Harperthe 6-week postnatal period, although this does not meanthat all of these women’s lives would have been saved. Inmost cases, the outcome was inevitable, but for 12 it mighthave been different had the infection been diagnosed andtreated more promptly. In six others, although the outcomewould not have changed, lessons remain <strong>to</strong> be learnt. Therewere also lessons <strong>to</strong> be learnt from the management of someof the women who died later in their postnatal period.The organisms involvedThe most common pathogen identified among thewomen’s <strong>deaths</strong> was the b-haemolytic strep<strong>to</strong>coccus LancefieldGroup A (Strep<strong>to</strong>coccus pyogenes), of which there were13 cases. There were five cases of Escherichia coli, one ofwhich also grew Enterococcus faecalis; three cases of Staphylococcusaureus, one of which also grew mixed coliforms;and one case each of Strep<strong>to</strong>coccus pneumoniae, Morganellamorganii and Clostridium septicum. One healthcare worker,known <strong>to</strong> be a methicillin-resistant Staphylococcus aureus(MRSA) carrier, died some days after caesarean sectionfrom septicaemia with Pan<strong>to</strong>n–Valentine leucocidin (PVL)-positive MRSA, which is a particularly virulent subtype.No pathogen was identified in four cases.Group A b-haemolytic strep<strong>to</strong>coccus (Strep<strong>to</strong>coccuspyogenes)There were 13 <strong>deaths</strong> from b-haemolytic strep<strong>to</strong>coccusLancefield Group A (Strep<strong>to</strong>coccus pyogenes) this trienniumcompared with eight in the last Report for 2003–05 andthree for <strong>maternal</strong> <strong>deaths</strong> from sepsis in 2000–02.This organism should not be confused with the b-haemolyticstrep<strong>to</strong>coccus Lancefield Group B (Strep<strong>to</strong>coccus agalactiae),which occasionally causes early neonatal mortality butis a much less common cause of <strong>maternal</strong> mortality.Group A strep<strong>to</strong>coccus is typically community based,and 5–30% of the population are asymp<strong>to</strong>matic carriers onskin or in throat. 1 It is easily spread by person-<strong>to</strong>-personcontact or by droplet spread from a person with infection.Strep<strong>to</strong>coccal sore throat is one of the most common bacterialinfections of childhood, and all of the 13 womenwho died from it either worked with, or had, young children.Several mothers also had a his<strong>to</strong>ry of recent sorethroat or respira<strong>to</strong>ry infection. Contamination of the perineumis more likely when a woman or her family or closecontacts have sore throats or other respira<strong>to</strong>ry symp<strong>to</strong>ms,as the organism may be transferred from the throat or nosevia her hands <strong>to</strong> her perineum. Antenatal education shouldraise awareness of this and the importance of good personalhygiene and avoiding contamination of the perineumby washing hands before and after using the lava<strong>to</strong>ry orchanging sanitary <strong>to</strong>wels. All except one mother had intactmembranes until shortly before delivery, although severalhad offensive, smelly or infected looking liquor when theirmembranes ruptured. Studies have shown that bacteriahave the ability <strong>to</strong> cross intact membranes. 3Group A strep<strong>to</strong>coccus can also cause serious illness suchas scarlet fever, bacteraemia, strep<strong>to</strong>coccal shock syndromeand necrotising fasciitis. His<strong>to</strong>rically it is the classic organismassociated with puerperal sepsis and was a major causeof <strong>maternal</strong> mortality before antiseptic practice was introducedand antibiotics became available.Increased levels of Group A strep<strong>to</strong>coccal infections tend<strong>to</strong> occur between December and April, which was true formost of the cases in this Report. Information from theHealth Protection Agency indicates that there were higherthan normal notifications of scarlet fever in some regionsof England from December 2007 <strong>to</strong> mid-<strong>March</strong> <strong>2008</strong>,which coincides with many of the cases reported here. 4 Formost of the 13 women who died, there was no informationabout subtype, but Types M, 12, T1 emm1 and emm11were all identified.The following vignette illustrates the typical symp<strong>to</strong>msand the rapid and relentless course of Group A strep<strong>to</strong>coccaldisease despite excellent care:A woman in mid-pregnancy called an out-of-hours GP as shewas feverish, shivery and unwell and had a sore throat butwas diagnosed as having a probable viral infection. A fewhours later the GP visited again as she had developed constantabdominal pain associated with vomiting, greenishblack diarrhoea, and reduced fetal movements but no vaginalbleeding. The GP suspected placental abruption, and,although she was rapidly transferred <strong>to</strong> hospital, on admissionshe was critically ill with marked tachycardia, breathlessness,cyanosis and confusion. The correct diagnosis ofseptic shock was quickly recognised, fluid resuscitation wasstarted, senior consultants were called, advice was soughtfrom haema<strong>to</strong>logy and microbiology consultants and appropriateintravenous antibiotics were commenced immediately.Despite intensive life support she died a few hours afteradmission <strong>to</strong> hospital.Sickle cell disease/traitSome of the women had underlying medical conditionsthat may have increased their susceptibility <strong>to</strong> infection,including three Black African women, two of whom diedfrom coliform and one from Staphylococcus aureus infectionfollowing spontaneous preterm prelabour rupture of membranes(PPROM) between 17 and 23 weeks of gestation.One had sickle cell trait, and two had known sickle cell disease.Women with sickle cell disease are at increased risk ofinfection because of poor splenic function as a result ofdamage from sickle cell disease, and any anaemia may alsoincrease the risk of infection. Maternal mortality in sicklecell disease is estimated <strong>to</strong> be around 1 in 220 (0.45%). 5Sickle cell disease in pregnancy is the subject of a UK88 ª <strong>2011</strong> Centre for Maternal and Child Enquiries (CMACE), BJOG 118 (Suppl. 1), 1–203
Chapter 7: SepsisObstetric Surveillance System (UKOSS) surveillance studyfrom February 2010 until February <strong>2011</strong>.As highlighted in Chapter 10, pregnant women withunderlying disease, including sickle cell disease, should bemanaged jointly under the care of a consultant obstetricianand a specialist consultant in their underlying condition, inthis case a haema<strong>to</strong>logist. All immunisations, includingagainst pneumococcus, should be up <strong>to</strong> date. Any infectionsshould be treated promptly and prophylactic penicillinis recommended. A clear plan of management shouldbe documented in the chart early in pregnancy. A nationalguideline would also be helpful.Sepsis in early pregnancyEight women, including seven counted in this Chapter andone Late death, died from complications of infections arisingbefore 24 completed weeks of gestation. Two women diedfrom septic miscarriage and two after a termination of pregnancy.Of these, one did not receive post-procedure prophylacticantibiotics and another died from Clostridium septicumsepticaemia and necrotising fasciitis. Clostridium infection isa rare but previously reported cause of <strong>maternal</strong> death,including after termination of pregnancy. Vaginal carriagewas the most likely source of infection and the inflamma<strong>to</strong>ryfocus in the uterus the most likely portal of entry. Necrotisingfasciitis is characterised by an overwhelming fulminantcourse with severe pain and muscle inflammation or necrosis;the majority of patients die within 24 hours of onset.Sepsis following pregnancy loss:learning pointsAll units should have an effective and robust system inplace <strong>to</strong> ensure that peri-abortion antibiotic prophylaxis(metronidazole 1 g rectally at the time of abortion plus,commencing on the day of abortion, either doxycycline100 mg orally twice daily for 7 days or azithromycin 1 gorally) is offered routinely in accordance with RCOGguidelines. 6Infection must be suspected and actively ruled out whenwomen who have had a recent termination of pregnancyor spontaneous miscarriage have pyrexia, persistentbleeding or abdominal pain, especially if the pain isconstant and severe. Vaginal swabs, ultrasound scan <strong>to</strong>exclude retained products of conception and diagnosticevacuation of uterus (evacuation of retained products ofconception) should be considered if there is still doubt;haemoglobin, white cell count, C-reactive protein, andblood cultures if pyrexia >38°C are minimum investigations;and high-dose broad-spectrum intravenousantibiotics should be commenced immediately, withoutwaiting for microbiology results.Four women, including a Late death, died from the consequencesof chorioamnionitis after spontaneous PPROM inthe second trimester. In one case the cause was Morganellamorganii. This is a Gram-negative rod bacterium oftenfound as part of the normal intestinal flora, but it can be arare cause of severe invasive disease and is naturally resistant<strong>to</strong> many b-lactam antibiotics. Chorioamnionitis andbrain abscess due <strong>to</strong> Morganella morganii have both beenreported previously. 7Sepsis before deliveryNine women, including eight counted in this Chapter andone Late death, developed sepsis before delivery after24 weeks of gestation. Seven women had group A strep<strong>to</strong>coccalinfection, one had Escherichia coli and for onewoman who was extremely unwell on admission therewas no information about whether any microbiologicalinvestigations were performed before antibiotics weregiven. Four had a caesarean section and five deliveredvaginally. All except two were extremely unwell on admission<strong>to</strong> hospital, and many received outstanding care onceadmitted, even though nothing more could have beendone <strong>to</strong> save them.Most of these women had similar symp<strong>to</strong>ms. Theyhad a short his<strong>to</strong>ry of feeling unwell; some had a recentsore throat, cough or flu-like illness; several had severediarrhoea; a few had vomiting; some felt hot and coldor shivery and had mild or severe pyrexia, although othershad no temperature. One woman was hypothermicand several were tachycardic and hypotensive on admission.All had contractions and abdominal pain that insome cases was constant, severe and not relieved by analgesia.Severe <strong>maternal</strong> infection also affects the fetus—fivebabies died in utero, and those delivered by emergencycaesarean section for abnormal fetal cardio<strong>to</strong>cographsneeded resuscitation after delivery, as did a baby bornvaginally <strong>to</strong> a woman who had complained of pelvic painin late pregnancy. In her case, when the membranes rupturedat delivery, the liquor was heavily meconium-stainedand smelt offensive. The combination of severe abdominalpain and abnormal or absent fetal heart is more usuallyassociated with placental abruption, but these cases demonstratethat when a woman presents with these symp<strong>to</strong>ms,genital tract sepsis must be considered in thedifferential diagnosis.Severe sepsis is often a cause of a<strong>to</strong>nic uterine haemorrhage,which may be further exacerbated by disseminatedintravascular coagulation. For example, one woman haduncontrollable bleeding after vaginal delivery and suffered acardiac arrest
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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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‘Top ten’ recommendationsMarch
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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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Oates, CantwellChild protection iss
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Oates, CantwellAll women who are su
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Oates, Cantwell4 Kendel RE, Chalmer
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Lewismaternal mortality rates or ra
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Annex 12.1. Domestic abuseAnnex 12.
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Annex 12.1. Domestic abuseshe could
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Garrod et al.supportive but challen
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Garrod et al.• Culture and system
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Garrod et al.the second stage and s
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Garrod et al.through the still heal
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ShakespeareChapter 14: General prac
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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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HulbertPre-eclampsia/eclampsia: lea
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HulbertTransfersWhen the obstetric
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Clutton-Brocksimply the case that s
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Clutton-BrockDiagnosis of sepsisTak
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Clutton-Brockpulseless electrical a
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Clutton-BrockImprovement Scotland (
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Lucas, Millward-Sadler95 mmHg. This
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Lucas, Millward-Sadleran agreed mai
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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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Knightbaseline incidence against wh
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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