Hydrops fetalis has there been a change in diagnostic spectrum and mortality?

Journal of Maternal-Fetal and Neonatal Medicine

Volumn 24, Issue 2, 2011, Pages 258-263

  Czernik, Christoph ^a   Proquitté, Hans ^a   Metze, Boris ^a   Bührer, Christoph ^a  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

live born infants' outcome; Medical progress; non immune hydrops fetalis; unexplained cases

Indexed keywords

APGAR SCORE; ARTICLE; AUTOIMMUNE HEMOLYTIC ANEMIA; BIRTH WEIGHT; CAUSAL ATTRIBUTION; CHROMOSOME ABERRATION; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE CLASSIFICATION; FATALITY; FEMALE; FETUS HYDROPS; FETUS MORTALITY; GENETIC ASSOCIATION; GESTATIONAL AGE; HEART FAILURE; HUMAN; IDIOPATHIC DISEASE; INFANT; LYMPHATIC SYSTEM DISEASE; MAJOR CLINICAL STUDY; MALE; NEWBORN; PRENATAL CARE; PRIORITY JOURNAL; PROGNOSIS; SURVIVAL RATE;

BIRTH RATE; COHORT STUDIES; FEMALE; FLORIDA; GESTATIONAL AGE; GREAT BRITAIN; HUMANS; HYDROPS FETALIS; INFANT MORTALITY; INFANT, NEWBORN; INFANT, NEWBORN, DISEASES; MALE; OUTCOME ASSESSMENT (HEALTH CARE); PREGNANCY; RETROSPECTIVE STUDIES; SURVIVAL ANALYSIS;

EID: 78651443067     PISSN: 14767058     EISSN: 14764954     Source Type: Journal    
DOI: 10.3109/14767058.2010.483522     Document Type: Article

References (62)

1. Huang HR, Tsay PK, Chiang MC, Lien R, Chou YH. Prognostic factors and clinical features in liveborn neonates with hydrops fetalis. Am J Perinatol 2007;24:33-38. (Pubitemid 46239713)
2. Oury JF, Fiblec BL, Nisand I, Muller F. Nonimmune fetal ascites: a series of 79 cases. Am J Obstet Gynecol 2004;190: 407-412. (Pubitemid 38249237)
3. Bukowski R, Saade GR. Hydrops fetalis. Clin Perinatol 2000;27:1007-1031.
4. Graves GR, Baskett TF. Nonimmune hydrops fetalis: antenatal diagnosis and management. Am J Obstet Gynecol 1984;148:563-565. (Pubitemid 14196271)
5. Andersen HM, Drew JH, Beischer NA, Hutchison AA, Fortune DW. Non-immune hydrops fetalis: changing contribution to perinatal mortality. Br J Obstet Gynaecol 1983;90:636-639.
6. Maidman JE, Yeager C, Anderson V, Makabali G, OGrady JP, Arce J, Tishler DM. Prenatal diagnosis and management of nonimmunologic hydrops fetalis. Obstet Gynecol 1980; 56:571-576. (Pubitemid 11238207)
7. Brown BS. The ultrasonographic features of nonimmune hydrops fetalis: a study of 30 successive patients. Can Assoc Radiol J 1986;37:164-168.
8. Swain S, Cameron AD, McNay MB, Howatson AG. Prenatal diagnosis and management of nonimmune hydrops fetalis. Aust N Z J Obstet Gynaecol 1999;39:285-290. (Pubitemid 29431484)
9. Thompson PJ, Greenough A, Brooker R, Nicolaides KH, Gamsu HR. Antenatal diagnosis and outcome in hydrops fetalis. J Perinat Med 1993;21:63-67. (Pubitemid 23106950)
10. Wafelman LS, Pollock BH, Kreutzer J, Richards DS, Hutchison AA. Nonimmune hydrops fetalis: fetal and neonatal outcome during 1983-1992. Biol Neonate 1999; 75:73-81. (Pubitemid 29012070)
11. Abrams ME, Meredith KS, Kinnard P, Clark RH. Hydrops fetalis: a retrospective review of cases reported to a large national database and identification of risk factors associated with death. Pediatrics 2007;120:84-89. (Pubitemid 47036244)
12. Ratanasiri T, Komwilaisak R, Sittivech A, Kleebkeaw P, Seejorn K. Incidence, causes and pregnancy outcomes of hydrops fetalis at Srinagarind Hospital, 1996-2005: a 10-year review. J Med Assoc Thai 2009;92:594-599.
13. Ng YP, Joseph R, Biswas A. Homozygous a-thalassemia in a growth retarded, non-hydropic premature newborn. J Perinatol 2008;28:158-159. (Pubitemid 351217645)
14. Wang C, Ryan G. Transfusion medicine illustrated: intrauterine transfusion for homozygous α(0) thalassemia reverses hydrops fetalis. Transfusion 2009;49:1043-1044.
15. Karnpean R, Fucharoen G, Fucharoen S, Sae-ung N, Sanchaisuriya K, Ratanasiri T. Accurate prenatal diagnosis of Hb Barts hydrops fetalis in daily practice with a doublecheck PCR system. Acta Haematol 2009;121:227-233.
16. Liu JZ, Yan M, Wang LR, Wang ZY, Fan YP, Xiao B, Zhou Y. Molecular prenatal diagnosis of a-thalassemia using real-time and multiplex polymerase chain reaction methods. Hemoglobin 2008;32:553-560.
17. Pornprasert S, Phusua A, Suanta S, Saetung R, Sanguansermsri T. Detection of a-thalassemia-1 Southeast Asian type using real-time gap-PCR with SYBR Green1 and high resolution melting analysis. Eur J Haematol 2008;80: 510-514. (Pubitemid 351695233)
18. Simpson JH, McDevitt H, Young D, Cameron AD. Severity of non-immune hydrops fetalis at birth continues to predict survival despite advances in perinatal care. Fetal Diagn Ther 2006;21:380-382. (Pubitemid 43875147)
19. Nakayama H, Kukita J, Hikino S, Nakano H, Hara T. Longterm outcome of 51 liveborn neonates with non-immune hydrops fetalis. Acta Paediatr 1999;88:24-28. (Pubitemid 29100194)
20. Wy CA, Sajous CH, Loberiza F, Weiss MG. Outcome of infants with a diagnosis of hydrops fetalis in the 1990s. Am J Perinatol 1999;16:561-567. (Pubitemid 30418255)
21. Trainor B, Tubman R. The emerging pattern of hydrops fetalis - incidence, aetiology and management. Ulster Med J 2006;75:185-186. (Pubitemid 44308988)
22. Hansmann M, Gembruch U, Bald R. New therapeutic aspects in nonimmune hydrops fetalis based on four hundred and two prenatally diagnosed cases. Fetal Ther 1989;4:29-36. (Pubitemid 20362486)
23. Bellini C, Hennekam RC, Bonioli E. A diagnostic flow chart for non-immune hydrops fetalis. Am J Med Genet A 2009;149A:852-853.
24. Jauniaux E, Van Maldergem L, De Munter C, Moscoso G, Gillerot Y. Nonimmune hydrops fetalis associated with genetic abnormalities. Obstet Gynecol 1990;75:568-572. (Pubitemid 20062334)
25. Machin GA. Hydrops revisited: literature review of 1,414 cases published in the 1980s. Am J Med Genet 1989;34:366-390.
26. Turkel SB. Conditions associated with nonimmune hydrops fetalis. Clin Perinatol 1982;9:613-625. (Pubitemid 13193778)
27. Kattner E, Schäfer A, Harzer K. Hydrops fetalis: manifestation in lysosomal storage diseases including Farber disease. Eur J Pediatr 1997;156:292-295. (Pubitemid 27142150)
28. Loren DJ, Campos Y, dAzzo A, Wyble L, Grange DK, Gilbert-Barness E, White FV, Hamvas A. Sialidosis presenting as severe nonimmune fetal hydrops is associated with two novel mutations in lysosomal α-neuraminidase. J Perinatol 2005;25:491-494. (Pubitemid 40975601)
29. Kepron C, Blumenthal A, Chitayat D, Cutz E, Superti-Furga A, Keating S. An autophagic vacuolar myopathy-like disorder presenting as nonimmune hydrops in a female fetus. Pediatr Dev Pathol 2009;12:53-58.
30. Spear GS, Beutler E, Hungs M. Congenital Gaucher disease with nonimmune hydrops/erythroblastosis, infantile arterial calcification, and neonatal hepatitis/fibrosis. Clinicopathologic report with enzymatic and genetic analysis. Fetal Pediatr Pathol 2007;26:153-168. (Pubitemid 47450901)
31. Burin MG, Scholz AP, Gus R, Sanseverino MT, Fritsh A, Magalhaes JA, Timm F, Barrios P, Chesky M, Coelho JC, et al. Investigation of lysosomal storage diseases in nonimmune hydrops fetalis. Prenat Diagn 2004;24:653-657. (Pubitemid 39108575)
32. Ghalamkarpour A, Debauche C, Haan E, Van Regemorter N, Sznajer Y, Thomas D, Revencu N, Gillerot Y, Boon LM, Vikkula M. Sporadic in utero generalized edema caused by mutations in the lymphangiogenic genes VEGFR3 and FOXC2. J Pediatr 2009;155:90-93.
33. Piraud M, Froissart R, Mandon G, Bernard A, Maire I. Amniotic fluid for screening of lysosomal storage diseases presenting in utero (mainly as non-immune hydrops fetalis). Clin Chim Acta 1996;248:143-155. (Pubitemid 26146774)
34. Stone DL, Tayebi N, Orvisky E, Stubblefield B, Madike V, Sidransky E. Glucocerebrosidase gene mutations in patients with type 2 Gaucher disease. Hum Mutat 2000;15:1881-1888. (Pubitemid 30078409)
35. Tasso MJ, Martinez-Gutierrez A, Carrascosa C, Vazquez S, Tebar R. GM1-gangliosidosis presenting as nonimmune hydrops fetalis: a case report. J Perinat Med 1996;24:445-449. (Pubitemid 26358595)
36. Sinelli MT, Motta M, Cattarelli D, Cardone ML, Chirico G. Fetal hydrops in GM(1) gangliosidosis: a case report. Acta Paediatr 2005;94:1847-1849. (Pubitemid 43155605)
37. Kooper AJ, Janssens PM, de Groot AN, Liebrand-van Sambeek ML, van den Berg CJ, Tan-Sindhunata GB, an den Berg PP, Bijlsma EK, Smits AP, Wevers RA. Lysosomal storage diseases in non-immune hydrops fetalis pregnancies. Clin Chim Acta 2006;371:176-182.
38. Meizner I, Levy A, Carmi R, Robinsin C. Niemann-Pick disease associated with nonimmune hydrops fetalis. Am J Obstet Gynecol 1990;163:128-129. (Pubitemid 20253075)
39. Vidgoff J. Nonimmune hydrops in fetal Niemann-Pick disease. Am J Obstet Gynecol 1991;164:231-232.
40. Colmant C, Picone O, Froissart R, Labrune P, Senat MV. Second-trimester diagnosis of mucopolysaccharidosis type IV a presenting as hydrops fetalis. Prenat Diagn 2006;26:750-752. (Pubitemid 44252256)
41. Geipel A, Berg C, Germer U, Krapp M, Kohl M, Gembruch U. Mucopolysaccharidosis VII (Sly disease) as a cause of increased nuchal translucency and non-immune fetal hydrops: study of a family and technical approach to prenatal diagnosis in early and late pregnancy. Prenat Diagn 2002;22:493-495. (Pubitemid 34716943)
42. Venkat-Raman N, Sebire NJ, Murphy KW. Recurrent fetal hydrops due to mucopolysaccharidoses type VII. Fetal Diagn Ther 2006;21:250-254.
43. Beck M, Bender SW, Reiter HL, Otto W, Bassler R, Dancygier H, Gehler J. Neuraminidase deficiency presenting as non-immune hydrops fetalis. Eur J Pediatr 1984;143:135-139. (Pubitemid 15222534)
44. Godra A, Kim DU, DCruz C. Pathologic quiz case: a 5-dayold boy with hydrops fetalis. Mucolipidoses I (Sialidosis III). Arch Pathol Lab Med 2003;127:1051-1052.
45. Lemyre E, Russo P, Melancon SB, Gagne R, Potier M, Lambert M. Clinical spectrum of infantile free sialic acid storage disease. Am J Med Genet 1999;82:385-391. (Pubitemid 29096147)
46. Haverkamp F, Jacobs D, Cantz M, Hansmann M, Fahnenstich H, Zerres K. Nonimmune hydrops fetalis with galactosialidosis: consequences for family planning. Fetal Diagn Ther 1996;11:114-119. (Pubitemid 26056055)
47. Ben-Haroush A, Yogev Y, Levit O, Hod M, Kaplan B. Isolated fetal ascites caused by Wolman disease. Ultrasound Obstet Gynecol 2003;21:297-298. (Pubitemid 36390718)
48. Cox PM, Brueton LA, Murphy KW, Worthington VC, Bjelogrlic P, Lazda EJ, Sabire NJ, Sewry CA. Early-onset fetal hydrops and muscle degeneration in siblings due to a novel variant of type IV glycogenosis. Am J Med Genet 1999;86:187-193. (Pubitemid 29400351)
49. Alegria A, Martins E, Dias M, Cunha A, Cardoso ML, Maire I. Glycogen storage disease type IV presenting as hydrops fetalis. J Inherit Metab Dis 1999;22:330-332. (Pubitemid 29259507)
50. Ferreira P, Morais L, Costa R, Resende C, Dias CP, Araujo F, Costa E, Barbot J, Vilarinho A. Hydrops fetalis associated with erythrocyte pyruvate kinase deficiency. Eur J Pediatr 2000;159:481-482. (Pubitemid 30418988)
51. Gallagher PG, Weed SA, Tse WT, Benoit L, Morrow JS, Marchesi SL, Mohandas N, Forget BG. Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte β-spectrin gene. J Clin Invest 1995;95:1174-1182.
52. Yetgin S, Aytac S, Gurakan F, Yurdakok M. Nonimmune hydrops fetalis in two cases of consanguineous parents and associated with hereditary spherocytosis and hemophagocytic hystiocytosis. J Perinatol 2007;27:252-254. (Pubitemid 46487721)
53. Carver C, Brice G, Mansour S, Ostergaard P, Mortimer P, Jeffery S. Three children with Milroy disease and de novo mutations in VEGFR3. Clin Genet 2007;71:187-189. (Pubitemid 46189225)
54. Fang J, Dagenais SL, Erickson RP, Arlt MF, Glynn MW, Gorski JL, Seaver LH, Glover TW. Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome. Am J Hum Genet 2000;67:1382-1388.
55. Irrthum A, Devriendt K, Chitayat D, Matthijs G, Glade C, Steijlen PM, Fryns JP, Van Steensel MA, Vikkula M. Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis- lymphedematelangiectasia. Am J Hum Genet 2003;72:1470-1478. (Pubitemid 36628386)
56. Hidaka N, Tsukimori K, Hojo S, Nakanami N, Fukushima K, Yamawaki K, Ohno T, Wake N. Transplacental digitalization for nonimmune hydrops fetalis caused by isolated noncompaction of the ventricular myocardium. J Ultrasound Med 2007;26:519-524. (Pubitemid 46542950)
57. Richards A, Mao CY, Dobson NR. Left ventricular noncompaction: a rare cause of hydrops fetalis. Pediatr Cardiol 2009;30:985-988.
58. Phibbs RH, Johnson P, Kitterman JA, Gregory GA, Tooley WH. Cardiorespiratory status of erythroblastotic infants. 1. Relationship of gestational age, severity of hemolytic diseases, and birth asphyxia to idiopathic respiratory distress syndrome and survival. Pediatrics 1972;49:5-14.
59. Carlson DE, Platt LD, Medearis AL, Horenstein J. Prognostic indicators of the resolution of nonimmune hydrops fetalis and survival of the fetus. Am J Obstet Gynecol 1990;163:1785-1787.
60. Castillo RA, Devoe LD, Hadi HA, Martin S, Geist D. Nonimmune hydrops fetalis: clinical experience and factors related to a poor outcome. Am J Obstet Gynecol 1986;155: 812-816.
61. Skoll MA, Sharland GK, Allan LD. Is the ultrasound definition of fluid collections in non-immune hydrops fetalis helpful in defining the underlying cause or predicting outcome? Ultrasound Obstet Gynecol 1991;1: 309-312.
62. Richardson DK, Corcoran JD, Escobar GJ, Lee SK. SNAP-II and SNAPPE-II: simplified newborn illness severity and mortality risk scores. J Pediatr 2001;138:92-100.