities: UK: 1985–<strong>2008</strong>Triennium Congenital Acquired TotalnIschaemicOtherRate95% CIn (%) n (%) n (%)1985–87 10 (43) 9 (39) 4 (17) 23 1.01 0.68 1.521988–90 9 (50) 5 (28) 4 (22) 18 0.76 0.48 1.211991–93 9 (24) 8 (22) 20 (54) 37 1.60 1.16 2.201994–96 10 (26) 6 (15) 23 (59) 39 1.77 1.30 2.431997–99 10 (29) 5 (14) 20 (57) 35 1.65 1.19 2.292000–02 9 (20) 8 (18) 27 (61) 44 2.20 1.64 2.962003–05 4 (8) 16 (33) 28 (58) 48* 2.27 1.67 2.96<strong>2006</strong>–08 3 (6) 8 (15) 42 (79) 53 2.31 1.77 3.03*Includes one woman for whom very little information was available.arising from cardiomyopathy: two from peripartum cardiomyopathy,one from arrhythmogenic right ventricularcardiomyopathy, one from cardiomyopathy related <strong>to</strong> systemiclupus erythema<strong>to</strong>sus, one secondary <strong>to</strong> anthrocyclineand one from dilated cardiomyopathy that could have beenperipartum cardiomyopathy or secondary <strong>to</strong> thyro<strong>to</strong>xicosis.There were two Late Coincidental <strong>deaths</strong> in intravenousdrug users because of infective endocarditis.Three other <strong>maternal</strong> <strong>deaths</strong> <strong>to</strong> which cardiac disease contributedare counted and considered in other Chapters. Oneassociated with ischaemic cardiac disease in early pregnancyis counted in Chapter 6, one with myocardial scarring fromcocaine use is counted in Chapter 8, and one from secondaryacute endocarditis is counted in Chapter 10.Summary of key findings: <strong>2006</strong>–08Table 9.2 shows the overall numbers of cardiac <strong>maternal</strong><strong>deaths</strong> by major cause for this, and previous, triennia. Theleading causes are sudden adult death syndrome (SADS),of which there has been a significant increase; myocardialinfarction, mostly related <strong>to</strong> ischaemic heart disease;dissection of the thoracic aorta and cardiomyopathy, mostcommonly peripartum cardiomyopathy. Deaths from pulmonaryhypertension and from congenital heart diseasecontinue <strong>to</strong> decrease. There were no <strong>deaths</strong> from rheumaticheart disease in the current triennium.Thirty of the 50 (60%) women who died from cardiacdisease and for whom a body mass index (BMI) was availablewere overweight or obese. Half of them had a BMI of30 or more.The assessors considered that some degree of substandardcare was present in 27 of the 53 (51%) <strong>deaths</strong>counted in this Chapter. In 13 <strong>deaths</strong>, there were major lessons<strong>to</strong> be learnt, and, if the care had been better, the outcomemay have been different. For 14 women, the carethey received was less than optimal and lessons can belearnt from their management, but the outcome wouldhave been inevitable. The varying reasons for this are discussedthroughout this Chapter.Congenital heart disease andpulmonary hypertensionThe <strong>deaths</strong> of four women who died from the complicationsof congenital heart disease or from pulmonaryvascular disease are counted in this Chapter, and onewoman whose cardiac disease complicated her pregnancy iscounted in Chapter 4. One died following heart transplantation,one from a thrombosed aortic valve and two frompulmonary hypertension. Of these latter two, one wasprobably the result of complications associated with anatrial septal defect.Even though these mothers’ <strong>deaths</strong> could not have beenprevented, care was considered suboptimal in somewomen. This was because of a lack of pre-pregnancy counselling,failure <strong>to</strong> refer <strong>to</strong> the cardiologists, a lack ofcommunication between specialists and inappropriate managemen<strong>to</strong>f anticoagulation.Maternal morbidity from pulmonary vasculardiseaseOver the 4-year period between <strong>March</strong> <strong>2006</strong> and February2010, 24 confirmed cases of pulmonary vascular diseasewere reported through the United Kingdom Obstetric SurveillanceSystem (UKOSS; Detailed information on theUKOSS is given in the Introduc<strong>to</strong>ry Chapter <strong>to</strong> thisreport), giving an estimated incidence of 0.8 (95% CI 0.5–1.2) per 100 000 maternities. 1 Eleven were due <strong>to</strong> the resul<strong>to</strong>f idiopathic pulmonary arterial hypertension, and nine110 ª <strong>2011</strong> Centre for Maternal and Child Enquiries (CMACE), BJOG 118 (Suppl. 1), 1–203
Chapter 9: Cardiac diseaseTable 9.2. Causes of <strong>maternal</strong> death from cardiac disease; UK: 1994–<strong>2008</strong>Type and cause of death 1994–96 1997–99 2000–02 2003–05 <strong>2006</strong>–08AcquiredAortic dissection 7 5 7 9 7Myocardial infarction (MI) 6 5 8 12 6Ischaemic heart disease (no MI) 0 0 0 4 5Sudden adult death syndrome (SADS) 0 0 4 3 10Peripartum cardiomyopathy 4 7 4 0* 9**Other cardiomyopathy 2 3 4 1 4Myocarditis or myocardial fibrosis 3 2 3 5 4Mitral stenosis or valve disease 0 0 3 3 0Thrombosed aortic or tricuspid valve 1 0 0 0 2Infective endocarditis 0 2 1 2 2Right or left ventricular hypertrophy or1 2 2 2 1hypertensive heart diseaseCongenitalPulmonary hypertension (PHT) 7 7 4 3 2Congenital heart disease (not PHT or3 2 2 3 1thrombosed aortic valve)Other 5 0 2 0 0Total 39 35 44 48*** 53*Twelve Late <strong>deaths</strong> reported in 2003–05.**Two Late <strong>deaths</strong> reported in <strong>2006</strong>–08.***Includes one woman for whom information on cause was not available.were attributed <strong>to</strong> congenital heart disease. There were tworelated <strong>to</strong> chronic thromboembolism, one <strong>to</strong> sleep apnoeaand one <strong>to</strong> connective tissue disease. Fourteen cases wereknown before pregnancy and ten were diagnosed duringpregnancy.Acquired heart diseaseMyocardial infarction and ischaemic heart diseaseEleven women died from acute myocardial infarction (MI)or chronic ischaemic heart disease (IHD), a rate of 0.48(95% CI 0.27–0.87) per 100 000 maternities compared withthe 16 whose <strong>deaths</strong> were considered in the last Report, arate of 0.76 (95% CI 0.46–1.2) per 100 000 maternities.Coronary atheroma was the underlying pathology in threeof the six women who died from MI; one of these <strong>deaths</strong>was the result of extensive coronary artery dissection, arecognised complication of pregnancy and in the two otherwomen the cause of death was undetermined. There werealso five <strong>deaths</strong> from IHD where no acute MI was demonstrated.Presumably death in these women related <strong>to</strong>arrhythmia or heart failure. In <strong>to</strong>tal, eight women died fromIHD compared with 12 in the previous triennium.The women who diedAgain, as shown in the last Report, the impact of lifestylefac<strong>to</strong>rs such as increasing <strong>maternal</strong> age, obesity and smokingwas dramatic, and all of the women who died had identifiablerisk fac<strong>to</strong>rs. The mothers’ ages ranged from 28 <strong>to</strong>46 years with a median of 36 years. Eight women were 35or older, of whom five were aged 40 years or more. All wereparous, and seven were para 4 or greater, of whom twowere of extremely high parity. Six smoked, four had knownhypertension, four were overweight and three were obese.Two had a family his<strong>to</strong>ry of cardiac disease, one had hypercholesterolaemia,one had gestational diabetes and one hadsickle cell disease. Three women were from black andminority ethnic groups. Three mothers also had social problems:two were known <strong>to</strong> the child protection services, oneof whom had also reported domestic violence, and anotherwoman abused cannabis and alcohol.All but two of these women died postnatally, althoughone had collapsed antenatally near term.Maternal morbidity from acute myocardialinfarctionThe UKOSS study of acute MI in pregnancy, undertakenbetween August 2005 and February 2010, 1 identified 23confirmed nonfatal cases occurring antenatally, giving anestimated incidence of 0.7 (95% CI 0.4–1.0) cases per100 000 maternities. Fourteen of the women with a confirmedMI had angiography: seven had coronary atheroma,three had coronary artery dissection, two hadcoronary arterial thrombosis and two had normal coro-ª <strong>2011</strong> Centre for Maternal and Child Enquiries (CMACE), BJOG 118 (Suppl. 1), 1–203 111
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AcknowledgementsSaving Mothers’ L
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AcknowledgementsAcknowledgementsCMA
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Forewordbeen written jointly by a m
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‘Top ten’ recommendationsServic
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‘Top ten’ recommendationscommun
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‘Top ten’ recommendationsof suc
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Oates et al.Back to basicsM Oates 1
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Oates et al.BreathlessnessBreathles
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Oates et al.appropriate pathway of
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LewisIntroduction: Aims, objectives
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LewisAn important limitation of ran
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Lewismaternal and public health-pol
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Lewisresult in a live birth at any
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LewisChapter 1: The women who died
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Lewiswho would not have been identi
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Lewis1098Rate per 100 000 materniti
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LewisTable 1.4. Numbers and rates o
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Lewis2.50Rate per 100 000 materniti
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LewisTable 1.9. Number of maternal
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LewisTable 1.12. Numbers and percen
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LewisThere were cases where a major
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LewisBox 1.5. Classifications of Bo
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LewisNew countries of the European
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LewisTable 1.26. Characteristics* o
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Lewis4 Lewis G (ed). The Confidenti
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DrifeTable 2.1. Direct deaths from
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Shakespeareemergency caesarean sect
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ShakespeareCardiac diseaseDeaths fr
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Shakespearereduce the risks to the
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ShakespeareManaging a maternal deat
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Hulbertin the ED was of a high qual
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Clutton-BrockDiagnosis of sepsisTak
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Lucas, Millward-Sadler95 mmHg. This
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Annex 17.1. The main clinico-tholog
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MillerAppendix 1: The method of Enq
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MillerDatanotificationNotificationR
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Knight• investigating different m
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LennoxAppendix 2B: Summary of Scott
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LennoxEvidence of effective managem
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Appendix 3: Contributors to the Mat
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Appendix 3: Contributors to the Mat