Medicine:Calcium channel blocker toxicity
Calcium channel blocker toxicity | |
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Other names | Calcium channel blocker poisoning, calcium channel blocker overdose |
A 20% lipid emulsion commonly used for calcium channel blocker toxicity | |
Specialty | Emergency medicine |
Symptoms | Slow heart rate, low blood pressure, nausea, vomiting, sleepiness[1][2] |
Complications | Cardiac arrest[2] |
Usual onset | Within 6 hours[2] |
Causes | Too much calcium channel blockers either by accident or on purpose[3] |
Differential diagnosis | Beta blocker toxicity[1] |
Treatment | Activated charcoal, whole bowel irrigation, intravenous fluids, calcium gluconate, glucagon, high dose insulin, vasopressors, lipid emulsion[1][2] |
Prognosis | High risk of death[2] |
Frequency | > 10,000 (US)[2] |
Calcium channel blocker toxicity is the taking of too much of the medications known as calcium channel blockers (CCBs), either by accident or on purpose.[3] This often causes a slow heart rate and low blood pressure.[1] This can progress to the heart stopping altogether.[2] Some CCBs can also cause a fast heart rate as a result of the low blood pressure.[4] Other symptoms may include nausea, vomiting, sleepiness, and shortness of breath.[2] Symptoms usually occur in the first six hours but with some forms of the medication may not start until 24 after hours.[2]
There are a number of treatments that may be useful.[1] These include efforts to reduce absorption of the drug including: activated charcoal taken by mouth if given shortly after the ingestion or whole bowel irrigation if an extended release formula was taken.[1] Efforts to bring about vomiting are not recommended.[1] Medications to treat the toxic effects include: intravenous fluids, calcium gluconate, glucagon, high dose insulin, vasopressors and lipid emulsion.[1][2] Extracorporeal membrane oxygenation may also be an option.[1]
More than ten thousand cases of calcium channel blocker toxicity were reported in the United States in 2010.[2] Along with beta blockers and digoxin calcium channel blockers have one of the highest rates of death in overdose.[2] These medications first became available in the 1970s and 1980s.[2] They are one of the few types of medication in which one pill can result in the death of a child.[2]
Signs and symptoms
Most people who have taken too much of a calcium channel blocker, especially diltiazem, get slow heart rate and low blood pressure (vasodilatory shock).[1] This can progress to the heart stopping altogether.[2] CCBs of the dihydropyridine group, as well as flunarizine, predominantly cause reflex tachycardia as a reaction to the low blood pressure.[4][5][6]
Other potential symptoms include: nausea and vomiting, a decreased level of consciousness, and breathing difficulties.[2] Symptoms usually begin within 6 hours of taking the medication by mouth.[2] With extended release formulations symptoms may not occur for up to a day.[2] Seizures are rare in adults but in children occur more often.[2] Hypocalcaemia may also occur.[7]
Cause
Calcium channel blockers, also known as calcium channel antagonists, are widely used for a number of health conditions.[8] Thus they are commonly present in many people's homes. In young children one pill may cause serious health problems and potentially death.[8] The calcium channel blocker that caused the greatest number of deaths in 2010 in the United States was verapamil.[2] This agent is believed to cause more heart problems than many of the others.[2]
Diagnosis
A blood or urine test to diagnose overdose is not generally available.[2] CCB overdose may cause high blood sugar levels, and this is often a sign of how severe the problem will become.[1]
Electrocardiogram
CCB toxicity can cause a number of electrocardiogram abnormalities with a low sinus rhythm being the most common.[1] Others include: QT prolongation, bundle branch block, first-degree atrioventricular block, and even sinus tachycardia.[1]
Differential
It may not be possible to tell the difference between beta blocker toxicity and calcium channel blocker overdose based on signs and symptoms.[1]
Management
The medical management of CCB toxicity may be difficult.[1] It may not improve with the usual treatments used for a low blood pressure and a slow heart rate.[9] Those who have no symptoms or signs six hours following taking an immediate release formulation and 24 hours after taking an extended release formulation generally need no further medical treatment.[2]
Detoxification
Activated charcoal is recommended if it can be given within an hour or two of taking the calcium channel blockers.[1] In those who have taken an extended release formulation of a CCB but are otherwise doing fine, whole bowel irrigation with polyethylene glycol may be useful.[1] Causing vomiting by the use of medications such as ipecac is not recommended.[1]
Insulin
High doses of intravenous insulin with glucose may be useful and are a first line treatment in overdoses.[1][10] As this treatment may cause a drop in blood sugar and blood potassium levels, these should be monitored closely.[11]
Other
Intravenous calcium gluconate or calcium chloride is considered a specific antidote.[12] Slow heart rate can be treated with atropine and sympathomimetics. Low blood pressure is treated with vasopressors such as adrenaline.[6][13]
There is tentative clinical evidence and good theoretical evidence of the benefit of lipid emulsion in severe overdoses of CCBs.[14] Methylene blue may also be used for those with low blood pressure that does not respond to other treatments.[10]
Epidemiology
More than 10,000 cases of potential calcium channel blocker toxicity occurred in the United States in 2010.[2] When death occurs in medicine overdose, heart medications are the cause more than 10% of time.[2] The three most common types of heart medications that result in this outcome are calcium channel blockers along with beta blockers and digoxin.[2]
References
- ↑ 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 1.13 1.14 1.15 1.16 1.17 1.18 Palatnick, Wesley (Feb 2014). "Emergency Department Management of Calcium-Channel Blocker, Beta Blocker, and Digoxin Toxicity". Emergency Medicine Practice 16 (2): 1-19; quiz 19-20. PMID 24883458. http://www.ebmedicine.net/topics.php?paction=showTopic&topic_id=396.
- ↑ 2.00 2.01 2.02 2.03 2.04 2.05 2.06 2.07 2.08 2.09 2.10 2.11 2.12 2.13 2.14 2.15 2.16 2.17 2.18 2.19 2.20 2.21 2.22 2.23 2.24 2.25 Marx, John A. Marx (2014). "Cardiovascular Drugs". Rosen's emergency medicine: concepts and clinical practice (8th ed.). Philadelphia, PA: Elsevier/Saunders. pp. Chapter 152. ISBN 978-1455706051.
- ↑ 3.0 3.1 "Calcium channel blocker overdose". ADAM. 2011-01-19. https://www.nlm.nih.gov/medlineplus/ency/article/002580.htm.
- ↑ 4.0 4.1 Wolfson, Allan B. (2010). Harwood-Nuss' clinical practice of emergency medicine (5th ed.). Philadelphia, PA: Lippincott Williams & Wilkins. p. 1454. ISBN 9780781789431. https://books.google.com/books?id=Idb0Z658lFQC&pg=PT1487. Retrieved 28 July 2016.
- ↑ Mutschler, Ernst (2013) (in de). Arzneimittelwirkungen (10 ed.). Stuttgart: Wissenschaftliche Verlagsgesellschaft. p. 1037. ISBN 978-3-8047-2898-1.
- ↑ 6.0 6.1 Haberfeld, H, ed (2015) (in de). Austria-Codex. Vienna: Österreichischer Apothekerverlag. Adalat; Norvasc; Sibelium; Zanidip.
- ↑ Soar, J; Perkins, GD; Abbas, G; Alfonzo, A; Barelli, A; Bierens, JJ; Brugger, H; Deakin, CD et al. (October 2010). "European Resuscitation Council Guidelines for Resuscitation 2010 Section 8. Cardiac arrest in special circumstances: Electrolyte abnormalities, poisoning, drowning, accidental hypothermia, hyperthermia, asthma, anaphylaxis, cardiac surgery, trauma, pregnancy, electrocution.". Resuscitation 81 (10): 1400–33. doi:10.1016/j.resuscitation.2010.08.015. PMID 20956045.
- ↑ 8.0 8.1 Olson, Kent (2011). "Calcium Channel Antagonists". Poisoning & drug overdose (6th ed.). New York: McGraw-Hill Medical. pp. Chapter 40. ISBN 978-0071668330.
- ↑ Shepherd, G (Oct 1, 2006). "Treatment of poisoning caused by beta-adrenergic and calcium-channel blockers.". American Journal of Health-System Pharmacy 63 (19): 1828–35. doi:10.2146/ajhp060041. PMID 16990629.
- ↑ 10.0 10.1 Graudins, A; Lee, HM; Druda, D (7 September 2015). "Calcium channel antagonist and beta-blocker overdose: antidotes and adjunct therapies.". British Journal of Clinical Pharmacology 81 (3): 453–61. doi:10.1111/bcp.12763. PMID 26344579.
- ↑ Engebretsen, KM; Kaczmarek, KM; Morgan, J; Holger, JS (Apr 2011). "High-dose insulin therapy in beta-blocker and calcium channel-blocker poisoning.". Clinical Toxicology 49 (4): 277–83. doi:10.3109/15563650.2011.582471. PMID 21563902.
- ↑ "Calcium channel blocker poisoning". https://www.uptodate.com/contents/calcium-channel-blocker-poisoning.
- ↑ Haberfeld, H, ed (2015) (in de). Austria-Codex. Vienna: Österreichischer Apothekerverlag. Verapabene.
- ↑ Rothschild, L; Bern, S; Oswald, S; Weinberg, G (Oct 5, 2010). "Intravenous lipid emulsion in clinical toxicology.". Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine 18: 51. doi:10.1186/1757-7241-18-51. PMID 20923546.
External links
Classification | |
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External resources |
- St-Onge, Maude; Anseeuw, Kurt; Cantrell, Frank Lee; Gilchrist, Ian C.; Hantson, Philippe; Bailey, Benoit; Lavergne, Valéry; Gosselin, Sophie et al. (October 2016). "Experts Consensus Recommendations for the Management of Calcium Channel Blocker Poisoning in Adults". Critical Care Medicine 45 (3): e306–e315. doi:10.1097/CCM.0000000000002087. PMID 27749343.
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