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1.
Ned Tijdschr Geneeskd ; 148(36): 1781-5, 2004 Sep 04.
Article de Néerlandais | MEDLINE | ID: mdl-15495942

RÉSUMÉ

OBJECTIVE: To assess the effect of extending the screening interval from 3 to 5 years on the detection of premalignant changes and invasive cervical carcinoma in the restructured population screening programme. DESIGN: Retrospective follow-up study. METHOD: The results were collected of the 1st round (1996-2000; 277, 377 women) and a part of the 2nd round (2001; 49,622 women; screening interval: 5 years) of the screening programme in Region West, the Netherlands. Histoscores for cervical intraepithelial neoplasia (CIN) 3 and squamous cell carcinoma (n/100 women investigated) and the hit count (sum of the histoscores for CIN 3, adenocarcinoma in situ and (micro)invasive cervical carcinoma) were calculated. Data of women with adenocarcinoma in situ and endocervical (adeno)carcinoma were recorded separately. The results of the 1st and 2nd round of the current screening programme (commenced in 1996) were compared with those of the historical screening programme that commenced in 1976 (screening interval: 3 years). RESULTS: From the 1st to the 2nd round of the historical screening programme that commenced in 1976, the histoscores for CIN 3 (3.33, 1.88) and squamous cell carcinoma (0.53, 0.19) and the hit count (3.92, 2.15) all diminished significantly. The current restructured programme, which commenced in 1996, showed low starting values for all three parameters, comparable to those in the 2nd round of the 1976 programme; a further reduction (0.16, 0.08; p < 0.01) was seen only in the histoscore for squamous cell carcinoma. In both rounds of both programmes, the histoscores for adenocarcinoma in situ (0.02, 0.02, 0.05, 0.04, respectively) and endocervical adenocarcinoma (0.04, 0.06, 0.05, 0.04) remained stable. CONCLUSION: In the current cervical carcinoma screening programme, with a screening interval of 5 years, the hit count of serious abnormalities remained constant while the incidence of squamous cell carcinoma decreased; this is in contrast to the historical screening programme (commenced in 1976), when both the hit count and the histoscore for CIN 3 diminished significantly. There were indications that cervical screening has no beneficial effect on the prevention of cervical adenocarcinoma.


Sujet(s)
Carcinomes/diagnostic , Dépistage de masse/méthodes , Tumeurs du col de l'utérus/diagnostic , Carcinomes/épidémiologie , Carcinomes/radiothérapie , Études de cohortes , Bases de données factuelles , Relation dose-effet des rayonnements , Femelle , Études de suivi , Humains , Incidence , Dépistage de masse/normes , Pays-Bas/épidémiologie , Surveillance de la population , Radium/effets indésirables , Radium/usage thérapeutique , Enregistrements , Études rétrospectives , Facteurs de risque , Facteurs temps , Tumeurs du col de l'utérus/épidémiologie , Tumeurs du col de l'utérus/radiothérapie
2.
Eur J Obstet Gynecol Reprod Biol ; 73(2): 145-8, 1997 Jun.
Article de Anglais | MEDLINE | ID: mdl-9228495

RÉSUMÉ

myotonic dystrophy, also called the Curschmann-Steinert syndrome, is an autosomal dominant inherited neuromuscular disorder characterized by progressive muscular dystrophy, muscle weakness and myotonia, which can affect both mother and child. Complications may arise during pregnancy, delivery, including anaesthetic problems, and in the neonatal period. During pregnancy hydramnion can be a first sign of the disease leading to premature labor and also muscle weakness and myotonia can aggravate complicating the course of delivery. The affected neonate may display severe hypotonia, facial diplegia and respiratory distress. The clinical diagnosis can be confirmed by direct DNA analysis in serum and in chorionvillus biopsy material. In this case report two sisters with myotonic dystrophy are described, their pregnancies, deliveries and the outcome of their affected babies.


Sujet(s)
Dystrophie myotonique/génétique , Complications de la grossesse/étiologie , Adulte , Femelle , Humains , Dystrophie myotonique/congénital , Pedigree , Grossesse
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