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- PMID: 30861511
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Article: Prenatal Diagnosis, Management, and Outcome of Fetal Subdural Haematoma: A Case Report and Systematic Review
Title | Prenatal Diagnosis, Management, and Outcome of Fetal Subdural Haematoma: A Case Report and Systematic Review |
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Authors | |
Keywords | Intracranial haemorrhage Haematoma Subdural haematoma Pregnancy Ultrasonography |
Issue Date | 2019 |
Publisher | S Karger AG. The Journal's web site is located at http://www.karger.com/FDT |
Citation | Fetal Diagnosis and Therapy: clinical advances and basic research, 2019, v. 46 n.5, p. 285-295 How to Cite? |
Abstract | Background: Fetal subdural haematoma (SDH) is associated with poor prognosis. Objective: The conflicting evidence from the literature presents a challenge in prenatal counselling. We present a case study and systematic review of the literature for the management and outcome of fetal SDH. Methods: Systematic search of electronic database. Results: A total 45 cases were extracted from 39 papers. Prenatal ultrasonographic features were intracranial echogenicity (42%), lateral ventriculomegaly (38%), presence of an intracranial mass (31%), macrocephaly (24%), midline deviation of cerebral falx (20%), and intracranial fluid collection (11%). Further secondary features were noted including reversed diastolic flow in the middle cerebral artery (11%), echogenic bowel (4%), hydrops fetalis (2%), and elevated middle cerebral artery peak systolic velocity (2%) (all highly likely to be associated with fetal anaemia). The rates of termination of pregnancy, stillbirth, and neonatal death were 18% (8/45), 16% (7/45), and 11% (5/45), respectively. Overall, therefore, the fetal and perinatal mortality was 32% (12/37). Amongst the 24 survivors with available neurological outcome, 42% (10/24) and 58% (14/24) had abnormal and normal neurological outcome, respectively. Underlying aetiology of fetal SDH was not identified in 47% (21/45). Fetal SDH with an identifiable underlying aetiology was the only factor associated with a higher chance of normal neurological outcome when compared to fetal SDH without a detectable cause (78.5 vs. 21.4%, p = 0.035). Conclusions: Stillbirth and neonatal death occurred in a significant proportion of fetal SDH. 58% of survivors had normal neurological outcome, and better prognosis was seen in SDH with identifiable underlying aetiology.
© 2019 S. Karger AG, Basel |
Persistent Identifier | http://hdl.handle.net/10722/269482 |
ISSN | 2023 Impact Factor: 1.6 2023 SCImago Journal Rankings: 0.767 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Cheung, KW | - |
dc.contributor.author | Tan, LN | - |
dc.contributor.author | Seto, MTY | - |
dc.contributor.author | Moholkar, S | - |
dc.contributor.author | Masson, G | - |
dc.contributor.author | Kilby, MD | - |
dc.date.accessioned | 2019-04-24T08:08:37Z | - |
dc.date.available | 2019-04-24T08:08:37Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | Fetal Diagnosis and Therapy: clinical advances and basic research, 2019, v. 46 n.5, p. 285-295 | - |
dc.identifier.issn | 1015-3837 | - |
dc.identifier.uri | http://hdl.handle.net/10722/269482 | - |
dc.description.abstract | Background: Fetal subdural haematoma (SDH) is associated with poor prognosis. Objective: The conflicting evidence from the literature presents a challenge in prenatal counselling. We present a case study and systematic review of the literature for the management and outcome of fetal SDH. Methods: Systematic search of electronic database. Results: A total 45 cases were extracted from 39 papers. Prenatal ultrasonographic features were intracranial echogenicity (42%), lateral ventriculomegaly (38%), presence of an intracranial mass (31%), macrocephaly (24%), midline deviation of cerebral falx (20%), and intracranial fluid collection (11%). Further secondary features were noted including reversed diastolic flow in the middle cerebral artery (11%), echogenic bowel (4%), hydrops fetalis (2%), and elevated middle cerebral artery peak systolic velocity (2%) (all highly likely to be associated with fetal anaemia). The rates of termination of pregnancy, stillbirth, and neonatal death were 18% (8/45), 16% (7/45), and 11% (5/45), respectively. Overall, therefore, the fetal and perinatal mortality was 32% (12/37). Amongst the 24 survivors with available neurological outcome, 42% (10/24) and 58% (14/24) had abnormal and normal neurological outcome, respectively. Underlying aetiology of fetal SDH was not identified in 47% (21/45). Fetal SDH with an identifiable underlying aetiology was the only factor associated with a higher chance of normal neurological outcome when compared to fetal SDH without a detectable cause (78.5 vs. 21.4%, p = 0.035). Conclusions: Stillbirth and neonatal death occurred in a significant proportion of fetal SDH. 58% of survivors had normal neurological outcome, and better prognosis was seen in SDH with identifiable underlying aetiology. © 2019 S. Karger AG, Basel | - |
dc.language | eng | - |
dc.publisher | S Karger AG. The Journal's web site is located at http://www.karger.com/FDT | - |
dc.relation.ispartof | Fetal Diagnosis and Therapy: clinical advances and basic research | - |
dc.rights | Fetal Diagnosis and Therapy: clinical advances and basic research. Copyright © S Karger AG. | - |
dc.rights | This is the peer-reviewed but unedited manuscript version of the following article: [insert full citation, e.g., Cytogenet Genome Res 2014;142:227–238 (DOI: 10.1159/000361001)]. The final, published version is available at http://www.karger.com/?doi=[insert DOI number]. OR This is the un-reviewed and unedited manuscript version of the following article: [insert full citation, e.g., Cytogenet Genome Res 2014;142:227–238 (DOI: 10.1159/000361001)]. The final, published version is available at http://www.karger.com/?doi=[insert DOI number]. | - |
dc.subject | Intracranial haemorrhage | - |
dc.subject | Haematoma | - |
dc.subject | Subdural haematoma | - |
dc.subject | Pregnancy | - |
dc.subject | Ultrasonography | - |
dc.title | Prenatal Diagnosis, Management, and Outcome of Fetal Subdural Haematoma: A Case Report and Systematic Review | - |
dc.type | Article | - |
dc.identifier.email | Cheung, KW: kawang@hku.hk | - |
dc.identifier.email | Seto, MTY: mimiseto@hku.hk | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1159/000496202 | - |
dc.identifier.pmid | 30861511 | - |
dc.identifier.scopus | eid_2-s2.0-85063456196 | - |
dc.identifier.hkuros | 297489 | - |
dc.identifier.volume | 46 | - |
dc.identifier.issue | 5 | - |
dc.identifier.spage | 285 | - |
dc.identifier.epage | 295 | - |
dc.identifier.isi | WOS:000497713700001 | - |
dc.publisher.place | Switzerland | - |
dc.identifier.issnl | 1015-3837 | - |