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Grau de subestimação histopatológica por core biopsy de lesões não palpáveis da mama 核心活检对乳腺不可触及病变的组织病理学低估程度
IF 1.2 Q3 Medicine Pub Date : 2011-03-31 DOI: 10.1590/S0100-72032011000700002
Aline Valadão Britto Gonçalves, Luiz Claudio Santos Thuler, Fabíola Procaci Kestelman, Pedro Carmo, C.F.F Lima, R. Cipolotti
OBJETIVO: Determinar o grau de subestimacao de core biopsy, guiada por imagem, de lesoes impalpaveis da mama subsequentemente submetidas a exerese cirurgica. METODOS: Foram revisados retrospectivamente 352 casos com biopsias de fragmento que foram submetidos a cirurgia entre fevereiro de 2000 e dezembro de 2005, cujo laudo histopatologico estava registrado no sistema interno de informacao. Os resultados foram comparados com os da cirurgia e a taxa de subestimacao foi calculada dividindo-se o numero de carcinoma in situ e/ou invasivo a cirurgia pelo numero de lesoes de alto risco ou carcinoma in situ que foram submetidas a cirurgia. O grau de concordância entre os resultados foi obtido pelo percentual de concordância e pelo coeficiente kappa de Cohen. A associacao das variaveis estudadas com a subestimacao do diagnostico foi verificada pelos testes do c2 exato de Fisher, ANOVA e Mann-Whitney U. O risco de subestimacao foi medido por meio do risco relativo acompanhado dos respectivos intervalos com 95% de confianca (IC95%). RESULTADOS: Core biopsy foi inconclusiva em 15,6%. O laudo histopatologico foi benigno em 26,4%, sugestivo de lesao de alto risco em 12,8% e maligno em 45,2%. A concordância entre a core biopsy e a cirurgia foi de 82,1% (kappa=0,75). A taxa de falso negativo foi de 5,4% e a lesao foi completamente removida em 3,4%. A taxa de subestimacao foi de 9,1% e esteve associada com BI-RADS® categoria 5 (p=0,01), microcalcificacoes (p < 0,001) e estereotaxia (p= 0,002). Todos os casos subestimados apresentavam diâmetro menor que 20 mm e em todos foram retirados pelo menos cinco fragmentos. A taxa de subestimacao para lesoes de alto risco foi de 31,1%, 41,2%, para hiperplasia ductal atipica, 31,2% para lesoes papiliferas, 16,7% para tumor filoides e 41,9% para carcinoma ductal in situ. CONCLUSOES: Core biopsy guiada por imagem e um procedimento confiavel, contudo permanece a recomendacao de resseccao cirurgica de lesoes de alto risco detectadas a biopsia de fragmento ja que nao foi possivel estabelecer caracteristicas clinicas, imaginologicas, do procedimento e patologicas que pudessem predizer subestimacao e evitar a cirurgia. Amostras representativas da lesao sao mais importantes que o numero de fragmentos.
摘要目的:探讨核活检在影像学引导下对乳腺隐性病变的低估程度。方法:回顾性回顾2000年2月至2005年12月接受手术的352例碎片活检,其组织病理学报告记录在内部信息系统中。将结果与手术结果进行比较,用原位癌和/或侵入性手术的数量除以手术后高危病变或原位癌的数量来计算低估率。通过一致性百分比和科恩kappa系数得到结果之间的一致性程度。通过Fisher精确c2检验、方差分析和Mann-Whitney u检验验证了研究变量与诊断低估的关联。低估风险是通过相对风险和95%置信区间(95% ci)来衡量的。结果:15.6%的核心活检不确定。组织病理学报告为良性26.4%,提示高危病变12.8%,恶性病变45.2%。核心活检与手术的一致性为82.1% (kappa= 0.75)。假阴性率为5.4%,损伤完全消除3.4%。低估率为9.1%,与BI-RADS®第5类(p= 0.01)、微钙化(p < 0.001)和立体定向(p= 0.002)有关。所有被低估的病例直径均小于20毫米,至少切除5个碎片。高危病变的低估率为31.1%,非典型导管增生的低估率为41.2%,乳头状病变的低估率为31.2%,叶状肿瘤的低估率为16.7%,原位导管癌的低估率为41.9%。CONCLUSOES:核心biopsy图像制导过程可靠,但陪伴我的建议resseccao被检测出损伤高风险手术活检片段,我们并不是躺下,imaginologicas诊所、步骤和特点能预测subestimacao patologicas,避免手术。具有代表性的lesao样本比碎片的数量更重要。
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引用次数: 6
Desenvolvimento das fissuras cerebrais fetais: avaliação com ultrassonografia tridimensional 胎儿脑裂的发展:三维超声评价
IF 1.2 Q3 Medicine Pub Date : 2011-03-01 DOI: 10.1590/S0100-72032011000300002
C. Alves, Edward Araújo Júnior, L. M. M. Nardozza, P. S. Oliveira, Suzan Menasce Goldman, S. Ajzen, A. F. Moron
OBJETIVO: avaliar a distância das fissuras cerebrais fetais a borda interna da calota craniana por meio da ultrassonografia tridimensional (US3D). METODOS: realizou-se um estudo de corte transversal em 80 gestantes normais entre a 21a e 34a semanas de gestacao. Avaliou-se a distância entre a tabua ossea interna da calota craniana fetal e as fissuras de Sylvius, parieto-occipital, hipocampo e calcarina. Para a obtencao desta distância para as tres primeiras fissuras, realizou-se uma varredura tridimensional atraves do plano axial (nivel dos ventriculos laterais). Para a obtencao da distância da fissura calcarina utilizou-se uma varredura coronal (nivel dos lobos occiptais). Para avaliar a correlacao entre as fissuras e a idade gestacional foram realizadas regressoes de primeiro grau, sendo os ajustes calculados pelo coeficiente de determinacao (R2). Foram determinados percentis 5, 50 e 95 para cada fissura. Avaliou-se ainda a correlacao entre a distância destas fissuras com os diâmetros biparietal (DBP) e circunferencia craniana (CC) utilizando o coeficiente de correlacao de Pearson (r). RESULTADOS: todas as medidas das fissuras apresentaram correlacao linear com a idade gestacional (Sylvius: R2=0,5; parieto-occipital: R2=0,7; hipocampo: R2=0,3 e calcarina: R2=0,3). A media da distância das fissuras variou de 7,0 a 14,0 mm, 15,9 a 28,7 mm, 15,4 a 25,4 mm e 15,7 a 24,8 mm para as fissuras de Sylvius, parieto-occipital, hipocampo e calcarina, respectivamente. As fissuras de Sylvius e parieto-occipital apresentaram as maiores correlacoes com o DBP (r=0,8 e 0,7, respectivamente) e a CC (r=0,7 e 0,8, respectivamente). CONCLUSOES: a distância das fissuras cerebrais fetais a borda interna da calota craniana por meio da US3D apresentou correlacao positiva com a idade gestacional.
摘要目的:利用三维超声(US3D)评价胎儿脑裂与颅骨内缘的距离。方法:对80名妊娠21 - 34周的正常孕妇进行横断面研究。评估胎儿颅骨内骨板与Sylvius、顶骨枕骨、海马和胼胝体裂缝之间的距离。为了获得前三个裂缝的距离,通过轴向平面(侧心室水平)进行三维扫描。为了获得钙石裂缝的距离,我们使用了冠状扫描(枕叶水平)。为了评估裂缝与胎龄之间的相关性,进行了一级回归,并通过决定系数(R2)计算调整。每个裂缝分别确定5、50和95百分位。我们还使用Pearson相关系数(r)评估了这些裂缝的距离与双顶骨直径(DBP)和颅骨周长(CC)之间的相关性。结果:所有裂缝测量均与胎龄呈线性相关(Sylvius: R2= 0.5; Sylvius: R2= 0.5)。枕顶叶:R2 = 0、7;海马体:R2= 0.3,钙素:R2= 0.3)。Sylvius、顶枕、海马和calcarina裂缝的平均距离分别为7.0 ~ 14.0 mm、15.9 ~ 28.7 mm、15.4 ~ 25.4 mm和15.7 ~ 24.8 mm。Sylvius和顶骨-枕裂与DBP (r= 0.8和0.7)和CC (r= 0.7和0.8)的相关性最大。结论:US3D测量的胎儿脑裂到颅骨内缘的距离与胎龄呈正相关。
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引用次数: 0
Comportamento do médico residente diante das questões sobre função sexual no ciclo gravídico-puerperal: comparação entre três especialidades - Ginecologia/Obstetrícia, Psiquiatria e Clínica Médica 住院医师在怀孕和产后性功能问题上的行为:妇产科、精神病学和临床医学三个专业的比较
IF 1.2 Q3 Medicine Pub Date : 2011-03-01 DOI: 10.1590/S0100-72032011000300009
T. C. Vieira
ObjetivO: comparar o comportamento do médico residente de Ginecologia e Obstetrícia (GO) com o de Clínica Médica (CM) e Psiquiatria (Psiq), perante as questões da função sexual, enfocando sua conduta profissional. MetOdOlOgia: estudo observacional,transversal, usando questionário adaptado, autorresponsivo e anônimo. ResultadOs: 154 questionários (92,5%) foram considerados válidos (74CM, 33 Psiq e 47GO). Somente 19,5 % dos médicos investigam queixas sexuais espontaneamente, apesar de que 68,2% concordam que estas questões devem fazer parte de todas as anamneses. Somente 22,7%, das 3 especialidades, afirmam ter segurança total para responder a questões sexuais; entretanto diante destas, 76% ouvem e orientam e 70,8% admitem faltar conhecimento específico sobre sexualidade. O GO foi o profissional mais indicado para tratar disfunções sexuais femininas (89%).Entretanto, o GO não conhece o ciclo de resposta sexual feminina (74,5%), além de que, ele se considera menos apto a tratar desejo hipoativo (25,5%) e anorgasmia (17%) comparado com o de psiquiatria (respectivamente, 69,7% e 57,6%). A maioria achou o estudo instigante e educativo: Clínica Médica (47,3%), Psiquiatria (69,7%) e Ginecologia/Obstetrícia (74,5%). A participação,neste trabalho aumentou o interesse pelo tema em todas as especialidades (60,4%). COnClusões: residentes de Psiquiatria investigaram espontaneamente e com maior frequência as queixas sexuais de suas pacientes, além de relatarem maior aptidão em tratar desejo hipoativo e anorgasmia, enquanto os GO sentiram maior habilidade para: lubrificação deficiente, sinussorragia e hipotonia e/ou rotura do assoalho pélvico. Os residentes de Clínica Médica, por seu lado, foram os que menos indagaram, menos atenderam e não se consideraram aptos a tratar queixas sexuais. Os médicos das 3 áreas de residência afirmaram não possuírem segurança, nem conhecimento específico suficiente para responder às questões sobre função sexual. A maioria dos residentes considerou este estudo instigante e educativo. Somente responder ao questionário despertou interesse em ampliar o conhecimento na área de Sexualidade.
摘要目的:比较妇产科住院医师与内科住院医师、精神科住院医师在性功能问题上的行为,重点比较其专业行为。方法:观察性、横断面研究,采用自反应性、匿名问卷。结果:154份问卷(92.5%)被认为是有效的(74CM, 33 Psiq和47GO)。只有19.5%的医生自发地调查性投诉,尽管68.2%的医生同意这些问题应该成为所有病史的一部分。在3个专业中,只有22.7%的人声称在回答性问题时完全安全;然而,面对这些,76%的人倾听和指导,70.8%的人承认缺乏关于性的具体知识。GO是治疗女性性功能障碍最合适的专业人员(89%)。然而,与精神病学(分别为69.7%和57.6%)相比,GO不知道女性的性反应周期(74.5%),而且它认为自己更不适合治疗性欲减退(25.5%)和性高潮障碍(17%)。大多数人认为这项研究具有启发性和教育性:内科(47.3%)、精神病学(69.7%)和妇产科(74.5%)。参与这项工作增加了所有专业对该主题的兴趣(60.4%)。结论:精神科住院医师自发地、更频繁地调查他们的患者的性主诉,并报告他们更有能力治疗性欲减退和性高潮障碍,而GO感觉更有能力:润滑不足、鼻窦撕裂、张力减退和/或盆底破裂。另一方面,医疗诊所的住院医生是那些询问最少、出席最少、认为自己不适合治疗性投诉的人。这三个地区的医生表示,他们没有足够的安全保障,也没有足够的专门知识来回答有关性功能的问题。大多数居民认为这项研究具有启发性和教育性。仅仅回答问卷就激发了拓宽性领域知识的兴趣。
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引用次数: 0
The sexuality in women undergoing total and subtotal hysterectomy 接受全子宫切除术和次全子宫切除术的妇女的性征
IF 1.2 Q3 Medicine Pub Date : 2011-03-01 DOI: 10.1590/S0100-72032011000300012
Nayara de Paula Faleiros
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引用次数: 0
Eficácia de dinoprostone e misoprostol para indução do trabalho de parto em nulíparas 地诺前列醇和米索前列醇对未分娩妇女引产的疗效
IF 1.2 Q3 Medicine Pub Date : 2011-03-01 DOI: 10.1590/S0100-72032011000300003
Tenilson Amaral Oliveira, Elisane Melo, Márcia Maria Auxiliadora de Aquino, Corintio Mariani Neto
PURPOSE: to determine the efficacy and safety of dinoprostone and misoprostol for the induction of vaginal childbirth, with or without the use of oxytocin in nulliparous women. METHODS: in this retrospective observational study, 238 patients were subjected to the induction of delivery from January 2008 to February 2010 with the use of misoprostol 25 mcg by the vaginal route or a pessary containing 10 mg of dinoprostone. A total of 184 patients were selected, with the following characteristics: nulliparous, gestational age of 37-42 weeks, singleton pregnancies, cephalic presentation, intact membranes, and Bishop score < 3. Obstetric and neonatal data were analyzed and compared between groups. The Student t-test, chi-square test and Fisher's exact test were used for statistical analysis, with the level of significance set at p<0.05. RESULTS: the rate of vaginal childbirth did not differ significantly in patients who used misoprostol and dinoprostone (43.2% versus 50%; p = 0.35, respectively). The ripening of cervix was higher in the group treated with misoprostol (87.3% versus 75.6%, p=0.04). The use of oxytocin was necessary in 58.8% of the misoprostol group and 57.3% in the dinoprostone group after the ripening of cervix. Failed induction was the primary indication of caesarean section delivery in both groups, with no significant difference between them. Fetal and maternal adverse events, such as tachysystole and Apgar scores were similar. CONCLUSION: dinoprostone and misoprostol are both effective for vaginal childbirth induction, although they need to be combined with oxytocin. They showed a similar safety profile, with misoprostol being more efficient regarding cervical ripening.
目的:确定迪诺前列酮和米索前列醇在未生育妇女中使用或不使用催产素诱导阴道分娩的有效性和安全性。方法:在这项回顾性观察性研究中,238例患者在2008年1月至2010年2月期间接受了米索前列醇25mcg阴道诱导分娩或含有10 mg迪诺前列醇的子宫托的诱导分娩。共入选184例患者,均为未产、胎龄37 ~ 42周、单胎、头位、胎膜完整、Bishop评分< 3分。分析和比较两组间的产科和新生儿数据。采用学生t检验、卡方检验和Fisher确切检验进行统计学分析,显著性水平为p<0.05。结果:使用米索前列醇和迪诺前列酮的患者阴道分娩率无显著差异(43.2% vs 50%;P = 0.35)。米索前列醇组宫颈成熟率较高(87.3%比75.6%,p=0.04)。米索前列醇组58.8%和迪诺前列酮组57.3%在子宫颈成熟后需要使用催产素。引产失败是两组剖宫产的主要指征,两组间差异无统计学意义。胎儿和母亲的不良事件,如心动过速和阿普加评分相似。结论:迪诺前列酮、米索前列醇均可有效诱导阴道分娩,但需与催产素合用。它们显示出相似的安全性,米索前列醇对宫颈成熟更有效。
{"title":"Eficácia de dinoprostone e misoprostol para indução do trabalho de parto em nulíparas","authors":"Tenilson Amaral Oliveira, Elisane Melo, Márcia Maria Auxiliadora de Aquino, Corintio Mariani Neto","doi":"10.1590/S0100-72032011000300003","DOIUrl":"https://doi.org/10.1590/S0100-72032011000300003","url":null,"abstract":"PURPOSE: to determine the efficacy and safety of dinoprostone and misoprostol for the induction of vaginal childbirth, with or without the use of oxytocin in nulliparous women. METHODS: in this retrospective observational study, 238 patients were subjected to the induction of delivery from January 2008 to February 2010 with the use of misoprostol 25 mcg by the vaginal route or a pessary containing 10 mg of dinoprostone. A total of 184 patients were selected, with the following characteristics: nulliparous, gestational age of 37-42 weeks, singleton pregnancies, cephalic presentation, intact membranes, and Bishop score < 3. Obstetric and neonatal data were analyzed and compared between groups. The Student t-test, chi-square test and Fisher's exact test were used for statistical analysis, with the level of significance set at p<0.05. RESULTS: the rate of vaginal childbirth did not differ significantly in patients who used misoprostol and dinoprostone (43.2% versus 50%; p = 0.35, respectively). The ripening of cervix was higher in the group treated with misoprostol (87.3% versus 75.6%, p=0.04). The use of oxytocin was necessary in 58.8% of the misoprostol group and 57.3% in the dinoprostone group after the ripening of cervix. Failed induction was the primary indication of caesarean section delivery in both groups, with no significant difference between them. Fetal and maternal adverse events, such as tachysystole and Apgar scores were similar. CONCLUSION: dinoprostone and misoprostol are both effective for vaginal childbirth induction, although they need to be combined with oxytocin. They showed a similar safety profile, with misoprostol being more efficient regarding cervical ripening.","PeriodicalId":47257,"journal":{"name":"Revista Brasileira de Ginecologia e Obstetricia","volume":null,"pages":null},"PeriodicalIF":1.2,"publicationDate":"2011-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67234497","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}
引用次数: 6
Endometriose em cicatriz cirúrgica: uma série de 42 pacientes 子宫内膜异位症手术疤痕:42例系列患者
IF 1.2 Q3 Medicine Pub Date : 2011-03-01 DOI: 10.1590/S0100-72032011000300004
F. Vilarino, Bianca Bianco, A. Martins, Denise Maria Christofolini, C. Barbosa
PURPOSE: to evaluate the frequency and clinical picture of patients with incisional endometriosis. METHODS: retrospective descriptive study performed from the medical records of patients that underwent nodules resection in the surgical scar at Faculdade de Medicina do ABC, from November 1990 to September 2003. The age, parity, number of cesarean sections, symptoms, tumor location, initial diagnosis, treatment, and recurrences were surveyed and analyzed. The results were reported as percentage, mean, and standard deviation. RESULTS: we found 42 patients that were diagnosed with scar endometriosis. From these 42 cases, 37 were of endometriosis on cesarean section scar; 3 cases of episiotomies and 2 cases on bladder in scar of hysterography. The mean age of the patients was 32.4 years old, standard deviation of ±6.2 years. All of them had previous obstetric surgery, and the main complaint was nodulation with perimenstrual pain in 40% of the cases. In 57% of the patients, the clinical evaluation was confirmed by pelvic or transvaginal ultrasonography. Patients were treated with total resection, and recurrence occurred in only two cases. CONCLUSION: scar surgical endometriosis is uncommon; however, the clinical diagnosis is easy when the signs and symptoms are known. The effective treatment is surgical resection.
目的:探讨切口子宫内膜异位症的发病频率及临床特点。方法:回顾性描述性研究对1990年11月至2003年9月在ABC医学院行手术瘢痕结节切除术的患者病历进行分析。调查和分析年龄、胎次、剖宫产次数、症状、肿瘤位置、初次诊断、治疗和复发情况。结果以百分比、平均值和标准差报告。结果:42例确诊为瘢痕性子宫内膜异位症。42例中,子宫内膜异位症伴剖宫产瘢痕37例;宫腔镜瘢痕外阴切开术3例,膀胱切开术2例。患者平均年龄32.4岁,标准差±6.2岁。所有患者既往均有产科手术史,其中40%的病例以结瘤伴经周疼痛为主要主诉。57%的患者通过盆腔或阴道超声检查证实了临床评价。患者均行全切除治疗,仅有2例复发。结论:瘢痕手术子宫内膜异位症少见;然而,当体征和症状已知时,临床诊断很容易。有效的治疗方法是手术切除。
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引用次数: 8
Presença de células da junção escamo-colunar em esfregaços cérvico-vaginais de mulheres acima de 40 anos 40岁以上女性宫颈-阴道涂片中鳞状柱状交界处细胞的存在
IF 1.2 Q3 Medicine Pub Date : 2011-03-01 DOI: 10.1590/S0100-72032011000300005
G. A. Nai, Karen Karina Gusmão de Souza, Eliane Rissato Rodrigues, Ricardo Luís Barbosa
PURPOSE: to evaluate the frequency of cells of the cervical transitional zone (CTZ) in cervicovaginal smears of women older than 40 years. METHODS: we conducted a retrospective study with review of 24,316 Pap smear reports during the period from January 2005 to December 2008, to evaluate the cases without material of the CTZ. Exclusion criteria were: total hysterectomy, smears with severe atrophy or unsatisfactory for analysis, cases without visualization of the cervix or the external orifice of the cervix closed during examination and records without the patient's age. A total of 21,866 cervical-vaginal cytology reports were included in this study. We evaluated the relationship between the presence of material of the CTZ and use of hormone replacement therapy (HRT) in patients aged 40 years or more and the relationship between presence of material of the CTZ and a moderate to intense inflammatory process in patients aged 39 years or less. Data were analyzed statistically by the χ2 test and Odds Ratio. RESULTS: only 11.2% of patients younger than 40 years had no material from the CTZ in their smears, while 47% patients older than 40 years had no material from the CTZ (p=0.0001). Most patients aged 40 years or more (92.1%) did not use HRT and this was not a predictor of incidence of CTZ material in these patients (p> 0.05). In contrast, most patients younger than 40 years without CTZ material (74.5%) had abundant inflammation in the smears (p=0.0001). CONCLUSION: patients aged 40 years or more had a lower incidence of material from the CTZ in cervicovaginal smears, and inflammation was a factor that contributed to the absence of CTZ material in the smears from patients younger than 40 years.
目的:评价40岁以上妇女宫颈阴道涂片中宫颈过渡带(CTZ)细胞的频率。方法:我们进行了一项回顾性研究,回顾了2005年1月至2008年12月期间24,316例巴氏涂片报告,以评估没有CTZ材料的病例。排除标准为:全子宫切除、涂片严重萎缩或不能用于分析、检查时未见宫颈或宫颈外孔闭合、无年龄记录者。本研究共纳入了21,866份宫颈阴道细胞学报告。我们评估了40岁及以上患者中CTZ物质的存在与激素替代疗法(HRT)的使用之间的关系,以及39岁及以下患者中CTZ物质的存在与中度至重度炎症过程之间的关系。采用χ2检验和比值比对资料进行统计学分析。结果:只有11.2%的40岁以下患者的涂片中没有来自CTZ的物质,而47%的40岁以上患者的涂片中没有来自CTZ的物质(p=0.0001)。大多数40岁或以上的患者(92.1%)没有使用HRT,这不是这些患者CTZ物质发生率的预测因子(p < 0.05)。相比之下,大多数40岁以下无CTZ物质的患者(74.5%)在涂片中有丰富的炎症(p=0.0001)。结论:40岁及以上患者宫颈阴道涂片中CTZ物质的发生率较低,炎症是导致40岁以下患者涂片中CTZ物质缺失的一个因素。
{"title":"Presença de células da junção escamo-colunar em esfregaços cérvico-vaginais de mulheres acima de 40 anos","authors":"G. A. Nai, Karen Karina Gusmão de Souza, Eliane Rissato Rodrigues, Ricardo Luís Barbosa","doi":"10.1590/S0100-72032011000300005","DOIUrl":"https://doi.org/10.1590/S0100-72032011000300005","url":null,"abstract":"PURPOSE: to evaluate the frequency of cells of the cervical transitional zone (CTZ) in cervicovaginal smears of women older than 40 years. METHODS: we conducted a retrospective study with review of 24,316 Pap smear reports during the period from January 2005 to December 2008, to evaluate the cases without material of the CTZ. Exclusion criteria were: total hysterectomy, smears with severe atrophy or unsatisfactory for analysis, cases without visualization of the cervix or the external orifice of the cervix closed during examination and records without the patient's age. A total of 21,866 cervical-vaginal cytology reports were included in this study. We evaluated the relationship between the presence of material of the CTZ and use of hormone replacement therapy (HRT) in patients aged 40 years or more and the relationship between presence of material of the CTZ and a moderate to intense inflammatory process in patients aged 39 years or less. Data were analyzed statistically by the χ2 test and Odds Ratio. RESULTS: only 11.2% of patients younger than 40 years had no material from the CTZ in their smears, while 47% patients older than 40 years had no material from the CTZ (p=0.0001). Most patients aged 40 years or more (92.1%) did not use HRT and this was not a predictor of incidence of CTZ material in these patients (p> 0.05). In contrast, most patients younger than 40 years without CTZ material (74.5%) had abundant inflammation in the smears (p=0.0001). CONCLUSION: patients aged 40 years or more had a lower incidence of material from the CTZ in cervicovaginal smears, and inflammation was a factor that contributed to the absence of CTZ material in the smears from patients younger than 40 years.","PeriodicalId":47257,"journal":{"name":"Revista Brasileira de Ginecologia e Obstetricia","volume":null,"pages":null},"PeriodicalIF":1.2,"publicationDate":"2011-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1590/S0100-72032011000300005","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67234537","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}
引用次数: 4
Clinical and epidemiological evaluation and quality of life in women with breast cancer 乳腺癌妇女的临床和流行病学评价及生活质量
IF 1.2 Q3 Medicine Pub Date : 2011-03-01 DOI: 10.1590/S0100-72032011000300010
P. B. M. Soares
{"title":"Clinical and epidemiological evaluation and quality of life in women with breast cancer","authors":"P. B. M. Soares","doi":"10.1590/S0100-72032011000300010","DOIUrl":"https://doi.org/10.1590/S0100-72032011000300010","url":null,"abstract":"","PeriodicalId":47257,"journal":{"name":"Revista Brasileira de Ginecologia e Obstetricia","volume":null,"pages":null},"PeriodicalIF":1.2,"publicationDate":"2011-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67234586","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}
引用次数: 1
Correlação entre as queixas de incontinência urinária de esforço e o pad test de uma hora em mulheres na pós-menopausa 绝经后妇女压力性尿失禁主诉与1小时pad试验的相关性
IF 1.2 Q3 Medicine Pub Date : 2011-02-01 DOI: 10.1590/S0100-72032011000200003
Maria Thereza Aragão Albuquerque, Barbosa Cabral Micussi, Elvira Maria Mafaldo Soares, T. Lemos, Tereza Neuma Sousa Brito, João Batista da Silva, Técia Maria do Oliveira Maranhão
OBJECTIVE: to correlate complaints of stress urinary incontinence and the results of a one-hour pad test in pre- and postmenopausal women. METHODS: cross-sectional study conducted on 60 postmenopausal volunteers divided into two groups: one consisting of 34 women with involuntary loss of urine due to stress incontinence and the other consisting of 26 women without involuntary loss of urine. A control group of 15 premenopausal women with normal menstrual cycles and no urinary complaints was also used. All women underwent clinical and laboratory analysis as well as the one-hour pad test. Patients were considered to be incontinent when sanitary pad weight post-test was more than 1 g. Data were submitted to descriptive statistics, parametric ANOVA, post-hoc Tukey test and Pearson's correlation. RESULTS: all postmenopausal women presented with stress urinary incontinence during the pad test, both those with urinary loss (4 g) and with no previous loss (3.5 g). A strong correlation was observed between urinary loss and time since menopause (r=0.8; p<0.01) and body mass index (r=0.7; p=0.01). Premenopausal women were continent during the pad test (0.4 g). CONCLUSIONS: the results of the one-hour pad test showed that all postmenopausal women exhibited stress urinary incontinence, including those without urine loss on effort. Urine loss was correlated with time since menopause and body mass index.
目的:探讨绝经前和绝经后妇女应激性尿失禁的主诉与1小时尿垫试验结果的相关性。方法:对60名绝经后志愿者进行横断面研究,分为两组:一组有34名因压力性尿失禁而非自愿尿失禁的妇女,另一组有26名无非自愿尿失禁的妇女。对照组为15名月经周期正常且无泌尿系统疾病的绝经前妇女。所有女性都接受了临床和实验室分析以及一小时尿垫试验。当卫生巾重量大于1 g时,患者被认为是失禁。数据进行描述性统计、参数方差分析、事后Tukey检验和Pearson相关分析。结果:所有绝经后妇女在尿垫试验中都出现了应激性尿失禁,包括尿丢失(4 g)和之前没有尿丢失(3.5 g)的妇女。尿丢失与绝经后时间之间存在很强的相关性(r=0.8;P <0.01)和体重指数(r=0.7;p = 0.01)。结论:1小时尿垫试验结果显示,所有绝经后妇女均表现为应激性尿失禁,包括未因用力而失尿的妇女。尿量与绝经时间和体重指数相关。
{"title":"Correlação entre as queixas de incontinência urinária de esforço e o pad test de uma hora em mulheres na pós-menopausa","authors":"Maria Thereza Aragão Albuquerque, Barbosa Cabral Micussi, Elvira Maria Mafaldo Soares, T. Lemos, Tereza Neuma Sousa Brito, João Batista da Silva, Técia Maria do Oliveira Maranhão","doi":"10.1590/S0100-72032011000200003","DOIUrl":"https://doi.org/10.1590/S0100-72032011000200003","url":null,"abstract":"OBJECTIVE: to correlate complaints of stress urinary incontinence and the results of a one-hour pad test in pre- and postmenopausal women. METHODS: cross-sectional study conducted on 60 postmenopausal volunteers divided into two groups: one consisting of 34 women with involuntary loss of urine due to stress incontinence and the other consisting of 26 women without involuntary loss of urine. A control group of 15 premenopausal women with normal menstrual cycles and no urinary complaints was also used. All women underwent clinical and laboratory analysis as well as the one-hour pad test. Patients were considered to be incontinent when sanitary pad weight post-test was more than 1 g. Data were submitted to descriptive statistics, parametric ANOVA, post-hoc Tukey test and Pearson's correlation. RESULTS: all postmenopausal women presented with stress urinary incontinence during the pad test, both those with urinary loss (4 g) and with no previous loss (3.5 g). A strong correlation was observed between urinary loss and time since menopause (r=0.8; p<0.01) and body mass index (r=0.7; p=0.01). Premenopausal women were continent during the pad test (0.4 g). CONCLUSIONS: the results of the one-hour pad test showed that all postmenopausal women exhibited stress urinary incontinence, including those without urine loss on effort. Urine loss was correlated with time since menopause and body mass index.","PeriodicalId":47257,"journal":{"name":"Revista Brasileira de Ginecologia e Obstetricia","volume":null,"pages":null},"PeriodicalIF":1.2,"publicationDate":"2011-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67234392","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}
引用次数: 13
Análise do polimorfismo Fok1 do gene VDR em mulheres inférteis com endometriose 子宫内膜异位症不孕妇女VDR基因Fok1多态性分析
IF 1.2 Q3 Medicine Pub Date : 2011-02-01 DOI: 10.1590/S0100-72032011000200002
F. Vilarino, Bianca Bianco, Denise Maria Christofolini, T. G. Lerner, C. Barbosa
PURPOSE: to evaluate the frequency of VDR gene polymorphism Fok1 in infertile women with endometriosis and Control and its relation to the disease. METHODS: a case-control study that included 147 infertile women with endometriosis and 154 fertile women without endometriosis as Control. Fok1 polymorphism (rs10735810, T2C), which promotes a T/C exchange in exon 2 of the VDR gene, was identified by the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP), that involves the combination of amplification by PCR and digestion with restriction endonuclease. The χ2 test was used to compare allele and genotype frequencies between groups. All p-values were two-tailed and a p-value < 0.05 was considered statistically significant. RESULTS: the TT, TC and CC genotype frequencies of VDR Fok1 polymorphism were 44.2%, 46.9% and 8.9% in infertile women with endometriosis and 41.6%, 50% and 8.4% in the Control Group. No significant difference was found (p=0.8), even when the patients were subdivided according to the stage of endometriosis (p=0.3 for minimal and mild endometriosis and p=0.2 for moderate and severe endometriosis). Alleles T and C were present, respectively, in 67.6% and 32.3% of infertile women with endometriosis (p=0.8), in 63.5% and 36.5% of women with minimal/mild endometriosis (p=0.5), in 72.5% and 27.5% of women with moderate/severe endometriosis (p=0.2), and in 66.6% and 33.4% of the Control Group. No statistically significant difference was found among any groups and the Control. CONCLUSION: the results suggest that VDR gene polymorphism Fok1 does not confer genetic susceptibility to endometriosis-associated infertility in the Brazilian population.
目的:探讨子宫内膜异位症不孕妇女VDR基因多态性Fok1的频率及其与该病的关系。方法:一项病例对照研究,纳入147例伴有子宫内膜异位症的不孕妇女和154例无子宫内膜异位症的有生育能力妇女作为对照。Fok1多态性(rs10735810, T2C)在VDR基因外显子2上促进T/C交换,通过聚合酶链反应-限制性片段长度多态性(PCR- rflp)鉴定,该多态性涉及PCR扩增和限制性内切酶酶切相结合。采用χ2检验比较各组间等位基因和基因型频率。所有p值均为双尾,p值< 0.05认为具有统计学意义。结果:子宫内膜异位症不孕妇女VDR Fok1多态性TT、TC和CC基因型频率分别为44.2%、46.9%和8.9%,对照组分别为41.6%、50%和8.4%。即使按照子宫内膜异位症的分期进行细分(轻度和轻度子宫内膜异位症p=0.3,中度和重度子宫内膜异位症p=0.2),也没有发现显著差异(p=0.8)。等位基因T和C分别存在于67.6%和32.3%的子宫内膜异位症不孕妇女中(p=0.8), 63.5%和36.5%的轻度/轻度子宫内膜异位症妇女中(p=0.5), 72.5%和27.5%的中度/重度子宫内膜异位症妇女中(p=0.2), 66.6%和33.4%的对照组。在任何组与对照组之间均未发现统计学上的显著差异。结论:研究结果表明,VDR基因多态性Fok1不赋予巴西人群子宫内膜异位症相关不孕症的遗传易感性。
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引用次数: 4
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Revista Brasileira de Ginecologia e Obstetricia
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