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succinylcholine and Inborn Errors of Metabolism

succinylcholine has been researched along with Inborn Errors of Metabolism in 61 studies

Succinylcholine: A quaternary skeletal muscle relaxant usually used in the form of its bromide, chloride, or iodide. It is a depolarizing relaxant, acting in about 30 seconds and with a duration of effect averaging three to five minutes. Succinylcholine is used in surgical, anesthetic, and other procedures in which a brief period of muscle relaxation is called for.
succinylcholine : A quaternary ammonium ion that is the bis-choline ester of succinic acid.

Research Excerpts

ExcerptRelevanceReference
" Rarely, patients with butyrylcholinesterase deficiency may show marked sensitivity to succinylcholine, manifested clinically by severely prolonged neuromuscular paralysis and apnea."7.77Prolonged neuromuscular paralysis following rapid-sequence intubation with succinylcholine. ( Aiken, DC; Donnell, RW; Kaufman, SE; Magee, C, 2011)
"Ventricular tachycardia was defibrillated and Gordon syndrome, which was diagnosed subsequently, was treated successfully."5.33Gordon syndrome and succinylcholine. ( Puura, A; Schultz, R, 2005)
" BChE deficiency induces a slower hydrolysis of the drug and consequently prolonged neuromuscular block, leading to apnea."3.83[Prolonged neuromuscular block in a patient with butyrylcholinesterase deficiency]. ( Ceppa, F; Courcelle, S; Delacour, H; Hary, B; Mabboux, I, 2016)
" Rarely, patients with butyrylcholinesterase deficiency may show marked sensitivity to succinylcholine, manifested clinically by severely prolonged neuromuscular paralysis and apnea."3.77Prolonged neuromuscular paralysis following rapid-sequence intubation with succinylcholine. ( Aiken, DC; Donnell, RW; Kaufman, SE; Magee, C, 2011)
"We describe a child who developed a malignant hyperthermia-like syndrome after exposure to succinylcholine and halothane."3.75Malignant hyperthermia-like syndrome and carnitine palmitoyltransferase II deficiency with heterozygous R503C mutation. ( Hogan, KJ; Vladutiu, GD, 2009)
"The mitochondrial disturbance in Reye syndrome is well documented but the pathophysiologic sequence linking the antecedent viral illness to the mitochondrial injury remains obscure."2.37Reye syndrome. ( De Vivo, DC, 1985)
"Ventricular tachycardia was defibrillated and Gordon syndrome, which was diagnosed subsequently, was treated successfully."1.33Gordon syndrome and succinylcholine. ( Puura, A; Schultz, R, 2005)
" Atypical pseudocholinesterases were identified using quantitative dosage of enzymatic activity and inhibition of atypical pseudocholinesterases by dibucaine, fluoride, chloride, scoline and urea."1.27[Congenital anomaly of serum pseudocholinesterase originating in neonatal respiratory distress]. ( Canis, M; Gutknecht, JL; Haberer, JP; Monteillard, C; Schoeffler, P; Viallard, JL, 1984)

Research

Studies (61)

TimeframeStudies, this research(%)All Research%
pre-199042 (68.85)18.7374
1990's2 (3.28)18.2507
2000's3 (4.92)29.6817
2010's12 (19.67)24.3611
2020's2 (3.28)2.80

Authors

AuthorsStudies
Acharya, S1
Bhattarai, S1
Shrimanker, I1
Gupta, SS1
Cornelius, BW1
Jacobs, TM1
Robles, A1
Michael, M1
McCallum, R1
Andersson, ML1
Møller, AM1
Wildgaard, K1
Dillon, D1
Lee, P1
Yuksel, E1
Sergin, D1
Tanatti, B1
Alper, I1
Zoller, M1
Walther, S1
Cassel, J1
Staehr-Rye, AK1
Nielsen, CV2
Gätke, MR2
Brozović, G1
Mazul Sunko, B1
Hafner, T1
Bekavac, I1
Thomsen, JL1
Palmqvist, DF1
Alvarellos, ML1
McDonagh, EM1
Patel, S1
McLeod, HL1
Altman, RB1
Klein, TE1
Mabboux, I1
Hary, B1
Courcelle, S1
Ceppa, F1
Delacour, H1
Binkley, C1
Hogan, KJ1
Vladutiu, GD1
Kaufman, SE1
Donnell, RW1
Aiken, DC1
Magee, C1
HODGES, RJ1
HARKNESS, J1
LEHMANN, H2
LIDDELL, J2
HARRIS, H1
PORTER, IH1
KAUFMAN, L1
SILK, E1
RUDDELL, JS1
Puura, A1
Schultz, R1
Williams, J1
Rosenquist, P1
Arias, L1
McCall, WV1
Deam, D1
Emmanuel, ER1
Schoeffler, P1
Viallard, JL1
Monteillard, C1
Canis, M1
Gutknecht, JL1
Haberer, JP1
Dell, DD1
Kehoe, C1
Ho, VW1
Osiovich, H1
Skakun, NP1
Oleĭnik, AN1
Shendevitskiĭ, VI1
Brown, BR1
Walson, PD1
Taussig, LM1
Pronk, IR1
van der Wal, SJ1
Thé, TH1
De Vivo, DC1
La Du, BN2
Bush, GH1
Lemaire, WJ1
Nagel, EL1
Smith, JC1
Maurer, HJ1
Hald, J1
Cherington, M1
Lasater, G1
Baraka, A1
Bikhazi, G1
Abu-Haidar, G1
Ernst, FW1
Pembrey, ME1
Prince, LC2
Garry, PJ2
Lubin, AH1
Rink, RA1
Husain, M1
Purry, NA1
Jardine, WI1
Ferguson, AS1
Mukuno, K1
Ishikawa, S1
Tanaka, R1
Cousin, MT1
Viars, P1
Notari, RE1
Du, BN1
Mogensen, JV1
Hanel, HK1
Peck, AW1
Garcia, CH1
Diaz, PM1
Szeinberg, A1
Pipano, S1
Assa, M1
Medalie, JH1
Neufeld, HN1
Baer, G1
Litwiller, RW1
Whittaker, M1
Vickers, MD1
Jenkins, T1
Balinsky, D1
Patient, DW1
Zsigmond, EK1
Eilderton, TE1
Schimke, RN1
Neitlich, HW1
Schärli, A1
Bettex, M1

Reviews

13 reviews available for succinylcholine and Inborn Errors of Metabolism

ArticleYear
Pseudocholinesterase Deficiency: What the Proceduralist Needs to Know.
    The American journal of the medical sciences, 2019, Volume: 357, Issue:3

    Topics: Anesthesia, General; Apnea; Butyrylcholinesterase; Dilatation; Endoscopy; Esophageal Achalasia; Huma

2019
Butyrylcholinesterase deficiency and its clinical importance in anaesthesia: a systematic review.
    Anaesthesia, 2019, Volume: 74, Issue:4

    Topics: Anesthesia; Apnea; Butyrylcholinesterase; Humans; Metabolism, Inborn Errors; Mivacurium; Neuromuscul

2019
PharmGKB summary: succinylcholine pathway, pharmacokinetics/pharmacodynamics.
    Pharmacogenetics and genomics, 2015, Volume: 25, Issue:12

    Topics: Apnea; Butyrylcholinesterase; Calcium Channels; Calcium Channels, L-Type; Humans; Hyperkalemia; Mali

2015
GENETIC BASIS OF DRUG METABOLISM IN MAN.
    Toxicology and applied pharmacology, 1964, Volume: 6

    Topics: Barbiturates; Catalase; Drug Tolerance; Genetics, Medical; Humans; Isoniazid; Metabolism; Metabolism

1964
Plasma cholinesterase deficiency.
    Journal of perianesthesia nursing : official journal of the American Society of PeriAnesthesia Nurses, 1996, Volume: 11, Issue:5

    Topics: Cholinesterases; Humans; Metabolism, Inborn Errors; Neuromuscular Depolarizing Agents; Neuromuscular

1996
Reye syndrome.
    Neurologic clinics, 1985, Volume: 3, Issue:1

    Topics: Aflatoxins; Anesthesia, General; Animals; Child; Child, Preschool; Disease Models, Animal; Disease O

1985
Pharmacogenetics: defective enzymes in relation to reactions to drugs.
    Annual review of medicine, 1972, Volume: 23

    Topics: Acetylation; Cholinesterases; Coumarins; Dicumarol; Dose-Response Relationship, Drug; Female; Geneti

1972
Pharmacogenetics and anaesthesia.
    Proceedings of the Royal Society of Medicine, 1968, Volume: 61, Issue:2

    Topics: Anemia, Sickle Cell; Anesthetics; Animals; Barbiturates; Cholinesterases; Fever; Genetics, Medical;

1968
Genetic determimants in drug action.
    Advances in biology of skin, 1972, Volume: 12

    Topics: Acetylation; Acetyltransferases; Cholinesterases; Coumarins; Dealkylation; Drug Resistance; Genes; G

1972
Pharmacogenetics.
    The Practitioner, 1974, Volume: 213, Issue:1277

    Topics: Acetyltransferases; Administration, Topical; Alleles; Analgesics; Anemia, Hemolytic; Anti-Inflammato

1974
Pharmacogenetics. Cholinesterase variants and suxamethonium apnoea.
    Proceedings of the Royal Society of Medicine, 1968, Volume: 61, Issue:2

    Topics: Alleles; Apnea; Cholinesterase Inhibitors; Cholinesterases; Dibucaine; Drug Hypersensitivity; Electr

1968
Pharmacogenetics.
    The Medical clinics of North America, 1969, Volume: 53, Issue:4

    Topics: Biotransformation; Cholinesterases; Coumarins; Genetic Variation; Genetics, Medical; Humans; Isoniaz

1969
[Cholinesterase. A survey with particular reference to inherited increase in sensitivity to suxamethonium].
    Nordisk medicin, 1970, Nov-05, Volume: 84, Issue:45

    Topics: Apnea; Blood Transfusion; Cholinesterases; Drug Hypersensitivity; Genes, Recessive; Humans; Metaboli

1970

Other Studies

48 other studies available for succinylcholine and Inborn Errors of Metabolism

ArticleYear
A prolonged paralysis with succinylcholine in pseudocholinesterase deficiency: an undesired effect.
    QJM : monthly journal of the Association of Physicians, 2022, 08-13, Volume: 115, Issue:8

    Topics: Apnea; Butyrylcholinesterase; Humans; Metabolism, Inborn Errors; Paralysis; Succinylcholine

2022
Pseudocholinesterase Deficiency Considerations: A Case Study.
    Anesthesia progress, 2020, 09-01, Volume: 67, Issue:3

    Topics: Apnea; Butyrylcholinesterase; Female; Humans; Metabolism, Inborn Errors; Mivacurium; Succinylcholine

2020
Patient information sheet for plasma cholinesterase deficiency.
    Anaesthesia, 2013, Volume: 68, Issue:10

    Topics: Apnea; Butyrylcholinesterase; Cholinesterases; Documentation; Drug Hypersensitivity; Follow-Up Studi

2013
Rocuronium-sugammadex use in electroconvulsive therapy of patients with pseudocholinesterase enzyme deficiency.
    Journal of clinical anesthesia, 2013, Volume: 25, Issue:8

    Topics: Androstanols; Apnea; Butyrylcholinesterase; Contraindications; Electroconvulsive Therapy; gamma-Cycl

2013
[Residual relaxant block due to pseudocholinesterase deficiency - First manifestation in an elderly patient].
    Anasthesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie : AINS, 2014, Volume: 49, Issue:1

    Topics: Aged; Anesthesia Recovery Period; Anesthesia, General; Apnea; Butyrylcholinesterase; Humans; Intraop

2014
Use of neuromuscular monitoring to detect prolonged effect of succinylcholine or mivacurium: three case reports.
    Acta anaesthesiologica Scandinavica, 2014, Volume: 58, Issue:8

    Topics: Accelerometry; Aged; Antidotes; Apnea; Appendicitis; Butyrylcholinesterase; Cholecystectomy, Laparos

2014
Allergic reaction to suxamethonium during emergency caesarean section and pseudocholinesterase deficiency in the same patient.
    Wiener klinische Wochenschrift, 2014, Volume: 126, Issue:13-14

    Topics: Anesthesia, Obstetrical; Apnea; Butyrylcholinesterase; Cesarean Section; Diagnosis, Differential; Dr

2014
Premature awakening and underuse of neuromuscular monitoring in a registry of patients with butyrylcholinesterase deficiency.
    British journal of anaesthesia, 2015, Volume: 115 Suppl 1

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Apnea; Butyrylcholinesterase; Child; Child, Preschool; F

2015
[Prolonged neuromuscular block in a patient with butyrylcholinesterase deficiency].
    Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 2016, Volume: 23, Issue:5

    Topics: Adolescent; Apnea; Butyrylcholinesterase; Humans; Male; Metabolism, Inborn Errors; Neuromuscular Dep

2016
Unknown Pseudocholinesterase Deficiency in a Patient Undergoing TIVA with Planned Motor Evoked Potential Monitoring: A Case Report.
    AANA journal, 2016, Volume: 84, Issue:3

    Topics: Aged, 80 and over; Anesthesia, Intravenous; Apnea; Butyrylcholinesterase; Cervical Vertebrae; Diskec

2016
Malignant hyperthermia-like syndrome and carnitine palmitoyltransferase II deficiency with heterozygous R503C mutation.
    Anesthesia and analgesia, 2009, Volume: 109, Issue:4

    Topics: Amino Acid Substitution; Anesthetics, Inhalation; Arginine; Carnitine O-Palmitoyltransferase; Child,

2009
Prolonged neuromuscular paralysis following rapid-sequence intubation with succinylcholine.
    The Annals of pharmacotherapy, 2011, Volume: 45, Issue:4

    Topics: Apnea; Butyrylcholinesterase; Female; Humans; Intubation, Intratracheal; Metabolism, Inborn Errors;

2011
Suxamethonium sensitivity in health and disease; a clinical evaluation of pseudo-cholinesterase levels.
    British medical journal, 1954, Jul-03, Volume: 2, Issue:4878

    Topics: Apnea; Butyrylcholinesterase; Cholinesterases; Drug Hypersensitivity; Health; Humans; Metabolism, In

1954
SUXAMETHONIUM SENSITIVITY.
    British medical journal, 1964, Feb-22, Volume: 1, Issue:5381

    Topics: Apnea; Blood; Butyrylcholinesterase; Cholinesterases; Drug Hypersensitivity; Fluorides; Genetics, Me

1964
ENZYMES AND DRUG SENSITIVITY. THE GENETICS OF SERUM CHOLINESTERASE 'DEFICIENCY' IN RELATION TO SUXAMETHONIUM APNOEA.
    Proceedings of the Royal Society of Medicine, 1964, Volume: 57

    Topics: Apnea; Blood; Cholinesterases; Drug Tolerance; Genetics, Medical; Humans; Metabolism, Inborn Errors;

1964
Suxamethonium apnoea in an infant; expression of familial pseudocholinesterase deficiency in three generations.
    British medical journal, 1960, Jan-16, Volume: 1, Issue:5167

    Topics: Apnea; Bis-Trimethylammonium Compounds; Butyrylcholinesterase; Child; Cholinesterases; Humans; Infan

1960
Apnoea due to suxamethonium associated with familial pseudocholinesterase deficiency.
    Lancet (London, England), 1962, Apr-21, Volume: 1, Issue:7234

    Topics: Apnea; Butyrylcholinesterase; Cholinesterases; Humans; Metabolism, Inborn Errors; Muscular Diseases;

1962
Gordon syndrome and succinylcholine.
    Journal of inherited metabolic disease, 2005, Volume: 28, Issue:6

    Topics: Child; Humans; Hyperkalemia; Male; Metabolism, Inborn Errors; Potassium; Pseudohypoaldosteronism; Ri

2005
Pseudocholinesterase deficiency and electroconvulsive therapy.
    The journal of ECT, 2007, Volume: 23, Issue:3

    Topics: Aged; Butyrylcholinesterase; Depressive Disorder; Electroconvulsive Therapy; Humans; Male; Metabolis

2007
A family with the silent cholinesterase gene.
    Anaesthesia and intensive care, 1983, Volume: 11, Issue:3

    Topics: Adult; Alleles; Anesthesia, Endotracheal; Apnea; Cholinesterases; Female; Heterozygote; Humans; Meta

1983
[Congenital anomaly of serum pseudocholinesterase originating in neonatal respiratory distress].
    Annales francaises d'anesthesie et de reanimation, 1984, Volume: 3, Issue:3

    Topics: Anesthesia, Obstetrical; Butyrylcholinesterase; Cholinesterases; Female; Humans; Infant, Newborn; Me

1984
A case of pseudocholinesterase deficiency in the neonate.
    American journal of perinatology, 1999, Volume: 16, Issue:7

    Topics: Apnea; Butyrylcholinesterase; Humans; Infant, Newborn; Male; Metabolism, Inborn Errors; Neuromuscula

1999
[Adverse effect of muscle relaxants and narcotics in hereditary diseases (literature survey)].
    Khirurgiia, 1976, Issue:11

    Topics: Arrhythmias, Cardiac; Barbiturates; Butyrylcholinesterase; Drug Synergism; Drug Tolerance; Dysautono

1976
Congenital metabolic diseases of pediatric patients: anesthetic implications.
    Anesthesiology, 1975, Volume: 43, Issue:2

    Topics: Acidosis; Anesthesia; Child; Cystic Fibrosis; Dysautonomia, Familial; Glycogen Storage Disease Type

1975
[Familial examinations for the presence of atypical cholinesterase].
    Nederlands tijdschrift voor geneeskunde, 1975, Oct-04, Volume: 119, Issue:40

    Topics: Adolescent; Anesthesia, General; Apnea; Appendectomy; Child, Preschool; Cholinesterase Inhibitors; C

1975
Suxamethonium apnoea.
    Lancet (London, England), 1973, Feb-03, Volume: 1, Issue:7797

    Topics: Anesthesia; Apnea; Cholinesterase Inhibitors; Cholinesterases; Drug Synergism; Humans; Liver; Metabo

1973
Plasma cholinesterase deficiency. A possible complication during anesthesia.
    Obstetrics and gynecology, 1972, Volume: 39, Issue:4

    Topics: Adolescent; Anesthesia, General; Apnea; Cholinesterases; Endoscopy; Female; Genotype; Humans; Intuba

1972
[Contrast reaction--reaction to anaesthetic?].
    Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin, 1972, Volume: 116, Issue:3

    Topics: Adolescent; Anesthesia, Inhalation; Angiography; Bone Cysts; Contrast Media; Creatine Kinase; Femur

1972
Prolonged paralysis in pseudocholinesterase deficiency.
    Archives of neurology, 1973, Volume: 28, Issue:4

    Topics: Cholecystectomy; Cholinesterases; Electric Stimulation; Erythrocytes; Evoked Potentials; Female; Hum

1973
Succinylcholine block in a patient with atypical serum cholinesterase.
    Middle East journal of anaesthesiology, 1974, Volume: 4, Issue:1

    Topics: Child; Cholinesterases; Humans; Metabolism, Inborn Errors; Pedigree; Phenotype; Succinylcholine

1974
Abnormal response to a muscle relaxant. Report of three cases.
    The Journal of the American Association of Nurse Anesthetists, 1973, Volume: 41, Issue:5

    Topics: Apnea; Cholinesterases; Metabolism, Inborn Errors; Succinylcholine

1973
Silent cholinesterase gene--report of a family.
    Anesthesiology, 1972, Volume: 37, Issue:6

    Topics: Adult; Cholinesterases; Female; Humans; Metabolism, Inborn Errors; Succinylcholine

1972
Apnea and atypical pseudocholinesterase.
    Southern medical journal, 1973, Volume: 66, Issue:5

    Topics: Adult; Apnea; Cholinesterases; Female; Humans; Male; Metabolism, Inborn Errors; Succinylcholine

1973
Scoline apnoea.
    South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 1973, Jun-02, Volume: 47, Issue:21

    Topics: Anesthesia, General; Apnea; Cholinesterases; Humans; Male; Metabolism, Inborn Errors; Middle Aged; S

1973
[Hypocholinesterasemia with oculomuscular paralysis].
    Nihon rinsho. Japanese journal of clinical medicine, 1973, Volume: 31, Issue:2

    Topics: Adult; Cholinesterases; Drug Hypersensitivity; Humans; Male; Metabolism, Inborn Errors; Ophthalmople

1973
[Prolonged curarization with succinylcholine].
    La Revue du praticien, 1974, Feb-21, Volume: 24, Issue:11

    Topics: Anesthesia; Cholinesterases; Humans; Metabolism, Inborn Errors; Muscle Contraction; Neuromuscular Ju

1974
Half-life of human serum cholinesterase following blood transfusion.
    Research communications in chemical pathology and pharmacology, 1974, Volume: 8, Issue:2

    Topics: Adult; Albumins; Apnea; Blood Proteins; Blood Transfusion; Cholinesterases; Female; Half-Life; Human

1974
Aspects of suxamethonium hydrolysis in man and animals.
    Proceedings of the Royal Society of Medicine, 1970, Volume: 63, Issue:2

    Topics: Acetylcholine; Acetylcholinesterase; Alleles; Animals; Apnea; Cats; Cholinesterase Inhibitors; Choli

1970
Atypical cholinesterase: frequency in a Puerto Rican population.
    Anesthesiology, 1972, Volume: 36, Issue:1

    Topics: Adjuvants, Anesthesia; Cholinesterases; Genetics, Population; Humans; Mass Screening; Metabolism, In

1972
High frequency of atypical pseudocholinesterase gene among Iraqi and Iranian Jews.
    Clinical genetics, 1972, Volume: 3, Issue:2

    Topics: Adult; Cholinesterases; Chromosome Aberrations; Chromosome Disorders; Drug Hypersensitivity; Female;

1972
[Pseudocholinesterase].
    Duodecim; laaketieteellinen aikakauskirja, 1972, Volume: 88, Issue:5

    Topics: Anesthesia; Apnea; Cholinesterase Inhibitors; Cholinesterases; Enzyme Activation; Genotype; Humans;

1972
A family study of atypical plasma cholinesterase activity.
    Southern medical journal, 1970, Volume: 63, Issue:7

    Topics: Adult; Apnea; Child; Cholinesterases; Clinical Enzyme Tests; Diagnosis, Differential; Dibucaine; Fem

1970
Initial experiences with the Cholinesterase Research Unit.
    British journal of anaesthesia, 1970, Volume: 42, Issue:11

    Topics: Apnea; Child; Cholinesterases; Dibucaine; Female; Fluorides; Genotype; Heterozygote; Humans; Male; M

1970
Cholinesterase in plasma: first reported absence in the Bantu; half-life determination.
    Science (New York, N.Y.), 1967, Jun-30, Volume: 156, Issue:3783

    Topics: Adolescent; Black People; Cholinesterases; Dibucaine; Female; Fluorides; Genes, Regulator; Heterozyg

1967
Abnormal reaction to procaine and succinylcholine in a patient with inherited atypical plasma cholinesterase: case report.
    Canadian Anaesthetists' Society journal, 1968, Volume: 15, Issue:5

    Topics: Abdomen; Adjuvants, Anesthesia; Adult; Anesthesia, Local; Apnea; Cholinesterases; Drug Hypersensitiv

1968
Drugs and heredity. Pharmacogenetics--the study of heritable variations in drug response.
    The Journal of the Kansas Medical Society, 1969, Volume: 70, Issue:3

    Topics: Drug Hypersensitivity; Genetics, Medical; Humans; Isoniazid; Metabolic Diseases; Metabolism, Inborn

1969
Increased plasma cholinesterase activity and succinylcholine resistance: a genetic variant.
    The Journal of clinical investigation, 1966, Volume: 45, Issue:3

    Topics: Adult; Cholinesterases; Humans; Isoflurophate; Male; Metabolism, Inborn Errors; Succinylcholine

1966
[Prolonged apnea caused by atypical pseudocholinesterase].
    Der Anaesthesist, 1966, Volume: 15, Issue:3

    Topics: Adolescent; Anesthesia, General; Apnea; Appendectomy; Cholinesterases; Female; Homozygote; Humans; M

1966