Pub Date : 2001-12-01DOI: 10.1016/S0306-5456(01)00293-5
Mira Harrison-Woolrych , David Purdie
{"title":"Breast and pelvic examination in women taking hormone replacement therapy","authors":"Mira Harrison-Woolrych , David Purdie","doi":"10.1016/S0306-5456(01)00293-5","DOIUrl":"10.1016/S0306-5456(01)00293-5","url":null,"abstract":"","PeriodicalId":75620,"journal":{"name":"British journal of obstetrics and gynaecology","volume":"108 12","pages":"Pages 1201-1203"},"PeriodicalIF":0.0,"publicationDate":"2001-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0306-5456(01)00293-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"56578393","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2001-12-01DOI: 10.1016/S0306-5456(01)00299-6
Tariq Miskry, Adam Magos
A variety of methods of management of the vaginal vault have been described, all of which maintain certain principles. In techniques that advocate closure of the vault, the peritoneum and vaginal epithelium are treated with separate sutures. This leaves a potential space above the vaginal closure. We describe a simple technique of mass closure which obliterates this space and incorporates the pedicles to provide support for the vault. This method may hold potential advantages in terms of haemostasis, risk of vault haematoma, and post-operative vaginal cuff infections.
{"title":"Mass closure: a new technique for closure of the vaginal vault at vaginal hysterectomy","authors":"Tariq Miskry, Adam Magos","doi":"10.1016/S0306-5456(01)00299-6","DOIUrl":"https://doi.org/10.1016/S0306-5456(01)00299-6","url":null,"abstract":"<div><p>A variety of methods of management of the vaginal vault have been described, all of which maintain certain principles. In techniques that advocate closure of the vault, the peritoneum and vaginal epithelium are treated with separate sutures. This leaves a potential space above the vaginal closure. We describe a simple technique of mass closure which obliterates this space and incorporates the pedicles to provide support for the vault. This method may hold potential advantages in terms of haemostasis, risk of vault haematoma, and post-operative vaginal cuff infections.</p></div>","PeriodicalId":75620,"journal":{"name":"British journal of obstetrics and gynaecology","volume":"108 12","pages":"Pages 1295-1297"},"PeriodicalIF":0.0,"publicationDate":"2001-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0306-5456(01)00299-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134663850","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2001-12-01DOI: 10.1016/S0306-5456(01)00298-4
M.F. Reznikoff-Etiévant , V. Cayol , B. Carbonne , A. Robert , F. Coulet , J. Milliez
Objective To determine whether there is an association between early recurrent miscarriage (before 10 weeks of pregnancy) and Factor V Leiden and G20210A prothrombin mutations.
Design A prospective study.
Setting Department of Gynaecology and Obstetrics, Saint Antoine Hospital, Paris, France.
Population Two groups of women: those with early unexplained recurrent miscarriage before 10 weeks of pregnancy (n=260) and control healthy women without a previous history of thromboembolism (n=240).
Methods Screening for defects in the protein C anticoagulant pathway was performed using the anticoagulant response to agkistrodon confortrix venom (ACV test). Protein C and Factor V Leiden mutation testing was performed for each low ACV level. Each sample was tested for the G20210A prothrombin mutation.
Results Factor V Leiden and G20210A mutations were found to be associated with early recurrent spontaneous miscarriage before 10 weeks of pregnancy, the odds ratios being 2.4 (95% CI 1–5) and 2.7 (95% CI 1–7), respectively. Similar results were found whether or not women had had a previous live birth.
Conclusions Early recurrent miscarriage before 10 weeks of pregnancy is significantly associated with Factor V or G20210A prothrombin mutations. These results indicate a possible role for anticoagulant prevention in these early miscarriages.
目的探讨早期复发性流产(妊娠10周前)与凝血酶原V Leiden和G20210A突变是否存在相关性。前瞻性研究。背景:法国巴黎圣安东尼医院妇产科。两组妇女:妊娠10周前有早期不明原因复发性流产的妇女(n=260)和对照组无血栓栓塞史的健康妇女(n=240)。方法采用蝮蛇蛇毒抗凝反应试验(ACV试验)筛选蛋白C抗凝途径缺陷。蛋白C和因子V Leiden突变检测在每低ACV水平。每个样本检测G20210A凝血酶原突变。结果因子V Leiden和G20210A突变与妊娠10周前早期复发性自然流产相关,优势比分别为2.4 (95% CI 1-5)和2.7 (95% CI 1-7)。无论女性之前是否有过活产,都发现了类似的结果。结论妊娠10周前早期复发性流产与因子V或G20210A凝血酶原突变显著相关。这些结果表明抗凝剂预防这些早期流产的可能作用。
{"title":"Factor V Leiden and G20210A prothrombin mutations are risk factors for very early recurrent miscarriage","authors":"M.F. Reznikoff-Etiévant , V. Cayol , B. Carbonne , A. Robert , F. Coulet , J. Milliez","doi":"10.1016/S0306-5456(01)00298-4","DOIUrl":"https://doi.org/10.1016/S0306-5456(01)00298-4","url":null,"abstract":"<div><p><strong>Objective</strong> To determine whether there is an association between early recurrent miscarriage (before 10 weeks of pregnancy) and Factor V Leiden and G20210A prothrombin mutations.</p><p><strong>Design</strong> A prospective study.</p><p><strong>Setting</strong> Department of Gynaecology and Obstetrics, Saint Antoine Hospital, Paris, France.</p><p><strong>Population</strong> Two groups of women: those with early unexplained recurrent miscarriage before 10 weeks of pregnancy (<em>n</em>=260) and control healthy women without a previous history of thromboembolism (<em>n</em>=240).</p><p><strong>Methods</strong> Screening for defects in the protein C anticoagulant pathway was performed using the anticoagulant response to agkistrodon confortrix venom (ACV test). Protein C and Factor V Leiden mutation testing was performed for each low ACV level. Each sample was tested for the G20210A prothrombin mutation.</p><p><strong>Results</strong> Factor V Leiden and G20210A mutations were found to be associated with early recurrent spontaneous miscarriage before 10 weeks of pregnancy, the odds ratios being 2.4 (95% CI 1–5) and 2.7 (95% CI 1–7), respectively. Similar results were found whether or not women had had a previous live birth.</p><p><strong>Conclusions</strong> Early recurrent miscarriage before 10 weeks of pregnancy is significantly associated with Factor V or G20210A prothrombin mutations. These results indicate a possible role for anticoagulant prevention in these early miscarriages.</p></div>","PeriodicalId":75620,"journal":{"name":"British journal of obstetrics and gynaecology","volume":"108 12","pages":"Pages 1251-1254"},"PeriodicalIF":0.0,"publicationDate":"2001-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0306-5456(01)00298-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134663877","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2001-12-01DOI: 10.1016/S0306-5456(01)00289-3
Allison Martin , Anthony J O'Sullivan , Mark A Brown
Objective To determine whether the insulin resistance syndrome and altered body composition are features of hypertensive pregnancy.
Design Women were recruited in the third trimester of pregnancy from the antenatal clinic, day assessment unit, and maternity ward of St George Hospital, Sydney.
Population Women with pre-eclampsia (n=12), gestational hypertension (n=12), essential hypertension in pregnancy (n=11), and normotensive pregnancy (n=10).
Methods Energy metabolism was assessed by indirect calorimetry to measure basal metabolic rate and diet-induced thermogenesis. Body composition was measured as lean body mass, total body water and fat mass by bio-electrical impedance. Blood was collected for measurement of glucose, insulin and lipid profiles. Insulin resistance was indirectly assessed by the insulin and glucose concentrations and diet-induced thermogenesis.
Results Women with essential hypertension and gestational hypertension were heavier than women with normotensive pregnancies both pre-pregnancy and in the third trimester, whereas women with pre-eclampsia were similar to those with normotensive pregnancy. Women with essential hypertension were otherwise similar to normotensive pregnancy but women with gestational hypertension had a reduced diet-induced thermogenesis and almost double insulin levels. Women with pre-eclampsia had a similar body composition and insulin levels but reduced basal metabolic rate, diet-induced thermogenesis and glucose levels compared with normotensive pregnancy.
Conclusions Women who develop gestational hypertension, but not pre-eclampsia, are more likely to be overweight. Women with essential hypertension are similar to women with normotensive pregnancy throughout pregnancy. Both gestational hypertension and pre-eclampsia appear to be associated with some degree of insulin resistance, greater than that occurring in normal pregnancy.
{"title":"Body composition and energy metabolism in normotensive and hypertensive pregnancy","authors":"Allison Martin , Anthony J O'Sullivan , Mark A Brown","doi":"10.1016/S0306-5456(01)00289-3","DOIUrl":"https://doi.org/10.1016/S0306-5456(01)00289-3","url":null,"abstract":"<div><p><strong>Objective</strong> To determine whether the insulin resistance syndrome and altered body composition are features of hypertensive pregnancy.</p><p><strong>Design</strong> Women were recruited in the third trimester of pregnancy from the antenatal clinic, day assessment unit, and maternity ward of St George Hospital, Sydney.</p><p><strong>Population</strong> Women with pre-eclampsia (<em>n</em>=12), gestational hypertension (<em>n</em>=12), essential hypertension in pregnancy (<em>n</em>=11), and normotensive pregnancy (<em>n</em>=10).</p><p><strong>Methods</strong> Energy metabolism was assessed by indirect calorimetry to measure basal metabolic rate and diet-induced thermogenesis. Body composition was measured as lean body mass, total body water and fat mass by bio-electrical impedance. Blood was collected for measurement of glucose, insulin and lipid profiles. Insulin resistance was indirectly assessed by the insulin and glucose concentrations and diet-induced thermogenesis.</p><p><strong>Results</strong> Women with essential hypertension and gestational hypertension were heavier than women with normotensive pregnancies both pre-pregnancy and in the third trimester, whereas women with pre-eclampsia were similar to those with normotensive pregnancy. Women with essential hypertension were otherwise similar to normotensive pregnancy but women with gestational hypertension had a reduced diet-induced thermogenesis and almost double insulin levels. Women with pre-eclampsia had a similar body composition and insulin levels but reduced basal metabolic rate, diet-induced thermogenesis and glucose levels compared with normotensive pregnancy.</p><p><strong>Conclusions</strong> Women who develop gestational hypertension, but not pre-eclampsia, are more likely to be overweight. Women with essential hypertension are similar to women with normotensive pregnancy throughout pregnancy. Both gestational hypertension and pre-eclampsia appear to be associated with some degree of insulin resistance, greater than that occurring in normal pregnancy.</p></div>","PeriodicalId":75620,"journal":{"name":"British journal of obstetrics and gynaecology","volume":"108 12","pages":"Pages 1263-1271"},"PeriodicalIF":0.0,"publicationDate":"2001-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0306-5456(01)00289-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134663836","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2001-12-01DOI: 10.1016/S0306-5456(01)00263-7
John M.J Kirwan , C.Simon Herrington
{"title":"Human papillomavirus and cervical cancer: where are we now?","authors":"John M.J Kirwan , C.Simon Herrington","doi":"10.1016/S0306-5456(01)00263-7","DOIUrl":"https://doi.org/10.1016/S0306-5456(01)00263-7","url":null,"abstract":"","PeriodicalId":75620,"journal":{"name":"British journal of obstetrics and gynaecology","volume":"108 12","pages":"Pages 1204-1213"},"PeriodicalIF":0.0,"publicationDate":"2001-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0306-5456(01)00263-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134663879","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2001-12-01DOI: 10.1016/S0306-5456(01)00275-3
Kevin G Cooper , Stuart A Jack , David E Parkin , Adrian M Grant
Objective To assess clinical status, changes in health related quality of life, and subsequent management five years after medical management or transcervical resection of the endometrium for treatment of heavy menstrual loss.
Design Five year follow up using postal questionnaires and operative databank review.
Setting Gynaecology department of a large UK teaching hospital.
Population Women referred to the gynaecologist for treatment of heavy menstrual loss.
Methods Eligible women, without a treatment preference, were randomised equally to either medical treatment or transcervical resection of the endometrium.
Main outcome measures Women's satisfaction with treatment, menstrual status, changes in health related quality of life, and additional treatments received at five years.
Results One hundred and forty-four patients completed questionnaires, achieving 77% follow up (medical n=71/94; transcervical resection of the endometrium n=73/93). At five-year follow up, 7/71 (10%) of those randomised to the medical arm still used medical treatment, while 72/94 (77%) had undergone surgical treatment and 17/94 (18%) a hysterectomy. Twenty-five (27%) women allocated to transcervical resection of the endometrium had undergone further surgery, 18/93 (19%) a hysterectomy. At five years women initially randomised to medical treatment were significantly less likely to be totally satisfied (P<0.01, difference 21%, 95% CI –37% to –4%), or to recommend their allocated treatment to a friend (P<0.001, difference 59%, 95% CI –73% to –45%). Bleeding and pain scores were similar in both groups and highly significantly reduced. Significantly more women in the transcervical resection of the endometrium arm had no bleeding or very light bleeding (P<0.02, difference -22%, CI –31% to –4%), and they had significantly less days heavy bleeding (P<0.02). Short Form 36 health survey scores were significantly improved from baseline for all eight health scales in the transcervical resection of the endometrium arm, and four in the medical arm.
Conclusions A policy of immediate transcervical resection of the endometrium for women referred to a gynaecologist for treatment of heavy menstrual loss achieves higher levels of satisfaction, better menstrual status, and greater improvements in health related quality of life than medical treatment. In addition, transcervical resection of the endometrium is safe and does not lead to an increase in the number of hysterectomies. An effective endometrial ablative technique should be offered to all eligible women seeking treatment of their heavy menses from a gynaecologist.
目的评价内科治疗或经宫颈子宫内膜切除术治疗重度月经减少患者5年后的临床状况、健康相关生活质量变化及后续处理。设计采用邮寄问卷和可操作的数据库审查进行为期五年的随访。设置英国某大型教学医院妇科。人口妇女因月经严重减少而向妇科医生求诊。方法:无治疗偏好的符合条件的妇女被随机分为药物治疗组和经宫颈子宫内膜切除术组。主要结果衡量妇女对治疗的满意度、月经状况、与健康相关的生活质量的变化以及五年内接受的额外治疗。结果144例患者完成问卷调查,随访率为77%(医学n=71/94;经宫颈子宫内膜切除术(n=73/93)。在5年随访中,7/71(10%)随机分配到医疗组的患者仍然使用药物治疗,72/94(77%)接受了手术治疗,17/94(18%)接受了子宫切除术。25名(27%)经宫颈子宫内膜切除术的妇女接受了进一步的手术,18/93(19%)的妇女接受了子宫切除术。在5年时,最初被随机分配到药物治疗组的妇女完全满意的可能性(P<0.01,差异21%,95% CI -37%至-4%)或向朋友推荐其分配的治疗方法的可能性显著降低(P<0.001,差异59%,95% CI -73%至-45%)。两组患者的出血和疼痛评分相似,均显著降低。经宫颈切除子宫内膜臂的女性明显更多的没有出血或非常轻微的出血(P<0.02,差值-22%,CI -31%至-4%),并且她们的大出血天数明显减少(P<0.02)。经宫颈子宫内膜切除术组的短表36健康调查得分在所有8个健康量表的基线上都有显著提高,在医疗组的4个健康量表上有显著提高。结论经宫颈子宫内膜切除术治疗重度月经丢失的妇女比内科治疗获得更高的满意度、更好的月经状况和更大的健康相关生活质量改善。此外,经宫颈子宫内膜切除术是安全的,不会导致子宫切除术数量的增加。一个有效的子宫内膜消融技术应提供给所有符合条件的妇女寻求治疗她们的重度月经从妇科医生。
{"title":"Five-year follow up of women randomised to medical management or transcervical resection of the endometrium for heavy menstrual loss: clinical and quality of life outcomes","authors":"Kevin G Cooper , Stuart A Jack , David E Parkin , Adrian M Grant","doi":"10.1016/S0306-5456(01)00275-3","DOIUrl":"https://doi.org/10.1016/S0306-5456(01)00275-3","url":null,"abstract":"<div><p><strong>Objective</strong> To assess clinical status, changes in health related quality of life, and subsequent management five years after medical management or transcervical resection of the endometrium for treatment of heavy menstrual loss.</p><p><strong>Design</strong> Five year follow up using postal questionnaires and operative databank review.</p><p><strong>Setting</strong> Gynaecology department of a large UK teaching hospital.</p><p><strong>Population</strong> Women referred to the gynaecologist for treatment of heavy menstrual loss.</p><p><strong>Methods</strong> Eligible women, without a treatment preference, were randomised equally to either medical treatment or transcervical resection of the endometrium.</p><p><strong>Main outcome measures</strong> Women's satisfaction with treatment, menstrual status, changes in health related quality of life, and additional treatments received at five years.</p><p><strong>Results</strong> One hundred and forty-four patients completed questionnaires, achieving 77% follow up (medical <em>n</em>=71/94; transcervical resection of the endometrium <em>n</em>=73/93). At five-year follow up, 7/71 (10%) of those randomised to the medical arm still used medical treatment, while 72/94 (77%) had undergone surgical treatment and 17/94 (18%) a hysterectomy. Twenty-five (27%) women allocated to transcervical resection of the endometrium had undergone further surgery, 18/93 (19%) a hysterectomy. At five years women initially randomised to medical treatment were significantly less likely to be totally satisfied (<em>P</em><0.01, difference 21%, 95% CI –37% to –4%), or to recommend their allocated treatment to a friend (<em>P</em><0.001, difference 59%, 95% CI –73% to –45%). Bleeding and pain scores were similar in both groups and highly significantly reduced. Significantly more women in the transcervical resection of the endometrium arm had no bleeding or very light bleeding (<em>P</em><0.02, difference -22%, CI –31% to –4%), and they had significantly less days heavy bleeding (<em>P</em><0.02). Short Form 36 health survey scores were significantly improved from baseline for all eight health scales in the transcervical resection of the endometrium arm, and four in the medical arm.</p><p><strong>Conclusions</strong> A policy of immediate transcervical resection of the endometrium for women referred to a gynaecologist for treatment of heavy menstrual loss achieves higher levels of satisfaction, better menstrual status, and greater improvements in health related quality of life than medical treatment. In addition, transcervical resection of the endometrium is safe and does not lead to an increase in the number of hysterectomies. An effective endometrial ablative technique should be offered to all eligible women seeking treatment of their heavy menses from a gynaecologist.</p></div>","PeriodicalId":75620,"journal":{"name":"British journal of obstetrics and gynaecology","volume":"108 12","pages":"Pages 1222-1228"},"PeriodicalIF":0.0,"publicationDate":"2001-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0306-5456(01)00275-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134663883","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2001-12-01DOI: 10.1016/S0306-5456(01)00291-1
Wilco C. Graafmans , Jan-Hendrik Richardus , Alison Macfarlane , Marisa Rebagliato , Beatrice Blondel , S. Pauline Verloove-Vanhorick , Johan P. Mackenbach
Objective To quantify the impact of publication criteria on differences in published national perinatal mortality rates among Western European countries.
Design Descriptive study of perinatal mortality rates in Western European countries with adjustments for international differences in publication data.
Population All live births and perinatal deaths in 1994 in Western European countries.
Methods The 1994 perinatal mortality rates were obtained from national and Eurostat publications for Belgium, Denmark, Finland, France, Germany, Greece, The Netherlands, Norway, Portugal, Spain, Sweden, United Kingdom (England, Wales, Scotland, Northern Ireland). Two methods, one direct and one indirect, were used for adjusting these officially published rates for differences in registration laws or publication practices. For the indirect method adjustment factors were derived from an analysis of a large Finnish database using different cutoff points for gestational age and birthweight. For the direct method a common cutoff point was imposed for birthweight (1000g) and gestational age (28 completed weeks) on national perinatal mortality data, obtained from civil registration or hospital/obstetrics databases in each country.
Results The published perinatal mortality rates ranged from 5.4 per 1000 total births in Sweden and Finland to 9.7 in Greece and Northern Ireland. The indirect adjustment method showed that some countries apply cutoff points for registration or publication of perinatal mortality which may raise the perinatal mortality rate by up to 17% above the most commonly used threshold for including live and stillbirths. The direct adjustment method showed that a common lower limit of 1000g for birthweight or 28 weeks for gestational age would reduce the perinatal mortality rate, but by a differing extent ranging from 14% to 40%. Both adjustment methods reduced the contrast between the countries’ perinatal mortality rates, and changed their rank order.
Conclusion These quantitative results confirm that international differences in countries’ published perinatal mortality rates partly reflect differences between countries’ criteria for registration and publication of perinatal deaths.
{"title":"Comparability of published perinatal mortality rates in Western Europe: the quantitative impact of differences in gestational age and birthweight criteria","authors":"Wilco C. Graafmans , Jan-Hendrik Richardus , Alison Macfarlane , Marisa Rebagliato , Beatrice Blondel , S. Pauline Verloove-Vanhorick , Johan P. Mackenbach","doi":"10.1016/S0306-5456(01)00291-1","DOIUrl":"https://doi.org/10.1016/S0306-5456(01)00291-1","url":null,"abstract":"<div><p><strong>Objective</strong> <!-->To quantify the impact of publication criteria on differences in published national perinatal mortality rates among Western European countries.</p><p><strong>Design</strong> <!-->Descriptive study of perinatal mortality rates in Western European countries with adjustments for international differences in publication data.</p><p><strong>Population</strong> <!-->All live births and perinatal deaths in 1994 in Western European countries.</p><p><strong>Methods</strong> <!-->The 1994 perinatal mortality rates were obtained from national and Eurostat publications for Belgium, Denmark, Finland, France, Germany, Greece, The Netherlands, Norway, Portugal, Spain, Sweden, United Kingdom (England, Wales, Scotland, Northern Ireland). Two methods, one direct and one indirect, were used for adjusting these officially published rates for differences in registration laws or publication practices. For the indirect method adjustment factors were derived from an analysis of a large Finnish database using different cutoff points for gestational age and birthweight. For the direct method a common cutoff point was imposed for birthweight (1000g) and gestational age (28 completed weeks) on national perinatal mortality data, obtained from civil registration or hospital/obstetrics databases in each country.</p><p><strong>Results</strong> <!-->The published perinatal mortality rates ranged from 5.4 per 1000 total births in Sweden and Finland to 9.7 in Greece and Northern Ireland. The indirect adjustment method showed that some countries apply cutoff points for registration or publication of perinatal mortality which may raise the perinatal mortality rate by up to 17% above the most commonly used threshold for including live and stillbirths. The direct adjustment method showed that a common lower limit of 1000g for birthweight or 28 weeks for gestational age would reduce the perinatal mortality rate, but by a differing extent ranging from 14% to 40%. Both adjustment methods reduced the contrast between the countries’ perinatal mortality rates, and changed their rank order.</p><p><strong>Conclusion</strong> <!-->These quantitative results confirm that international differences in countries’ published perinatal mortality rates partly reflect differences between countries’ criteria for registration and publication of perinatal deaths.</p></div>","PeriodicalId":75620,"journal":{"name":"British journal of obstetrics and gynaecology","volume":"108 12","pages":"Pages 1237-1245"},"PeriodicalIF":0.0,"publicationDate":"2001-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0306-5456(01)00291-1","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134663885","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2001-12-01DOI: 10.1016/S0306-5456(01)00290-X
G. Lieberman , A.B. MacLean , J.R. Buscombe , A.J.W. Hilson , K. Adamson , W.M. Reid , A. Green , R.H. Begent
Objective To assess the effectiveness of a dual head coincidence gamma camera in identifying ovarian cancer as a less expensive alternative to the traditional 2-[18F] fluoro-2-deoxy-D-glucose (18FDG) system using positron emission tomography.
Design Prospective study.
Population Twenty consecutive women suspected of having ovarian carcinoma. Inclusion was based on abnormal serum CA125 (reference range is 0–35 units/L), ultrasound, computerised tomography or clinical findings.
Methods Women underwent assessment before staging laparotomy. Two nuclear medicine physicians, who were blinded to the pre-operative assessment, reported on 18FDG- dual head coincidence gamma camera imaging.
Main outcomemeasures The histology and operative staging were compared with the 18FDG- dual head coincidence gamma camera findings.
Results Twelve women had pelvic malignancies (nine primary and three recurrences), seven women had benign pathology and one patient had a borderline malignancy. We were able to image accurately all malignant pelvic masses with dual head coincidence gamma camera, as well as accurately demonstrate disease spread. Two of the benign pelvic masses localised 18FDG. The positive predictive value for detecting malignancy was 86%.
Conclusions Dual head coincidence gamma camera offers accurate and affordable imaging in suspected ovarian masses, with improved specificity over CA125, ultrasound and computerised tomography. These results are similar to those obtained on more expensive dedicated PET systems. We report on a series of patients believed to have primary or recurrent carcinoma and recognise the need to include patients more likely to have benign lesions to assess false positive results. However, we believe that dual head coincidence gamma camera is useful in the pre-operative assessment of women with suspected ovarian cancer.
{"title":"The clinical application of a dual head gamma camera with coincidence detection in 20 women with suspected ovarian cancer","authors":"G. Lieberman , A.B. MacLean , J.R. Buscombe , A.J.W. Hilson , K. Adamson , W.M. Reid , A. Green , R.H. Begent","doi":"10.1016/S0306-5456(01)00290-X","DOIUrl":"https://doi.org/10.1016/S0306-5456(01)00290-X","url":null,"abstract":"<div><p><strong>Objective</strong> To assess the effectiveness of a dual head coincidence gamma camera in identifying ovarian cancer as a less expensive alternative to the traditional 2-[<sup>18</sup>F] fluoro-2-deoxy-D-glucose (<sup>18</sup>FDG) system using positron emission tomography.</p><p><strong>Design</strong> Prospective study.</p><p><strong>Population</strong> Twenty consecutive women suspected of having ovarian carcinoma. Inclusion was based on abnormal serum CA125 (reference range is 0–35 units/L), ultrasound, computerised tomography or clinical findings.</p><p><strong>Methods</strong> Women underwent assessment before staging laparotomy. Two nuclear medicine physicians, who were blinded to the pre-operative assessment, reported on <sup>18</sup>FDG- dual head coincidence gamma camera imaging.</p><p><strong>Main outcome</strong> <strong>measures</strong> The histology and operative staging were compared with the <sup>18</sup>FDG- dual head coincidence gamma camera findings.</p><p><strong>Results</strong> Twelve women had pelvic malignancies (nine primary and three recurrences), seven women had benign pathology and one patient had a borderline malignancy. We were able to image accurately all malignant pelvic masses with dual head coincidence gamma camera, as well as accurately demonstrate disease spread. Two of the benign pelvic masses localised <sup>18</sup>FDG. The positive predictive value for detecting malignancy was 86%.</p><p><strong>Conclusions</strong> Dual head coincidence gamma camera offers accurate and affordable imaging in suspected ovarian masses, with improved specificity over CA125, ultrasound and computerised tomography. These results are similar to those obtained on more expensive dedicated PET systems. We report on a series of patients believed to have primary or recurrent carcinoma and recognise the need to include patients more likely to have benign lesions to assess false positive results. However, we believe that dual head coincidence gamma camera is useful in the pre-operative assessment of women with suspected ovarian cancer.</p></div>","PeriodicalId":75620,"journal":{"name":"British journal of obstetrics and gynaecology","volume":"108 12","pages":"Pages 1229-1236"},"PeriodicalIF":0.0,"publicationDate":"2001-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0306-5456(01)00290-X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134663884","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2001-12-01DOI: 10.1016/S0306-5456(01)00294-7
A.G Sutcliffe , N.J Sebire , A.J Pigott , B Taylor , P.R Edwards , K.H Nicolaides
Objective To examine the postnatal development of a group of children born after in utero laser ablation therapy for severe twin-to-twin transfusion syndrome.
Design Retrospective cohort outcome study involving assessment of neurodevelopment and physical well being.
Setting Harris Birthright Centre, King’s College Hospital, London.
Participants Twins and singleton survivors treated via laser ablation therapy for twin-to-twin transfusion syndrome over a four-year period.
Methods Of 54 families contacted to participate in the study, who had been treated for twin-to-twin transfusion syndrome during a four-year period, 24 families attended for paediatric assessment; 12 pairs of twins and 12 singleton survivors were assessed for perinatal, neurological and neurodevelopmental outcome using the Griffiths scales of mental development. A further 20 families were assessed via a proforma after contact with their general practitioner. A comparison of these groups showed no significant differences in sociodemographic factors or severity of disease between responders (44 families, 81.5%) and non-responders (10 families).
Results The group of children assessed by a paediatrician had low birthweight (1619g donor, 1814g recipient, 1877g singleton) and had been born preterm (33 weeks twins, 31.2 weeks singleton) with attendant increased resuscitation, neonatal unit admission (mean 40 days) and instrumental delivery. Mean Griffiths scores were within the normal range of ability (91.2 donor vs 97.7 recipient and 101.6 singletons) with the only significant difference being in the locomotor subscale where donor (82.6) and recipient (85.3) were less than singletons: -99.1 (P<0.05). There was no cerebral palsy in the singleton survivors, but there were five cases in the twin group. All except one affected child (with quadriplegia) had mean Griffiths scores in the normal range. In the GP proforma group there was one case, in a twin, of cerebral palsy.
Conclusion The overall cerebral palsy rate was 9%: 0% in the singleton survivors group and 13.3% in the twin survivors group. This pilot data highlights the need for careful long term follow up of children affected by twin-to-twin transfusion syndrome.
{"title":"Outcome for children born after in utero laser ablation therapy for severe twin-to-twin transfusion syndrome","authors":"A.G Sutcliffe , N.J Sebire , A.J Pigott , B Taylor , P.R Edwards , K.H Nicolaides","doi":"10.1016/S0306-5456(01)00294-7","DOIUrl":"https://doi.org/10.1016/S0306-5456(01)00294-7","url":null,"abstract":"<div><p><strong>Objective</strong> To examine the postnatal development of a group of children born after <em>in utero</em> laser ablation therapy for severe twin-to-twin transfusion syndrome.</p><p><strong>Design</strong> <!-->Retrospective cohort outcome study involving assessment of neurodevelopment and physical well being.</p><p><strong>Setting</strong> <!-->Harris Birthright Centre, King’s College Hospital, London.</p><p><strong>Participants</strong> <!-->Twins and singleton survivors treated via laser ablation therapy for twin-to-twin transfusion syndrome over a four-year period.</p><p><strong>Methods</strong> Of 54 families contacted to participate in the study, who had been treated for twin-to-twin transfusion syndrome during a four-year period, 24 families attended for paediatric assessment; 12 pairs of twins and 12 singleton survivors were assessed for perinatal, neurological and neurodevelopmental outcome using the Griffiths scales of mental development. A further 20 families were assessed via a proforma after contact with their general practitioner. A comparison of these groups showed no significant differences in sociodemographic factors or severity of disease between responders (44 families, 81.5%) and non-responders (10 families).</p><p><strong>Results</strong> The group of children assessed by a paediatrician had low birthweight (1619g donor, 1814g recipient, 1877g singleton) and had been born preterm (33 weeks twins, 31.2 weeks singleton) with attendant increased resuscitation, neonatal unit admission (mean 40 days) and instrumental delivery. Mean Griffiths scores were within the normal range of ability (91.2 donor <em>vs</em> 97.7 recipient and 101.6 singletons) with the only significant difference being in the locomotor subscale where donor (82.6) and recipient (85.3) were less than singletons: -99.1 (<em>P</em><0.05). There was no cerebral palsy in the singleton survivors, but there were five cases in the twin group. All except one affected child (with quadriplegia) had mean Griffiths scores in the normal range. In the GP proforma group there was one case, in a twin, of cerebral palsy.</p><p><strong>Conclusion</strong> The overall cerebral palsy rate was 9%: 0% in the singleton survivors group and 13.3% in the twin survivors group. This pilot data highlights the need for careful long term follow up of children affected by twin-to-twin transfusion syndrome.</p></div>","PeriodicalId":75620,"journal":{"name":"British journal of obstetrics and gynaecology","volume":"108 12","pages":"Pages 1246-1250"},"PeriodicalIF":0.0,"publicationDate":"2001-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0306-5456(01)00294-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134663887","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}