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Amniocentesis early assessment in an institution of prenatal diagnosis in Brazil

Evaluación de la amniocentesis precoz en una institución brasileña de diagnóstico prenatal




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Bernal Parra, L. M. (2012). Amniocentesis early assessment in an institution of prenatal diagnosis in Brazil. NOVA, 10(17). https://doi.org/10.22490/24629448.513

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NOVA by http://www.unicolmayor.edu.co/publicaciones/index.php/nova is distributed under a license creative commons non comertial-atribution-withoutderive 4.0 international.

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Luz Mery Bernal Parra

    Although mid-trimester amniocentesis (MA) is a safety and reliability procedure, cytogenetic diagnosis report is only informed in an advanced period of pregnancy. First trimester amniocentesis  (12-14 weeks) shows some advantages on MA and others of chorionic villus sampling (CVS), but its safety requires careful analysis. The aim of this study was to evaluate the fetal loss and congenital anomalies in a population of 479 pregnant women (single gestations) who underwent first trimester amniocentesis (12-14+6/7 weeks). Under ultrasound-guided procedures approximately 1ml of amniotic fluid per gestational week was collected. Mean maternal age was 35.7± 1 4.58. The main indication for the test was maternal age 35 or greater (66.1%). Follow up was successful in 90.2% (432/479) patients. Amniotic fluid was successfully aspirated in the first attempt in 406 cases (94%). Fetal loss rate was 4.9%, 2.9% were observed before 28 weeks. Differences in fetal loss rates associated to different categories of maternal age were not statistically significant. The distribution of fetal losses by different categories of gestational age showed no significant differences. No association between fetal loss and collected volume of amniotic fluid was observed. 5.1% and 2.3% of patients reported amniotic fluid loss and bleeding, respectively. Such complications were significantly associated with fetal loss. Eight cases (2%) of respiratory problems and two (0.5%) of musculo-skeletal anomalies were observed. Our data suggest increased complications and fetal losses at earlier gestational ages, especially at less than 13 weeks. Amniocentesis at 14 weeks poses low risk of fetal loss or congenital anomalies and may be routinely offered to patients, provided that operators are experienced, technical measures taken, and collected volume of amniotic fluid is minimized.


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    1. Tabor A., Madsen M, Obel E.B., Philip J., Bang J., Noergard-Peterson B. (1986). Randomised controlled trial of genetic amniocentesis in 4606 low-risk women. Lancet i: 1287-1293.
    2. Dallaire L., Lortie G., Des Rochers M., Clermont R., Vachon C. (1995). Parental reaction and adaptability to the prenatal diagnosis of fetal defect or genetic disease leading to pregnancy interruption. Prenat. Diagn., 15:249-259.
    3. Hanson F.W., Zom E.M., Tennant F.R., Marionos S., Samuels S. (1987). Amniocentesis before 15 weeks gestation: Outcome, risks, and technical problems. Am. J. Obstet. GynecoI., 156:1524-1531.
    4. Eiben B., Goebel R., Hansen S., Hammans W. (1994). Early amniocentesis. A cytogenetic evaluation of over 1500 cases. Prenat. Diagn., 14:497-501.
    5. Elejalde B.R., de Elejalde M.M., Acuna J.A., Thelen D., Tiujillo C., Kamnann M. (1990).
    6. Prospective study of amniocentesis performed between weeks 9 and 16 of gestation: Its feasibility, risks, complications and use in early genetic prenatal diagnosis. Am. J. Med. Genet., 35:188-196.
    7. Gollop T.R., Naccache N.F., Pieri P.C. (1993). Amniocentese Precoce (12-15 semanas) com resultados rápidos: Uma realidade no lnstituto de Medicina Fetal. Femina., 21:680- 682.
    8. Henry G.P., Miller W.A. (1992). Early Amniocentesis. J. Repmd. Med., 37(5):396-402.
    9. Nadyr Fernandes Naccache, Instituto de Medicina Fetal y Genética Humana
    10. Nicolaides K.H., Brizot M.L., Patel F., Snijders R.J. (1996). Comparison of Chorion Villus Sampling and Early Amniocentesis for karyotyping in 1492 singlenton pregnancies. Fetal. Diagn. Ther., 11:9-15.
    11. Cederholm M., Axelsson O. (1997). A prospective comparative study on transabdominal chorionic villus sampling and amniocentesis performed at 10-13 weeks gestation. Prenat. Diagn., 17(4):311-317..
    12. Nagel H.T.C., Vandenbussche F.P., Keirse M.J., Oepkes D., Oostewijk J.C., Beverstock G., Kanhai H.H. (1998). Amniocentesis before 14 completed weeks as an altemative to transabdominal chorionic villus sampling: A controlled trial with infant follow-up. Prenat. Diagn., 18:465-475.
    13. The Canadian Early and Mid-Trimester Amniocentesis Trial (CEMAT) Group. (1998). Randomised trial to asses safety and fetal outcome of early and midtrimester amniocentesis. Lancet, 351:242-247.
    14. Crandall B. F., Kulch P., Khalil T. (1994). Risk assessment of amniocentesis between 11 and 15 weeks: Comparison to later amniocentesis controls. Prenat. Diagn., 14:913-919.
    15. Eiben B., Hammans W., Hansen S., Trawicki W., Osthelder B., Stelzer A., Jaspers KD., Goebel R. (1997). On the complication risk of Early Amniocentesis versus Standard Amniocentesis. Fetal. Diagn. Ther., 12:140-144.
    16. Tavares P., Tavares A., Rendeiro P., Palmares C. (1998). Comparison between CVS and early amniocentesis. Prenat. Diagn., 18(1):87. Letters to editor.
    17. Sato K., lzuta M., Kojima T., Miyakawa T., Yokoo l., Takahashi K, Tametika S., Okuno T.,
    18. Saitou R., Toubai H. (1992). Early amniocentesis risk and laboratory evaluation. Acta.Obstet.
    19. Gynaecol. Jpn., 44:1285-1288.
    20. Stripparo L., Buscaglia M., Longatti L., Ghisoni L., Dambrosio F., Guemeri S., Roselia
    21. F., Lituania M., Cordones M., De Biasio P., Passamonti U., Gimeiii G., Cuoco C. (1990). Genetic amniocentesis; 505 cases performed before the sixteenth week of gestation. Prenat. Diagn., 10:359-364.
    22. Hanson F.W., Tennant F.R, Hune S., Brookhyser K. (1992). Early amniocentesis: Outcome, risk, and technical problems at 12.8 weeks or less. Am. J. Obstet. GynecoI., 166:1707-1711.
    23. Johnson J.M., Wilson R.D., Singer J., Winsor E., Harman C., Armson B.A., Benzie
    24. R., Dansereau J., Ho M.F., Mohide P., Natale R., Okun N. (1999). Technical factors in early amniocentesis predict adverse outcome. Results of the Canadiam Early (EA) versus Mid-trimester (MA) Amniocentesis Trial. Prenat. Diagn., 19:732-738.
    25. Daniel A., NG A., Kuah K.B., Reiha S., Malafiej P. (1998). A study of early amniocentesis for prenatal cytogenetic diagnosis. Prenat. Diagn., 18(1):21-28.
    26. Schulman L.P., Elias 8., Simpson J.L. (1991). Early amniocentesis: Complications in initial 150 cases compared to complications in initial 150 cases of transabdominal chorioric villus sampling. Am. J. Hum. Genet, 49:231.
    27. Opitz, J.M. Tópicos recentes de genética clinica. (1984). Sociedade Brasileira de Genética Ribeirão Preto. São Paulo.
    28. Boué J., Boué A., Lazar P. (1975). Retrospective and prospective epidemiological studies of 1500 karyotyped spontaneous human abortions. Teratology., 12:11-26.
    29. Fitzsimmons J., Jackson D., Wapner R. Jackson L. (1983). Subsequent reproductive outcome in couples with repeated pregnancy loss. Am. J. Med. Genet., 16:583-587.
    30. Stray-Pederson B., Stray-Pederson S. (1984). Etiologic factors and subsequent reproductive performance in 195 couples with a prior history of habitual abortion. Am. J. Obstet. Gynecol., 148:140-146.
    31. Goldberg J.D., Porter A.E., Golbus M.S. (1990). Current assessment of fetal losses as a direct consequence of chorionic villus sampling. Am. J. Med. Genet, 35:174-177.
    32. Nevin J., Nevin N.C., Doman J.C., Sim D., Armstrong M.J. (1990). Early amniocentesis:
    33. Experience of 222 consecutive patients, 1987- 1988. Prenat. Diagn., 10:79-83.
    34. Schulman L.P., Elias 8., Phillips O.P., Grevengood C., Dungan J.S., Simpson J.L. (1994).
    35. Amniocentesis performed at 14 weeks gestation or earlier. Comparison with first-trimester
    36. transabdominal chorionic villus sampling. Obstet. Gynecol., 83:543-548.
    37. Frates M.C., Benson C.B., Doubilet M. (1993). Pregnancy outcome after a first trimester sonogram demonstrating fetal cardiac activity. J.
    38. Ultrasound. Med., 12:383-386.
    39. Wilson R.D., Kendrick V., Wittmann B.K., McGiIIivray B.C. (1986). Spontaneous abortion and pregnancy outcome after normal firsttrimester ultrasound examination. Am.J.Obstet. Gynecol., 67:352-355.
    40. Brumfield C.G., Lin S., Conner W., Cosper P., Davis R.O., Owen J. (1996). Pregnancy outcome following genetic amniocentesis al 11-14 versus 16-19 weeks gestation. Obstet. Gynecol., 88(1): 114-118.
    41. Sundberg K., Bang J., Smidt-Jensen 8., Brocks V., Lundsteen C., Pamer J., Keiding N.,
    42. Philip J. (1997). Randomised study of risk of fetal loss related to early amniocentesis versus chorionic villus sampling. Lancet., 350:697-703.
    43. Eiben B., Hammans W., Trawicki W., Goebel R. (1998). Early Amniocentesis versus Chorionic Villus Sampling. Prenat. Diagn., 18:405-406, Letters to the editor.
    44. Tharmaratnam S., Sadek S., Steele E.K., Harper M.A., Stewart F.J., Nevin J., Nevin N.C.,
    45. Doman J.C. (1998). Early amniocentesis: Efect of removing a reduced volume of amniotic fluid on pregnancy outcome. Prenat. Diagn., 18:1773-778.
    46. Tharmaratnam S., Sadek S., Steele E.K., Harper M.A., Nevin N.C., Doman JACI
    47. (1998). Transplacental early amniocentesis and pregnancy outcome. Br. J. Obstet. Gynaecol., 105(2):228-230.
    48. Diaz M., De la Cueva P., Leal C_, Aisa F. (1996). Early Amniocentesis at 10-12 weeks gestation. Prenat. Diagn., 16:307-312.
    49. Aula P., Karjalinen 0., Terano N., Vaara L., Seppala M. (1979). Safety and accuracy of
    50. midtrimester amniocentesis for prenatal diagnosis of genetic disorders. Ann. Clin. Res., 11:156-159.
    51. Simpson N., Dallaire L., Miller J., Siminovich L., Hammnerton J., Miller J., McKeen C. (1976). Prenatal diagnosis of genetic disease of Canada; report of a collaborative study. Can. Med. Ass. J., 115:739-745.
    52. Reece E.A. (1997). Amniocentese genética precoce e nos trimestres intermediarios.
    53. Segurança e resultados. In: Clinicam Obstétricas e Ginecológicas da América do Norte. Diagnóstico e Tratamento Fetal. Reece E.A. Vol 1. lnterlivros. Rio de Janeiro.
    54. Mennuti M., Brummond W., Criombleholme W., Shwartz R. (1980). Fetal maternal bleeding associated with genetic amniocentesis. Obstet. GynecoI., 55:48.
    55. Zolnierczyk P., Raczynski A., Lisawa J., Chazan B. (1997). Early amniocentesis transplacental needle passage safer than nontransplacental? Acta. Obstet. Gynecol. Scand., Supplement, 76(167):51.
    56. DATASUS. (1997). Banco de dados do Sistema Único de Saúde. Disponível na lnternet.
    57. http://www.datasus.saude.gov.brmarco2000
    58. -----------------------------------------------------------------------------------
    59. DOI: http://dx.doi.org/10.22490/24629448.513
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