The DOI matches its Crossref record; 73 of the 73 references it cites were found in a registry or an index.
Vagal stimulation and prevention of sudden death in conscious dogs with a healed myocardial infarction.
Open accessAbstract
The interest for the antifibrillatory effect of vagal stimulation has been largely limited by the fact that this concept seemed restricted to acute experiments in anesthetized animals. To explore the potentially protective role of vagal stimulation in conscious animals we developed a chronically implantable device to be placed around the cervical right vagus. An anterior myocardial infarction was produced in 161 dogs; 1 month later an exercise stress test was performed on the 105 survivors. Toward the end of the test the circumflex coronary artery was occluded for 2 minutes. Fifty-nine (56%) dogs developed ventricular fibrillation and, before this test was repeated, were assigned either to a control group (n = 24) or to be instrumented with the vagal device (n = 35). Five dogs were excluded because of electrode malfunction. Compared with the heart rate level attained after 30 seconds of occlusion during exercise in the control test, vagal stimulation led to a decrease of approximately 75 beats/min (from 255 +/- 33 to 170 +/- 36 beats/min, p less than 0.001). In the control group 22 (92%) of 24 dogs developed ventricular fibrillation during the second exercise and ischemia test. By contrast, during vagal stimulation ventricular fibrillation occurred in only 3 (10%) of the 30 dogs tested and recurred in 26 (87%) during an additional exercise and ischemia test in the control condition (p less than 0.001 versus the vagal stimulation test; internal control analysis). Combined analysis of the tests performed in the control condition showed that ventricular fibrillation was reproducible in 48 (89%) of the 54 dogs tested. The protective effect of vagal stimulation was also significant in the group comparison analysis and even after exclusion of those four dogs in which ventricular fibrillation was not reproducible (92% versus 11.5%, control versus vagal stimulation, p less than 0.001). When heart rate was kept constant by atrial pacing, the vagally mediated protection was still significant (p = 0.015) as five (55%) of nine dogs survived the test. This study shows that vagal stimulation, performed shortly after the onset of an acute ischemic episode in conscious animals with a healed myocardial infarction, can effectively prevent ventricular fibrillation. This striking result seems to depend on multiple mechanisms having a synergistic action. The decrease in heart rate is an important but not always essential protective mechanism. The electrophysiological effects secondary to the vagally mediated antagonism of the sympathetic activity on the heart are likely to play a major role.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In particular, post-exercise recovery is a critical phase for sudden cardiovascular events, predominantly in the 30 minutes immediately following vigorous exercise, 5 which is attributable to increased sympathetic and decreased parasympathetic nerve activity.6”
From Caffeine delays autonomic recovery following acute exercise (2015) · cites this paper as [6]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Kleiger, R. E., Miller, J. P., Bigger, J. T., & Moss, A. J. (1987) · The American Journal of Cardiology · doi:10.1016/0002-9149(87)90795-8 · Cited by 3,995
Paradoxical Vasoconstriction Induced by Acetylcholine in Atherosclerotic Coronary Arteries
Ludmer, P. L., Selwyn, A. P., Shook, T., Wayne, R. R., Mudge, G. H., Alexander, R. W., & Ganz, P. (1986) · New England Journal of Medicine · doi:10.1056/nejm198610233151702 · Cited by 2,422
G proteins and dual control of adenylate cyclase
Gilman, A. G. (1984) · Cell · doi:10.1016/0092-8674(84)90336-2 · Cited by 1,772
Factors Influencing Infarct Size Following Experimental Coronary Artery Occlusions
Maroko, P. R., KJEKSHUS, J. K., Sobel, B. E., Watanabe, T., Covell, J. W., Ross, J., & D, E. B. M. (1971) · Circulation · doi:10.1161/01.cir.43.1.67 · Cited by 1,486
Levy, M. N. (1971) · Circulation Research · doi:10.1161/01.res.29.5.437 · Cited by 798
Rovere, M. T. L., Specchia, G., Mortara, A., & Schwartz, P. J. (1988) · Circulation · doi:10.1161/01.cir.78.4.816 · Cited by 631
Self-citationSchwartz, P. J., Vanoli, E., Stramba‐Badiale, M., Ferrari, G. M. D., Billman, G. E., & Foreman, R. D. (1988) · Circulation · doi:10.1161/01.cir.78.4.969 · Cited by 577
Self-citationA sympathetic reflex elicited by experimental coronary occlusion
Malliani, A., Pj, S., & Zanchetti, A. (1969) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1969.217.3.703 · Cited by 509
Schwartz, P. J., Billman, G. E., & STONE, H. L. (1984) · Circulation · doi:10.1161/01.cir.69.4.790 · Cited by 434
Self-citationTemporal dispersion of recovery of excitability in atrium and ventricle as a function of heart rate
Han, J., Millet, D., Chizzonitti, B., & Moe, G. K. (1966) · American Heart Journal · doi:10.1016/0002-8703(66)90213-4 · Cited by 394
Research works printed but not linked: 13
- [4]4. Janse MJ, Schwartz PJ, Wilms-Schopman F, Peters RJG, Durrer D: Effects of unilaterate stellate ganglion stimulation and ablation on electrophysiologic changes induced by acute myocardial ischemia in dogs. Circulation 1985;72:585-595
- [11]11. Kleiger RE, Miller JP, Bigger JT Jr, Moss AJ, Multicenter Postinfarction Research Group: Heart rate variability: A variable predicting mortality following acute myocardial infarction. Am J Cardiol 1987;59:256-262
- [20]20. Kent KM, Smith ER, Redwood DR, Epstein SE: Electrical stability of acutely ischemic myocardium: Influences of heart rate and vagal stimulation. Circulation 1973;47:291-298
- [21]21. Myers RW, Pearlman AS, Hyman RM, Goldstein RA, Kent KM, Goldstein RE, Epstein SE: Beneficial effect of vagal stimulation and bradycardia during experimental acute myo- cardial ischemia. Circulation 1974;49:943-947
- [22]22. Verrier RL, Lown B: Sympathetic-parasympathetic interac- tions and ventricular electrical stability, in Schwartz PJ, Brown AM, Malliani A, Zanchetti A (eds): Neural Mechanisms in Cardiac Arrhythmias. New York, Raven Press, Publishers, 1978, pp 75-85
- [38]38. Verrier RL, Hohnloser SH: How is the nervous system impli- cated in the genesis of cardiac arrhythmias?, in Hearst DG, Manning AS, Janse MJ (eds): Life-Threatening Arrhythmias During Ischemia and Infarction. New York, Raven Press, Publishers, 1987, pp 153-168
- [48]48. Gonzales-Serrato H, Alanis J: La acci6n de los nervios cardi- acos y de la acetilacolina sobre el automatismo del coraz6n. Acta Physiol Latinoam 1962;12:139-152
- [50]50. Carrier GO, Bishops VS: The interaction of acetylcholine and norepinephrine on heart rate. JPharmacol Exp Ther 1972;180: 31-37
- [51]51. Fleming JW, Watanabe AM: Biochemical mechanisms of parasympathetic regulation of cardiac function, in Fozzard HA, Haber E, Jennings RB, Katz AM, Morgan HE (eds): The Heart and Cardiovascular System. New York, Raven Press, Publishers, 1986, pp 1679-1688
- [59]59. Levy MN: Sympathetic-parasympathetic interactions in the heart. Circ Res 1972;29:437-445
- [64]64. Waxman MB, Wald RW: Termination of ventricular tachycar- dia by increase in cardiac vagal drive. Circulation 1977;56: 385-394
- [66]66. Schwartz PJ, Pagani M, Lombardi F, Malliani A, Brown AM: A cardio-cardiac sympatho-vagal reflex in the cat. Circ Res 1973;32:215-220
- [82]82. Redwood DR, Smith ER, Epstein SE: Coronary artery occlu- sion in the conscious dog: Effects of alterations in heart rate and arterial pressure on the degree of myocardial ischemia. Circulation 1972;46:323-332
Cited by
Sorted by citations
Items 601–680 of 680
When the heart sleeps... Is the vagus resetting the myocardial 'redox clock'?
Vecoli, C., & Paolocci, N. (2008) · INFM-OAR (INFN Catania) · doi:10.1093/cvr/cvn009
Risk for Sudden Cardiac Death in Heart Failure: Underlying Mechanisms and Therapeutic Modalities
Adamson, P. B., Vanoli, E., & Gronda, E. (2015) · Springer eBooks · doi:10.1007/978-3-319-15961-4_7
Self-citationStabilization of the Cardiac Nervous System During Cardiac Stress Induces Cardioprotection
Gibbons, D. D. (2012) · Digital Commons - East Tennessee State University (East Tennessee State University)
Аурикулярная вагусная стимуляция в лечении больных с левожелудочковой дисфункцией
Николаевна, П. Е., Kuzmichkina, M. A., Александрович, А. С., & Сергеевич, К. Р. (2013) · CyberLeninK (CyberLeninka)
Schwartz, P. J. (2009) · doi:10.1002/9780470561416.ch19
Self-citationChoi, E., Shen, M. J., Lin, S., Fishbein, M. C., Chen, L. S., & Chen, P. (2012) · doi:10.1002/9781118481585.ch19
Kimotsuki, T., Niwa, N., Hicks, M. N., Dunne, M., Cobbe, S. M., & Watanabe, M. (2009) · arXiv (Cornell University) · doi:10.48550/arxiv.0906.5028
Assessment of autonomic tonus and reflexes in patients after myocardial infarction
Hohnloser, S. H., & Klingenheben, T. (1994) · Steinkopff eBooks · doi:10.1007/978-3-642-72505-0_17
Menz, V., Hoffmann, J., Grimm, W., BORN, S., Mey, N., Glaveris, C., & Maisch, B. (1999) · Annals of Noninvasive Electrocardiology · doi:10.1111/j.1542-474x.1999.tb00367.x
Hong, G., Shin, D. G., Kang, J., Bae, J. H., Chung, H. J., Park, J., Kim, Y. J., & Shim, B. S. (2005) · Korean Circulation Journal · doi:10.4070/kcj.2005.35.7.539
Pathophysiology of Vulnerability Caused by Thrombogenic (Vulnerable) Blood
Cimmino, G., Ibáñez, B., & Badimón, J. J. (2010) · Humana Press eBooks · doi:10.1007/978-1-60327-179-0_4
Accentuated antagonism in canine subendocardium is not altered by chronic exercise
Hamra, M., & McNeil, R. S. (1997) · Medicine & Science in Sports & Exercise · doi:10.1097/00005768-199708000-00005
Choi, C. Q. (2006) · Scientific American · doi:10.1038/scientificamerican0706-32b
CARDIOVASCULAR REGULATION AND VASCULAR STRUCTURE IN PREHYPERTENSION AND CORONARY HEART DISEASE
Myredal, A. (2009) · Gothenburg University Publications Electronic Archive (Gothenburg University)
Frequenza cardiaca e rischio cardiovascolare
Rovere, M. T. L., & Tavazzi, L. (2006) · Giornale italiano di cardiologia · doi:10.1714/710.8104
Lujan, H. L., Janbaih, H., & DiCarlo, S. E. (2015)
Physiologic Effect of Relaxation Therapies on Autonomic Tone Early After Acute Coronary Syndromes
Friedman, R. S. C. (2009)
Heart Failure and Changes at the Periphery: Vascular, Inflammation, Neurohormonal, and Renal Systems
Marı́n-Garcı́a, J. (2010) · Humana Press eBooks · doi:10.1007/978-1-60761-147-9_12
What Is the Predictive Value of Heart Rate Variability and Baroreflex Sensitivity?
Pedretti, R. F. E. (1998) · Springer eBooks · doi:10.1007/978-88-470-2288-1_25
Chronische zervikale vagale Stimulation
Kuschyk, J., Doesch, C., Akın, İ., Borggrefe, M., & Roeger, S. (2015) · Herz · doi:10.1007/s00059-015-4364-6
Heart Rate Recovery Index Was Deteriorated In Diastolic Dysfunction
Aksoy, M., Akdemir, R., Kılıç, H., Vural, M. G., Saygısunar, U., Sarı, M., & Aytürk, M. (2016) · DergiPark (Istanbul University)
Shirai, T., Kasao, M., & Inoue, K. (1997) · Japanese Journal of Electrocardiology · doi:10.5105/jse.17.284
Circadian rhythm of heart rate variability in dilated cardiomyopathy.
Saitou, Y. (1999) · Japanese Journal of Electrocardiology · doi:10.5105/jse.19.694
Machhada, A. (2015) · UCL Discovery (University College London)
[Autonomous pharmacodynamics of organic nitrates in patients with unstable angina].
Аркадьевна, С. Э., Tf, M., & Im, S. (2013) · PubMed
Autonomic Pathophysiology After Myocardial Infarction Falling into Heart Failure
D’Elia, E., Ferrero, P., Mongillo, M., & Vanoli, E. (2015) · Springer eBooks · doi:10.1007/978-3-319-24993-3_6
Self-citationCostea, A., & Zardkoohi, O. (2015) · Springer eBooks · doi:10.1007/978-3-319-24993-3_4
Mourot, L. (2004) · OpenGrey (Institut de l'Information Scientifique et Technique)
Budowa łącza przedsionkowo-komorowego - od Paladino do ablacji
Koźluk, E., Kozłowski, D., Szufladowicz, E., & Walczak, F. (1998) · Via Medica Journals
Autonomic Regulation and Cardiac Risk
Malík, M. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-44733-1.00068-7
Heart and Autonomic Nervous System : Learn from the Past, Create the Future
Inoue, H. (2016) · Japanese Journal of Electrocardiology · doi:10.5105/jse.36.315
Shi, C. L., Zhao, J., Gao, J.-H., Zhang, J., Zhu, B., Yu, X., & Rong, P. (2017) · Acupuncture & Electro-Therapeutics Research · doi:10.3727/036012917x15118029263229
Gomes, B. F. D. O., Benchimol‐Barbosa, P. R., & Nadal, J. (2019) · World Congress on Medical Physics and Biomedical Engineering, September 7 - 12, 2009, Munich, Germany · doi:10.1007/978-981-13-2517-5_16
Neuromodulation of Cardiac Repolarization and Arrhythmogenesis
Extramiana, F., & Maison‐Blanche, P. (2019) · Springer eBooks · doi:10.1007/978-3-030-22672-5_2
Peculiarities of Cardiohemodynamics and its Autonomic Regulation in Elderly People
Нестеров, В. П., Бурдыгин, А. И., Nesterov, S. V., Ivanov, K., Korotkov, S. M., Sobol, K. V., & Шемарова, И. В. (2019) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093019060061
Dias, A. R. L., Cambri, L. T., de Araújo, J. A., Tricot, G. K., de Souza, K. A., Meireles, K., & Arsa, G. (2018) · Revista Brasileira de Educação Física e Esporte · doi:10.11606/issn.1981-4690.v32i4p533-546
Raddatz, C. (2020) · Spectrum Research Repository (Concordia University)
Neuromodulation in Heart Failure
Keaney, J., & Singh, J. P. (2020) · Elsevier eBooks · doi:10.1016/b978-0-323-60987-6.00042-9
Device Autonomic Regulation Therapy in Patients with Heart Failure and Reduced Ejection Fraction
Lakkireddy, D. (2020) · Journal of Atrial Fibrillation · doi:10.4022/jafib.2409
Detecting and Reversing Myocardial Ischemia Using an Artificially Intelligent Bioelectronic MedicinePreprint
Ganzer, P. D., Loeian, M. S., Roof, S. R., Teng, B., Lin, L., Friedenberg, D. A., Baumgart, I., Meyers, E., Chun, K., Rich, A., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.12.30.424900
Kuschyk, J., Doesch, C., Akın, İ., Borggrefe, M., & Roeger, S. (2015) · Herz
Vagusstimulation: Mechanismen und momentaner klinischer Stellenwert bei der Herzinsuffizienz
Kuschyk, J., & Borggrefe, M. (2011) · Herzschrittmachertherapie + Elektrophysiologie
Neurocardiac Interactions in Sudden Unexpected Death in Epilepsy
Verrier, R. L., & Schachter, S. C. (2010) · CRC Press eBooks · doi:10.1201/b10317-44
Neural Regulation of the Heart in Health and Disease
Verrier, R. L., & Tan, A. Y. (2013) · Springer eBooks · doi:10.1007/978-1-4471-4881-4_5
Yap, Y. G., & Camm, A. J. (1998) · Springer eBooks · doi:10.1007/978-94-017-1057-2_15
Device-Based Approaches to Modulate the Autonomic Nervous System and Cardiac Electrophysiology
Hucker, W. J., Singh, J. P., Parks, K. A., & Armoundas, A. A. (2011) · Arrhythmia & Electrophysiology Review · doi:10.15420/articles/device-based-approaches-modulate-autonomic-nervous-system-and-cardiac-electrophysiology
Fernandes, O., da Silva, R. M., Ramos, L. R., Gama, T. M., Lobo, I., Souza, G. G. L., & Sanchez, T. A. (2022) · Journal of Community Psychology · doi:10.1002/jcop.22877 · Cited by 1
Blok, M., Jongbloed, M. R. M., & Boukens, B. J. (2022) · Physiological Reports · doi:10.14814/phy2.15511
Nitric Oxide and the Heart Autonomic Nervous System
Buchholz, B., Riveros, V. B. F., Diodati, N. M., & Gelpi, R. J. (2023) · Advances in biochemistry in health and disease · doi:10.1007/978-3-031-24778-1_4
The Neuro-cardiac Axis in Arrhythmogenesis: Role and Impact of Autonomic Modulation
Chin, S. H., & Ng, G. A. (2023) · Springer eBooks · doi:10.1007/978-3-031-33588-4_9 · Cited by 2
Cardiopulmonary Mechanoreflexes
Takahashi, T. (2024) · Springer eBooks · doi:10.1007/978-981-99-8486-2_4
Vagal Activity and Duration of Recovery Exercise
Takahashi, T. (2024) · Springer eBooks · doi:10.1007/978-981-99-8486-2_3
Vagus Nerve Stimulation for Treatment of Chronic Heart Failure
Karibova, M., Кручинова, С. В., Shvartz, V. A., Нургалиевна, Г. М., & Kosmacheva, E. D. (2025) · Innovative medicine of Kuban · doi:10.35401/2541-9897-2025-10-1-136-143
The Autonomic Nervous System and Ventricular Arrhythmias
Dusi, V., & Ferrari, G. M. D. (2025) · Springer eBooks · doi:10.1007/978-3-031-81762-5_3
Did George Floyd Die of Cardioinhibition From Pressure on His Neck?
Weedn, V. W., Steinberg, A. A., & Speth, P. (2025) · Academic Forensic Pathology · doi:10.1177/19253621251327721
Use of baroreceptor reflex sensitivity in the prediction of risk after myocardial infarction
Ferrari, G. M. D., & Schwartz, P. J. (1996) · Developments in cardiovascular medicine · doi:10.1007/978-94-009-0219-0_10
Self-citationStructural Determinants of T Wave Alternans in Patients with Cardiomyopathy
Suszko, A. M. (2012) · TSpace (University of Toronto)
Consequences of Arterial Switch Operation in Children Born with Transposition of the Great Arteries
Falkenberg, C. (2013) · Gothenburg University Publications Electronic Archive (Gothenburg University)
Cai, C., Wu, N., Yang, G., Yang, S., Liu, W., Chen, M., & Po, S. S. (2023) · Figshare · doi:10.6084/m9.figshare.24425614
Huffman, W. J., Musselman, E. D., Pelot, N. A., & Grill, W. M. (2024) · Figshare · doi:10.6084/m9.figshare.26569084
Ventricular Arrhythmias and Heart Failure
Keane, S., Ellis, E. R., Josephson, M. E., & Callans, D. J. (2026) · Springer eBooks · doi:10.1007/978-3-032-12626-9_21
Cardiovascular risks and implications of epilepsy: The epileptic heart
Massarwa, M., Fennig, U., Loebenstein, R., Altman, K., Gofrit, S. G., Boxer, M., Katz, M., & Maggio, N. (2026) · Health Sciences Review · doi:10.1016/j.hsr.2026.100266
Bussmann, B. M., George, B., Robinson, M., Grist, J. T., Sukumar, P., Chinherende, E., Sheerin, F., Enzhil, V., Rider, O. J., Jones, B., et al. (2026) · BMJ Open · doi:10.1136/bmjopen-2025-110958
Alber, B. R., Gill, A., Dyavanpalli, J., Mendelowitz, D., & Kay, M. W. (2026) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2026.1814067
Zhao, Y., Shen, T., & Jia, S. (2026) · Frontiers in Neurology · doi:10.3389/fneur.2026.1933117
Sikorska, A., Nowiński, A., Niedzwiedz, M., Kryński, T., Gawalkiewicz-Mazanska, A., Baran, J. M., & Kułakowski, P. (2026) · Heart Rhythm · doi:10.1016/j.hrthm.2026.10.053
Concomitant Therapy and Autonomic Tests
Copie, X., Guize, L., & Heuzey, J. L. (1998) · Springer eBooks · doi:10.1007/978-94-017-1057-2_12
Therapeutical Options to Influence the Autonomic Nervous System
Vanoli, E., Valentini, P., & Pedretti, R. F. E. (2000) · Developments in cardiovascular medicine · doi:10.1007/978-94-011-4090-4_7
Self-citationLeite, S., Martinelli, F., Madruga, V. A., Catai, A. M., Júnior, L. G., & Chacon‐Mikahil, M. P. T. (2008)
Metadata
- Authors
- Vanoli, E., De Ferrari, G. M., Stramba-Badiale, M., Hull, S. S., Foreman, R. D., & Schwartz, P. J.
- Affiliations
- University of Oklahoma (US)
- Department of Physiology and Biophysics, University of Oklahoma, Oklahoma City.
- Venue
- Circulation Research
- Published
- 1991-05
- Volume
- 68
- Issue
- 5
- Pages
- 1471-1481
- ISSN
- 0009-7330 (ISSN-L)
- 1524-4571
- OpenAlex
- W2123181530
- Cited by
- 681
- References
- 73
- Citations by year
- 2026: 8 · 2025: 11 · 2024: 10 · 2023: 22 · 2022: 18 · 2021: 19 · 2020: 20 · 2019: 23 · 2018: 16 · 2017: 22 · 2016: 29 · 2015: 42 · 2014: 35 · 2013: 28 · 2012: 25
- FWCI
- 8.20
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Circulation Research (publishedVersion)
- PubMed (publishedVersion)
- Institutional Research Information System University of Turin (University of Turin) (submittedVersion)
- Funders
- National Institutes of Health (5p01hl033727-03)
- National Heart, Lung, and Blood Institute (HL33727)
- Topics
- Life Sciences › Neuroscience › Neurology › Vagus Nerve Stimulation Research
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Heart Rate Variability and Autonomic Control
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac pacing and defibrillation studies
- Keywords
- vagus nerve stimulation, sudden cardiac death prevention, ventricular fibrillation, myocardial infarction, anterior myocardial infarction, coronary artery occlusion, exercise stress testing, heart rate reduction, atrial pacing, conscious dogs, ischemia-induced arrhythmia, antifibrillatory effect, atrial fibrillation prevention
- MeSH terms
- Animals, Blood Pressure, Cardiac Pacing, Artificial, Death, Sudden, Dogs, Electric Stimulation, Electrocardiography, Heart Rate, Hemodynamics, Myocardial Infarction, Vagus Nerve, Ventricular Fibrillation
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review