Back Atriale fibrillasie Afrikaans رجفان أذيني Arabic Qulaqcıqların fibrilyasiyası Azerbaijani آتریال فیبریلاسیون AZB Pretkomorska fibrilacija BS Fibril·lació auricular Catalan Fibrilace síní Czech Vorhofflimmern German Κολπική μαρμαρυγή Greek Fibrilación auricular Spanish

Atrial fibrillation

Atrial fibrillation
Other namesAuricular fibrillation[1]
Electrocardiogram samples displaying atrial fibrillation in the upper recording with absence of P waves (red arrow), an erratic baseline between QRS complexes, and elevated heart rate. Bottom recording shows normal sinus rhythm with P waves (purple arrow)
SpecialtyCardiology
SymptomsNone, heart palpitations, fainting, dizziness, decreased level or total loss of consciousness, shortness of breath, chest pain[2][3]
ComplicationsHeart failure, dementia, stroke[3]
Usual onset> age 50[4]
Risk factorsHigh blood pressure, valvular heart disease, coronary artery disease, cardiomyopathy, congenital heart disease, COPD, obesity, smoking, sleep apnea[3][5][6][7]
Diagnostic methodFeeling the pulse, electrocardiogram[8]
Differential diagnosisIrregular heartbeat[9]
TreatmentLifestyle modifications, rate control, rhythm control, anticoagulation[5]
Frequency3.5% (developed world), 1.5% (developing world)[4]
Deaths315,000 with atrial flutter (2019)[10]

Atrial fibrillation (AF, AFib or A-fib) is an abnormal heart rhythm (arrhythmia) characterized by rapid and irregular beating of the atrial chambers of the heart.[11][12] It often begins as short periods of abnormal beating, which become longer or continuous over time.[4] It may also start as other forms of arrhythmia such as atrial flutter that then transform into AF.[13]

Episodes can be asymptomatic.[3] Symptomatic episodes may involve heart palpitations, fainting, lightheadedness, loss of consciousness, shortness of breath, or chest pain.[2] Atrial fibrillation is associated with an increased risk of heart failure, dementia, and stroke.[3][12] It is a type of supraventricular tachycardia.[14]

Atrial fibrillation frequently results from bursts of tachycardia that originate in muscle bundles extending from the atrium to the pulmonary veins.[15] Pulmonary vein isolation by transcatheter ablation can restore sinus rhythm.[15] The ganglionated plexi (autonomic ganglia of the heart atrium and ventricles) can also be a source of atrial fibrillation, and is sometimes also ablated for that reason.[16] Not only the pulmonary vein, but the left atrial appendage can be a source of atrial fibrillation and is also ablated for that reason.[17] As atrial fibrillation becomes more persistent, the junction between the pulmonary veins and the left atrium becomes less of an initiator and the left atrium becomes an independent source of arrhythmias.[18]

High blood pressure and valvular heart disease are the most common modifiable risk factors for AF.[5][6] Other heart-related risk factors include heart failure, coronary artery disease, cardiomyopathy, and congenital heart disease.[5] In low- and middle-income countries, valvular heart disease is often attributable to rheumatic fever.[19] Lung-related risk factors include COPD, obesity, and sleep apnea.[3] Cortisol and other stress biomarkers (including vasopressin, chromogranin A, and heat shock proteins), as well as emotional stress, may play a role in the pathogenesis of atrial fibrillation.[20]

Other risk factors include excess alcohol intake, tobacco smoking, diabetes mellitus, and thyrotoxicosis.[3][7][19] However, about half of cases are not associated with any of these aforementioned risks.[3] Moreover, thyrotoxicosis seems to be an especially rare risk factor.[21] Healthcare professionals might suspect AF after feeling the pulse and confirm the diagnosis by interpreting an electrocardiogram (ECG).[8] A typical ECG in AF shows irregularly spaced QRS complexes without P waves.[8]

Healthy lifestyle changes, such as weight loss in people with obesity, increased physical activity, and drinking less alcohol, can lower the risk for AF and reduce its burden if it occurs.[22] AF is often treated with medications to slow the heart rate to a near-normal range (known as rate control) or to convert the rhythm to normal sinus rhythm (known as rhythm control).[5] Electrical cardioversion can convert AF to normal heart rhythm and is often necessary for emergency use if the person is unstable.[23] Ablation may prevent recurrence in some people.[24] For those at low risk of stroke, AF does not necessarily require blood-thinning though some healthcare providers may prescribe an anti-clotting medication.[25] Most people with AF are at higher risk of stroke.[26] For those at more than low risk, experts generally recommend an anti-clotting medication.[25] Anti-clotting medications include warfarin and direct oral anticoagulants.[25] While these medications reduce stroke risk, they increase rates of major bleeding.[27]

Atrial fibrillation is the most common serious abnormal heart rhythm and, as of 2020, affects more than 33 million people worldwide.[3][22] As of 2014, it affected about 2 to 3% of the population of Europe and North America.[4] This was an increase from 0.4 to 1% of the population around 2005.[28] In the developing world, about 0.6% of males and 0.4% of females are affected.[4] The percentage of people with AF increases with age with 0.1% under 50 years old, 4% between 60 and 70 years old, and 14% over 80 years old being affected.[4] A-fib and atrial flutter resulted in 193,300 deaths in 2015, up from 29,000 in 1990.[29][30] The first known report of an irregular pulse was by Jean-Baptiste de Sénac in 1749.[3] Thomas Lewis was the first doctor to document this by ECG in 1909.[3]

  1. ^ "Atrial fibrillation or flutter: MedlinePlus Medical Encyclopedia". medlineplus.gov. Retrieved 28 May 2019.
  2. ^ a b Gray D (2010). Chamberlain's Symptoms and Signs in Clinical Medicine: An Introduction to Medical Diagnosis (13th ed.). London: Hodder Arnold. pp. 70–71. ISBN 978-0-340-97425-4.
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  7. ^ a b Cite error: The named reference Staerk2017 was invoked but never defined (see the help page).
  8. ^ a b c Ferguson C, Inglis SC, Newton PJ, Middleton S, Macdonald PS, Davidson PM (May 2014). "Atrial fibrillation: stroke prevention in focus". Australian Critical Care. 27 (2): 92–98. doi:10.1016/j.aucc.2013.08.002. PMID 24054541.
  9. ^ Hui D, Leung AA, Padwal R (2015). Approach to Internal Medicine: A Resource Book for Clinical Practice. Springer. p. 45. ISBN 978-3-319-11821-5. Archived from the original on 8 September 2017.
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  16. ^ Stavrakis S, Po S (2017). "Ganglionated Plexi Ablation: Physiology and Clinical Applications". Arrhythmia & Electrophysiology Review. 6 (4): 186–190. doi:10.15420/aer2017.26.1. PMC 5739885. PMID 29326833.
  17. ^ Naksuk N, Padmanabhan D, Asirvatham SJ (2016). "Left Atrial Appendage: Embryology, Anatomy, Physiology, Arrhythmia and Therapeutic Intervention". JACC: Clinical Electrophysiology. 2 (4): 403–412. doi:10.1016/j.jacep.2016.06.006. PMID 29759858.
  18. ^ Eranki A, Wilson-Smith A, Manganas C (2023). "Mid term freedom from atrial fibrillation following hybrid ablation, a systematic review and meta analysis". Journal of Cardiothoracic Surgery. 18 (1): 155. doi:10.1186/s13019-023-02189-2. PMC 10114378. PMID 37076929.
  19. ^ a b Mischke K, Knackstedt C, Marx N, Vollmann D (April 2013). "Insights into atrial fibrillation". Minerva Medica. 104 (2): 119–130. PMID 23514988.
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  29. ^ GBD 2015 Mortality and Causes of Death Collaborators (October 2016). "Global, regional, and national life expectancy, all-cause mortality, and cause-specific mortality for 249 causes of death, 1980-2015: a systematic analysis for the Global Burden of Disease Study 2015". Lancet. 388 (10053): 1459–1544. doi:10.1016/s0140-6736(16)31012-1. PMC 5388903. PMID 27733281.
  30. ^ GBD 2013 Mortality and Causes of Death Collaborators (January 2015). "Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013". Lancet. 385 (9963): 117–171. doi:10.1016/S0140-6736(14)61682-2. PMC 4340604. PMID 25530442.
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