-
Something wrong with this record ?
The Hypothesis of Circulus Hypoxicus and Its Clinical Relevance in Patients With Methanol Poisoning - An Observational Study of 35 Patients
E. Drangsholt, M. Vangstad, S. Zakharov, KE. Hovda, D. Jacobsen,
Language English Country England, Great Britain
Document type Journal Article, Observational Study
Grant support
NV16-27075A
MZ0
CEP Register
Digital library NLK
Full text - Article
NLK
Medline Complete (EBSCOhost)
from 2004-01-01 to 1 year ago
PubMed
29923671
DOI
10.1111/bcpt.13074
Knihovny.cz E-resources
- MeSH
- Acid-Base Equilibrium drug effects MeSH
- Acidosis chemically induced MeSH
- Blood Gas Analysis MeSH
- Adult MeSH
- Formates blood MeSH
- Lactic Acid blood MeSH
- Middle Aged MeSH
- Humans MeSH
- Methanol blood poisoning MeSH
- Adolescent MeSH
- Young Adult MeSH
- Acid-Base Imbalance chemically induced MeSH
- Aged MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Observational Study MeSH
Methanol mass poisoning is a global problem with high fatality rates and often severe sequelae in survivors. Patients typically present late to the hospital with severe metabolic acidosis followed by a rapid deterioration in their clinical status. The hypothesis 'Circulus hypoxicus' describes the metabolic acidosis following methanol poisoning as a self-enhancing hypoxic circle responsible for methanol toxicity. We wanted to test the validity of this hypothesis by an observational study based on 35 patients from the methanol outbreaks in Norway (2004) and the Czech Republic (2012). Comprehensive laboratory values, including S(serum)-methanol, S-formate, S-lactate, arterial blood gases, anion and osmolal gaps, were used in the calculations. Laboratory values and calculated gaps were compared to each other using linear regression. S-lactate and S-formate correlated better with the increased base deficit and anion gap than did S-formate alone. Base deficit rose to about 20 mmol/L and S-formate rose to 12 mmol/L prior to a significant rise in S-lactate - most likely caused by formate inhibition of mitochondrial respiration (type B lactacidosis). The further rise in S-lactate was not linear to S-formate most likely due to the self-enhancing pathophysiology, but may also be associated with hypotension in critically ill patients and variable ethanol drinking habits. Our study suggests that the primary metabolic acidosis leads to a secondary lactic acidosis mainly due to the toxic effects of formate. The following decline in pH will further increase this toxicity. As such, a vicious and self-enhancing acidotic circle may explain the pathophysiology in methanol poisoning, namely the 'Circulus hypoxicus'.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc19012602
- 003
- CZ-PrNML
- 005
- 20190409161423.0
- 007
- ta
- 008
- 190405s2018 enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1111/bcpt.13074 $2 doi
- 035 __
- $a (PubMed)29923671
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Drangsholt, Elise $u Department of Acute Medicine, Division of Medicine, Oslo University Hospital, Oslo, Norway. University of Oslo, Oslo, Norway.
- 245 14
- $a The Hypothesis of Circulus Hypoxicus and Its Clinical Relevance in Patients With Methanol Poisoning - An Observational Study of 35 Patients / $c E. Drangsholt, M. Vangstad, S. Zakharov, KE. Hovda, D. Jacobsen,
- 520 9_
- $a Methanol mass poisoning is a global problem with high fatality rates and often severe sequelae in survivors. Patients typically present late to the hospital with severe metabolic acidosis followed by a rapid deterioration in their clinical status. The hypothesis 'Circulus hypoxicus' describes the metabolic acidosis following methanol poisoning as a self-enhancing hypoxic circle responsible for methanol toxicity. We wanted to test the validity of this hypothesis by an observational study based on 35 patients from the methanol outbreaks in Norway (2004) and the Czech Republic (2012). Comprehensive laboratory values, including S(serum)-methanol, S-formate, S-lactate, arterial blood gases, anion and osmolal gaps, were used in the calculations. Laboratory values and calculated gaps were compared to each other using linear regression. S-lactate and S-formate correlated better with the increased base deficit and anion gap than did S-formate alone. Base deficit rose to about 20 mmol/L and S-formate rose to 12 mmol/L prior to a significant rise in S-lactate - most likely caused by formate inhibition of mitochondrial respiration (type B lactacidosis). The further rise in S-lactate was not linear to S-formate most likely due to the self-enhancing pathophysiology, but may also be associated with hypotension in critically ill patients and variable ethanol drinking habits. Our study suggests that the primary metabolic acidosis leads to a secondary lactic acidosis mainly due to the toxic effects of formate. The following decline in pH will further increase this toxicity. As such, a vicious and self-enhancing acidotic circle may explain the pathophysiology in methanol poisoning, namely the 'Circulus hypoxicus'.
- 650 _2
- $a acidobazická rovnováha $x účinky léků $7 D000136
- 650 _2
- $a poruchy acidobazické rovnováhy $x chemicky indukované $7 D000137
- 650 _2
- $a acidóza $x chemicky indukované $7 D000138
- 650 _2
- $a mladiství $7 D000293
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a analýza krevních plynů $7 D001784
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a formiáty $x krev $7 D005561
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a kyselina mléčná $x krev $7 D019344
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a methanol $x krev $x otrava $7 D000432
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a mladý dospělý $7 D055815
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a pozorovací studie $7 D064888
- 700 1_
- $a Vangstad, Marie $u Department of Acute Medicine, Division of Medicine, Oslo University Hospital, Oslo, Norway.
- 700 1_
- $a Zakharov, Sergey $u Toxicological Information Center, Department of Occupational Medicine, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic.
- 700 1_
- $a Hovda, Knut Erik $u Norwegian CBRNE Centre of Medicine, Department of Acute Medicine, Division of Medicine, Oslo University Hospital, Oslo, Norway.
- 700 1_
- $a Jacobsen, Dag $u Department of Acute Medicine, Division of Medicine, Oslo University Hospital, Oslo, Norway. University of Oslo, Oslo, Norway.
- 773 0_
- $w MED00007578 $t Basic & clinical pharmacology & toxicology $x 1742-7843 $g Roč. 123, č. 6 (2018), s. 749-755
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/29923671 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20190405 $b ABA008
- 991 __
- $a 20190409161437 $b ABA008
- 999 __
- $a ok $b bmc $g 1391912 $s 1050907
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2018 $b 123 $c 6 $d 749-755 $e 20180723 $i 1742-7843 $m Basic & clinical pharmacology & toxicology $n Basic Clin Pharmacol Toxicol $x MED00007578
- GRA __
- $a NV16-27075A $p MZ0
- LZP __
- $a Pubmed-20190405