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2.
Phys Rev Lett ; 94(14): 147201, 2005 Apr 15.
Article in English | MEDLINE | ID: mdl-15904099

ABSTRACT

Employing the density matrix renormalization group method and strong-coupling perturbation theory, we study the phase diagram of the SU(2)xSU(2) Kondo lattice model in one dimension. We show that, at quarter filling, the system can exist in two phases depending on the coupling strength. The weak-coupling phase is dominated by RKKY exchange correlations, while the strong-coupling phase is characterized by strong antiferromagnetic correlations of the channel degree of freedom. These two phases are separated by a quantum critical point. For conduction-band fillings of less than one-quarter, we find a paramagnetic metallic phase at weak coupling and a ferromagnetic phase at moderate to strong coupling.

3.
BJOG ; 109(2): 212-3, 2002 Feb.
Article in English | MEDLINE | ID: mdl-11911102

ABSTRACT

As part of the Confidential Enquiry into the Causes of Maternal Deaths in The Netherlands, substandard care was assessed in immigrant versus indigenous maternal deaths. Except for substandard care related to the women's and relatives' decisions, substandard care factors were hypothesised to occur in similar frequency among both groups of women. The results, however, indicate that substandard care factors related to all aspects of care were disproportionately more frequent in immigrant women. More research into the interpretation of these worrying data is needed.


Subject(s)
Emigration and Immigration , Maternal Health Services/standards , Maternal Mortality , Quality of Health Care/classification , Ethnicity , Female , Humans , Netherlands/epidemiology , Pregnancy
4.
Eur J Obstet Gynecol Reprod Biol ; 89(1): 81-4, 2000 Mar.
Article in English | MEDLINE | ID: mdl-10733029

ABSTRACT

A case of severe shoulder dystocia is reported in which, after other methods had failed, cephalic replacement succeeded but was very difficult. The infant suffered severe damage. A review of methods to relieve shoulder dystocia is given, with special attention to published cases of the Zavanelli manoeuvre. It could only be used when all other methods fail.


Subject(s)
Delivery, Obstetric/methods , Dystocia/therapy , Shoulder , Adult , Birth Injuries/etiology , Cerebral Palsy/etiology , Delivery, Obstetric/adverse effects , Female , Fetal Weight , Humans , Obstetric Surgical Procedures , Pregnancy , Version, Fetal
5.
Aliment Pharmacol Ther ; 13(11): 1493-7, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10571606

ABSTRACT

BACKGROUND: Prucalopride (PR) is a novel 5-HT4 agonist enterokinetic compound. AIM: To evaluate its effect on bowel function, gut transit and anorectal function in healthy volunteers using a double-blind, placebo-controlled crossover study. METHODS: Twenty-four healthy volunteers (12 men, 12 women, mean age 25 years, range 20-53 years) were randomly assigned to 1 mg/placebo or 2 mg/placebo (PL). The trial consisted of five consecutive 1 week periods: no drug treatment, PR treatment or PL, washout, PL or PR, no treatment. Subjects maintained a diary of bowel function during the entire study period. Total intestinal transit time (TITT), mean colonic transit time (MCTT) and anorectal function (anal manometry, rectal sensitivity and rectal compliance) were assessed at the end of both treatment periods. Electrocardiography and blood sampling were performed for safety analysis; blood sampling was also used to check compliance. RESULTS: No subjects withdrew from the study. Treatment with PR 2 mg showed a statistically significant increase in mean number of weekly stools (11.5 vs. 7.1 compared to PL, P = 0.04) and in the percentage of loose/watery stools (48 vs. 12% compared to PL, P = 0.005). Within 1 week, stool frequency and consistency returned to baseline values when treatment was stopped. MCTT was shortened significantly with both doses, i.e. from 35 h on PL to 25 h on PR 1 mg (P = 0.01) and from 43 h on PL to 22 h on PR 2 mg (P = 0.02). Anorectal function was unaffected by PR. Transient and moderate headache occurred in nine subjects during PR treatment and in six subjects during PL treatment. CONCLUSION: Prucalopride is well tolerated by healthy subjects and has a marked and consistent effect on stool frequency and consistency, and on colonic transit. In the present study prucalopride did not affect visceral sensitivity or sphincter function. It holds promise for patients with slow transit constipation.


Subject(s)
Anal Canal/drug effects , Benzofurans/pharmacology , Gastrointestinal Agents/pharmacology , Gastrointestinal Transit/drug effects , Rectum/drug effects , Serotonin Antagonists/pharmacology , Adult , Benzofurans/adverse effects , Colon/drug effects , Cross-Over Studies , Defecation/drug effects , Double-Blind Method , Female , Gastrointestinal Agents/adverse effects , Humans , Male , Middle Aged , Serotonin Antagonists/adverse effects
6.
Eur J Obstet Gynecol Reprod Biol ; 84(1): 77-82, 1999 May.
Article in English | MEDLINE | ID: mdl-10413232

ABSTRACT

OBJECTIVE: To determine the incidence and correlation of joint hypermobility (HM) and peripartum pelvic pain (PPPP) in an homogeneous pregnant South African population. STUDY DESIGN: A cross-sectional study among Cape Coloured pregnant women. Joint mobility was measured by Beighton score; PPPP with a specially developed PPPP score. RESULTS: Using the Beighton scores with a cut-off point of HM > or = 5/9, only 4.9% of the 509 pregnant women were hypermobile. Hyperextension of the elbow was the largest contributor to HM (35.4%). No correlation of HM with the incidence of PPPP was established. Only 20 very mild cases of PPPP were recorded. Back pain increased significantly during pregnancy to a mean of 38%. Right handedness occurred in 95.9%. No significant relation was found between HM and the non-dominant side. CONCLUSION: Hypermobility in pregnant Cape Coloured women was surprisingly low (4.9%) with a decrease with age, but no increase during pregnancy. Peripartum pelvic pain is virtually absent and has no correlation with joint laxity. Back pain increased during pregnancy to a mean of 38%. Right handedness was high (96%) in comparison with the world-wide figure of 85%. No correlation was found between the dominant body side and hypermobility.


Subject(s)
Joint Instability/epidemiology , Pelvic Pain/epidemiology , Adolescent , Adult , Age Factors , Back Pain/physiopathology , Cross-Sectional Studies , Elbow/physiopathology , Female , Functional Laterality , Gestational Age , Gravidity , Humans , Joint Instability/ethnology , Joint Instability/physiopathology , Parity , Pelvic Pain/ethnology , Pelvic Pain/physiopathology , Postpartum Period , Pregnancy , South Africa/epidemiology , South Africa/ethnology
7.
Eur J Obstet Gynecol Reprod Biol ; 82(1): 69-72, 1999 Jan.
Article in English | MEDLINE | ID: mdl-10192488

ABSTRACT

OBJECTIVE: To investigate the prevalence of joint hypermobility in non-pregnant nulliparous women and the influences of age and Quetelet-index in a rural, female population in Tanzania. STUDY DESIGN: A cross-sectional study. Joint mobility was measured according to the scoring systems of Beighton and Biro. RESULTS: According to the Beighton criteria with a score of 0 to 9 points, 50.5% of 705 non-pregnant nulliparous women scored 3, while 30.8% scored > or =4 and 18.6% > or =5. There were no correlations between hypermobility and age or Quetelet-index. The prevalence of hypermobility at the dominant body side was significantly lower (19.2%) than at the non-dominant side (23.4%) (p<0.001). CONCLUSION: This study confirms that there are ethnic differences in the prevalence of hypermobility. The prevalence of hypermobility in Tanzanian non-pregnant nulliparous women is about 1.5-times higher as compared to Dutch non-pregnant nulliparous women. Prevalence of hypermobility was higher at the non-dominant body side. The most predictive test for the diagnosis of hypermobility was the hyperextension of the elbows >10 degrees.


Subject(s)
Joint Instability/epidemiology , Adolescent , Adult , Age Factors , Body Mass Index , Child , Cross-Sectional Studies , Elbow/physiopathology , Female , Fingers/physiopathology , Hand/physiopathology , Humans , Joint Instability/physiopathology , Knee/physiopathology , Parity , Predictive Value of Tests , Prevalence , Rural Population , Tanzania/epidemiology , Thumb/physiopathology
8.
Eur J Obstet Gynecol Reprod Biol ; 80(2): 279-81, 1998 Oct.
Article in English | MEDLINE | ID: mdl-9846685

ABSTRACT

A case report of gunshot uterine rupture from which the mother and fetus survived is presented for the first time. Management was guided by pre-operative ultrasound diagnosis of traumatic anhydramnios.


Subject(s)
Pregnancy Complications , Prenatal Injuries , Uterine Rupture/etiology , Wounds, Gunshot , Adult , Arm Injuries , Female , Gestational Age , Humans , Oligohydramnios/diagnostic imaging , Oligohydramnios/etiology , Pregnancy , Ultrasonography, Prenatal , Uterine Rupture/surgery
9.
Drugs ; 56(4): 523-35, 1998 Oct.
Article in English | MEDLINE | ID: mdl-9806101

ABSTRACT

Ergot alkaloids are well known preparations. Ergot alkaloids used in obstetrics and gynaecology are ergometrine (ergonovine; EM), methylergometrine (methergine; ME) and bromocriptine. The pharmaceutical properties of ME EM) are critical. To guarantee stability, ME and EM ampoules should be stored in a cool, dark place. ME and EM tablets are unstable in all conditions and they show an unpredictable bioavailability, which prevents oral use of the drugs for any purpose. ME and EM are known for their strong uterotonic effect and, compared with other ergot alkaloids, for their relatively slight vasoconstrictive abilities. ME and EM do have a place in the management of the third stage of labour as they are strong uterotonics. They act differently from oxytocin and prostaglandins, and have different adverse effects. Oxytocin should be used as prophylaxis or a the drug of first choice; next, ME or EM should be used, and if none of these drugs produce the desired effects, prostaglandins should be used to control bleeding. Ergot alkaloid use in gynaecology has been limited and today is discouraged even in essential menorrhagia. It is suggested that EM and ME be used (parenterally) only in first trimester abortion curettage, to reduce blood loss. Bromocriptine has been used for lactation suppression. However, alternatives such as cabergoline, which possess fewer adverse effects, are now available and therefore preferred for this indication. In sum, there is no place for the prophylactic use of ME and EM in obstetrics or gynaecology. They can be used for therapeutic purposes in the third stage of labour. During use, the practitioner must be alert for adverse effects.


Subject(s)
Ergot Alkaloids/pharmacology , Oxytocics/pharmacology , Ergonovine/pharmacokinetics , Ergonovine/pharmacology , Ergonovine/therapeutic use , Ergot Alkaloids/chemistry , Ergot Alkaloids/pharmacokinetics , Ergot Alkaloids/therapeutic use , Female , Humans , Methylergonovine/analogs & derivatives , Methylergonovine/pharmacokinetics , Methylergonovine/pharmacology , Methylergonovine/therapeutic use , Oxytocics/chemistry , Oxytocics/pharmacokinetics , Oxytocics/therapeutic use , Postpartum Hemorrhage/prevention & control , Pregnancy , Pregnancy Complications/prevention & control
10.
Clin Genet ; 53(6): 440-6, 1998 Jun.
Article in English | MEDLINE | ID: mdl-9712532

ABSTRACT

Ehlers Danlos syndrome (EDS) comprises ten types. EDS IV is the most severe type because of its often lethal complications, such as arterial rupture. EDS IV is caused by an abnormality of collagen type III as a result of mutations in the corresponding gene COL3A1. A collagen type III abnormality is also seen in patients with EDS without the classical severe EDS IV phenotype. We report on 11 patients with type III collagen abnormality and normal collagen V in whom clinically EDS II, III, and IV were diagnosed. There is no correlation between the type of collagen III anomaly and the clinical phenotype. It is concluded that type III collagen abnormality may lead to a phenotypic spectrum and that it does not predict the severity and course of the disease.


Subject(s)
Collagen/metabolism , Ehlers-Danlos Syndrome/metabolism , Adult , Cells, Cultured , Child, Preschool , Collagen/genetics , Ehlers-Danlos Syndrome/genetics , Female , Fibroblasts/metabolism , Humans , Male , Middle Aged
11.
Eur J Obstet Gynecol Reprod Biol ; 79(1): 57-62, 1998 Jul.
Article in English | MEDLINE | ID: mdl-9643405

ABSTRACT

OBJECTIVE: To determine the causes of maternal death in The Netherlands. STUDY DESIGN: Nationwide Confidential Enquiry into the Causes of Maternal Deaths during the period 1983-1992. RESULTS: Of 192 direct and indirect maternal deaths, 154 (80%) were available for the Enquiry. The most frequent direct causes were (pre-)eclampsia, thrombo-embolism, obstetrical haemorrhage and sepsis. Cerebro- and cardiovascular disorders were the most frequent indirect causes of death. Age above 35 years and parity 3 or more are related to higher maternal mortality. Women from non-caucasian origin are more prone to death in comparison to caucasian women. Autopsy was performed in 88 cases (57%). Of the 24 women where labour started at home, the place of birth played a significant role in delay in four. CONCLUSIONS: More efforts should be made to have a higher percentage than 80% available for the Confidential Enquiry as in the UK where only 1-4% of deaths are not available for similar purposes. Also, the autopsy rate of 57% is much lower than in the UK (82%). Special strategies should be developed to improve maternal health of populations at higher risk such as women of high age and parity and immigrant populations.


Subject(s)
Cause of Death , Confidentiality , Maternal Mortality , Adolescent , Adult , Cross-Sectional Studies , Female , Humans , Maternal Age , Middle Aged , Netherlands/epidemiology , Pregnancy , Pregnancy, High-Risk , Surveys and Questionnaires
12.
Am J Perinatol ; 15(5): 295-7, 1998 May.
Article in English | MEDLINE | ID: mdl-9643634

ABSTRACT

Chemotherapeutic agents administered to the mother during pregnancy may severely jeopardize the fetus. We describe a newborn girl who had been exposed to idarubicin and cytosine-arabinoside during the second and third trimesters of pregnancy due to treatment of newly diagnosed acute myeloid leukemia in the mother. The child had no structural congenital abnormalities. Adverse effects observed were prematurity, growth retardation, mildly disturbed transaminases and erythroblastosis, all of which were self-limiting with no permanent sequelae.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/adverse effects , Fetal Growth Retardation/etiology , Leukemia, Monocytic, Acute/drug therapy , Pregnancy Complications, Neoplastic/drug therapy , Prenatal Exposure Delayed Effects , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Cytarabine/administration & dosage , Cytarabine/adverse effects , Female , Humans , Idarubicin/administration & dosage , Idarubicin/adverse effects , Infant, Newborn , Infant, Premature , Pregnancy , Pregnancy Outcome , Pregnancy Trimester, Second , Pregnancy Trimester, Third
13.
Eur J Obstet Gynecol Reprod Biol ; 77(2): 181-7, 1998 Apr.
Article in English | MEDLINE | ID: mdl-9578276

ABSTRACT

OBJECTIVE: To determine the maximum tolerated dose (MTD) of carbetocin (a long-acting synthetic analogue of oxytocin), when administered immediately after vaginal delivery at term. MATERIALS AND METHODS: Carbetocin was given as an intramuscular injection immediately after the birth of the infant in 45 healthy women with normal singleton pregnancies who delivered vaginally at term. Dosage groups of 15, 30, 50, 75, 100, 125, 150, 175 or 200 microg carbetocin were assigned to blocks of three women according to the continual reassessment method (CRM). RESULTS: All dosage groups consisted of three women, except those with 100 microg (n=6) and 200 microg (n=18). Recorded were dose-limiting adverse events: hyper- or hypotension (three), severe abdominal pain (0), vomiting (0) and retained placenta (four). Serious adverse events occurred in seven women: six cases with blood loss > or = 1000 ml, four cases of manual placenta removal, five cases of additional oxytocics administration and five cases of blood transfusion. Maximum blood loss was greatest at the upper and lower dose levels, and lowest in the 70-125 microg dose range. Four out of six cases with blood loss > or = 1000 ml occurred in the 200 microg group. The majority of additional administration of oxytocics (4/5) and blood transfusion (3/5) occurred in the dose groups of 200 microg. All retained placentae were found in the group of 200 microg. CONCLUSION: The MTD was calculated to be at 200 microg carbetocin.


Subject(s)
Oxytocics/administration & dosage , Oxytocin/analogs & derivatives , Postpartum Hemorrhage/prevention & control , Abdominal Pain/chemically induced , Female , Humans , Hypertension/chemically induced , Hypotension/chemically induced , Injections, Intramuscular , Oxytocics/adverse effects , Oxytocics/therapeutic use , Oxytocin/administration & dosage , Oxytocin/adverse effects , Oxytocin/therapeutic use , Placenta, Retained/chemically induced , Pregnancy , Vomiting/chemically induced
14.
Eur J Obstet Gynecol Reprod Biol ; 76(1): 61-4, 1998 Jan.
Article in English | MEDLINE | ID: mdl-9481549

ABSTRACT

OBJECTIVE: To assess genital tract sepsis-related maternal mortality in The Netherlands during 1983-1992. STUDY DESIGN: A nationwide Confidential Enquiry into the causes of maternal death. RESULTS: Genital tract sepsis-related maternal mortality during 1983-1987 was 0.11 per 100,000 live births (1/893,998) and 0.93 per 100,000 live births (9/968,990) during 1988-1992. The relative risk of dying due to sepsis in the second 5-year period as compared to the first period was 10.1 (1/72 versus 9/72 maternal deaths; 95% CI 1.3-82.3; P < 0.01). CONCLUSIONS: Also in The Netherlands an increase of death due to genital tract sepsis has been observed since the 1980s.


Subject(s)
Pregnancy Complications, Infectious/microbiology , Streptococcal Infections/mortality , Streptococcus pyogenes , Female , Fetal Death , Genital Diseases, Female/microbiology , Gestational Age , Humans , Infant Mortality , Infant, Newborn , Netherlands , Pregnancy , Pregnancy Complications, Infectious/mortality , Pregnancy Outcome
16.
Eur J Obstet Gynecol Reprod Biol ; 74(1): 1-6, 1997 Jul.
Article in English | MEDLINE | ID: mdl-9243191

ABSTRACT

OBJECTIVES: This study was performed to assess the intra-operative surgical complications and postoperative maternal morbidity rate of caesarean section. STUDY DESIGN: A total of 2647 women, delivered by caesarean section in our department between 1983 and 1992, were studied retrospectively. Three caesarean section groups were formed: (1) primary elective, (2) primary acute, without any effort to deliver vaginally, and (3) secondary acute, due to a failed vaginal delivery. The Student's-t-, Fisher-exact- and chi 2-test were used for statistical analysis. RESULTS: The overall maternal intra-operative complication rate was 14.8%. The most common complications were lacerations of the uterine corpus (10.1%) and bloodloss > or = 1000 ml (7.3%). The complication rate of the secondary group (23.4%) was significantly higher (p < 0.001) compared to both primary groups (7.4%). The overall maternal postoperative morbidity rate was 35.7%. Fever (24.6%), bloodloss between 1000 and 1500 ml (4%), haematoma (3.5%) and urinary tract infections (3.0%) were the most frequent complications. The primary elective group showed significantly (p < 0.001) lower major (2.6%) and minor (23.7%) complication rates compared to the emergency groups (major 5.2%, minor 34%). CONCLUSION: Emergency caesarean sections carried the greatest risks regarding maternal complications compared to elective procedures.


Subject(s)
Cesarean Section/adverse effects , Intraoperative Complications/epidemiology , Postoperative Complications/epidemiology , Cesarean Section/mortality , Female , Fever , Hematoma/epidemiology , Hemorrhage/epidemiology , Humans , Obstetric Labor Complications , Pregnancy , Retrospective Studies , Urinary Tract Infections/epidemiology , Uterus/injuries
17.
Obstet Gynecol ; 90(1): 78-82, 1997 Jul.
Article in English | MEDLINE | ID: mdl-9207818

ABSTRACT

OBJECTIVE: To establish the actual number of maternal deaths in The Netherlands by determining the degree of underreporting. METHODS: We conducted a nationwide, retrospective cross-check of the three available maternal mortality registration systems and issued a questionnaire to senior obstetricians in all hospitals during the years 1983-1992. RESULTS: The officially reported maternal mortality rate during the study period was 7.1 per 100,000 live births (133 maternal deaths per 1,862,985 live births). After completion of the study, our data indicate that the rate should be at least 9.7 per 100,000 live births (180 maternal deaths). Early pregnancy and indirect deaths were more likely to be underreported than direct deaths during labor and the puerperium. Failure to register the recent pregnancy on the death certificate was a frequent problem. Misclassification was particularly evident for cerebrovascular disorders, cardiovascular disorders, and eclampsia. CONCLUSION: The level of underreporting of maternal mortality in The Netherlands was estimated at 26%. The pregnancy status of women should be registered on death certificates. Officially reported maternal mortality rates are unreliable and international comparisons using these data thus are less meaningful.


Subject(s)
Maternal Mortality , Cross-Sectional Studies , Female , Humans , Netherlands/epidemiology , Pregnancy , Retrospective Studies
18.
Trop Med Int Health ; 2(6): 558-67, 1997 Jun.
Article in English | MEDLINE | ID: mdl-9236823

ABSTRACT

In a hospital-based study, birthweights of 3162 consecutive births were related to perinatal mortality, multiple birth, and gestational age. Independent associations between 15 potential determinants and low birthweight, prematurity and small-at-term factors were also assessed. A newly constructed local curve of birthweight-for-gestational age is compared with the existing curves. The variables positively associated with low birthweight (< 2500 g) were nulliparity, vomiting as a self-reported complaint, spleen enlargement, sex of the infant and previous perinatal mortality. Nulliparity and spleen enlargement were positively associated with preterm birth, while small-at-birth was mostly associated with nulliparity and sex of the infant. Further study on spleen enlargement, the only modifiable factor in this study of possible public health importance, is warranted. Other factors of potential importance which deserve further investigations are hard physical work, maternal morbidity and antenatal care.


Subject(s)
Infant, Low Birth Weight , Female , Gestational Age , Humans , Infant, Newborn , Infant, Small for Gestational Age , Logistic Models , Male , Parity , Pregnancy , Pregnancy Complications , Risk Factors , Sex Factors , Splenic Diseases , Tanzania
19.
Eur J Obstet Gynecol Reprod Biol ; 73(2): 189-92, 1997 Jun.
Article in English | MEDLINE | ID: mdl-9228503

ABSTRACT

OBJECTIVE: To determine the presence of hypermobility and differences between females and males in a Dutch population. STUDY DESIGN: Joint mobility was measured in a primary and a secondary school population. Beighton and Biro measurements were used. The data were evaluated statistically. RESULTS: Using the Beighton score, 15.5% of group I (n = 252; 4-13 years) and 13.4% of group II (n = 658; 12-17 years) were hypermobile. Hypermobility was found more in females than in males, the difference being significant in the older group. Overall, hypermobility did not significantly diminish with ageing, although the individual joints did not show a significant decrease in mobility with ageing. Hypermobility was significantly more pronounced at the non-dominant body side in both groups. The Quetelet-index did not show a significant relation to hypermobility. CONCLUSION: Hypermobility was found more in females than in males, with a trend of decrease of hypermobility with ageing. The non-dominant body side proved to be more hypermobile and the Quetelet-index did not show a relation to hypermobility. Beighton's measurements proved best, since Biro considers the two body sides being equal.


Subject(s)
Joint Instability/epidemiology , Schools , Adolescent , Child , Child, Preschool , Female , Functional Laterality/physiology , Humans , Incidence , Joint Instability/physiopathology , Male , Netherlands/epidemiology
20.
Acta Obstet Gynecol Scand ; 76(4): 332-4, 1997 Apr.
Article in English | MEDLINE | ID: mdl-9174426

ABSTRACT

BACKGROUND: To assess cesarean section-related maternal mortality in The Netherlands during 1983-1992. METHODS: A nationwide confidential enquiry into the causes of maternal death. RESULTS: The risk of dying after vaginal birth was 0.04 per 1000 vaginal births (65/1.763.999) compared to 0.53 per 1000 cesarean births (57/108.587). The direct risk of dying from cesarean section was 0.13 per 1000 operations (14/108.587). In some women cesarean section did not initiate, but contributed to, the train of events leading to death. Adding this associated risk to the direct risk gives a fatality rate of 0.28 per 1000 cesarean births (30/108.587). CONCLUSIONS: Although cesarean section is a relatively safe procedure nowadays, birth by cesarean section in The Netherlands is seven times more hazardous than vaginal birth. Keeping the cesarean birth rate as low as possible is therefore in the interest of women of reproductive age.


Subject(s)
Cesarean Section/adverse effects , Maternal Mortality , Adult , Delivery, Obstetric/methods , Female , Humans , Maternal Age , Netherlands/epidemiology , Pregnancy , Pregnancy Complications/mortality , Risk Factors
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