Literature DB >> 2509811

Acute metabolic encephalopathy: a review of causes, mechanisms and treatment.

R Surtees1, J V Leonard.   

Abstract

Acute encephalopathy is a relatively common problem: one of the causes is metabolic disorders. A detailed history, examination and investigations performed during the acute illness (blood sugar, blood gases, plasma ammonia, blood lactate, plasma ketones, plasma amino acids, liver function tests, and urinary organic acids) should identify those patients in whom a metabolic disorder is likely. More detailed studies may be needed to establish a precise diagnosis. The mechanism of the acute brain dysfunction is multifactorial. Factors that contribute include changes in blood flow and, initially, a disturbance in neurotransmitter function followed by failure of energy metabolism and cellular depolarization. Treatment of these conditions is largely supportive, with special attention to the management of cerebral perfusion pressure.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2509811     DOI: 10.1007/bf01799285

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  38 in total

1.  Inhibition of brain glutamic acid decarboxylase by phenylalanine, valine, and leucine derivatives: a suggestion concerning the etiology of the neurological defect in phenylketonuria and branched-chain ketonuria.

Authors:  R E TASHIAN
Journal:  Metabolism       Date:  1961-05       Impact factor: 8.694

Review 2.  Synaptic transmission in ammonia intoxication.

Authors:  W Raabe
Journal:  Neurochem Pathol       Date:  1987 Feb-Apr

3.  Neural dysfunction during hypoglycaemia.

Authors:  T H Koh; A Aynsley-Green; M Tarbit; J A Eyre
Journal:  Arch Dis Child       Date:  1988-11       Impact factor: 3.791

4.  Hypoglycaemia complicating feeding regimens for glycogen-storage disease.

Authors:  J V Leonard; D B Dunger
Journal:  Lancet       Date:  1978-12-02       Impact factor: 79.321

5.  Cerebral oxidative metabolism and blood flow during acute hypoglycemia and recovery in unanesthetized rats.

Authors:  J B Ghajar; F Plum; T E Duffy
Journal:  J Neurochem       Date:  1982-02       Impact factor: 5.372

6.  Central nervous system lesions in disorders of amino-acid metabolism. A neuropathological study.

Authors:  J J Martin; W Schlote
Journal:  J Neurol Sci       Date:  1972       Impact factor: 3.181

7.  Pathophysiology of ammonia intoxication.

Authors:  W Raabe; S Lin
Journal:  Exp Neurol       Date:  1985-03       Impact factor: 5.330

8.  Variation in plasma ketone bodies during a 24-hour fast in normal and in hypoglycemic children: relationship to age.

Authors:  J M Saudubray; C Marsac; J M Limal; E Dumurgier; C Charpentier; H Ogier; F X Coudè
Journal:  J Pediatr       Date:  1981-06       Impact factor: 4.406

Review 9.  Hyperketotic states due to inherited defects of ketolysis.

Authors:  J M Saudubray; N Specola; B Middleton; A Lombes; J P Bonnefont; C Jakobs; A Vassault; C Charpentier; R Day
Journal:  Enzyme       Date:  1987

10.  Effect of acute ammonia intoxication on energy stores in the cerebral reticular activating system.

Authors:  D W McCandless; S Schenker
Journal:  Exp Brain Res       Date:  1981       Impact factor: 1.972

View more
  10 in total

Review 1.  Genetic hypoglycaemia in infancy and childhood: pathophysiology and diagnosis.

Authors:  J M Saudubray; P de Lonlay; G Touati; D Martin; M C Nassogne; P Castelnau; C Sevin; C Laborde; C Baussan; M Brivet; A Vassault; D Rabier; J P Bonnefont; P Kamoun
Journal:  J Inherit Metab Dis       Date:  2000-05       Impact factor: 4.982

2.  Arginosuccinate synthetase deficiency: good outcome despite severe neonatal hyperammonaemia.

Authors:  J H Walter; J T Allen; J B Holton
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

3.  Maple syrup urine disease: interrelations between branched-chain amino-, oxo- and hydroxyacids; implications for treatment; associations with CNS dysmyelination.

Authors:  E Treacy; C L Clow; T R Reade; D Chitayat; O A Mamer; C R Scriver
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

4.  Cerebral energy metabolism in isovaleric acidaemia.

Authors:  A K Lorek; J M Penrice; E B Cady; J V Leonard; J S Wyatt; R A Iles; S P Burns; E O Reynolds
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  1996-05       Impact factor: 5.747

5.  Pipecolic Acid, a Putative Mediator of the Encephalopathy of Cerebral Malaria and the Experimental Model of Cerebral Malaria.

Authors:  Tarun Keswani; Aisha Obeidallah; Edward Nieves; Simone Sidoli; Melissa Fazzari; Terrie Taylor; Karl Seydel; Johanna P Daily
Journal:  J Infect Dis       Date:  2022-02-15       Impact factor: 5.226

Review 6.  Alternative pathway therapy for urea cycle disorders.

Authors:  F Feillet; J V Leonard
Journal:  J Inherit Metab Dis       Date:  1998       Impact factor: 4.982

7.  Cerebral activity during the anesthesia-like state induced by mesopontine microinjection of pentobarbital.

Authors:  Ruth Abulafia; Vladimir Zalkind; Marshall Devor
Journal:  J Neurosci       Date:  2009-05-27       Impact factor: 6.167

8.  [Ornithine transcarbamylase deficiency in adolescence and adulthood: first manifestation with life-threatening decompensation].

Authors:  M Bürle; H Mende; U Plum; M Bluthardt; M Walka; G Geldner
Journal:  Anaesthesist       Date:  2009-06       Impact factor: 1.041

9.  Frequency of inborn errors of metabolism screening for children with unexplained acute encephalopathy at an emergency department.

Authors:  Mamdouh Abdel Maksoud; Solaf Mohamed ELsayed; Rania H Shatla; Abdulbasit Abdulhalim Imam; Riad M Elsayed; Amira Aa Mosabah; Ashraf M Sherif
Journal:  Neuropsychiatr Dis Treat       Date:  2018-06-29       Impact factor: 2.570

10.  Hashimoto's Thyroiditis Presents as an Acute Encephalopathy: A Case Report of Unusual Presentation.

Authors:  Sohaib Khatib; Fouad Jaber; Marwa Elsayed; Islam M Shatla; Majdi S Hamarshi
Journal:  Cureus       Date:  2022-01-11
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.