Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 13 de 13
Filter
1.
J Low Genit Tract Dis ; 22(1): 1-7, 2018 Jan.
Article in English | MEDLINE | ID: mdl-29271849

ABSTRACT

OBJECTIVE: The aim of the study was to describe the screening history in postmenopausal women diagnosed with cervical cancer during 1990-2013 by age and screening period. MATERIALS AND METHODS: This hospital-based cohort study included women 55 years and older diagnosed with cervical cancer at Aarhus University Hospital, Denmark, during 1990-2013. Information on their previous history of cervical cancer screening was obtained from the Danish Pathology Databank. RESULTS: Overall, 47.0% (95% CI = 42.6-51.4) had no record of screening before their cervical cancer diagnosis. This proportion declined over calendar time from 69.8% (95% CI = 61.4-77.3) in 1990-1994 to 20.0% (95% CI = 12.7-29.2) in 2010-2013 and increased by age from 22.5% (95% CI = 14.6-32.0) in women aged 55 to 59 years to 63.2% (95% CI = 49.3-75.6) in women 80 years and older. Cases living in the organized screening era (i.e., birth cohorts 1943-1960) were more likely to have a record of screening than women in the preorganized screening era (i.e., birth cohorts 1901-1942) (p < .001). Of all cases, 17.7% (n = 91) had a record of screening within 5 years of diagnosis and the proportion was highest in the most recent periods and in women aged 55 to 64 years. Of cases with a record of screening within 5 years, 84.6% (95% CI = 14.5-21.2) had a normal cytology result, whereas only 8.8% (95% CI = 2.9-14.7) had high-grade squamous intraepithelial lesion or worse. CONCLUSIONS: Cervical cancer in older women may partly be attributed to a lack of screening or due to a failure in screening. However, older women were in general less screened because screening was unavailable.


Subject(s)
Early Detection of Cancer , Uterine Cervical Neoplasms/diagnosis , Age Factors , Aged , Cohort Studies , Denmark , Female , Health Services Accessibility , Humans , Middle Aged , Retrospective Studies , Time Factors
3.
Acta Obstet Gynecol Scand ; 95(8): 850-60, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27258798

ABSTRACT

INTRODUCTION: Bacterial vaginosis (BV) is characterized by a dysbiosis of the vaginal microbiota with a depletion of Lactobacillus spp. In pregnancy, prevalence's between 7 and 30% have been reported depending on the study population and the definition. BV may be associated with an increased risk of spontaneous preterm delivery (sPTD). However, it is controversial whether or not BV-positive pregnant women will benefit from treatment to reduce the risk of sPTD. We could not identify any good-quality guideline addressing this issue. Consequently we aimed to produce this clinical recommendation based on GRADE. MATERIAL AND METHODS: Systematic literature searches were conducted in the following databases: Guidelines International Network: G-I-N, Medline, Embase, The Cochrane Database of Systematic Reviews, Web of Science and http://www.clinicaltrials.gov from 1999 to 3 October 2014. Hence, nine guidelines, 34 reviews, 18 randomized controlled trials and 12 observational studies were included. RESULTS: The GRADE quality of evidence was consistently low or very low, primarily because none of the risk ratios (RR) for the risk of sPTD at <37 weeks were statistically significant. Concerning treatment with metronidazole, RR was 1.11 (95% CI 0.93-1.34) in low-risk pregnancies and 0.96 (95% CI 0.78-1.18) in high risk pregnancies. Concerning treatment with clindamycin at any gestational age, the RR was 0.87 (95% CI 0.73-1.05). CONCLUSION: This systematic review gives a strong recommendation against treatment with metronidazole and a weak recommendation against treatment with clindamycin to reduce the sPTD rate in both high-risk and low-risk pregnancies with BV.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Clindamycin/therapeutic use , Metronidazole/therapeutic use , Pregnancy Complications, Infectious/drug therapy , Premature Birth/prevention & control , Vaginosis, Bacterial/drug therapy , Female , Humans , Pregnancy , Pregnancy Complications, Infectious/therapy , Premature Birth/etiology , Probiotics/therapeutic use , Risk Factors , Treatment Outcome , Vaginosis, Bacterial/therapy
4.
Acta Obstet Gynecol Scand ; 95(7): 717-23, 2016 07.
Article in English | MEDLINE | ID: mdl-26946059

ABSTRACT

The article serves to review the literature on the human uterine cervix based on a new distension technology named functional luminal imaging probe. This technology was originally developed to study the biomechanical competence of the gastro-esophageal junction where it provides a geometric profile of the lumen during distension, which can be related to sensory data. We searched and reviewed publications on cervical distention from 2002. The functional luminal imaging probe technology has been used for studying the mechanical and mechano-sensory properties of the cervix in non-pregnant women. In early pregnant women and in term pregnant women, the technique provides geometric measurements from the whole cervical canal during distension, which changes dramatically during pregnancy. Furthermore, it has been demonstrated that the technique predicts the outcome of labor induction better than the Bishop score does. The functional luminal imaging probe technology has potential as a research tool as well as for clinical use in gynecology and obstetrics.


Subject(s)
Cervix Uteri , Labor, Induced , Female , Humans , Obstetrics , Pain
5.
Acta Obstet Gynecol Scand ; 93(12): 1219-37, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25174701

ABSTRACT

OBJECTIVE: To give an overview of the methods available for biomechanical testing of the non-pregnant and pregnant uterine cervix in vivo. METHODS: The following databases were searched. PubMed, Embase, and Cochrane Library. Additional studies were identified from reference lists. Only studies on in vivo biomechanical testing on both pregnant and non-pregnant women were included. MAIN OUTCOME MEASURES: Estimation of distensibility, compressibility, and biochemical composition of the uterine cervix. RESULTS: The distensibility methods evaluated a physiologic variable and might serve as a gold standard; however, they may never be clinically useful as they involve instrumentation of the cervical canal. The compression methods evaluated an unphysiological variable but despite that, they seemed to evaluate biologically relevant figures and were non-invasive. Of the methods evaluating the biomechanical properties indirectly, those based on ultrasound may be clinically useful. Other indirect methods only measured variables within the most superficial layer of the distal uterine cervix, so further studies are needed to evaluate whether these measurements reflect the entire organ. Both compression methods and indirect methods were similar or superior to the Bishop score and to cervical length measurements regarding prediction of spontaneous preterm delivery and successful induction of labor in small studies. CONCLUSION: The methods may have the potential to detect the biomechanical changes in the uterine cervix before the cervical length has shortened. The most promising methods need large-scale clinical testing regarding induction of labor and preterm delivery before they can be used in the clinic.


Subject(s)
Cervical Ripening , Cervix Uteri/physiology , Diagnostic Techniques, Obstetrical and Gynecological/instrumentation , Obstetric Labor, Premature/prevention & control , Biomechanical Phenomena/physiology , Elasticity Imaging Techniques/methods , Female , Humans , In Vitro Techniques , Palpation/methods , Pregnancy
6.
J Mech Behav Biomed Mater ; 39: 27-37, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25084120

ABSTRACT

BACKGROUND AND AIMS: The course and outcome of pregnancy is closely correlated to change of biomechanical properties of the uterine cervix. The aim of this study was to build a non-linear, fiber reinforced mechanical model of the cervix for estimation of mechanical characteristics of the cervix in early- and term-pregnant women based on recordings of in vivo pressure and diameter by means of the Functional Luminal Imaging Probe (FLIP) technology. MATERIALS AND METHODS: Five early- and six term-pregnant women were examined with a FLIP probe. The bag on the probe was inserted into the cervical canal for concomitant measurement of diameters at 16 serial locations along the canal and the bag pressure. The bag was inflated to a maximum volume of 50 ml. A three-fiber-families model including isotropic elastin-dominated matrix and anisotropic collagen was introduced to describe the mechanical behavior of the cervical canal. The unknown geometric and mechanical parameters were calculated on the basis of the mid-cervical diameters and the intraluminal pressures during the inflation. RESULTS: The wall thickness in the unloaded state (zero pressure applied) and mechanical properties of the matrix material (c) and collagens (c1, c2) were estimated with good fits of the calculated intraluminal pressures to the FLIP recordings during the cervical canal distension. No significant difference in the wall thickness was found between the early- and term-pregnant women (10.3 ± 0.8mm vs. 11.7 ± 2.2mm, p=0.30). The cervical matrix material and the collagen in the early-pregnant women were much stiffer than that in the term-pregnant women (p<0.05). CONCLUSIONS: The cervical mechanical properties can be obtained from recorded pressure and diameter data in vivo via the established mechanical model. Matrix material and collagens of the cervix wall were remodeled during pregnancy. The mechanical model can be applied to other tubular visceral organs where concomitant measures of pressure and diameter can be obtained for better understanding diseases and their evolution or treatment.


Subject(s)
Cervix Uteri/pathology , Cervix Uteri/physiology , Adult , Anisotropy , Biomechanical Phenomena , Collagen/chemistry , Diagnostic Imaging/methods , Elasticity , Female , Humans , Imaging, Three-Dimensional , Models, Biological , Pregnancy , Pressure , Stress, Mechanical , Time Factors , Viscosity
7.
Acta Obstet Gynecol Scand ; 93(7): 684-90, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24702544

ABSTRACT

OBJECTIVE: To evaluate how the approximate Young's modulus of the uterine cervix assessed by quantitative sonoelastography in patients undergoing induction of labor is associated with the cervical dilation time and to evaluate the approximate Young's modulus as a predictor of prolonged cervical dilation time. DESIGN: Cross-sectional study. SETTING: Aarhus University Hospital, Aarhus, Denmark. POPULATION: Term-pregnant women. METHODS: A total of 49 term-pregnant women were included before induction of labor. The approximate Young's modulus of the anterior cervical lip was determined by the use of a reference cap applied on the end of the transvaginal transducer during sonoelastography. MAIN OUTCOME MEASURES: Cervical dilation time during active labor. RESULTS: The approximate Young's modulus was associated with the cervical dilation time during active labor (R(2) log  = 0.24, p < 0.01) and predicted prolonged duration of cervical dilation time (>330 min) with the area under the receiver operating characteristic (ROC) curve of 0.71, sensitivity 74%, and specificity 69%. Equivalent figures for the Bishop's score were R(2) log  = 0.02 (p = 0.37), the area under the ROC curve 0.53, sensitivity 53%, and specificity 46%. For the cervical length measurements the corresponding results were: R(2) log  = 0.02, p = 0.35, area under the ROC curve 0.57, sensitivity 66% and specificity 54%. The intra-observer and inter-observer intraclass correlations were 88% and 58%, respectively, with quantitative elastography. CONCLUSIONS: The approximate Young's modulus is superior to the Bishop score and the cervical length measurements concerning the prediction of cervical dilation time and the risk of prolonged dilation time after induction of labor.


Subject(s)
Cervix Uteri/physiology , Elasticity Imaging Techniques/methods , Labor Stage, First/physiology , Labor, Induced , Cervix Uteri/diagnostic imaging , Cross-Sectional Studies , Elastic Modulus , Female , Humans , Predictive Value of Tests , Pregnancy , ROC Curve , Sensitivity and Specificity , Time Factors
8.
PLoS One ; 9(3): e91121, 2014.
Article in English | MEDLINE | ID: mdl-24603859

ABSTRACT

OBJECTIVE: To determine the stiffness of the pregnant uterine cervix in vivo. METHOD: Five women in early pregnancy and six women in late pregnancy were included. The EndoFlip is a 1-m-long probe with a 12-cm-long bag mounted on the tip. The tip of the probe was inserted into the cervical canal. Sensors spaced at 0.5-cm intervals along the probe were used to determine 16 serial cross-sectional areas of the bag. The diameter of the cervical canal could thereby be determined during inflation with up to 50 ml saline solution. Tissue stiffness was calculated from the geometric profiles and the pressure-strain elastic modulus (EP) at each sensor site. Three parts of the cervix were defined: the uterus-near part, the middle and the vaginal part. The EPmax was defined as the highest EP detected along the cervical canal. RESULTS: The EPmax was always found in the middle part of the cervix. The median EPmax was 243 kPa (IQR, 67-422 kPa) for the early pregnant women and 5 kPa (IQR, 4-15 kPa) for those at term. In the early pregnant women the stiffness differed along the cervical length (p<0.05) whereas difference along the cervix was not found for late pregnant women. A positive correlation coefficient (Spearman's rho) was established between the EPs of the uterus-near and the middle part (0.84), between the vaginal and the middle part (0.81), and between the uterus-near and the vaginal part (0.85). CONCLUSION: This new method can estimate the stiffness along the cervical canal in vivo. This method may be useful in the clinical examination of the biomechanical properties of the uterine cervix.


Subject(s)
Cervix Uteri/physiology , Ultrasonography, Prenatal/methods , Biomechanical Phenomena , Cervix Uteri/diagnostic imaging , Elastic Modulus , Female , Humans , Phantoms, Imaging , Pregnancy , Pressure , Reproducibility of Results , Vagina/diagnostic imaging , Vagina/physiology
10.
Acta Obstet Gynecol Scand ; 92(11): 1244-9, 2013 Nov.
Article in English | MEDLINE | ID: mdl-24032689

ABSTRACT

OBJECTIVE: To develop a reference material that allows quantitative elastography of the uterine cervix using the calculation of the approximate tissue stiffness expressed as Young's modulus (N/mm(2) ). Further, to test the elastography equipment on phantoms from a clinical perspective regarding the distance dependence and the influence of a heterogeneous material. DESIGN: Methodological study. SETTING: Aarhus University Hospital, Denmark. POPULATION: Six mid- and five full-term pregnant women. METHODS: Reference caps and phantoms with Young's moduli between 0.07 and 0.40 N/mm(2) were made of silicone and oil. By using reference caps, the approximate Young's moduli of the cervixes were calculated from strain ratios obtained by elastography. MAIN OUTCOME MEASURES: Approximate Young's modulus of the cervix. RESULTS: The recordings of the phantoms revealed that the calculation of the approximate Young's moduli became unreliable at distances above 10-15 mm from the transducer. This was further increased for a phantom which included a soft layer imitating the cervical canal. The approximate Young's modulus obtained from the anterior cervical lip was 0.08 N/mm(2) in mid-term and 0.03 N/mm(2) in full-term pregnant women (Wilcoxon rank-sum test, p = 0.01). CONCLUSION: The reference cap constitutes a promising tool for quantitative elastography of the anterior cervical lip. Figures obtained from the posterior cervical lip are less plausible due to the distance from the transducer and the heterogeneity introduced by the cervical canal. The method has the potential to be used to supplement cervical length assessment when evaluating women at risk of preterm delivery and when planning induction of labor.


Subject(s)
Cervix Uteri/diagnostic imaging , Elasticity Imaging Techniques/methods , Phantoms, Imaging , Silicones/chemistry , Adult , Cervix Uteri/physiology , Elastic Modulus , Female , Humans , Pregnancy , Reference Values
11.
Acta Obstet Gynecol Scand ; 92(2): 125-36, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23083413

ABSTRACT

OBJECTIVE: To describe the effects and side-effects of the continuous use of oral contraceptives. DESIGN: A review of articles concerning oral contraceptives taken continuously or in cycles with hormones taken for more than 21 days per cycle. METHODS: We searched publications in PubMed and Embase. Randomized controlled trials were selected if possible, otherwise case-control studies or cohort studies with controls were chosen. A level of evidence as described by the Centre for Evidence Based Medicine (Oxford University, Oxford, UK) was assigned to all selected studies. MAIN OUTCOME MEASURES: Clinical and paraclinical effects and side-effects of oral contraceptives administered continuously. RESULTS: The studies suggest that the endometrium is inactive during continuous use of oral contraceptives and the risk of endometrial hyperplasia is not increased. Numbers of bleeding days are halved with continuous use; however, spotting and irregular bleeding are more often seen in the beginning of use, decreasing with time. Hemostatic parameters and serum lipid and carbohydrate profiles in continuous and conventional users do not differ. Menstrual cycle-related symptoms are relieved better by continuous treatment. After surgery for endometriosis, the effect of continuously used oral contraceptives on the risk of recurrence of pain has been found to be less than that of gonadotropin-releasing hormone (GnRH) analogues, but better than the rate seen during conventional cyclic use. CONCLUSION: Oral contraceptives taken continuously or in long cycles seem to offer benefits with regard to menstrual symptoms and the recurrence of symptoms related to endometriosis. Long-term studies, comprising large groups of women, are lacking.


Subject(s)
Contraceptives, Oral/administration & dosage , Contraceptives, Oral/adverse effects , Blood Pressure/physiology , Body Weight/physiology , Bone Density/physiology , Contraceptives, Oral/therapeutic use , Endometriosis/surgery , Endometrium/drug effects , Endometrium/physiology , Female , Humans , Menstruation/drug effects , Menstruation/physiology , Pelvic Pain/drug therapy , Secondary Prevention , Venous Thromboembolism/chemically induced
12.
Acta Obstet Gynecol Scand ; 90(11): 1189-99, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21568946

ABSTRACT

OBJECTIVE: To conduct a literature search for selected biomarkers on preterm delivery and estimate their likelihood ratios (LR). DESIGN: Structured review. POPULATION: Low and high-risk populations and women with symptoms of preterm delivery. METHODS. Publications were identified in PubMed. MAIN OUTCOME MEASURES: LR on selected biomarkers for preterm delivery. RESULTS: In asymptomatic women with low risk of preterm delivery, the following biomarkers gave major shifts in probability (LR above 5): twins (LR+ 10), Ureaplasma urealyticum in amniotic fluid (LR+ of 10), cervical length <25mm (LR+ 6), salival estriol (LR+ 5) and various combined tests. In asymptomatic women with high risk of preterm delivery, short cervical length (LR+ 11, LR- 0.7), high serum tumor necrosis factor-alpha (LR+ 10, LR- 0.6) gave major shifts in probability. In women with symptoms of preterm delivery, major shifts in probability can be obtained from the following amniotic fluid biomarkers: high matrix metalloproteinase-8 (LR+ 23, LR- 0.6), Ureaplasma urealyticum (LR+ 19, LR- 0.8), high interleukin (IL)-6 (LR+ 9, LR- 0.2), IL-8 (LR+10, LR- 0.2) and tumor necrosis factor-alpha (LR+ 8, LR- 0.4). In serum IL-6 (LR+ 12, LR- 0.2), Cluster of Differentiation 163 (LR+9, LR-0.8) and various combined tests. Vaginal fetal fibronectin (LR+ 3 and LR- 0.5) and short cervical length (LR+ 2, LR- 0.3) gave LRs of some importance (LR below 5). CONCLUSION: Several biomarkers have been identified for assessment of risk of preterm delivery. Their clinical relevance depends on the efficacy of the interventions which can be offered to these patients.


Subject(s)
Amniotic Fluid/metabolism , Biomarkers/metabolism , Obstetric Labor, Premature/diagnosis , Premature Birth/diagnosis , Female , Humans , Obstetric Labor, Premature/metabolism , Predictive Value of Tests , Pregnancy , Premature Birth/metabolism
13.
Acta Obstet Gynecol Scand ; 90(1): 92-6, 2011 Jan.
Article in English | MEDLINE | ID: mdl-21275921

ABSTRACT

OBJECTIVE: To study maternal serum interleukin-17 (IL-17) during normal pregnancy and evaluate the association with preterm delivery. DESIGN: Prospective study. SETTING: Aarhus University Hospital, Denmark. POPULATION: Three cohorts: (a) low-risk cohort of 1,069 women who had serum drawn in weeks 12 and 19, (b) subgroup of the low-risk cohort, consisting of 40 women, who had serum drawn at 12, 19, 26, 33 and 39 weeks of gestation and (c) a symptomatic cohort of 93 women admitted with symptoms of preterm delivery at a gestational age of 24(+ 0) weeks to 33(+ 6) weeks. METHODS: Serum IL-17 determined by an in-house developed multiplex sandwich immunoassay. MAIN OUTCOME MEASURES: Preterm delivery <37(+0) weeks gestation. RESULTS: Serum IL-17 did not change during normal pregnancy. At admission to hospital, women with preterm contractions had significantly decreased serum IL-17 as compared with normal pregnancies (median <4 [interquartile ranges, IQR, <4-10 pg/ml] vs. 174 pg/ml [IQR, 92 - 485 pg/ml]); this difference was enhanced and highly significant for women delivering preterm versus term (median <4 [IQR, <4-7.9 pg/ml] vs. median 6.0 [IQR, <4-221 pg/ml]; p-value 0.03). Serum IL-17 was also lower in women with preterm prelabor rupture of membranes. A slightly, but not statistically significant decrease was found in weeks 12 and 19 in low-risk women who subsequently delivered preterm. CONCLUSION: Maternal serum IL-17 may be involved in preterm delivery.


Subject(s)
Interleukin-17/blood , Premature Birth/blood , Case-Control Studies , Cohort Studies , Denmark , Female , Gestational Age , Humans , Labor, Obstetric/blood , Pregnancy , Risk Factors
SELECTION OF CITATIONS
SEARCH DETAIL
...