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Artículos de revistas sobre el tema "Prenatal diagnosis"

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Autor: Grafiati

Publicado: 4 de junio de 2021

Última modificación: 11 de marzo de 2023

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1

Gorbunov, D. V. y L. S. Abikeeva. "Prenatal diagnosis of critical congenital heart defects in Kazakhstan: a single-center 8 years’ experience". Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) 67, n.º 5 (18 de noviembre de 2022): 96–102. http://dx.doi.org/10.21508/1027-4065-2022-67-5-96-102.

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Purpose. To give a quantitative and qualitative assessment of the results of prenatal diagnosis of critical congenital heart defects in the Republic of Kazakhstan based on the treatment of newborns at the head cardiac surgery center.Methods. A retrospective analysis of the medical records of 511 newborns with critical congenital heart defects treated at the National Research Cardiac Surgery Center (NRCSC) in 2012–2019 was performed. The proportion of those operated on was 474/511 (92.8%). The studied parameters were the presence of prenatal diagnosis of critical congenital heart defects (yes/no); prenatal diagnosis formulation; postnatal diagnosis formulation; discrepancy between pre- and postnatal diagnoses (yes/no); for a prenatally diagnosed newborn — the gestational age at the time of the diagnosis and the region where the diagnosis was firstly made.Results. Prenatally, 297/511 (58.1%) newborns were diagnosed. The rate of discrepancies between pre- and postnatal diagnoses was 62/288 (21.5%). According to the timing of the prenatal diagnosis, newborns were distributed as follows: first trimester screening — 20/272 (7.4%), second trimester screening — 139/272 (51.1%), third trimester screening — 113/272 (41.5%). Up to 22 weeks of gestation, 71/272 (26.1%) patients were diagnosed. Among the newborns treated at the NRCSC, the proportion of those diagnosed prenatally in different regions of the Kazakhstan varies from 20% to 100%.Conclusions. 1) Prenatal diagnosis of critical congenital heart defects is carried out in all regions of Kazakhstan, providing an acceptable level of detection; 2) in half of the cases, critical congenital heart defects are diagnosed during the second screening, however, there is an experience of their accurate detection as early as during the first screening; 3) individually, doctors of ultrasound diagnostics in Kazakhstan apply an extended protocol for examining the fetal heart; 4) a significant proportion of fetuses diagnosed before the 22nd week of gestation shows the choice of families in favor of carrying of a pregnancy when a critical congenital heart defects is detected; 5) the greatest difficulty for prenatal diagnosis is presented by patients with total anomalous pulmonary veins return.

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2

DiLiberti, J. H., M. A. Greenstein y S. S. Rosengren. "Prenatal Diagnosis". Pediatrics in Review 13, n.º 9 (1 de septiembre de 1992): 334–42. http://dx.doi.org/10.1542/pir.13-9-334.

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3

Begum, Rashida. "Prenatal Diagnosis". Bangladesh Journal of Obstetrics & Gynaecology 31, n.º 2 (12 de octubre de 2017): 61–62. http://dx.doi.org/10.3329/bjog.v31i2.34211.

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4

Baumiller, Robert. "Prenatal Diagnosis". Ethics & Medics 20, n.º 11 (1995): 3–4. http://dx.doi.org/10.5840/em1995201122.

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5

Hafner, Erich. "Prenatal diagnosis". Hamdan Medical Journal 5, n.º 3 (2012): 213. http://dx.doi.org/10.7707/hmj.v5i3.196.

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6

DiLiberti, John H., Mark A. Greenstein y Sally Shulman Rosengren. "Prenatal Diagnosis". Pediatrics In Review 13, n.º 9 (1 de septiembre de 1992): 334–42. http://dx.doi.org/10.1542/pir.13.9.334.

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The enormous progress witnessed in the field of prenatal diagnosis during the past two decades is likely to continue into the future. Improved imaging techniques are likely to enhance the resolution of noninvasively obtained fetal images considerably over their current excellent quality. Although this undoubtedly will be true for ultrasonography, the increased speed of magnetic resonance equipment may offer a new realm of imaging possibilities. Computerized image processing, analysis, and three-dimensional reconstructions all should make interpretation of fetal images easier and more understandable to the nonspecialist. Advances in molecular genetics will continue to accelerate, greatly expanding the range and accuracy of prenatal diagnosis. The alert pediatrician who is sensitive to genetic issues may, by early detection of pediatric disorders and careful family history assessment, be in a position to identify families at risk for serious genetic conditions and provide the opportunity to make informed decisions on reproductive options that avert a major tragedy. The pediatrician, working with obstetric colleagues, should be part of a team effort to support families going through prenatal testing. Familiarity with these rapidly changing technologies will make it far easier to support the family needing additional explanation about prenatal diagnosis issues.

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7

Texler, K. C. "Prenatal diagnosis". Medical Journal of Australia 152, n.º 3 (febrero de 1990): 149. http://dx.doi.org/10.5694/j.1326-5377.1990.tb125125.x.

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8

Lippman, A. "Prenatal diagnosis." American Journal of Public Health 89, n.º 10 (octubre de 1999): 1592–93. http://dx.doi.org/10.2105/ajph.89.10.1592.

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9

WILLIAMSON, ROGER A. "PRENATAL DIAGNOSIS". Clinical Obstetrics and Gynecology 31, n.º 2 (junio de 1988): 231. http://dx.doi.org/10.1097/00003081-198806000-00003.

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10

&NA;. "Prenatal Diagnosis". Clinical Obstetrics and Gynecology 31, n.º 2 (junio de 1988): 419–20. http://dx.doi.org/10.1097/00003081-198806000-00015.

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11

De Ponte, Francesco Saverio, Davide Johan Bottini, Eugenio Maggi, Emanuele Marchetti, Piero Cascone y Giorgio lannetti. "Prenatal Diagnosis". Journal of Craniofacial Surgery 9, n.º 2 (marzo de 1998): 190–95. http://dx.doi.org/10.1097/00001665-199803000-00020.

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12

Johnson, Timothy R. B. "Prenatal diagnosis". Current Opinion in Obstetrics and Gynecology 3, n.º 2 (abril de 1991): 219–20. http://dx.doi.org/10.1097/00001703-199104000-00009.

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13

&NA;. "Prenatal diagnosis". Current Opinion in Obstetrics and Gynecology 5, n.º 2 (abril de 1993): 267???288. http://dx.doi.org/10.1097/00001703-199304000-00016.

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14

Ludmir, Jack. "Prenatal diagnosis". Current Opinion in Obstetrics and Gynecology 8, n.º 2 (abril de 1996): 129???132. http://dx.doi.org/10.1097/00001703-199604000-00009.

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15

Ludmir, Jack. "Prenatal diagnosis". Current Opinion in Obstetrics and Gynecology 9, n.º 2 (abril de 1997): 107–8. http://dx.doi.org/10.1097/00001703-199704000-00006.

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16

Chescheir, Nancy. "Prenatal diagnosis". Current Opinion in Obstetrics and Gynecology 16, n.º 2 (abril de 2004): 151. http://dx.doi.org/10.1097/00001703-200404000-00009.

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17

Desforges, Jane F., Mary E. D'Alton y Alan H. DeCherney. "Prenatal Diagnosis". New England Journal of Medicine 328, n.º 2 (14 de enero de 1993): 114–20. http://dx.doi.org/10.1056/nejm199301143280208.

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18

Langford, K. "Prenatal diagnosis". Current Obstetrics & Gynaecology 11, n.º 5 (octubre de 2001): 313–14. http://dx.doi.org/10.1054/cuog.2001.0202.

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19

Saili, Arvind, Savita Jha y Babu Madarkar. "Prenatal Diagnosis". Journal of Neonatology 28, n.º 1 (marzo de 2014): 28–32. http://dx.doi.org/10.1177/0973217920140106.

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20

Chueh, Jane. "Prenatal diagnosis". Current Opinion in Obstetrics and Gynecology 29, n.º 2 (abril de 2017): 71–72. http://dx.doi.org/10.1097/gco.0000000000000352.

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21

Chueh, Jane. "Prenatal diagnosis". Current Opinion in Obstetrics and Gynecology 30, n.º 2 (abril de 2018): 102–3. http://dx.doi.org/10.1097/gco.0000000000000446.

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22

Davis, Alison. "PRENATAL DIAGNOSIS". Lancet 334, n.º 8671 (noviembre de 1989): 1104. http://dx.doi.org/10.1016/s0140-6736(89)91122-7.

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23

Carlson, Laura M. y Neeta L. Vora. "Prenatal Diagnosis". Obstetrics and Gynecology Clinics of North America 44, n.º 2 (junio de 2017): 245–56. http://dx.doi.org/10.1016/j.ogc.2017.02.004.

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24

Mackie Ogilvie, Caroline y Frances Flinter. "Prenatal diagnosis". Lancet 366, n.º 9492 (octubre de 2005): 1159–60. http://dx.doi.org/10.1016/s0140-6736(05)67471-5.

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25

Eiben, Bernd y Ralf Glaubitz. "Prenatal diagnosis". Lancet 366, n.º 9492 (octubre de 2005): 1161–62. http://dx.doi.org/10.1016/s0140-6736(05)67473-9.

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26

Somerville, Margaret. "Prenatal diagnosis". Lancet 366, n.º 9492 (octubre de 2005): 1162. http://dx.doi.org/10.1016/s0140-6736(05)67474-0.

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27

Arensman, Robert M. "Prenatal Diagnosis". Journal of the American College of Surgeons 204, n.º 1 (enero de 2007): A36. http://dx.doi.org/10.1016/j.jamcollsurg.2006.10.020.

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28

Eiben, B. y W. Hammans. "Prenatal diagnosis". Reproduktionsmedizin 15, n.º 5 (octubre de 1999): 372–77. http://dx.doi.org/10.1007/s004440050127.

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29

Kabra, Madhulika. "Prenatal diagnosis". Indian Journal of Pediatrics 70, n.º 1 (enero de 2003): 81–85. http://dx.doi.org/10.1007/bf02722749.

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30

Paek, Bettina, James D. Goldberg y Craig T. Albanese. "Prenatal Diagnosis". World Journal of Surgery 27, n.º 1 (1 de enero de 2003): 27–37. http://dx.doi.org/10.1007/s00268-002-6734-5.

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31

Rodeck, C. H. "PRENATAL DIAGNOSIS". Lancet 341, n.º 8843 (febrero de 1993): 468–69. http://dx.doi.org/10.1016/0140-6736(93)90213-z.

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32

Ghai, Anita y Rachana Johri. "Prenatal Diagnosis". Indian Journal of Gender Studies 15, n.º 2 (mayo de 2008): 291–316. http://dx.doi.org/10.1177/097152150801500205.

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33

Reddy, Pramod P. y James Mandell. "PRENATAL DIAGNOSIS". Urologic Clinics of North America 25, n.º 2 (mayo de 1998): 171–80. http://dx.doi.org/10.1016/s0094-0143(05)70005-7.

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34

Rodrigo, Nalinda. "Prenatal diagnosis". Sri Lanka Journal of Child Health 33, n.º 4 (8 de julio de 2009): 97. http://dx.doi.org/10.4038/sljch.v33i4.618.

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35

BAUMANN, P. y B. MCFARLIN. "Prenatal diagnosis". Journal of Nurse-Midwifery 39, n.º 2 (marzo de 1994): S35—S51. http://dx.doi.org/10.1016/0091-2182(94)90063-9.

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36

Bobrow, Martin. "Prenatal diagnosis". Journal of Chemical Technology & Biotechnology 43, n.º 4 (24 de abril de 2007): 285–91. http://dx.doi.org/10.1002/jctb.280430408.

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37

Gordon, Jon W. "Prenatal diagnosis today: The morality of prenatal diagnosis". Human Reproduction 10, n.º 4 (abril de 1995): 767–68. http://dx.doi.org/10.1093/oxfordjournals.humrep.a136034.

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38

Lazow, Stefanie P., Danielle M. Richman, Beatrice Dionigi, Steven J. Staffa, Carol B. Benson y Terry L. Buchmiller. "Prenatal Imaging Diagnosis of Suprarenal Lesions". Fetal Diagnosis and Therapy 48, n.º 3 (2021): 235–42. http://dx.doi.org/10.1159/000512689.

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<b><i>Introduction:</i></b> Prenatal suprarenal lesions represent diverse pathologies. This study investigated prenatal imaging features and regression patterns associated with specific lesion diagnoses. <b><i>Methods:</i></b> This is a multicenter retrospective review of fetuses with prenatally diagnosed suprarenal lesions between 2001 and 2019. Prenatal ultrasound and MRI characteristics, postnatal imaging, and clinical course were reviewed<i>.</i> Prenatal imaging findings were compared by the most common diagnoses and regression patterns. <b><i>Results:</i></b> Forty-four fetuses were prenatally diagnosed with suprarenal lesions. Diagnoses included pulmonary sequestration (<i>n</i> = 12; 27.3%), adrenal hemorrhage (<i>n</i> = 12; 27.3%), upper quadrant cyst (including 2 duplication cysts, 1 splenic cyst, and 3 indeterminate cysts), neuroblastoma (<i>n</i> = 4), adrenal hyperplasia (<i>n</i> = 3), bilateral adrenal calcifications (<i>n</i> = 1), and indeterminate lesions (<i>n</i> = 6). Sequestrations were uniformly left-sided (100 vs. 50%; <i>p</i> = 0.014) and diagnosed earlier in gestation than adrenal hemorrhages (<i>p</i> = 0.025). Sequestrations were also significantly more likely to have a prenatal feeding vessel (<i>p</i> = 0.005), low T1 MRI signal (<i>p</i> = 0.015), and no MRI blood products (<i>p</i> = 0.018) compared to adrenal hemorrhages. When comparing all 44 patients, a prenatal feeding vessel and low T1 signal on prenatal MRI were significantly associated with lesion persistence (<i>p</i> = 0.003; <i>p</i> = 0.044). <b><i>Discussion/Conclusion:</i></b> Imaging findings on prenatal ultrasound and MRI aid in the diagnosis of suprarenal lesions, including differentiating pulmonary sequestrations and adrenal hemorrhages.

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39

Zvanca, Mona y Cristian Andrei. "Prenatal Diagnosis of Neuroblastoma". Donald School Journal of Ultrasound in Obstetrics and Gynecology 8, n.º 3 (2014): 321–27. http://dx.doi.org/10.5005/jp-journals-10009-1371.

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ABSTRACT Fetal malignancies are rare complications during pregnancies, but when they appear, they are very challenging for the perinatology team. Because of their low incidence, the information is limited, with data provided from individual case reports or small case series. Although neuroblastoma is the most frequent extracranial solid tumor in childhood, prenatal diagnosis by ultrasound is very rare and almost always discovered during routine third trimester ultrasound. Expectant management is usually indicated prenatally, with serial ultrasound examination. Delivery should be planned in a tertiary center together with pediatric oncologists and surgeons to allow appropriate postnatal management. We present two cases of neuroblastoma diagnosed at 36 and 33 weeks of gestation with multiple aspects of this tumor identified by ultrasound. Both cases needed surgery and had a favorable outcome. The key role of ultrasound in diagnosis and follow-up of neuroblastoma in pregnancy is discussed, together with the management options recommended in literature. How to cite this article Andrei C, Vladareanu R, Zvanca M, Vladareanu S. Prenatal Diagnosis of Neuroblastoma. Donald School J Ultrasound Obstet Gynecol 2014;8(3):321-327.

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40

Schäfer, D., J. Arnemann, E. Brude y R. Baumann. "Prenatal diagnosis today: Society must decide about prenatal diagnosis". Human Reproduction 10, n.º 4 (abril de 1995): 768–69. http://dx.doi.org/10.1093/oxfordjournals.humrep.a136035.

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41

Shields, Lisa B. E., Jeffrey T. White, Dennis S. Peppas y Eran Rosenberg. "Challenges in the Prenatal Diagnosis of Cloaca". Global Pediatric Health 7 (enero de 2020): 2333794X2095892. http://dx.doi.org/10.1177/2333794x20958929.

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Background: Cloaca is a common excretory channel for the genital, urinary, and gastrointestinal tracts. It is considered a severe anorectal malformation caused by failed partitioning of the genital, rectal, and urinary tracts. Methods: We report 5 infants with cloaca at birth who were identified prenatally by one or more of the following on prenatal ultrasound (US): ambiguous genitalia, a cystic pelvic/abdominal mass, hydronephrosis, ascites, a single umbilical artery, and oligohydramnios. Results: A cystic pelvic/abdominal mass and ambiguous genitalia were each observed in 3 cases by prenatal US. Ambiguous genitalia was observed in all 5 neonates at birth. There were 2 twin pregnancies (dichorionic/diamniotic and monochorionic/monoamniotic), with only 1 twin in a set affected with cloaca. Conclusion: Pediatricians should be alert to the prenatal US findings that may raise suspicion of a persistent cloaca to improve both prenatal counseling and family preparation.

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42

Wolter, Aline, Marie Gebert, Christian Enzensberger, Andrea Kawecki, Rüdiger Stessig, Jan Degenhardt, Jochen Ritgen et al. "Outcome and Associated Findings in Individuals with Pre- and Postnatal Diagnosis of Tetralogy of Fallot (TOF) and Prediction of Early Postnatal Intervention". Ultraschall in der Medizin - European Journal of Ultrasound 41, n.º 05 (19 de noviembre de 2018): 504–13. http://dx.doi.org/10.1055/a-0753-0008.

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AbstractPurpose The aim of our retrospective evaluation was to compare the outcome of patients with prenatal and postnatal diagnosis of Tetralogy of Fallot (TOF) and to analyze prenatal echocardiographic parameters predicting intervention within 30 days postnatal.Materials and Methods We evaluated 142 patients in our pediatric heart center and prenatal diagnosis center and prenatal practice Praenatal plus in Cologne between 01/08–06/16.Results Within the prenatal diagnosis group, 6/74 fetuses (8.1 %) had TOF with pulmonary atresia (TOF-PA), and 6 (8.1 %) had absent pulmonary valve syndrome (TOF-APVS). 14 (18.9 %) had an abnormal karyotype including 9/14 (64.3 %) with microdeletion 22q11.2. 25 (33.8 %) had extracardiac malformation. 4 (5.4 %) had agenesis of ductus arteriosus (DA), 22 (29.7 %) had right aortic arch (RAA) and 9 (12.2 %) had major aortopulmonary collateral arteries (MAPCAs). Within the postnatal diagnosis group, no patient had TOF-PA, 4/68 (5.9 %) had TOF-APVS. 12 (17.6 %) had extracardiac malformations, 9 (13.2 %) had an abnormal karyotype including 2/9 with microdeletion 22q11.2. 10 (14.7 %) had RAA, 9 (13.2 %) had MAPCAs. There were no cases with agenesis of DA. Increasing z-score values of the left/right pulmonary artery (LPA/RPA) prenatally were associated with a lower probability for early postnatal intervention (RPA: p = 0.017; LPA: p = 0.013). Within the prenatal diagnosis group, 12 of 41 (29.3 %) live-born patients with follow-up and intention to treat needed early intervention versus 7 (10.3 %) in the postnatal diagnosis group (p = 0.02). Within the postnatal diagnosis group, there were no deaths, while 2 (4.9 %) post-intervention deaths occurred in the prenatal diagnosis group.Conclusion There are no significant differences concerning post-intervention survival in the prenatal diagnosis group versus the postnatal diagnosis group. Complex cases may be underrepresented in the postnatal diagnosis group. Smaller RPA/LPA values prenatally seem to be associated with early postnatal intervention.

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43

Stryker, Richard N. "Poor Prenatal Diagnosis". National Catholic Bioethics Quarterly 14, n.º 1 (2014): 31–37. http://dx.doi.org/10.5840/ncbq201414145.

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44

Jones, Warren R. "Prenatal genetic diagnosis". Medical Journal of Australia 143, n.º 2 (julio de 1985): 55. http://dx.doi.org/10.5694/j.1326-5377.1985.tb122793.x.

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45

Jones, Robert A. "Prenatal genetic diagnosis". Medical Journal of Australia 143, n.º 3 (agosto de 1985): 127. http://dx.doi.org/10.5694/j.1326-5377.1985.tb122845.x.

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46

Fisk, Nicholas M., John C. Anderson y Arabella Smith. "Prenatal genetic diagnosis". Medical Journal of Australia 143, n.º 7 (septiembre de 1985): 316–17. http://dx.doi.org/10.5694/j.1326-5377.1985.tb123026.x.

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47

Smith, Arabella, Nicholas M. Fisk y John C. Anderson. "Prenatal cytogenetic diagnosis". Medical Journal of Australia 143, n.º 8 (octubre de 1985): 368. http://dx.doi.org/10.5694/j.1326-5377.1985.tb123070.x.

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48

Khan, Md Mahbub Ul Karim. "Prenatal Diagnosis (PND)". Community Based Medical Journal 1, n.º 2 (19 de febrero de 2013): 1–2. http://dx.doi.org/10.3329/cbmj.v1i2.13855.

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49

McGowan, Kathryn D. "PREIMPLANTATION PRENATAL DIAGNOSIS". Obstetrics and Gynecology Clinics of North America 20, n.º 3 (septiembre de 1993): 599–610. http://dx.doi.org/10.1016/s0889-8545(21)00544-1.

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50

Poidevin, Leslie O. S. "Prenatal cytogenetic diagnosis". Medical Journal of Australia 144, n.º 1 (enero de 1986): 56. http://dx.doi.org/10.5694/j.1326-5377.1986.tb113651.x.

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