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1.
Arch Dis Child Fetal Neonatal Ed ; 94(4): F268-74, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19000995

ABSTRACT

OBJECTIVES: To investigate prognosis of the fetus with isolated gastroschisis and bowel dilatation from a systematic review of the literature. We aimed to compare the incidence of (a) intrauterine death, (b) death within 4 weeks of delivery, (c) bowel resection, (d) length of time to oral feeds and (e) time as inpatient in fetuses with gastroschisis with and without evidence of bowel dilatation. METHODS: Literature was identified by searching two bibliographical databases between 1980 and 2007. Studies were assessed for quality and stratified according to the definition of bowel dilatation. The data extracted were inspected for clinical and methodological heterogeneity. RESULTS: The search strategy yielded 1335 potentially relevant citations. Full manuscripts were retrieved for 92 citations. 10 studies (273 patients) were finally included in the systematic review. No difference was found between groups for death within 4 weeks of delivery (OR = 0.62 (95% CI 0.11 to 3.32); heterogeneity p = 0.39) or bowel resection (OR = 3.35 (95% CI 0.82 to 13.74); heterogeneity p = 0.39). There were insufficient data to compare the risk of intrauterine death and length of time to oral feeds. The mean inpatient stay was not significantly different between groups (OR = 16.63 (95% CI 0.98 to 32.28); heterogeneity p = 0.23). CONCLUSION: Current available evidence suggests that fetuses with isolated gastroschisis and bowel dilatation are not at increased risk of adverse perinatal outcome compared to those without bowel dilatation. However, there is a paucity of studies, and a randomised controlled trial is urgently needed.


Subject(s)
Fetal Diseases/mortality , Gastroschisis/mortality , Intestines , Birth Weight , Dilatation, Pathologic/diagnosis , Dilatation, Pathologic/mortality , Dilatation, Pathologic/surgery , Gastroschisis/surgery , Gestational Age , Humans , Infant , Infant Nutritional Physiological Phenomena , Infant, Newborn , Intestines/pathology , Intestines/surgery , Prognosis
2.
Fetal Diagn Ther ; 21(5): 471-4, 2006.
Article in English | MEDLINE | ID: mdl-16912498

ABSTRACT

OBJECTIVE: A foetus with an echodense, microcystic lung lesion complicated by non-immune hydrops has a high mortality rate. Because of the limited treatment options available, laser ablation was offered in an attempt to reduce the size of the lesion and reduce hydrops fetalis. METHODS AND RESULTS: A 25-year-old nulliparous woman presented at 21 weeks gestation. Ultrasound revealed a male foetus with a large microcystic right sided lung lesion that completely occupied the right hemithorax causing marked mediastinal deviation. The foetus was hydropic with polyhydramnios. Percutaneous laser ablation of the large microcystic lung lesion was performed under direct ultrasound control. At a power setting of 45 W, and using a 400 microm Nd:YAG laser fibre, the core of the lesion was photocoagulated in pulses lasting 5 s at 5 s intervals. The total target dose was 1683 J. This led to a marked but temporary reduction in amniotic fluid volume. The patient was commenced on sulindac and amniodrainage was performed at 27 weeks as reaccumulation of the polyhydramnios occurred. Pre-eclampsia complicated the pregnancy at 38 weeks gestation and an emergency caesarean section was performed. The baby underwent a thoracotomy and lobectomy at 48 h of age, made a good recovery, and is currently well 8 weeks post-delivery. CONCLUSIONS: In cases of cystic lung lesion complicated by hydrops, laser ablation should be considered as a treatment option.


Subject(s)
Adenoma/surgery , Fetal Diseases/surgery , Laser Coagulation , Lung Neoplasms/surgery , Adenoma/complications , Adenoma/diagnostic imaging , Adult , Cesarean Section , Female , Fetal Diseases/diagnostic imaging , Gestational Age , Humans , Hydrops Fetalis , Laser Coagulation/methods , Lung Neoplasms/complications , Lung Neoplasms/diagnostic imaging , Male , Polyhydramnios , Pre-Eclampsia , Pregnancy , Treatment Outcome , Ultrasonography, Prenatal
3.
BJOG ; 113(9): 992-8, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16903844

ABSTRACT

BACKGROUND: Following single-twin death, the perinatal mortality and morbidity for the surviving co-twin is increased but difficult to quantify. We present data on prognosis from a systematic review. OBJECTIVES: We aimed to determine the incidence of a) co-twin death, b) neurological abnormality and c) preterm delivery for the surviving co-twin following single-twin death after 14 weeks of gestation. SEARCH STRATEGY: Literature was identified by searching two bibliographical databases and specialist journals between 1990 and 2005. SELECTION CRITERIA: The selected studies of > or = 5 cases reported on perinatal death and/or neurodevelopmental delay of the surviving co-twin. DATA COLLECTION AND ANALYSIS: Studies were assessed for quality and data extracted to allow computation of rates. The data were inspected for heterogeneity using a Forrest plot and examined statistically using the chi-square test. Data from individual studies were pooled within subgroups defined by prognosis. MAIN RESULTS: The search strategy yielded 632 potentially relevant citations. Full manuscripts were retrieved for 54 citations and 28 studies were finally included in the review. Following the death of one twin, the risk of monochorionic and dichorionic co-twin demise was 12% (95% CI 7-11) and 4% (95% CI 2-7), respectively. The risk of neurological abnormality in the surviving monochorionic and dichorionic co-twin was 18% (95% CI 11-26) and 1% (95% CI 0-7), respectively. The risk of preterm delivery was 68% (95% CI 56-78) and 57% (95% CI 34-77), respectively. Where there was comparative data within studies, the odds of monochorionic co-twin intrauterine death was six times that of dichorionic twins (OR 6.04 [95% CI 1.84-19.87]). Neurological abnormality was also higher in monochorionic compared with dichorionic pregnancies (OR 4.07 [95% CI 1.32-12.51]). AUTHOR'S CONCLUSIONS: More prospective research is required to inform decision making on this subject, especially with data that allow stratification based upon chorionicity.


Subject(s)
Fetal Death , Twins , Child , Developmental Disabilities/etiology , Female , Humans , Infant Mortality , Infant, Newborn , Pregnancy , Pregnancy Outcome , Premature Birth/etiology
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