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Year : 2009  |  Volume : 57  |  Issue : 4  |  Page : 375-380

Management of the trigeminocardiac reflex: Facts and own experience

1 Department of Neurosurgery, University of Paris, France, and Department of Neurology, Addis Ababa University, Ethiopia
2 Department of Neurosurgery, University of Lausanne, Switzerland
3 Department of Neurosurgery, University of Paris, France
4 Department of Neuroanesthesiology, Neurosciences Center, All India Institute of Medical Sciences, New Delhi, India

Date of Acceptance24-Jul-2009
Date of Web Publication10-Sep-2009

Correspondence Address:
Bernhard Schaller
Department of Neurosurgery, University of Paris
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0028-3886.55577

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 » Abstract 

The trigeminocardiac reflex (TCR) is defined as the sudden onset of parasympathetic dysrhythmia, sympathetic hypotension, apnea, or gastric hyper-motility during stimulation of any of the sensory branches of the trigeminal nerve. The proposed mechanism for the development of TCR is-the sensory nerve endings of the trigeminal nerve send neuronal signals via the Gasserian ganglion to the sensory nucleus of the trigeminal nerve, forming the afferent pathway of the reflex arc. It has been demonstrated that the TCR may occur with mechanical stimulation of all the branches of the trigeminal nerve anywhere along its course (central or peripheral). The reaction subsides with cessation of the stimulus. But, some patients may develop severe bradycardia, asystole, and arterial hypotension which require intervention. The risk factors already known to increase the incidence of TCR include: Hypercapnia; hypoxemia; light general anesthesia; age (more pronounced in children); the nature of the provoking stimulus (stimulus strength and duration); and drugs: Potent narcotic agents (sufentanil and alfentanil); beta-blockers; and calcium channel blockers. Because of the lack of full understanding of the TCR physiology, the current treatment options for patients with TCR include: (i) risk factor identification and modification; (ii) prophylactic measures; and (iii) administration of vagolytic agents or sympathomimetics.

Keywords: Atropine, cardiac reflex, oculocardiac reflex, skull base surgery, treatment, trigemino

How to cite this article:
Arasho B, Sandu N, Spiriev T, Prabhakar H, Schaller B. Management of the trigeminocardiac reflex: Facts and own experience. Neurol India 2009;57:375-80

How to cite this URL:
Arasho B, Sandu N, Spiriev T, Prabhakar H, Schaller B. Management of the trigeminocardiac reflex: Facts and own experience. Neurol India [serial online] 2009 [cited 2022 Oct 6];57:375-80. Available from: https://www.neurologyindia.com/text.asp?2009/57/4/375/55577

 » Introduction Top

The trigeminal nerve is the largest of the cranial nerves, and it provides sensory supply to the face, scalp, and mucosa of the nose and mouth. [1],[2],[3] Stimulation of the trigeminal receptors that innervate the nose and nasal passages is thought to provide an important stimulus for the initiation of the trigeminorespiratory reflex and cardiac arrhythmias which could arise with it. This has been studied in animals and known for more than a century, [4],[5],[6] and is now considered as the trigeminocardiac reflex (TCR). In the early 20 th century, this TCR has gained much clinical attention, in the form of the oculocardiac reflex (OCR) which is the cardiac response (mainly bradycardia) associated with stimulation of the ophthalmic division of the trigeminal nerve during ocular surgeries. [7],[8] Then, Schaller, for the first time, demonstrated that a similar reflex occurs with stimulation of the intracranial portion of the trigeminal nerve. [1] Again Schaller was the first who subsummarized all these reflexes under the term TCR. [2],[9] Since then, there has been much discussion about the reflex itself and the prophylaxis and treatment of the TCR when it occurs during intracranial or extracranial procedures. But until now, there exists no clear recommendations how to treat the TCR. So, the aim of the present work is to update knowledge about currently available treatment options for patients with TCR.

Definition and pathophysiology of the trigeminocardiac reflex

The TCR is defined as the sudden onset of parasympathetic dysrhythmia, sympathetic hypotension, apnea, or gastric hyper-motility during stimulation of any of the sensory branches of the trigeminal nerve. [1] The proposed mechanism for the development of the TCR is that the sensory nerve endings of the trigeminal nerve send neuronal signals via the  Gasserian ganglion More Details to the sensory nucleus of the trigeminal nerve, forming the afferent pathway of the reflex arc. [1],[2] This afferent pathway continues along the short internuncial nerve fibres in the reticular formation to connect with the efferent pathway in the motor nucleus of the vagus nerve. Several lines of experimental evidence demonstrate that trigeminally induced cardiovascular reflexes could be mediated initially in the trigeminal nucleus caudalis and subsequently in the parabrachial nucleus, the rostral ventrolateral medulla oblongata, the dorsal medullary reticular field, and the paratrigeminal nucleus in animal models. [3],[10],[11]

The TCR occurs during both, the peripheral and the central manipulations of the trigeminal nerve. The OCR, which is a subform of the TCR, has long been reported in patients with ocular surgeries and manipulations.[7],[8],[12] In 1999, Schaller et al ., for the first time, reported the occurrence of the TCR in skull base and neurological surgeries. [1] The underlying responsible mechanism is not yet fully understood, but is believed to be the same as the OCR reported earlier on, i.e., activation of the central or intracranial portions of the trigeminal nerve. [2]

Epidemiology of the trigeminocardiac reflex

It has been demonstrated that the TCR may occur with manipulation of all the branches of the trigeminal nerve anywhere along its (intracranial or extracranial) course.[7],[8],[12],[13],[14],[15],[16] The OCR, which is a subvariant of the TCR, and studied far earlier, was said to occur in up to 67% of the patients operated for strabismus, [17] but a lot of authors only studied the heart rate and a reduction in heart rate by 10% or more was taken as a positive OCR, so that the real incidence may be substantially smaller. According to Schaller's experience, the TCR occurs in 10-18% of the patients. [1],[18],[19],[20] In a retrospective review of 125 patients operated for tumors of the cerebello-pontine angle, Schaller et al . noticed the occurrence of the TCR in 11% of the operated patients. [4] Three of the patients in this series developed asystole which lasted from 30-70 seconds.0[1] In contrast to the studies on OCR, Schaller take into consideration the heart rate and blood pressure into account and defined TCR as heart rate less than 60 beats per minute and mean arterial blood pressure (MABP) 20% lower than the baseline. [1]

In another study, Schaller also showed the occurrence of TCR during microvascular decompression of the trigeminal nerve for trigeminal neuralgia. [20] In this review on 28 patients, the incidence of TCR was 18% with the same definition used as in his prior study, i.e., heart rate less than 60 beats per minute and MABP 20% lower than the baseline. [20] TCR was also reported during transsphenoidal surgery for pituitary adenoma. [9],[19],[21] Among 117 patients who underwent transsphenoidal surgery for pituitary adenoma, 10% developed a TCR during the surgical procedure. [19] Peripheral stimulation of the naso-pharynx may also lead to TCR. [9]

Risk factors for occurrence of the trigeminocardiac reflex

As there is a lack of detailed knowledge of the physiology of the TCR and since we cannot treat in whole the TCR, the risk factors gain increased importance. The risk factors already known to increase the incidence of TCR include: (i) hypercapnia; (ii) hypoxemia; (iii) light general anesthesia; (iv) age (more pronounced in children); (v) the nature of the provoking stimulus (stimulus strength and duration); and (vi) drugs. Drugs known to increase the TCR include: (i) potent narcotic agents (sufentanil and alfentanil); [22],[23] (ii) beta-blockers; and (iii) calcium channel blockers. [24] Narcotics may augment vagal tone through their inhibitory action on the sympathetic nervous system. [1],[25],[26],[27] Beta-blockers reduce the sympathetic response of the heart and by so doing, augment the vagal cardiac response resulting in bradycardia. Calcium channel blockers result in peripheral arterial smooth muscle relaxation and vasodilatation causing reduction in blood pressure. In patients undergoing trigeminal manipulations, this worsens the vagal effect that occurs in some patients.

 » Case Report Top

A 60-year-old male patient with a diagnosis of right-sided vestibular schwannoma underwent tumor resection via a retrosigmoid (suboccipital approach) approach. His medical history was significant for long standing hypertension for which he is taking irbesartan (an angiotensin receptor blocker) and a 14-pack-year history of smoking. Otherwise, he has no history of diabetes, cardiac problems, and was not on beta blockers or calcium channel blockers. His baseline MABP was 73.2mm Hg and heart rate was 65 beats per minute. Two hours after skin incision, his MABP dropped to 43.3mm Hg (40.8% drop from the baseline) and concomitantly, his heart rate dropped to 40 beats per minute (38% drop from the baseline). Then, the procedure was discontinued; he was given epinephrine and crystalloid fluids. After five minutes, his MABP and heart rate stabilized and the surgical procedure was carried out successfully to the end without any further episodes of TCR. His oxygen saturation was 100% and no hypercarbia occurred. The postoperative course was uneventful.

Clinical significance of the trigeminocardiac reflex and why it should be treated

Most authors recognized that the TCR is a transient response to the trigeminal nerve manipulation in its extra or intracranial course which subsides with cessation of the stimulus. But, in the most serious forms of severe bradycardia and asystole, administration of vagolytic agents is warranted in addition to cessation of the stimulus. Rath et al . reported a case of asystole occuring in a patient who was undergoing percutaneous retrogasserian glycerol rhizolysis for trigeminal neuralgia.[28] Immediately after injection of anhydrous glycerol, the patient became unresponsive, the pulse became impalpable, blood pressure unrecordable, the ECG showed asystole, and had a respiratory arrest. The patient regained consciousness and heart rate and blood pressure returned to normal after 30 seconds with oxygen and IV atropine. [28] Prabhakar et al . also reported a case of sudden asystole without prior bradycardia which occurred during surgery for cerebellopontine angle tumor. [29] This case was just managed by cessation of the manipulation without administration of vagolytic agents. [30] Fayol et al . also reported a five-year-old boy who was operated for strabismus and possibly died due to OCR which developed on underlying myocarditis.[30] These cases demonstrate the (clinical) importance of the TCR which may range from mild bradycardia which responds to simple cessation of the stimulus to asystole and severe bradycardia requiring additional intervention with vagolytics. In some rare but serious cases, it may lead to death if not detected early and appropriate measures taken.

In addition, hypotension which occurs during the TCR may lead to myocardial and cerebral infarction in those who are at risk for these conditions. It has also been shown that the hypotension may lead to worse outcomes in hearing function in patients operated for vestibular schwannoma compared to those who do not develop the reflex. [18],[31] In a prospective study of 100 patients after vestibular schwannoma surgery, Gharabaghi et al . found out that the occurrence of TCR was 11%. [18] With an overall hearing preservation of 47%, 11.1% of the patients in the TCR group and 51.4% of those in the nonTCR group, experienced preserved hearing function postoperatively. [18] In addition, in cases involving larger tumors, an intraoperative TCR was associated with a significantly worse postoperative hearing function during vestibular schwannoma surgery suggesting that the hypotension following TCR is-in addition to the tumor size-a negative prognostic factor for hearing preservation in patients undergoing VS surgery. [18] In another study, Schaller et al . compared the occurrence and persistence of tinnitus in patients with and without TCR. [32] Among 36 patients operated for vestibular schwannoma, TCR occurred in 17% and influenced the occurrence of postoperative ipsilateral tinnitus: The overall incidence of postoperative ipsilateral tinnitus was 22%. A total of 60% patients in the TCR subgroup and only 17% of in the nonTCR subgroup experienced ipsilateral tinnitus postoperatively. [32] These studies show that there is a tendency for increased complication rates in patients who developed TCR compared to those without it, again stressing the importance of looking it carefully during neurosurgical and especially skull base surgical procedures.

Management of the trigeminocardiac reflex

There has been a lot of discussion about the best and more effective treatment for TCR. [33],[34],[35],[36],[37],[38],[39],[40],[41],[42] It is beyond the scope of this manuscript to discuss all these influences. Without any doubt, application of atropine is not the only modality of treatment, based on physiological knowledge of the reflex and based on clinical experience. To the authors opinion, the first and the most important "management option" for the TCR is to be aware of its potential danger and minimize any mechanical stimulation of the nerve.

According to the clinical experience on this topic, the management of patients with TCR can be classified into the following categories which are illustrated in the flow-chart [Figure 1]:

  1. Risk factor identification and modification.
  2. Prophylactic treatment with either vagolytic agents or peripheral nerve blocks in case of peripheral manipulations of the trigeminal nerve.
  3. Careful cardiovascular monitoring during anesthesia especially in those with risk factors for TCR.
  4. Treatment of the condition when it occurs:

  1. cessation of the manipulation, and;
  2. administration of vagolytic agents or adrenaline.
The risk of TCR should be considered in any neurosurgical intervention, especially at the skull base. If any mechanical stimulation to the trigeminal nerve is necessary, which is a rather "robust" nerve, should be as gentle as possible. If working in the vicinity of the nerve or its branches, the anesthesiologist should be notified by the surgeon. Continuous intraoperative monitoring of hemodynamic parameters has been shown to allow the surgeon to interrupt surgical maneuvers immediately upon the occurrence of TCR. This technique has been proven sufficient in most cases for the heart rate and the arterial blood pressure to return to normal levels without the necessity of additional anticholinergic medication. Following this strategy, an uneventful further intraoperative and postoperative course may be achieved. However, the intraoperative reaction of the surgeon to the TCR may be too late to prevent postoperative neurological deficits under certain circumstances. [33],[34]

If controlled arterial hypotension is planned, the prophylaxis of TCR is better accomplished with local anesthetic infiltration or block of the nerve(s) which convey afferent stimuli. Shende et al . studied the efficacy of peribulbar block with bupivacaine in patients operated for retinal detachment. [35] They collected 60 patients who were randomly assigned to receive either bupivacaine or IV morphine and studied the incidence and severity of the OCR. Apart from significantly reducing the incidence of OCR (30% vs . 70%), peribulbar bupivacaine also attenuated the severity of the reflex. [35] Gupta et al. studied the effect of peribulbar block in comparison to topical application of local anesthetic in children scheduled for strabismus surgery. They found out that the incidence and severity of OCR intraoperatively was significantly reduced in children who received a peribulbar block. [36] Misurya et al. studied the effectiveness of prophylactic intravenous atropine sulphate which blocks the peripheral muscarinic receptors at the heart and retrobulbar xylocaine hydrochloride, which blocks the conduction at ciliary ganglion on the afferent limb of OCR. In this study, both atropine and retrobulbar xylocaine reduced the rate of OCR to 10-20%. But, when both methods were used together, they were able to completely suppress the OCR. [37]

If there is no contraindication to intravenous anticholinergics, atropine and/or glycopyrrolate IV may be used to partially prevent a TCR. [38] Hunsley et al . evaluated the efficacy of IV atropine and glycopyrrolate in the prevention of the OCR in children operated for strabismus. They tested different doses of the two drugs, glycopyrrolate 5 and 7.5 mg/kg and atropine 10 and 15 mg/kg. Overall, there is a reduction in the rate of bradycardia to 23.8% to 33.3%. [39] But, they noticed that even higher doses of the two drugs, atropine 15mg/kg and glycopyrrolate 7.5mg/kg i.v., given 5min before induction of anesthesia, are not sufficient to protect completely against the OCR in children.

In a study done to evaluate the efficacy of IV or IM vagolytic agents (atropine and glycopyrrpolate), in children undergoing squint surgery, Mirakhur et al . evaluated them in a controlled study and found out that the administration of the anticholinergic agents in both the IV and the IM forms may decrease the occurrence of the OCR. [40] The overall frequency was approximately 40% (62 of 160 patients), but was 90% in those patients who did not receive anticholinergic drugs. [40] The authors concluded that, administration of anticholinergic drugs, even by the IM route, decreased the frequency, and glycopyrrolate 10 mg per kg being the most efficacious by this route. [40]

Intramuscular administration of anticholinergics has shown to be ineffective in preventing the TCR. [29,43] The use of atropine is, nowadays, questioned because cholinergic blockage reduces but does not totally prevent either bradycardia or hypotension in animals. [41] Another reason is that, a trigeminal depressor response includes both activation of vagal cardioinhibitory fibres and inhibition of adrenergic vasoconstriction as demonstrated after electrical stimulation of the spinal trigeminal tract and trigeminal nuclear complex. In addition, atropine may cause serious cardiac arrhythmias itself, especially when halothane is the primary anaesthetic agent and hence the dose must be carefully chosen. [42]

Prabhakar et al . reported a 48-year-old female who developed severe bradycardia and hypotension during craniotomy for parietal convexity meningioma; she was unresponsive to atropine and successfully managed with epinephrine. [44] The action of adrenaline is to increase peripheral resistance via alpha-1 adrenoceptor vasoconstriction, so that blood is shunted to the body's core, and the alpha-1 adrenoceptor response which is to increase cardiac rate and output. [44] This important case report underscores the fact that TCR may be refractory to atropine and other vagolytics and may rather need to be managed with epinephrine. [44]

In general and with special reference to our case reported here, the treatment of TCR deserves more attention. If a TCR is elicited, the surgeon must stop the stimulus and wait until the pulse recovers its normal rhythm. Occurrence of the TCR corresponds to the intensity of the mechanical stimulation on the trigeminal pathway. Abrupt and sustained traction is more likely to evoke the TCR than smooth and gentle manipulations. [34],[45],[46],[47]

 » Conclusion Top

In the present paper, we illustrated the clinical relevance of the TCR and discussed its management. The most important aspects of management which were detailed above are: (i) awareness of its possible occurrence in every patient undergoing head surgery (as there exist no identified risk factors); (ii) prophylactic peripheral nerve block in some type of surgeries (for example, strabismus surgery); (iii) avoidance of traction and gentle manipulation around the nerve, if any necessary intraoperatively; (iv) interaction between surgeon and anethesiologists; (v) careful and continuous monitoring of the heart rate and blood pressure to detect its occurrence; (vi) cessation of the mechanical stimulus upon recovery of pulse rate and arterial blood pressure; (vii) in severe cases of bradycardia and asystole, administration of vagolytic agents such as atropine; (viii) if unresponsive to atropine, epinephrine administration may be considered as ultima ratio.

Further anatomical studies may help to describe the reflex arc in more detail on the one hand and to develop more precise prophylactic treatment options on the other hand.

 » References Top

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[Pubmed] | [DOI]
2 Atypical trigeminocardiac reflex during intranasal dexmedetomidine sedation of a 6-month-old premature baby
Denise Bayard, Friedrich Lersch, Gesar Ugen, Bernhard Schaller
BMJ Case Reports. 2022; 15(5): e247292
[Pubmed] | [DOI]
3 Prevention of trigeminocardiac reflex-induced severe bradycardia during cerebral aneurysm clipping surgery by topical anesthesia of the dura surface and atropine administration: a case report
Akari Yoshida, Takafumi Seki, Yuichi Aratani, Tadashi Tanioku, Tomoyuki Kawamata
JA Clinical Reports. 2022; 8(1)
[Pubmed] | [DOI]
4 Cardiovascular response to Gasserian ganglion ablation on trigeminal neuralgia under local anesthesia: a retrospective single-blind case–control study
Dingliang Zhao, Jing Li, Chao Ma, Ying Huang, Gaojian Tao
BMC Anesthesiology. 2022; 22(1)
[Pubmed] | [DOI]
5 Profound trigeminocardiac reflex from lingual nerve stimulation: a case report
Allen Champion, John Masi
Journal of Dental Anesthesia and Pain Medicine. 2022; 22(1): 61
[Pubmed] | [DOI]
6 Severe Bradycardia Occurring After Assisted Mouth Opening: A Case Report
Yoshio Hayakawa, Keiko Fujii-Abe, Takuya Nakano, Masayuki Suzuki, Hiroshi Kawahara
Anesthesia Progress. 2022; 69(1): 46
[Pubmed] | [DOI]
Venu Sameera Panthagada, Ravi Raja Kumar Saripalli, Manoj Kumar Kanta
[Pubmed] | [DOI]
8 Asystole During Reduction of a Zygomaticomaxillary Complex Fracture
Chloe Warinner, Nicholas B. Abt, David A. Shaye
Facial Plastic Surgery & Aesthetic Medicine. 2021; 23(2): 148
[Pubmed] | [DOI]
9 Trigeminal Nerve Repair: Is the Trigeminocardiac Reflex a Concern?
Yousef Hammad, Allison Mootz, Kevin Klein, John R. Zuniga
Journal of Oral and Maxillofacial Surgery. 2021; 79(11): 2355
[Pubmed] | [DOI]
10 In-office endoscopic nasal polypectomy: prospective analysis of patient tolerability and efficacy
Jaime Viera-Artiles, Patricia Corriols-Noval, Eugenia López-Simón, Rocío González-Aguado, David Lobo, Roberto Megía
European Archives of Oto-Rhino-Laryngology. 2020; 277(12): 3341
[Pubmed] | [DOI]
11 Anestesia en cirugía oftalmológica
P.J. Zetlaoui
EMC - Anestesia-Reanimación. 2020; 46(1): 1
[Pubmed] | [DOI]
12 Reflejo trigémino cardíaco durante artroscopia de la articulación temporomandibular. Reporte de caso clínico
José Ernesto Miranda Villasana, Diego Armando Ayala Gonzalez, Lidia Araceli Campos Ramírez, Edith Jocelyn Hernández Sánchez, Gabriel Galindo Velázquez
Acta Odontológica Colombiana. 2020; 10(2): 147
[Pubmed] | [DOI]
13 Effects of General Anesthesia Using Remifentanil on Hemodynamics during Oral Surgery
Hidenori Yamaguchi, Masatoshi Suzuki, Mami Nakamura, Rika Okamura, Ayako Tsuji, Takahiro Sasaki, Koh Shibutani
International Journal of Oral-Medical Sciences. 2020; 19(2): 88
[Pubmed] | [DOI]
14 Relationship between trigeminocardiac reflex, QT, QTc and anesthesia in septorhinoplasty surgeries
I?smail KONUK, I?lknur Suidiye YORULMAZ, Onur OZLU, Derya ÖZÇELIK, Fatih Alper AKCAN, Pelin ÇETIN
Konuralp Tip Dergisi. 2020;
[Pubmed] | [DOI]
15 Anesthetic management of functional endoscopic endonasal rhinosinus surgery in children
T. A. Ovchar, V. V. Lazarev
Anesteziologiya i Reanimatologiya. 2020; (1): 55
[Pubmed] | [DOI]
16 Trigeminocardiac Reflex Induced by Maxillary Nerve Stimulation during Sphenopalatine Ganglion Implantation: A Case Series
Yousef Hammad, Allison Mootz, Kevin Klein, John R. Zuniga
Brain Sciences. 2020; 10(12): 973
[Pubmed] | [DOI]
17 Photic sneeze reflex: another variant of the trigeminocardiac reflex?
Tumul Chowdhury, Zohara Sternberg, Eugene Golanov, Riccardo Gelpi, Thomas Rosemann, Bernhard J Schaller
Future Neurology. 2019; 14(4): FNL32
[Pubmed] | [DOI]
18 Does Surgical Release of TMJ Bony Ankylosis Increase the Risk of Trigeminocardiac Reflex? A Retrospective Cohort Study
Shadia Abdel-Hameed Elsayed, Ayman F. Hegab, Saeed Salem Youssif Alkatsh
Journal of Oral and Maxillofacial Surgery. 2019; 77(2): 391
[Pubmed] | [DOI]
19 Asystole During Onyx Embolization of a Pediatric Arteriovenous Malformation: A Severe Case of the Trigeminocardiac Reflex
Kasra Khatibi,Omar Choudhri,Ian D. Connolly,Ryan A. McTaggart,Huy M. Do
World Neurosurgery. 2017; 98: 884.e1
[Pubmed] | [DOI]
20 Trigeminocardiac reflex during non-surgical root canal treatment of teeth with irreversible pulpitis
James I.-Sheng Huang,Hao-Hueng Chang,Chun-Pei Lin,Wan-Chuen Liao,Chia-Tze Kao,Tsui-Hsien Huang
Journal of the Formosan Medical Association. 2017;
[Pubmed] | [DOI]
21 Trigemino-Cardiac Reflex: A Phenomenon Neglected in Maxillofacial Surgery?
Udupikrishna M. Joshi,Ashwini Munnangi,Kundan Shah,Satishkumar G. Patil,Nitin Thakur
Journal of Maxillofacial and Oral Surgery. 2017; 16(2): 181
[Pubmed] | [DOI]
22 Oculocardiac reflex elicited by orbital floor fracture and inferior globe displacement
Chau M. Pham,Steven M. Couch
American Journal of Ophthalmology Case Reports. 2017; 6: 4
[Pubmed] | [DOI]
23 Chronic Trigemino-Cardiac Reflex: An Underestimated Truth
Tumul Chowdhury,Bernhard Schaller
Frontiers in Neurology. 2017; 8
[Pubmed] | [DOI]
24 Editorial: The Trigeminocardiac Reflex: Beyond the Diving Reflex
Bernhard Schaller,Tumul Chowdhury,Thomas Rosemann
Frontiers in Neuroscience. 2017; 11
[Pubmed] | [DOI]
25 The negative chronotropic effect during lumbar spine surgery
Tumul Chowdhury,Bernhard Schaller
Medicine. 2017; 96(1): e5436
[Pubmed] | [DOI]
26 The clinical surrogate definition of the trigeminocardiac reflex
Cyrill Meuwly,Tumul Chowdhury,Ricardo Gelpi,Paul Erne,Thomas Rosemann,Bernhard Schaller
Medicine. 2017; 96(49): e9033
[Pubmed] | [DOI]
27 Trigeminocardiac reflex in cerebrovascular surgery: a review and an attempt of a predictive analysis
Nora Sandu,Tumul Chowdhury,Cyrill Meuwly,Bernhard Schaller
Expert Review of Cardiovascular Therapy. 2017; 15(3): 203
[Pubmed] | [DOI]
28 Sudden Infant Death Syndrome – Role of Trigeminocardiac Reflex: A Review
Gyaninder Pal Singh,Tumul Chowdhury,Barkha Bindu,Bernhard Schaller
Frontiers in Neurology. 2016; 7
[Pubmed] | [DOI]
29 How to apply case reports in clinical practice using surrogate models via example of the trigeminocardiac reflex
Nora Sandu,Tumul Chowdhury,Bernhard J. Schaller
Journal of Medical Case Reports. 2016; 10(1)
[Pubmed] | [DOI]
30 Trigeminocardiac reflex and haemodynamic changes during Le Fort I osteotomy
M.T. Kiani,G. Tajik,M. Ajami,H. Fazli,M.J. Kharazifard,A. Mesgarzadeh
International Journal of Oral and Maxillofacial Surgery. 2016;
[Pubmed] | [DOI]
31 Herpes zoster infection and cardiac arrest
Nader Wansa,Joseph Shaffu,Mounir Khoury,Luc De Roy,Salah Chouairi
Heart & Lung: The Journal of Acute and Critical Care. 2015; 44(2): 170
[Pubmed] | [DOI]
32 Trigeminocardiac Reflex
Tumul Chowdhury,David Mendelowith,Eugene Golanov,Toma Spiriev,Belachew Arasho,Nora Sandu,Pooyan Sadr-Eshkevari,Cyrill Meuwly,Bernhard Schaller
Journal of Neurosurgical Anesthesiology. 2015; 27(2): 136
[Pubmed] | [DOI]
33 Trigeminocardiac reflex during cerebellopontine angle surgery: anatomical location as a new risk factor
Nora Sandu,Tumul Chowdhury,Pooyan Sadr-Eshkevari,Andreas Filis,Belachew Arasho,Toma Spiriev,Bernhard Schaller
Future Neurology. 2015; 10(1): 7
[Pubmed] | [DOI]
34 Trigeminal Cardiac Reflex
C. Meuwly,E. Golanov,T. Chowdhury,P. Erne,B. Schaller
Medicine. 2015; 94(5): e484
[Pubmed] | [DOI]
35 Anesthetic Influence on Occurrence and Treatment of the Trigemino-Cardiac Reflex
Cyrill Meuwly,Tumul Chowdhury,Nora Sandu,Martin Reck,Paul Erne,Bernhard Schaller
Medicine. 2015; 94(18): e807
[Pubmed] | [DOI]
36 Functional Outcome Changes in Surgery for Pituitary Adenomas After Intraoperative Occurrence of the Trigeminocardiac Reflex
T. Chowdhury,C. Nöthen,A. Filis,N. Sandu,M. Buchfelder,Bernhard Schaller
Medicine. 2015; 94(37): e1463
[Pubmed] | [DOI]
37 Trigeminocardiac reflex: current trends
Tumul Chowdhury,Nora Sandu,Pooyan Sadr-Eshkevari,Cyrill Meuwly,Bernhard Schaller
Expert Review of Cardiovascular Therapy. 2014; 12(1): 9
[Pubmed] | [DOI]
38 Trigeminocardiac reflex: differential behavior and risk factors in the course of the trigeminal nerve
Tumul Chowdhury,Nora Sandu,Cyrill Meuwly,Ronald B Cappellani,Bernhard Schaller
Future Neurology. 2014; 9(1): 41
[Pubmed] | [DOI]
39 Slowdown during Parotidectomy
Ankush Gupta,Cecil Thankachan Thomas,Pranay Gaikwad
Otolaryngology-Head and Neck Surgery. 2013; 149(2): 345
[Pubmed] | [DOI]
40 Isolated Bradycardia Due to Skull Pin Fixation
Rudrashish Haldar,Prakhar Gyanesh,Guruprasad Bettaswamy
Journal of Neurosurgical Anesthesiology. 2013; : 1
[Pubmed] | [DOI]
41 Topical lidocaine to suppress trigemino-cardiac reflex
C. Meuwly,T. Chowdhury,B. Schaller
British Journal of Anaesthesia. 2013; 111(2): 302
[Pubmed] | [DOI]
42 Trigeminocardiac Reflex: A Reappraisal with Relevance to Maxillofacial Surgery
Darpan Bhargava,Shaji Thomas,Nupur Chakravorty,Ashutosh Dutt
Journal of Maxillofacial and Oral Surgery. 2013;
[Pubmed] | [DOI]
43 In reply
Haldar, R. and Gyanesh, P. and Bettaswamy, G.
Journal of Neurosurgical Anesthesiology. 2013; 25(2): 207-208
44 Two cases of trigeminocardiac reflex during sagittal split ramus osteotomy
Kumasaka, A. and Miura, Y.
Journal of Japanese Dental Society of Anesthesiology. 2013; 41(1): 47-48
45 Therapeutic approach to chordoid glioma of the third ventricle
Kobayashi, T. and Tsugawa, T. and Hashizume, C. and Arita, N. and Hatano, H. and Iwami, K. and Nakazato, Y. and Mori, Y.
Neurologia Medico-Chirurgica. 2013; 53(4): 249-255
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46 Chordoid glioma of the third ventricle: Four cases including one case with papillary features
Ni, H.-C. and Piao, Y.-S. and Lu, D.-H. and Fu, Y.-J. and Ma, X.-L. and Zhang, X.-J.
Neuropathology. 2013; 33(2): 134-139
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47 CD99 is expressed in chordoid glioma and suggests ependymal origin
Romero-Rojas, A.E. and Díaz-Pérez, J.A. and Ariza-Serrano, L.M.
Virchows Archiv. 2012; 460(1): 119-122
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48 Comparison of the effects of atropine and labetalol on trigeminocardiac reflex-induced hemodynamic alterations during percutaneous microballoon compression of the trigeminal ganglion
Chen, C.-Y. and Luo, C.-F. and Hsu, Y.-C. and Chen, J.-F. and Day, Y.-J.
Acta Anaesthesiologica Taiwanica. 2012; 50(4): 153-158
49 Oculocardiac reflex induced by an orbital floor fracture: Report of a case and review of the literature
Kim, B.B. and Qaqish, C. and Frangos, J. and Caccamese Jr., J.F.
Journal of Oral and Maxillofacial Surgery. 2012; 70(11): 2614-2619
50 A case of trigeminocardiac reflex in the pterional approach
Kitabayashi, M. and Nakamura, K. and Murata, T.
Neurological Surgery. 2012; 40(10): 903-907
51 Bradycardia and hypotension during laryngoscopy for intubation in maxillofacial trauma
Srivastava, V. and Agrawal, S. and Kumar, R. and Misra, P.
Saudi Journal of Anaesthesia. 2012; 6(4): 436-437
52 Preliminary experience with the percutaneous embolization of juvenile angiofibromas using only ethylene-vinyl alcohol copolymer (Onyx) for preoperative devascularization prior to surgical resection
Gemmete, J.J. and Patel, S. and Pandey, A.S. and Sullivan, S.E. and McKean, E.L. and Marentette, L.J. and Chaudhary, N.
American Journal of Neuroradiology. 2012; 33(9): 1669-1675
53 Comparison of the effects of atropine and labetalol on trigeminocardiac reflex-induced hemodynamic alterations during percutaneous microballoon compression of the trigeminal ganglion
Chun-Yu Chen,Chiao-Fen Luo,Yi-Chun Hsu,Jyi-Feng Chen,Yuan-Ji Day
Acta Anaesthesiologica Taiwanica. 2012; 50(4): 153
[Pubmed] | [DOI]
54 Preliminary Experience with the Percutaneous Embolization of Juvenile Angiofibromas Using Only Ethylene-Vinyl Alcohol Copolymer (Onyx) for Preoperative Devascularization Prior to Surgical Resection
J. J. Gemmete,S. Patel,A. S. Pandey,S. E. Sullivan,E. L. McKean,L. J. Marentette,N. Chaudhary
American Journal of Neuroradiology. 2012; 33(9): 1669
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55 The Trigeminocardiac Reflex and Dermatologic Surgery
William D. Holmes, Justin J. Finch, Daniel Snell, S. Brett Sloan
Dermatologic Surgery. 2011; : n/a
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56 Trigeminocardiac reflex during the percutaneous injection of ethylene vinyl alcohol copolymer (Onyx) into a juvenile nasopharyngeal angiofibroma: A report of two cases
Potti, T.A. and Gemmete, J.J. and Pandey, A.S. and Chaudhary, N.
Journal of NeuroInterventional Surgery. 2011; 3(3): 263-265
57 Chordoid glioma of the third ventricle: A case report with review of literature
Vij, M. and Jaiswal, S. and Jaiswal, A. and Jain, M. and Behari, S.
Neurology India. 2011; 59(3): 469-471
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58 Chordoid glioma: A case report and literature review
Liu, W.-P. and Cheng, J.-X. and Yi, X.-C. and Zhen, H.-N. and Fei, Z. and Li, Q. and Zhang, X.
Neurologist. 2011; 17(1): 52-56
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59 Trigeminocardiac Reflex, Bilateral Sagittal Split Ramus Osteotomy, Gow-Gates Block: A Randomized Controlled Clinical Trial
Behnam Bohluli, Bernhard J. Schaller, Reza Khorshidi-Khiavi, Mohsen Dalband, Pooyan Sadr-Eshkevari, Peter Maurer
Journal of Oral and Maxillofacial Surgery. 2011;
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60 Is Prevention or Knowledge Better Than a Cure for the Trigeminal Cardiac Reflex?
Gyaninder Pal Singh, Hemanshu Prabhakar, Zulfiqar Ali
Journal of Oral and Maxillofacial Surgery. 2010; 68(8): 2035
[VIEW] | [DOI]
61 Chordoid glioma: A case report of unusual location and neuroradiological characteristics
Kim, J.W. and Kim, J.H. and Choe, G. and Kim, C.
Journal of Korean Neurosurgical Society. 2010; 48(1): 62-65
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62 Chordoid glioma: Ten years of a low-grade tumor with high morbidity
DeSouza, R.-M. and Bodi, I. and Thomas, N. and Marsh, H. and Crocker, M.
Skull Base. 2010; 20(2): 125-138
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63 Editorial: The trigemino-cardiac reflex in adults: Own experience
Cornelius, J.F. and Sadr-Eshkevari, P. and Arasho, B.D. and Sandu, N. and Spiriev, T. and Lemaitre, F. and Schaller, B.
Expert Review of Cardiovascular Therapy. 2010; 8(7): 895-898
64 Cerebral hemodynamic changes during the trigeminocardiac reflex: Description of a new animal model protocol
Sandu, N., Cornelius, J., Filis, A., Nöthen, C., Rasper, J., Kulinsky, V.I., Schaller, B.J.
TheScientificWorldJournal. 2010; 10: 1416-1423
65 The trigemino-cardiac reflex in adults: own experience
Jan F Cornelius,Pooyan Sadr-Eshkevari,Belachew D Arasho,Nora Sandu,Toma Spiriev,Frederic Lemaitre,Bernhard Schaller
Expert Review of Cardiovascular Therapy. 2010; 8(7): 895
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66 Chordoid glioma with calcification and neurofilament expression: case report and review of the literature (Iwami et al. Surg Neurol 2008;10.1016/j.surneu.2007.07.032)
Kim, C.H.
Surgical Neurology. 2009; 72(5): 554-555
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67 Radiologic features of the chordoid glioma: A report of three cases
Jia, C.-H. and Lu, G.-M. and Zhu, Z.-M. and Xu, Y. and Bai, Z.-J. and Huang, Q.-L. and Zhang, Z.-J. and Zhang, F.
Chinese Journal of Radiology. 2009; 43(11): 1139-1141
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68 Chordoid glioma: A case report and molecular characterization of five cases
Horbinski, C. and Dacic, S. and McLendon, R.E. and Cieply, K. and Datto, M. and Brat, D.J. and Chu, C.T.
Brain Pathology. 2009; 19(3): 439-448
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69 Chordoid glioma of the third ventricle: Case report and literature review [Glioma cordoide del III ventrículo: Descripción de un nuevo caso y revisión de la literatura]
Ferri-íguez, B. and Amparo Torroba-Carón, M. and Sola-Pérez, J. and Piqueras-Pérez, C.
Revista Espanola de Patologia. 2009; 42(3): 214-220
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70 Chordoid glioma of the third ventricle attached to the optic chiasm. Successful removal through a trans-lamina terminalis approach
Carrasco, R. and Pascual, J.M. and Reina, T. and Nieto, S. and Linera, J. and Sola, R.G.
Clinical Neurology and Neurosurgery. 2008; 110(8): 828-833
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71 Chordoid glioma of the third ventricle
Vanhauwaert, D.J. and Clement, F. and Van Dorpe, J. and Deruytter, M.J.
Acta Neurochirurgica. 2008; 150(11): 1183-1191
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