Early amniocentesis and chorionic villus biopsy. Fetal losses and congenital anomalies in a group of Brazilian pregnant women
Amniocentesis precoz y biopsia de vellosidad corial. Pérdidas fetales y anomalías congénitas en un grupo de gestantes brasileñas
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.
Furthermore, the authors keep their property intellectual rights over the articles.
Show authors biography
In the Institute of Fetal Medicine and Human Genetics of São Paulo are offered, pregnant women have an increased risk for chromosomal abnormalities, different techniques, among them, Transabdominal Corial Vellosity Biopsy (BVCTA) and Precocious Amniocentesis (AP). The objective of this study is to compare the frequency of Hepatitis and congenital anomalies presented in all procedures, both performed by operators, in the same gestational age (12-14 6/7 weeks) and under a transabdominal approach. 432 AP and 418 BVCTA were analyzed retrospectively. All collection procedures were monitored by ultrasonography. The spontaneous fetal frequency was 4.9% in AP and 5.3% in BVCTA, a non-significant difference. There is no difference in results compared to gestation times. Bleeding and loss of amniotic fluid were more frequent in AP than in BVCTA. That difference was significant in the case of the loss of amniotic fluid. In some cases, this finding was related to fetal loss. The incidence of prematurity and birth weight without difference between the two procedures. The highest frequency of respiratory problems recorded in AP was not significant compared to BVCTA. There is no significant difference in the incidence of musculoskeletal abnormalities. Amniocentesis after 14 weeks presents a low risk of fetal loss or congenital anomalies. The BVCTA should be close to the twelfth week of gestation.
Article visits 311 | PDF visits 168
Downloads
1. Tabor A, Madsen M, Obel E, Philip J, Bang J, Noergard-Pe- terson B. Randomised controlled trial of genetic amniocen- tesis in 4606 low-risk women. Lancet.1986; 1: 1287-1293.
2. Reece E. Amniocentese genética precoce e nos trimestres intermediários. Segurança e resultados. Clínicas Obstétricas e Ginecológicas da América do Norte. Diagnostico e Trata- mento Fetal. Vol 1. Rio de Janeiro: Interlivros; 1997.
3. Eddleman K, Malone F, Sullivan L, Dukes K, Berkowitz R, Kharbutli Y, and others. Pregnancy loss rates after mi- dtrimester amniocentesis. Obstet Gynecol. 2006; 108(5): 1067–72.
4. Kong C, Leung T, Leung T, Chan L, Sahota D, Fung T, and others. Risk factors for procedure-related fetal losses after mid-trimester genetic amniocentesis. Prenat Diagn. 2006; 26(10): 925–30.
5. Anuwutnavin S, Chanprapaph P, Ruangvutilert P, Eammatta M, Tontisirin P. Short-term outcomes after second-trimester genetic amniocentesis in Siriraj Hospital. International Jour- nal of Gynecology and Obstetrics. 2014; 124: 222–225. doi: 10.1016/j.ijgo.2013.09.019.
6. Connolly K, Eddleman K. Amniocentesis: A contemporary review. World J Obstet Gynecol. 2016; 5(1): 58-65.
7. Bernal L. Evaluación de la amniocentesis precoz en una ins- titución brasileña de diagnóstico prenatal. NOVA. 2012; 10(17): 12-24.
8. Naccache N, GollopT, Auler-Bittencourt E, Vianna-Mor- gante A, Eigier A. Cytogenetic analysis of first trimester cho- rionic villi sampling. Rev. Brasil. Genet. 1987; 10: 277-287.
9. Gollop T, Pieri P, Naccache N, Auler-Bittencourt E, Eigier A, Hauschild D. Transabdominal Chorionic Villus Sampling: experience with 70 cases. Rev. Brasil. Genet. 1990; 13(3): 591-597.
10. Gollop T, Naccache N, Campos I, Fieri P. Amostra de Vilo Corial: 1.290 casos. Rev. Brasil. Ginecol. Obstet. 1993; 15(2): 84-87.
11. Cederholm M, Axelsson O. A prospective comparati- ve study on transabdominal chorionic villus sampling and amniocentesis performed at 10-13 weeks gestation. Prenat Diagn. 1997; 17(4): 311-317.
12. CEMAT, The Canadian Early and Mid-Trimester Amnio- centesis Trial Group. Randomised trial to asses safety and fetal outcome of early and midtrimester amniocentesis. Lan- cet. 1998; 351:242-247.
13. Al Ibrahim A, Zidan M, Obaidly S, Khenyab N, Al Jenahi N, Al Mansori Z, Bolushi M, and others. Early Amniocentesis: The Resurrection. Qatar Foundation Annual Research Con- ference Proceedings. 2016.
14. Gollop T, Eigier A, Vianna-Morgante A, Naccache, N. Cho- rionic villi sampling for early prenatal genetic diagnosis. Rev. Brasil. Genet.. 1986; 9: 381-385.
15. Nicolaides K, Brizot M, Patel F, Snijders R. Comparison of Chorion Villus Sampling and Early Amniocentesis for karyo- typing in 1492 singlenton preqnancies. Fetal. Diagn. Ther. 1996; 11: 9-15.
16. Chuet J, Goldberg J, Wohlferd M, Golbus M. Comparision of transcervical and transabdominal chorionic villus sam- pling loss rate in nine thousand from a single center. Am. J. Obstet. Gynecol. 1995; 173: 1277-1282.
17. Smidt-Jensen S, Permin M, Phillip J, Lundsteen, C, Zachary, J, Fowler S et al. Randomized comparison of amniocentesis and transabdominal and transcervical chorionis villus sam- pling. Lancet. 1992; 340: 1237-1244.
18. Brambati B, Terzian E, Tognoni G. Randomized clinical trial of transaddominal versus transcervical chorionic villus sam- pling methods. Prenat. Diagn. 1991; 11: 285 293.
19. Fortuny A, Borrell A, Soler A, Casals E, Costa D, Carrio A, and others. Chorionic villus sampling by forceps. Results of 1580 procedures from single centre. Prenat. Diagn. 1995; 15: 541-550.
20. Penso C, Sandstrom M, Garber M, Ladoulis M, Stryker J, Benacerraf, B. Early Amniocentesis: Report of 407 cases with neonatal follow-up. Obstet. Gynecol. 1990; 76: 1032-1036.
21. Sato K, Izuta M, Kojima T, Miyakawa T, Yokoo I, Takahashi K, and others. Early amniocentesis risk and laboratory eva- luation. Acta. Obstet. Gynaecol. Jpn. 1992; 44: 1285-1288.
22. Stripparo L, Buscaglia M, Longatti L, Ghisoni L, Dambrosio F, Guerneri, S, and others. Genetic amniocentesis: 505 ca- ses performed before the sixteenth week of gestation. Prenat. Diagn. 1990; 10: 359-364.
23. Bravo R, Schulman L, Phillips O. Transplacental needle pas- sage in early amniocentesis and pregnancy loss. Obstet. Gy- necol. 1995; 86: 437-440.
24. Johnson J, Wilson R, Winsor E, Singer J, Dansereau J, Ka- lousek, D. The Early Amniocentesis Study: A randomized clinical trial of early amniocentesis versus midtrimester am- niocentesis. Fetal. Diagn. Ther. 1996; 11: 85-93.
25. Elejalde B, de Elejalde M, Acuna J, Thelen D, Trujillo C, Karrmann M. Prospective study of amniocentesis performed between weeks 9 and 16 of gestation: Its feasibility, risks, complications and use in early genetic prenatal diaqnosis. Am. J. Med. Genet.. 1990; 35: 188-196.
26. Brumfield C, Lin S, Conner W, Cosper P, Davis R, Owen J. Pregnancy outcome following genetic amniocentesis at 11-14 versus 16 -19 weeks gestation. Obstet. Gynecol. 1996; 88(1): 114-118.
27. Eiben B, Hammans W, Hansen S, Trawicki W, Osthelder B, Stelzer A, and others. On the complication risk of Early Amniocentesis versus Standard Amniocentesis. Fetal. Diagn. Ther. 1997; 12: 140-144.
28. Daniel A, N, Kuah K, Reiha S, Malafiej P. A study of ear- ly amniocentesis for prenatal cytogenetic diagnosis. Prenat. Diagn. 1998; 18(1): 21-28.
29. Schulman L, Elias S, Simpson, J. Early amniocentesis: Com- plications in initial 150 cases compared to complication in initial 150 cases transabdominal chorionic villus sampling. Am. J. Human. Genet. 1991; 49: 231.
30. Nagel H, Vandenbussche F, Keirse M, Oepkes D, Oosterwijk J, Beverstock G, and others. Amniocentesis before 14 com- pleted weeks as an alternative to transabdominal chorionic villus sampling: A controlled trial with infant follow-up. Pre- nat Diagn. 1998; 18: 465-475.
31. Philip J, Silver R, Wilson R, Thom E, Zachary J, Mohide P, and others. Late First-Trimester Invasive Prenatal Diagnosis: Results of an International Randomized Trial.
Obstetrica and Gynecology. 2004; 103(6): 1164-117
32. Liu D, Jeavons B, Preston C, Pearson D. A prospective study of spontaneous miscarriage in intrasonically normal preg- nancies and relevance to chorionic villus sampling. Pnenat. Diagn. 1987; 7: 223-226.
33. Frates M, Benson C, Doubilet M. Pregnancy outcome after a first trimester sonogram demonstrating fetal cardiac activity. J. Ultrasound. Med. 1993; 12: 383-386.
34. Tharmaratnam S, Sadek S, Steele E, Harper M, Stewart F, Nevin J, and others. Early amniocentesis: Effect of removing a reduced volume of amniotic fluid on pregnancy outcome. Prenat. Diagn. 1998; 18:773-778.
35. Wulff C, Gerds T, Rode L, Ekelund C, Petersen O, Tabor A. Risk of fetal loss associated with invasive testing following combined first-trimester screening for Down syndrome: a national cohort of 147987 singleton pregnancies. Ultra- sound Obstet Gynecol. 2016; 47: 38-44.
36. Sundberg K, Jorgensen F, Bang J. Experience with early am- ncentesis. J Perinat Med. 1995; 23: 149-158.
37. Tharmaratnam S, Sadek S, Steele E, Harper M, Nevin N, Dornan C. Transplacental early amniocentesis and pregnan- cy outcome. British Journal of Obstetrics and Gynaecology. 1998; 105(2): 228-230.
38. Zelig C, Knutzen D, Ennen C, Dolinsky B, Napolitano P. Chorionic Villus Sampling, Early Amniocentesis, and Ter- mination of Pregnancy Without Diagnostic Testing: Compa- rison of Fetal Risk Following Positive Non-invasive Prenatal Testing. J Obstet Gynaecol Can. 2016; 38(5): 441-445
39. Hanson F, Tennant F, Hune S, Brookhyser K. Early amnio- centesis: Outcome, risk, and technical problems at 12.8 wee- ksor less. Am. J. Obstet. Gynecol. 1992; 166: 1707-1711.
40. Sundberg K, Bang J, Smidt-Jensen S, Brocks V, Lundsteen C, Pamer J, and others. Randomised study of risk of fetal loss related to early amniocentesis versus chorionic villus sam- pling. Lancet. 1997; 350: 697-703.
41. Akolekar R, Beta J, Picciarelli G, Ogilvie C, D’Antonio F. Procedure-related risk of miscarriage following amniocente- sis and chorionic villus sampling: a systematic review and meta-analysis. Ultrasound Obstet Gynecol. 2015; 45: 16–26
42. Tara F, Lotfalizadeh M, Moeindarbari S. The effect of diag- nostic amniocentesis and its complications on early spon- taneous abortion. Electronic Physician. 2016; 8(8): 2787- 2792.
43. Ghi T, Sotiriadis A, Calda P, Da Silva Costa F, Raine-Fen- ning N, Alfirevic Z, McGillivray G, on behalf of the Interna- tional Society of Ultrasound in Obstetrics and Gynecology. ISUOG Practice Guidelines: invasive procedures for prenatal diagnosis in obstetrics. Ultrasound Obstet Gynecol. 2016; 48: 256–268.
44. Firth H, Boyd P, Chamberlain P, Mackenzie I, Lindenbaum R, Huson S. Severe limb abnormalities after chorionic villus sampling at 56-66 days gestation. Lancet. 1991; 337: 762- 763.
45. Hoyme H, Jones K, Van Allen M, Saunders B, Benirschke K. Vascular pathogenesis of transverse limb reduction defects. J. Pediatr 1982; 101: 839-843.
46. Wapner, R. Amostragem do Vilo Coriónico. Clínicas Obs- tétricas e Ginecológicas da América do Norte. Diagnóstico e Tratamento Fetal. Reece E.A. Vol 1. Rio de Janeiro: Inter- livros; 1997.
47. Lochmiller C, Johnston D, Scott A,Risman N,Hecht T. Ge- netic epidemiology study of idiopathic talipes equinovarus. Am J Med Genet. 1998; 79: 90–96.
48. Bernal Luz Mery, López Greizy. Diagnóstico prénatal: retros- pectiva. Nova. 2014; 12( 21 ): 23-36.
49. Márquez Gómez Marco Antonio, Gómez Díaz Graciela Ma- ría. Accidente ofídico en el departamento de Sucre, Colom- bia. Nova. 2015; 13( 24 ): 39-46.
50. Pinilla B Gladys, Chavarro P Bibiana, Moreno A Natalia, Navarrete O Jeannette, Muñoz M Liliana. Determinación de los genes, 16S ADNr, polA, y TpN47, en la detección de Treponema pallidum subsp. pallidum para el diagnóstico de sífilis congénita. Nova. 2015; 13( 24 ): 17-25.
51. Corrales Lucia Constanza, Antolinez Romero Diana Mar- cela, Bohórquez Macías Johanna Azucena, Corredor Vargas Aura Marcela. Bacterias anaerobias: procesos que realizan y contribuyen a la sostenibilidad de la vida en el planeta. Nova. 2015; 13( 24 ): 55-81.
52. González Yuri Lilian. Evaluación de la percepción del riesgo ocupacional en trabajadores de una empresa del sector de la construcción en Bogotá D.C. Nova. 2015; 13( 23 ): 93-107.
53. Thompson P, Greenough A, Nicolaides K. Lung function measured by functional residual capacity in infants following first trimester amniocentesis or chorion villus sampling. Br. J. Obstet. Gynaecol. 1992; 99: 479-482.
54. Carrero Sandra Helena Suescún, HerediaMontoya Dina Pao- la, Bolaños Yoryany Mulato, Medellín Martín Orlando Puli- do. Seroprevalencia de infección por Leptospira y factores de riesgo en estudiantes de una universidad de Colombia. Nova. 2017; 15( 27 ): 131-138.
55. Naranjo Flórez Ricardo Andrés. Avances y perspectivas en Síndrome de Asperger. Nova. 2014; 12( 21 ): 81-101.
56. Zuluaga Martha, Robledo Sebastian, Osorio-Zuluaga Ger- man A, Yathe Laura, Gonzalez Diana, Taborda Gonzalo. Me- tabolomics and pesticides: systematic literature review using graph theory for analysis of references. Nova. 2016; 14( 25): 121-138.
57. Almonacid Urrego Carmen Cecilia, Camarillo Romero Ma- ría del Socorro, Gil Murcia Zulay, Medina Medina Claudia Yasmin, Rebellón Marulanda Jennifer Viviana, Mendieta Zerón Hugo. Evaluación de factores de riesgo asociados a enfermedad cardiovascular en jóvenes universitarios de la Lo- calidad Santafé en Bogotá, Colombia. Nova. 2016; 14(25): 9-17.
58. González Devia Johanna L., Monroy Romero Paola A., Al- monacid Urrego Carmen C.. Homocisteína y otros factores de riesgo cardiovascular en niños de educación básica pri- maria del Colegio Distrital Manuel Elkin Patarroyo, Bogo- tá, D.C.Colombia. Estudio piloto. Nova. 2017 ; 15( 27 ): 103-117.