catastrophic haemorrhage due to vascular anomalies of the gut in a preterm neonate

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gestation in 10 study regions in 2003. Regions were Flanders in Belgium, the Eastern Region of Denmark, 6 of 8 districts in the Ile-de-France region of France, Hesse in Germany, Lazio in Italy, the Central-Eastern region of the Netherlands, the Wielkopolska/Lubuskie region in Poland, the Northern region of Portugal and the Northern and former Trent regions of the UK. Inclusions were crossed-checked with birth registers. Outcomes included terminations of pregnancy, stillbirths, neonatal deaths and respiratory and neurological morbidity (intraventricular hemorrhage (IVH) grade III and IV or cystic periventricular leukomalacia (PVL) and bronchopulmonary dysplasia (BPD)). Results The MOSAIC cohort included 7222 babies. Terminations of pregnancy constituted 8.1% of the cohort, but ranged between 0.5% in the Polish study region to 17.5% in the French region. There were also large differences in rates of intrapartum and labor ward deaths. In the Danish and German study regions, few babies 2427 weeks of gestation died during labor or in the labor ward, while this proportion was much higher in the Dutch and French regions. In- hospital mortality after live birth, standardized for gestational age and sex, was doubled in high versus low mortality regions (1820% versus 79%). Morbidity among survivors varied significantly (IVH/PVL ranged from 2.6% to over 10% and BDP from 10.5 to 21.5%), but differed from mortality rankings. Conclusions Mortality and morbidity varied widely between European regions, raising questions about the differences in ethical decision making, medical practices and organization of care that are responsible for these variations. Our results also underscore the importance of collecting data on all pregnancy outcomes and suggest that substantial biases may exist in studies based only on NICU admissions. doi:10.1016/j.earlhumdev.2008.09.376 Abstract UENPS.361 Catastrophic haemorrhage due to vascular anomalies of the gut in a preterm neonate Kumar Swamy, Anu Paul, Brian Davies, Shailinder Singh, Dulip Jayasinghe Nottingham University Hospital, Nottingham, United Kingdom Background and aim Catastrophic upper gastrointestinal bleed due to vascular anomalies has not previously been reported in a preterm neonate. We present such a case in a 26 week neonate on the 8th day of life. Conservative measures failed to stop the bleeding hence laparotomy was performed and a bleeding gastric haemangioma was oversewn. At a subsequent laparotomy a partial gastrectomy was performed. Even at extreme prematurity, surgery is a treatment option for uncontrollable upper gastrointestinal bleeding. Materials and methods A baby girl, weighing 690 g, was born following 26 weeks of pregnancy. On day 8, she developed massive upper gastrointestinal bleed with a total blood loss of about 64 mL/kg. At laparotomy the bleed was found to be coming from a gastric haemangioma occupying a large part of the anterior stomach wall. The haemangioma was over sewn and stomach cavity was packed with Surgicel. Four days postoperatively (day 12) she developed abdominal distension with free air on abdominal X-ray. She was taken back to theatre and was found to have gastric perforation at the site of her previous surgery. The abnormal area of the stomach was excised in the form of a partial gastrectomy. Enteral feeds were started on day 23 and full NG feeding was established by day 29. Four weeks later (day 43), she suddenly deteriorated with overwhelming necrotising enterocolitis. Despite full resuscitation including a peritoneal drain she continued to deteriorate and died within a few hours. A post mortem examination was performed and found to have necrotising enterocolitis and foci of ectatic vascular spaces suggesting vascular malformation of the stomach and intestines. Results This case illustrates two points. Firstly, even at extreme pre-maturity, surgery should be considered for ongoing gastrointestinal bleeding. Secondly at both operations the rest of the intestine was inspected externally and further lesions were not seen. Four weeks later, after her death, post mortem showed multiple vascular malformations which may have led to necrotizing enterocolitis. This shows that either these lesions were small or not present and had developed with growth. Conclusions Vascular anomaly of the gastrointestinal tract is a source of acute blood loss but is a rare occurrence. It can arise in any part of the digestive system; however is extremely rare in neonates especially in a preterm neonate and not many have been reported in literature. This intraoperative photograph shows the stomach opened to reveal the vascular lesion with a single prolene stitch on the lesion. doi:10.1016/j.earlhumdev.2008.09.377 Abstract UENPS.362 Ethylglucuronide and ethylsulfate in meconium: New biomarkers of gestational ethanol exposure? Federica Vagnarelli,c , Luca Morini a , Emilia Marchei b , Manuela Pellegrini b , Angelo Groppi a , Cristiana Stramesi a , Oscar Garcia-Algar d , Roberta Pacifici b , Simona Pichini b a Department of Legal Medicine and Public Health, University of Pavia, Pavia, Italy b Istituto Superiore di Sanità, V.le Regina Elena 299, 00161, Rome, Italy c NICU, Arcispedale Santa Maria Nuova, Reggio Emilia, Italy d Unitad de Recerca Infància i Entorn (URIE), Paediatric Service, Hospital del Mar, Barcelona, Spain Background and aim In recent years, fatty acid ethyl esters (FAEEs) in meconium emerged as reliable, direct biological markers for establishing gestational alcohol exposure. Conversely, ethyl glucuronide (EtG) and ethyl sulfate (EtS), two ethanol metabolites already detected in blood, urine and hair have been never investigated in this neonatal biological matrix. We developed a sensitive and specific liquid chromatography-tandem mass spectrometric method which for the first time identified and quantified EtG and EtS in neonatal meconium. Materials and methods The validated method has been applied to analysis of specimens from two different European study cohorts: Reggio Emilia (Italy) and Barcelona Abstracts S145

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gestation in 10 study regions in 2003. Regions were Flanders in Belgium, theEastern Region of Denmark, 6 of 8 districts in the Ile-de-France region ofFrance, Hesse in Germany, Lazio in Italy, the Central-Eastern region of theNetherlands, the Wielkopolska/Lubuskie region in Poland, the Northernregion of Portugal and the Northern and former Trent regions of the UK.Inclusions were crossed-checked with birth registers. Outcomes includedterminations of pregnancy, stillbirths, neonatal deaths and respiratory andneurological morbidity (intraventricular hemorrhage (IVH) grade III and IV orcystic periventricular leukomalacia (PVL) and bronchopulmonary dysplasia(BPD)).

Results

The MOSAIC cohort included 7222 babies. Terminations of pregnancyconstituted 8.1% of the cohort, but ranged between 0.5% in the Polish studyregion to 17.5% in the French region. Therewere also large differences in rates ofintrapartum and labor ward deaths. In the Danish and German study regions,few babies 24–27 weeks of gestation died during labor or in the labor ward,while this proportion was much higher in the Dutch and French regions. In-hospital mortality after live birth, standardized for gestational age and sex, wasdoubled in high versus low mortality regions (18–20% versus 7–9%). Morbidityamong survivors varied significantly (IVH/PVL ranged from 2.6% to over 10% andBDP from 10.5 to 21.5%), but differed from mortality rankings.

Conclusions

Mortality and morbidity varied widely between European regions, raisingquestions about the differences in ethical decision making, medical practices andorganization of care that are responsible for these variations. Our results alsounderscore the importance of collecting data on all pregnancy outcomes andsuggest that substantial biasesmayexist in studies basedonlyonNICUadmissions.

doi:10.1016/j.earlhumdev.2008.09.376

Abstract UENPS.361Catastrophic haemorrhage due to vascular anomalies of the gut in apreterm neonate

Kumar Swamy⁎, Anu Paul, Brian Davies, Shailinder Singh, Dulip JayasingheNottingham University Hospital, Nottingham, United Kingdom

Background and aim

Catastrophic upper gastrointestinal bleed due to vascular anomalies hasnot previously been reported in a preterm neonate. We present such a case ina 26 week neonate on the 8th day of life. Conservative measures failed tostop the bleeding hence laparotomy was performed and a bleeding gastrichaemangioma was oversewn. At a subsequent laparotomy a partialgastrectomy was performed. Even at extreme prematurity, surgery is atreatment option for uncontrollable upper gastrointestinal bleeding.

Materials and methods

A baby girl, weighing 690 g, was born following 26 weeks of pregnancy.On day 8, she developed massive upper gastrointestinal bleed with a totalblood loss of about 64 mL/kg. At laparotomy the bleed was found to becoming from a gastric haemangioma occupying a large part of the anteriorstomach wall. The haemangioma was over sewn and stomach cavity waspacked with Surgicel. Four days postoperatively (day 12) she developedabdominal distension with free air on abdominal X-ray. She was taken backto theatre and was found to have gastric perforation at the site of herprevious surgery. The abnormal area of the stomach was excised in the formof a partial gastrectomy. Enteral feeds were started on day 23 and full NGfeeding was established by day 29.

Four weeks later (day 43), she suddenly deteriorated with overwhelmingnecrotising enterocolitis. Despite full resuscitation including a peritonealdrain she continued to deteriorate and died within a few hours.

A post mortem examination was performed and found to havenecrotising enterocolitis and foci of ectatic vascular spaces suggestingvascular malformation of the stomach and intestines.

Results

This case illustrates two points. Firstly, even at extreme pre-maturity,surgery should be considered for ongoing gastrointestinal bleeding. Secondlyat both operations the rest of the intestine was inspected externally andfurther lesions were not seen. Four weeks later, after her death, post mortemshowed multiple vascular malformations which may have led to necrotizingenterocolitis. This shows that either these lesions were small or not presentand had developed with growth.

Conclusions

Vascular anomaly of the gastrointestinal tract is a source of acute bloodloss but is a rare occurrence. It can arise in any part of the digestive system;however is extremely rare in neonates especially in a preterm neonate andnot many have been reported in literature.

This intraoperative photograph shows the stomach opened to reveal thevascular lesion with a single prolene stitch on the lesion.

doi:10.1016/j.earlhumdev.2008.09.377

Abstract UENPS.362Ethylglucuronide and ethylsulfate in meconium: New biomarkers ofgestational ethanol exposure?

Federica Vagnarelli⁎,c, Luca Morinia, Emilia Marcheib, Manuela Pellegrinib,Angelo Groppia, Cristiana Stramesia, Oscar Garcia-Algard,Roberta Pacificib, Simona PichinibaDepartment of Legal Medicine and Public Health, University of Pavia, Pavia,ItalybIstituto Superiore di Sanità, V.le Regina Elena 299, 00161, Rome, ItalycNICU, Arcispedale Santa Maria Nuova, Reggio Emilia, ItalydUnitad de Recerca Infància i Entorn (URIE), Paediatric Service, Hospital del Mar,Barcelona, Spain

Background and aim

In recent years, fatty acid ethyl esters (FAEEs) in meconium emerged asreliable, direct biological markers for establishing gestational alcoholexposure. Conversely, ethyl glucuronide (EtG) and ethyl sulfate (EtS), twoethanol metabolites already detected in blood, urine and hair have beennever investigated in this neonatal biological matrix.

We developed a sensitive and specific liquid chromatography-tandemmass spectrometric method which for the first time identified and quantifiedEtG and EtS in neonatal meconium.

Materials and methods

The validated method has been applied to analysis of specimens fromtwo different European study cohorts: Reggio Emilia (Italy) and Barcelona

Abstracts S145