Abstract
Background
Atrial tachycardia (AT) can be treated by medical or electrical cardioversion but the recurrence rate is high. Three‐dimensional electro‐anatomical mapping, recently described in horses, might be used to map AT to identify a focal source or reentry mechanism and to guide treatment by radiofrequency ablation.
Objectives
To describe the feasibility of 3D electro‐anatomical mapping and radiofrequency catheter ablation to characterize and treat sustained AT in horses.
Animals
Nine horses with sustained AT.
Methods
Records from horses with sustained AT referred for radiofrequency ablation at Ghent University were reviewed.
Results
The AT was drug resistant in 4 out of 9 horses. In 8 out of 9 horses, AT originated from a localized macro‐reentrant circuit (n = 5) or a focal source (n = 3) located at the transition between the right atrium and the caudal vena cava. In these 8 horses, local radiofrequency catheter ablation resulted in the termination of AT. At follow‐up, 6 out of 8 horses remained free of recurrence.
Conclusions and Clinical Importance
Differentiation between focal and macro‐reentrant AT in horses is possible using 3D electro‐anatomical mapping. In this study, the source of right atrial AT in horses was safely treated by radiofrequency catheter ablation.
Keywords: arrhythmia, atrial flutter, electrophysiology, focal atrial tachycardia, supraventricular tachyarrhythmia
Abbreviations
- AF
atrial fibrillation
- AT
atrial tachycardia
- EAM
electro‐anatomical mapping
- RA
right atrium
- RFCA
radiofrequency catheter ablation
- SR
sinus rhythm
- TVEC
transvenous electrical cardioversion
1. INTRODUCTION
Atrial tachycardia (AT), a subtype of supraventricular tachycardia, is occasionally found in horses. In general, AT refers to any rapid atrial rhythm with identifiable P′ waves on the surface electrocardiogram (ECG). 1 The underlying mechanisms are still poorly understood. 2 , 3 , 4 Differentiation between a macro‐reentrant circuit (eg, atrial flutter) and a focal source is based upon characteristics of the surface ECG but remains challenging. 5 , 6 , 7 In human medicine, invasive electrophysiological studies, such as endocardial mapping, are often required to identify the underlying AT mechanism. 5 , 8
The technique of 3D electro‐anatomical mapping (EAM) combines the recording of electrical activity from multielectrode, intracardiac catheters with a location tracking system that automatically determines the 3D position of the catheter in the heart. This 3D tracking of the catheter is based upon impedance sensing or on a magnetic sensor in the catheter in combination with an external magnetic field generator. By comparing the timing of multiple intracardiac depolarizations with a reference electrogram, the activation pattern underlying the AT (macro‐reentrant circuit or focus) can be identified. 9 3D mapping strategies are poorly developed in horses, mostly because the large thorax hampered the fluoroscopic positioning of catheters. However, recently 3D EAM of the right atrium 10 and entire heart 11 have been validated in horses to describe the electrical activation pattern during sinus rhythm.
In human medicine, 3D EAM is used to guide radiofrequency catheter ablation (RFCA) of drug‐resistant arrhythmias. More specifically, catheter ablation markedly reduces the recurrence rate of AT compared to pharmacological treatment. 12 In the present paper, we describe the first‐in‐horse experience with 3D EAM and catheter ablation of sustained AT. Until now, sustained AT in horses has been treated with medication (quinidine sulfate) or transvenous electrical cardioversion albeit with a high likelihood of recurrence. 2 , 13
2. METHODS
Medical records of 9 horses with sustained AT that were examined with 3D EAM for treatment by RFCA at Ghent University were reviewed. Case 6 underwent 3 ablations (referred to as cases 6, 6′, and 6″). Signalment, history, base‐apex, and 12‐lead ECG, and standard echocardiographic data were recorded. 14 , 15 , 16 Follow‐up was done by a telephone discussion with the owners or veterinarians. This included asking if the horse had returned to work after treatment and if the rhythm was regular on the last full clinical exam by the veterinarian.
3. MAPPING AND ABLATION PROCEDURE
The 3D EAM of the right atrium (RA) and venae cavae was performed under general anesthesia, as described using the Rhythmia mapping system (Boston Scientific, Machelen, Belgium). 17 In brief, a decapolar steerable catheter (Dynamic XT, Boston Scientific, Machelen, Belgium) was inserted through the jugular vein and placed in the coronary sinus in the standing horse under echocardiographic guidance. The electrograms from this catheter served as timing reference for the atrial activation during the EAM. Before induction of anesthesia, sodium penicillin was administered intravenously (20 000 IU/kg, Penicillin 5.000.000IE, KELA pharma, Hoogstraten, Belgium). After induction of anesthesia, during positioning on the table, the grounding patch of the RF ablation generator was placed under the left shoulder after shaving and degreasing the skin with alcohol. In the first 3 cases, the procedure was performed in dorsal recumbency and the magnetic field generator was fixated with tension straps at the left side of the thorax. From case 4 onward, mapping was performed with the horse in left lateral recumbency as it allowed easier fixation of the magnetic field generator upon the right thorax. The grounding patch of the RF ablation generator was placed under the left triceps muscle. From case 6′ on (because of left triceps myositis seen in cases 5 and 6) we opted for 2 in‐parallel grounding patches on the right dorsal thorax with the horse positioned in right lateral recumbency with the magnetic field generator placed in a 15‐cm thick wooden casing underneath the horse. Because of problems with tracking in cases 7 and 8 (compatible with magnetic interference from the metal from the surgery table), from case 9 onwards we used a 40‐cm high wooden construction between the magnetic field generator and the surgery table (Figure S1, Supporting Information).
The mapping catheter (Intellamap Orion, Boston Scientific, Machelen, Belgium) was inserted through the jugular vein and a 3D EAM was made of the RA as described. 17 The location and mechanism of the AT were determined by analysis of the activation pattern. Macro‐reentry was defined as activation recorded over the entire AT cycle length circling around an anatomic or functional line of block (large or localized) usually characterized by a passage of slow conduction consistent with an “isthmus” which was visually identified on the map. The direction of the reentry, clockwise or counterclockwise, was described from an outside view. Focal AT was defined as atrial activity originating from a discrete site activating the surrounding tissue centrifugally (not necessarily recorded over the entire AT cycle length). 12 , 18
After mapping, a 7.5 F irrigated, deflectable ablation catheter (Intellanav OI, Boston Scientific, Machelen, Belgium) was inserted into the RA. Depending on the mechanism, the target for ablation was either the isthmus or source. Radiofrequency energy was delivered in power‐ or temperature‐controlled mode (Stockert 70 generator, Biosense Webster, Machelen, Belgium) for 60 s with a target power of 30 to 40 W and an irrigation rate of 30 mL/min. The procedure was continued until the AT was terminated. In some horses, an extrastimulus pacing protocol was used to try to reintroduce the AT in order to confirm a successful ablation. This was not done by default because the pacing protocol could potentially induce AF. If required, the horse was converted to SR by transvenous electrical cardioversion (TVEC). 19
After conversion to SR, all catheters were removed and the horse was allowed to recover. No anti‐inflammatory drugs were administered.
4. RESULTS
4.1. Clinical characteristics and medical history of the 9 horses
Nine horses (2 mares, 6 geldings, and 1 stallion; 8 warmbloods and 1 trotter) underwent mapping of sustained AT between March 2018 and February 2020.
Most of the horses had previous treatment for AT or atrial fibrillation (AF) with medication or TVEC. Case 1 had been treated in our clinic for AT by transvenous electrical cardioversion (TVEC) but had AF 1 day later. The horse underwent a second TVEC. After 72 h of sinus rhythm, AF recurred, which was treated with quinidine sulfate to restore sinus rhythm. AT recurred after 3 months. Case 2 was referred because treatment with quinidine sulfate failed to restore SR. Cases 3 and 4 had been treated at our department for sustained AT with TVEC but both had recurrence after 3 and 30 days, respectively. Case 5 was referred because quinidine sulfate treatment had changed AF to sustained AT but failed to restore SR. Cases 6 to 8 were referred to our clinic for AT and were treated with ablation. Case 9 had been treated in our clinic for AT by transvenous electrical cardioversion (TVEC). Four years after the first treatment AF recurred which was treated by TVEC. One year after the last treatment, the horse had recurrence of AT and presented occasional signs of staggering and weakness, which seemed to be associated with stress. The horse was referred to our clinic.
Details about the horses and electrocardiographic and echocardiographic findings are summarized in Table 1. On auscultation, an irregular rhythm was noted in all cases although periods with a regular rhythm were also identified. A left‐sided systolic murmur was noted in case 1 (grade 1/6) and case 7 (grade 2/6). The atrial rate was averaged over 10 P′‐P′ intervals on the base‐apex surface ECG. The P′ waves had a bifid positive morphology in cases 1, 3, and 4, and a trifid positive morphology in all other cases (Figure 1). In cases 1, 2, 4, 5, 6, and 9 an iso‐electric line between the different P′ waves was identified on all leads of the 12‐lead ECG, suggestive for focal AT. 1
TABLE 1.
Case | 1 | 2 | 3 | 4 | 5 | 6 | 6′ | 6″ | 7 | 8 | 9 |
---|---|---|---|---|---|---|---|---|---|---|---|
Sex | Stallion | Gelding | Mare | Gelding | Gelding | Gelding | Gelding | Gelding | Gelding | Mare | Gelding |
Age (years) | 4 | 8 | 7 | 9 | 3 | 10 | 11 | 11 | 12 | 3 | 12 |
Bodyweight (kg) | 520 | 585 | 670 | 560 | 517 | 560 | 550 | 560 | 675 | 489 | 515 |
Height at withers (cm) | 167 | 167 | 175 | 167 | 165 | 170 | 170 | 170 | 172 | 162 | 175 |
Iso‐electric 12‐lead ECG | Yes | Yes | No | Yes | Yes | Yes | Yes | Yes | No | No | Yes |
Atrial rate (dpm) | |||||||||||
Base‐apex ECG (standing) | 217 | 160 | 213 | 200 | 200 | 165 | 129 | 135 | 219 | 201 | 162 |
CS electrogram (anesthesia) | 146 | 169 | 192 | 207 | 176 | 166 | 132 | 125 | 194 | 160 | 134 |
Variation in atrial rate (%) | 49 | 5 | 11 | 3 | 14 | 1 | 2 | 8 | 13 | 26 | 21 |
Echocardiography | |||||||||||
R‐LAAd4C (cm2) (36‐75) 47 | 70.7 | 74.9 | 68.1 | 74.4 | 56.7 | 62.7 | 68.3 | 70.3 | 82.2+ | 72.3 | 71.7 |
R‐LAAs4C (cm2) (62‐116) 47 | 92.8 | 98.3 | 101.6 | 99.7 | 71.4 | 81.6 | 81.3 | 81.3 | 95.5 | 94.0 | 99.5 |
R‐LA/AoSAX (1.05‐1.29) 48 | 1.24 | 1.31+ | 1.29 | 1.17 | 1.19 | 1.20 | 1.14 | 1.35+ | 1.18 | 1.26 | |
Color flow doppler 16 | |||||||||||
Mitral valve regurgitation | Trivial | Mild | Mild | Mild | Mild | Mild | Trivial | ||||
Aortic valve regurgitation | Trivial | Mild | |||||||||
Pulmonary valve regurgitation | Trivial | Trivial | |||||||||
Tricuspid valve regurgitation | Trivial | Mild |
Note: Variation in rate is the difference between the atrial rate when admitted to the hospital and the atrial rate during anesthesia. Echocardiographic measurements were made in sinus rhythm, 5 days after the ablation procedure.
Abbreviations: dpm, depolarizations per minute; iso‐electric, no deflections are visible between subsequent P waves on the surface ECG; R‐LAAd4C, end‐diastolic left atrial area from a right parasternal 4‐chamber view; R‐LAAs4C, end‐systolic left atrial area from a right parasternal 4‐chamber view; R‐LA/AoSAX, the ratio of the left atrium and aortic diameter measured from a right parasternal short‐axis view; 6′, 6″ characteristics of horse 6 during the second and third ablation procedure respectively; values between brackets, reference values; +, above reference values.
4.2. Mapping and ablation of sustained AT: Case description
In 8 out of 9 cases the AT originated in the caudal right atrium. Catheter ablation of the isthmus or source resulted in SR in all 8 cases (100%). Details of mapping and ablation data and follow‐up are given in Table 2. In the first 4 cases it was not possible to identify bipolar low voltage (<0.3 mV, mapping system default value) areas because of excessive noise on the catheter electrograms (technical error).
Case 1: The activation map of the RA was compatible with a focal source at the transition of the caudomedial right atrium to the caudal vena cava with a cycle length of 410 ms (Figure 2). Because the catheter could not be irrigated (technical error) we opted for temperature‐controlled ablation targeting 60 W with a temperature limit at 60°C (for 40 s). During the 5th application AT terminated with ensuing sinus rhythm. After termination 4 additional RF energy applications were given at 60 W. No AT could be induced by burst pacing (at a basic cycle length of 390 ms) followed by an extra stimulus at 300 ms. Recovery was uneventful and the horse remained free of AT/AF 42 months after the procedure.
Case 2: In the standing horse, AT was induced by burst pacing with an extra stimulus (S1‐S1 = 370 ms, S2 = 350 ms) on the decapolar CS catheter (Biosense Webster CS, Biosense Webster, Machelen, Belgium). Mapping under general anesthesia revealed a clockwise macro‐reentrant circuit confined to the transition between the medial region of the caudal RA and caudal vena cava with a cycle length of 355 ms (Figure 3). The dorsoventral line of block (12 mm) with doubled potentials was located 69 mm caudal to the intervenous tubercle. The first power‐controlled RF application (target 50 W, 20 s) at the isthmus of the macro‐reentrant circuit resulted in sinus rhythm. The extrastimulus pacing protocol no longer induced AT. Three years later the horse remained free of AT/AF.
Case 3: Sustained AT originated from the caudo‐dorsal right atrium at the transition with the caudal vena cava and was thought to be a focal source. After six 60 s applications (power‐controlled 30 W), the AT cycle length increased from 313 to 407 ms but AT did not terminate. A detailed remap revealed a counterclockwise, localized macro‐reentry with the isthmus at the dorsolateral aspect of the caudal RA with an area of block (5.4 cm2), 50 mm caudal of the intervenous tubercle. After another 6 RFCA applications (35 W, 60 s) AT terminated, and sinus rhythm was maintained. At 7 months after the procedure, the horse experienced recurrence of AT.
Case 4: After insertion of the decapolar coronary sinus catheter in the standing horse, the activation pattern from the coronary sinus catheter was from distal to proximal, which was opposite compared to cases 1 to 3, indicating a different left atrial activation. The procedure was continued. Mapping of the RA initially suggested a focal source from the dorsal interatrial septum with a cycle length of 289 ms. Ablation was attempted but AT could not be terminated. Failure to terminate the arrhythmia in combination with the different left atrial activation suggested a left atrial source with breakthrough via the interatrial septum. TVEC catheters were positioned as described. 20 A 150 J shock converted AT to SR. Recovery was uneventful, but the horse experienced AT recurrence after 13 months.
Case 5: Mapping revealed a clockwise macro‐reentrant circuit with a cycle length of 340 ms confined to the caudomedial RA near the transition to the caudal vena cava. A ventral and dorsal isthmus (Video S1) with a central low voltage area (7.5 cm2), 22 mm caudal to the intervenous tubercle, were observed. To ensure stable contact, a 92‐cm deflectable sheath (Zurpaz, Boston Scientific, Machelen, Belgium) was used to support the positioning of the ablation catheter. The first RFCA application at the isthmus (power‐controlled 35 W, 42 s) resulted in sinus rhythm after which the procedure was terminated. The horse remained free of AT/AF 17 months after the procedure.
Case 6: Mapping of the AT with a cycle length of 361 ms revealed stable counterclockwise reentry localized in the caudodorsal RA with a narrow, fast conducting area dorsally and slow conducting area ventrally (Figure 3). A line of block (50 mm) was present 75 mm caudal to the intervenous tubercle. The reentry also involved a low voltage area of 23 cm2, starting 41 mm caudal to the intervenous tubercle. During the 4th RF energy application (35 W, 60 s) at the dorsal isthmus sinus rhythm was restored. Because of recurrence of AT with a similar ECG morphology but slower atrial rate (AT cycle length of 447 ms) 8 months after the procedure, the patient was referred for repeat ablation (case 6′). Again, mapping was compatible with reentry at the transition from the right atrium to caudal vena cava, now in a clockwise direction and with a slow conducting area dorsally and ventrally. The dorsal slow conduction area, located at the previous ablation site, now showed double potentials, which had not been observed during the first ablation procedure. The ventral slow conducting area was targeted for irrigated RFCA since this area was narrower. Irrigated ablation restored SR during the second cycle of 60 s at 35 W. Because restoration of SR resulted in a slight change in cardiac position, an additional ablation point could not be added. One month after the second ablation procedure the horse experienced another recurrence of sustained AT (case 6″), with similar 12‐lead ECG characteristics and an even longer cycle length (478 ms) compared to the previous procedures. RA mapping revealed clockwise reentry with double potentials and neighboring fractionated potentials indicating slow conduction at the dorsal area. Power‐controlled ablation at the fractionated electrograms, now with higher power up to 45 W, resulted in SR after 4 s. To avoid catheter instability upon SR restoration, rapid atrial pacing at a cycle length of 480 ms was immediately started. To create a complete line of block, point‐by‐point ablation was performed from the area of double potentials (area of block because of prior ablation) caudally towards the nonconducting region of the caudal vena cava. An extrastimulus pacing protocol was performed to verify AT inducibility but resulted in AF. TVEC catheters were positioned and a single 150 J shock restored SR. After the last procedure, the horse remained free of AT 1 year after the last treatment.
Case 7: Mapping revealed a clockwise macro‐reentrant AT with a cycle length of 309 ms located near the transition of the caudomedial RA to the caudal vena cava. A mediodorsal and medioventral low voltage area (12.2 and 2.8 cm2, respectively) were found 42 and 76 mm caudal to the intervenous tubercle, with the isthmus of the reentry in between. Mapping took 62 minutes because the tracking of the mapping catheter was disrupted in different areas of the heart. During the first RFCA application (30 W, 40 s) AT terminated. At the time of conversion, a small change in cardiac position was noticed. As a result, during a second ablation cycle of 60 s at the same location, the ablation catheter tip appeared outside the electro‐anatomical map, indicating that the 3D anatomical position had slightly changed. No further ablation attempts were made and the horse recovered uneventfully with no recurrences at follow‐up 11 months after the procedure.
Case 8: Mapping revealed a focal source with a cycle length of 375 ms near the transition of the caudodorsal RA to the caudal vena cava (Video S2). However, no clear delineation could be made of the area of the first activation, partially because the tracking of the mapping catheter was again disrupted in different areas of the heart. Ablation with 35 W was performed at the assumed area of earliest activation. After 10 ablation cycles of 60 s, the AT cycle length remained unaltered. A remap was performed in 20 minutes. The remap revealed that during the first mapping, the catheter had not always been in contact with the endocardium at the site of earliest activation. The second map revealed a clear focal source of the AT caudomedial of the initially suspected region. This focal source was targeted with the ablation catheter and SR could be restored after 19 s of ablation at 35 W. At 6 months after the ablation, the horse experienced recurrence of AT. The owners chose not to treat the horse again.
Case 9: Mapping in case 9 showed a counterclockwise macro‐reentrant AT mechanism with a cycle length of 447 ms confined to the caudomedial RA near the transition to the caudal vena cava. The reentry was located around a low voltage area (12.5 cm2), 57 mm caudal to the intervenous tubercle. A line of block (45 mm) was present 86 mm caudal to the intervenous tubercle. Irrigated RFCA with 35 W at the dorsal isthmus could restore SR after 4 cycles of 60 s. Atrial pacing at the tachycardia cycle length was started after conversion to SR to avoid changes in atrial morphology. Seven additional locations were ablated in cycles of 60 s to ensure proper closure of the dorsal isthmus. As the horse developed an episode of AF during the extrastimulus pacing protocol, TVEC catheters were positioned and a single 150 J shock restored SR. The horse remained free of recurrence of AT and AF.
TABLE 2.
Case | 1 | 2 | 3 | 4 | 5 | 6 | 6° | 6°° | 7 | 8 | 9 |
---|---|---|---|---|---|---|---|---|---|---|---|
Mapping duration (min) | 43 | 25 | 53 | 42 | 33 | 47 | 34 | 27 | 62 | 52 | 40 |
Procedure duration (min) | 225 | 225 | 260 | 250 | 210 | 195 | 165 | 220 | 150 | 230 | 315 |
Focal (F) or reentry (R) AT | F | R | F + R | R | R | R | R | R | F | R | |
Length of reentry circuit (mm) | 33 | 140 | 66 | 81 | 40 | 43 | 128 | 76 | |||
Direction of reentry circuit | CW | CCW | CW | CCW | CW | CW | CW | CW | |||
Location | M | M | DM | LA | D | M | D | M | D | M | M |
Distance to IVT (mm) | 65 | 70 | 65 | 63 | 73 | 73 | 78 | 78 | 62 | 68 | |
Ablation | |||||||||||
Total duration (s) | 366 | 30 | 380 | 280 | 42 | 240 | 104 | 360 | 79 | 575 | 552 |
Number of applications | 6 | 1 | 6 | 8 | 1 | 4 | 2 | 6 | 2 | 11 | 9 |
Power (W) | 60 | 50 | 30 | 35 | 35 | 35 | 35 | 45 | 30 | 35 | 35 |
Max temperature (°C) | 60 | 48 | 28 | 24 | 22 | 27 | 27 | 48 | 28 | 31 | |
Irrigated | No | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
SR restoration | Yes | Yes | Yes | No | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Time of follow‐up (months) | 42 | 30 | 7 | 13 | 17 | 8 | 1 | 12 | 11 | 6 | 12 |
Recurrence | No | No | Yes | Yes | No | Yes | Yes | No | No | Yes | No |
Note: The direction of the macro‐reentrant circuit is described as seen from a left lateral view. As an anatomical marker, the distance to the intervenous tubercle (IVT) was measured on the electro‐anatomical map as the shortest distance between the arrhythmia focus/circuit and the IVT. The ablation duration is the total duration of the application of radiofrequency energy, in 4 cases sinus rhythm (SR) was restored before the end of the application. All arrhythmia origins, focal sources as well as localized reentry, were situated at the caudal right atrium adjacent to the caudal vena cava, with exception for case 4. The maximal temperature of the catheter tip was not registered by the recording system in case 3. Case 3 initially showed a focal AT, but after successful ablation of the focal source of the AT a macro‐reentrant AT mechanism was found with a different cycle length.
Abbreviations: AT, atrial tachycardia; (C)CW, (Counter)clockwise direction of the reentry wave; D, dorsocaudal RA; DM, dorsomedial caudal right atrium; IVT, intervenous tubercle; LA, suspected left atrial origin; M, caudomedial right atrium.
4.3. Complications
Case 4: After recovery the horse showed a transient left facial nerve paralysis which resolved after 3 days of treatment with 5 g of thiamine orally once a day and local application of prednisolone ointment (Ekyflogyl, Audevard, Clichy, France) 4 times a day. Oral treatment with 10 mg/kg phenytoin (Diphantoine, KELA pharma, Hoogstraten, Belgium) twice a day was administered for 6 weeks.
Case 5: At the time of recovery, the horse had a myopathy of the left triceps muscle at the height of the grounding patch of the ablation generator. The horse was treated with prednisolone (1 mg/kg i.v., Solu‐Delta‐Cortef, Zoetis, Zaventem, Belgium) followed by flunixin administration (1.1 mg/kg p.o., Finadyne, Intervet International, Brussels, Belgium) on the second day. The triceps muscle was locally treated with a prednisolone ointment every 6 hours and with daily physiotherapy. The clinical signs resolved gradually with full return of muscle function 6 days after the procedure.
Case 6: This horse had a left triceps myopathy at the height of the grounding patch after recovery. Clinical signs resolved after 5 days of treatment with local prednisolone ointment 4 times a day, daily physiotherapy, and phenylbutazone (2.2 mg/kg p.o., Butagran Equi, Dopharma, Raamsdonksveer, the Netherlands).
5. DISCUSSION
Atrial tachycardia is characterized by a rapid atrial activation that originates from a rapidly firing focus (focal AT) or a macro‐reentry circuit (macro‐reentry AT). In each situation, a depolarization wave moves over the atrial myocardium resulting in a clear, monomorphic P′ wave on the surface ECG. 21 Atrial fibrillation, on the other hand, consists of a large number of chaotically moving depolarization waves, resulting in F waves on the surface ECG. 22 An important finding in this study was that AT can change into AF. As such, in a horse with AF, it remains unknown whether or not the arrhythmia started with AT. This might, at least in part, contribute to the observed recurrence rates of AF and could lead to new treatment perspectives for AF in future.
RFCA is the recommended treatment for humans with either focal and macro‐reentry AT since this addresses the underlying cause of the arrhythmia thereby reducing the rate of recurrence. 12 In horses, no specific recommendations regarding AT treatment exist but the arrhythmia is treated similar to AF since RFCA was not available. 13 Current treatment options for AT in horses include biphasic TVEC, 2 administration of quinidine sulfate, 7 , 13 overdrive pacing, and administration of amiodarone. 3 , 4 Flecainide has been used for the cardioversion of AT but is potentially lethal and its issue is not advised in humans. 16 , 23 In humans, electrical cardioversion is mainly used when the patient is hemodynamically too unstable to perform an ablation procedure. Hemodynamic instability at rest because of AT, as observed in case 9 is unusual in horses because the AV node usually blocks most impulses from the atria, resulting in a normal heart rate but irregular rhythm. 24
The presence of iso‐electric lines on the surface ECG suggests focal AT in humans and small animals, while saw‐toothed P′ waves are rather associated with macro‐reentrant AT or typical flutter. 9 , 25 However, there is considerable overlap between ECG characteristics of focal and reentry AT as an iso‐electric line can result from conduction slowing. An invasive electrophysiological study is needed for proper diagnosis. 1 12‐lead ECG recording did not allow identification of the underlying mechanism in any of our cases 2. However, the 12‐lead ECG was useful to predict the anatomical site of origin of atrial ectopy. 25 , 26 In human patients, focal AT often has variations in atrial rate while this is less the case in macro‐reentrant AT. 27 If the irregularity exceeds 15% of the cycle length, a focal arrhythmia is likely to be present. In our horses, the variation in atrial rate because of anesthesia exceeded 15% in cases with focal atrial tachycardia while cases with macro‐reentrant AT remained below 15% variation. Theoretically, an exercise test could help to differentiate between focal AT and reentrant AT. In contrast to a macro‐reentrant AT, the heart rate of a focal AT might be overridden during an exercise test. However, because of the high atrial rates, an exercise test would probably have been inconclusive in our horses. 2
Macro reentrant circuits (flutter) in humans and dogs typically cover the entire atrium and have a length of 44 ± 7 mm. 28 The length of the reentrant circuits in the current cases is comparable to the length of macro reentrant circuits in humans, but because of the large atrium this circuit only covered a small area and could therefore be considered as a local macro‐re‐entrant circuit. In the current study 8 out of 9 ATs were located in the RA, all at the transition from caudal RA to caudal vena cava, which contrasts with AT in humans and small animals. The crista terminalis, tricuspid, and mitral valve annulus, and pulmonary veins are the most predominant predilection sites for focal AT in humans. 29 The cavotricuspid isthmus circuit in the RA and the peri‐mitral or roof‐dependent circuit in the LA are responsible for more than 90% of reentries in humans. 27 Atrial arrhythmias originating from the ostium of the coronary sinus are described in humans, but are considered rare. 30 In dogs, focal AT is more likely to occur in the RA, with a predilection for the crista terminalis and triangle of Koch, 31 and reentry has been described at the RA mid septum and free wall but is considered rare. 32 In humans, ectopic beats originating from the inferior (caudal) vena cava have been described, but are considered rare. 33 The superior (cranial) vena cava and ostia of the pulmonary veins are a more likely origin for atrial ectopy because of the arrhythmogenic properties of the irregularly delineated myocardial sleeves in these locations in humans. 34 The inferior vena caval myocardial sleeves are sharply delineated in human patients but, irregularly delineated electrical active tissues present in the caudal vena cava and pulmonary veins of horses. 11 , 35 , 36 The presence of myocardial sleeves in the equine caudal vena cava has been confirmed. 37 Because the medial wall of the caudal vena cava is closely located to the LA, it remains possible that “far field” LA electrical signals are picked up by the mapping system. Retrograde LA mapping via the aorta has been performed in horses 17 and would have allowed better differentiation between a caudal right atrial and left atrial origin by detecting the earliest depolarization. In human medicine, the transseptal puncture technique has been developed to overcome these limitations of the retrograde approach, but this technique has not been described in horses. Therefore mapping and ablation were not continued in case 4. In case 4, the site of earliest activation at the dorsal septum remained stable after ablation. The dorsal intercaval area is also a left‐to‐right atrial breakthrough site in humans, 38 indicating that this was most likely the breakthrough site from the left to the right atrium. The current system did not include contact force or local impedance measurement for ensuring contact with the myocardial wall which was an important limitation and which might have resulted in false low voltage areas because of inadequate contact. Therefore, low voltage areas were not used in the current study for determining the most optimal ablation target.
Conversion to SR during the ablation procedure was achieved in 10/11 procedures, which is in line with ablations of focal/macro‐reentrant AT in human medicine (75%‐100%). 12 In the current study, 2 of the 8 ablated horses had recurrence although the recurrence rate is difficult to compare with human medicine. In humans, the recurrence rate varies depending on the underlying mechanism of the AT. Typical atrial flutter and focal AT usually have a recurrence rate of <10% of ablation, 12 with the second treatment after relapse being curative in most cases. 39 On the other hand, nontypical atrial flutter can have a recurrence rate varying from 12% up to 84% if paroxysmal AF was detected during the period of AT. 39 , 40 , 41 The recurrence rate of the current cases was comparable to that of a previous small study in which AT was treated with TVEC (2/7, 28%). 2 The current numbers should be interpreted with caution because of the number of patients is too small to draw strong conclusions and the application of this technology in horses is still in its infancy. This is illustrated by the different adaptations made throughout the study period. It should also be noted that 2 cases (1 and 3) had undergone a successful TVEC procedure before a relapsed into AT within a short period while they now remained in SR for a long period (42 and 7 months). The 2 remaps of the recurrences of case 6 suggested reconnection of the previous ablation site because of insufficient ablation. Reconnection is also frequently observed in humans but is not necessarily accompanied by recurrence of the arrhythmia. 42 , 43 Lesion quality markers, such as ablation index, have been introduced in human medicine to deliver qualitative ablation lesions and prevent reconnection. 43 Unfortunately contact force‐sensing catheters which are necessary for scoring the ablation lesions were not used in our horses. In addition, since no features were available in both the mapping and ablation catheter to verify atrial wall contact, it was unknown if the 3D electro‐anatomical map was complete and whether or not the ablation catheter actually delivered the energy to the myocardium. This was especially applicable in cases 6 and 8 because of it was difficult to visualize the region of interest because of the interference problems with the electromagnetic field. This was demonstrated in case 8, where a missing part of the 3D electro‐anatomical map led to a failure of the first ablation attempts. Both cases 6 and 8 showed AT recurrence, indicating that the ablation lesion was not adequate, probably because of the tracking issues which were later resolved. Little is known about the optimal (safe) ablation settings in horses. In the current case series, different ablation settings were applied, making comparisons difficult. Delivery of ablation energy is a delicate balance between applying too little (lesion not deep enough) and too much power (perforating the atrial wall). In the first 2 cases, ablation was performed with relatively high power settings (60 and 50 W). After offline analysis of the maps of the first 2 cases we noticed that the ablation targets were very close to the caudal vena cava, which is a thin walled region. To reduce the potential risk of wall perforation, ablation settings were lowered to 35 W in the following horses, comparable to coronary sinus ablation in humans. 40 Because of the high recurrence rate in the cases which were ablated at lower power settings, the last cases (8, 9, and 6″) were again ablated with a higher setting of 45 W, which is more commonly used for ablation of the atria in humans and dogs. 32 , 40 Because of the small number of horses, no recommendations can be made for the power settings in horses. Further in vitro and in vivo studies are necessary to determine the most optimal ablation settings for horses. In most of our cases, the ablation was ended once the rhythm converted to SR, with exception of cases 1 and 6″ (2 cases without recurrence of AT). Postablation conduction over the isthmus in cases with macro‐reentrant AT was not tested and AT inducibility was only verified in a few cases. In addition, a point‐by‐point complete line of block was not created in most cases with macro‐reentrant AT 44 as ablation was usually ended as soon as sinus rhythm restored. Therefore, the arrhythmogenic substrate was probably not sufficiently neutralized, allowing AT and AF to recur. In future, these issues should be addressed.
In the current study, 2 out of 8 cases had signs of triceps myopathy after recovery. Both horses had a single grounding patch of the RF generator located at the triceps muscle. Similar complications have not been reported in human medicine. Usual complications of ablation include vascular complications, hematoma, perforation, and, rarely, skin burns, but not myopathy. 45 , 46 Complications were no longer encountered after adjusting the positioning of the horse and changing the location and increasing the area of the grounding patch. Recently, mapping of the right atrium was performed in the standing horse using impedance tracking to determine catheter position. Impedance tracking uses small, high‐frequency electrical currents between the surface electrodes and catheters for localization of the catheters. 10
6. CONCLUSION
Three‐dimensional EAM of the right atrium under general anesthesia is feasible in horses to differentiate focal from macro‐reentrant AT, and to guide the RFCA without the use of fluoroscopy. The caudal vena cava appears to be an anatomical predilection site for AT in horses. Ablation of both focal and macro‐reentrant AT is feasible in horses. Ongoing technical improvements, use of catheter contact‐force technology and gain of experience will further improve outcome in the future.
CONFLICT OF INTEREST DECLARATION
Authors declare no conflict of interest.
OFF‐LABEL ANTIMICROBIAL DECLARATION
Authors declare no off‐label use of antimicrobials.
INSTITUTIONAL ANIMAL CARE AND USE COMMITTEE (IACUC) OR OTHER APPROVAL DECLARATION
Authors declare no IACUC or other approval was needed.
HUMAN ETHICS APPROVAL DECLARATION
Authors declare human ethics approval was not needed for this study.
Supporting information
ACKNOWLEDGMENT
Funding provided by Bijzonder Onderzoeksfonds, BOF.BAS.2018.0022.01, and Fonds Wetenschappelijk Onderzoek, 1S56217N.
Van Steenkiste G, Boussy T, Duytschaever M, et al. Detection of the origin of atrial tachycardia by 3D electro‐anatomical mapping and treatment by radiofrequency catheter ablation in horses. J Vet Intern Med. 2022;36(4):1481‐1490. doi: 10.1111/jvim.16473
Funding information Bijzonder Onderzoeksfonds, Grant/Award Number: BOF.BAS.2018.0022.01; Fonds Wetenschappelijk Onderzoek, Grant/Award Number: 1S56217N
REFERENCES
- 1. van Loon G. Cardiac arrhythmias in horses. Vet Clin N Am Equine Pract. 2019;35(1):85‐102. [DOI] [PubMed] [Google Scholar]
- 2. van Steenkiste G, de Clercq D, Vera L, Decloedt A, van Loon G. Sustained atrial tachycardia in horses and treatment by transvenous electrical cardioversion. Equine Vet J. 2019;51:634‐640. [DOI] [PubMed] [Google Scholar]
- 3. Whelchel DD, Tennent‐Brown BS, Coleman AE, et al. Treatment of supraventricular tachycardia in a horse. J Vet Emerg Crit Care. 2017;27(3):362‐368. [DOI] [PubMed] [Google Scholar]
- 4. van Loon G, Jordaens L, Muylle E, Nollet G, Sustronck B. Intracardiac overdrive pacing as a treatment of atrial flutter in a horse. Vet Rec. 1998;142:301‐303. [DOI] [PubMed] [Google Scholar]
- 5. Saoudi N, Cosio F, Waldo A, et al. Classification of atrial flutter and regular atrial tachycardia according to electrophysiologic mechanism and anatomic bases: a statement from a Joint Expert Group from the Working Group of Arrhythmias of the European Society of Cardiology and the North American Society of Pacing and Electrophysiology. J Cardiovasc Electrophysiol. 2001;22(14):1162‐1182. [DOI] [PubMed] [Google Scholar]
- 6. van Loon G. Atrial premature complexes and atrial tachycardia. In: Durando M, ed. Clinical Veterinary Advisor. 6th ed. St. Louis, MO: Elsevier; 2012:54‐55. [Google Scholar]
- 7. van Loon G. Atrial flutter. In: Durando M, ed. Clinical Veterinary Advisor: The Horse. 6th ed. St. Louis, MO: Elsevier; 2011:52‐53. [Google Scholar]
- 8. Segal OR, Koa‐Wing M, Jarman J, Peters N, Markides V, Davies DW. Intracardiac mapping. In: Macfarlane PW, van Oosterom A, Pahlm O, Kligfield P, Janse M, Camm J, eds. Comprehensive Electrocardiology. London: Springer; 2011:1165‐1191. [Google Scholar]
- 9. Murgatroyd FD, Krahn AD. In: Krahn FD, Andrew M, eds. Handbook of Cardiac Electrophysiology. London: Remedica; 2003. 320 p. [Google Scholar]
- 10. Hesselkilde E, Linz D, Saljic A, et al. First catheter‐based high‐density endocardial 3D electroanatomical mapping of the right atrium in standing horses. Equine Vet J. 2020;13(10):1095‐1099. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11. van Steenkiste G, Vera L, Decloedt A, Schauvliege S, Boussy T, van Loon G. Endocardial electro‐anatomic mapping in healthy horses: Normal sinus impulse propagation in the left and right atrium and the ventricles. Vet J. 2020;258:105452. [DOI] [PubMed] [Google Scholar]
- 12. Katritsis DG, Boriani G, Cosio FG, et al. European heart rhythm association (EHRA) consensus document on the management of supraventricular arrhythmias, endorsed by Heart Rhythm Society (HRS), Asia‐Pacific Heart Rhythm Society (APHRS), and Sociedad Latinoamericana de Estimulación Cardiaca y Electrofisiologia (SOLAECE). Europace. 2017;19(3):465‐511. [DOI] [PubMed] [Google Scholar]
- 13. Reef VB, Bonagura J, Buhl R, et al. Recommendations for management of equine athletes with cardiovascular abnormalities. J Vet Intern Med. 2014;28(3):749‐761. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14. Hesselkilde EM, Isaksen JL, Petersen BV, et al. A novel approach for obtaining 12‐lead electrocardiograms in horses. J Vet Intern Med. 2021;35(1):521‐531. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15. Verheyen T, Decloedt A, De Clercq D, Deprez P, Sys SU, van Loon G. Electrocardiography in horses – part 1: how to make a good recording. Vlaams Diergeneeskundig Tijdschrift. 2010;79:331‐336. [Google Scholar]
- 16. Vernemmen I, van Steenkiste G, Dufourni A, Decloedt A, Loon G. Transvenous electrical cardioversion of atrial fibrillation in horses: horse and procedural factors correlated with success and recurrence. J Vet Intern Med. 2022;36(2):758‐769. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17. van Steenkiste G, de Clercq D, Boussy T, et al. Three dimensional ultra‐high‐density electro‐anatomical cardiac mapping in horses: methodology. Equine Vet J. 2020;52(5):765‐772. [DOI] [PubMed] [Google Scholar]
- 18. Maury P, Champ‐Rigot L, Rollin A, et al. Comparison between novel and standard high‐density 3D electro‐anatomical mapping systems for ablation of atrial tachycardia. Heart Vessels. 2019;34(5):801‐808. [DOI] [PubMed] [Google Scholar]
- 19. De Clercq D, van Loon G, Schauvliege S, Tavernier R, et al. Transvenous electrical cardioversion of atrial fibrillation in six horses using custom made cardioversion catheters. Vet J. 2008;177(2):198‐204. [DOI] [PubMed] [Google Scholar]
- 20. van Loon G, Van Steenkiste G, Vera L, Decloedt A. Catheter‐based electrical interventions to study, diagnose and treat arrhythmias in horses: from refractory period to electro‐anatomical mapping. Vet J. 2020;263:105519. [DOI] [PubMed] [Google Scholar]
- 21. Brugada J, Katritsis DG, Arbelo E, et al. 2019 ESC guidelines for the management of patients with supraventricular tachycardia. Eur Heart J. 2020;41(5):655‐720. [DOI] [PubMed] [Google Scholar]
- 22. Hindricks G, Potpara T, Dagres N, et al. ESC guidelines for the diagnosis and management of atrial fibrillation developed in collaboration with the European Association of Cardio‐Thoracic Surgery (EACTS): The Task Force for the diagnosis and management of atrial fibrillation of the European Society of Cardiology (ESC) Developed with the special contribution of the European Heart Rhythm Association (EHRA) of the ESC. Eur Heart J. 2020;42:373‐498. [DOI] [PubMed] [Google Scholar]
- 23. Dembek KA, Hurcombe SDA, Schober KE, Toribio RE. Sudden death of a horse with supraventricular tachycardia following oral administration of flecainide acetate. J Vet Emerg Crit Care. 2014;24(6):759‐763. [DOI] [PubMed] [Google Scholar]
- 24. Young LE, van Loon G. Diseases of the heart and vessels. In: Hinchcliff KW, Kaneps AJ, Geor RJ, eds. Equine Sports Medicine and Surgery: Basic and Clinical Sciences of the Equine Athlete. Saunders: Philadelphia PA USA; 2014:695‐743. [Google Scholar]
- 25. Santilli RA, Perego M, Crosara S, et al. Utility of 12‐lead electrocardiogram for differentiating paroxysmal supraventricular tachycardias in dogs. J Vet Intern Med. 2008;22(4):915‐923. [DOI] [PubMed] [Google Scholar]
- 26. Qian ZY, Hou XF, Xu DJ, et al. An algorithm to predict the site of origin of focal atrial tachycardia. Pacing Clin Electrophysiol. 2011;34(4):414‐421. [DOI] [PubMed] [Google Scholar]
- 27. Jaïs P, Matsuo S, Knecht S, et al. A deductive mapping strategy for atrial tachycardia following atrial fibrillation ablation: importance of localized reentry. J Cardiovasc Electrophysiol. 2009;20(5):480‐491. [DOI] [PubMed] [Google Scholar]
- 28. Yokokawa M, Latchamsetty R, Ghanbari H, et al. Characteristics of atrial tachycardia due to small vs large reentrant circuits after ablation of persistent atrial fibrillation. Heart Rhythm. 2013;10(4):469‐476. [DOI] [PubMed] [Google Scholar]
- 29. Teh AW, Kistler PM, Kalman JM. Using the 12‐lead ECG to localize the origin of ventricular and atrial tachycardias: part 1. Focal atrial tachycardia. J Cardiovasc Electrophysiol. 2009;20(6):706‐709. [DOI] [PubMed] [Google Scholar]
- 30. Kistler PM, Roberts‐Thomson KC, Haqqani HM, et al. P‐wave morphology in focal atrial tachycardia. J Am Coll Cardiol. 2006;48(5):1010‐1017. [DOI] [PubMed] [Google Scholar]
- 31. Santilli RA, Perego M, Perini A, Moretti P, Spadacini G. Electrophysiologic characteristics and topographic distribution of focal atrial tachycardias in dogs. Intergovernmental panel on climate change, editor. J Vet Intern Med. 2010;24(3):539‐545. [DOI] [PubMed] [Google Scholar]
- 32. Santilli RA, Ramera L, Perego M, Moretti P, Spadacini G. Radiofrequency catheter ablation of atypical atrial flutter in dogs. J Vet Cardiol. 2014;16(1):9‐17. [DOI] [PubMed] [Google Scholar]
- 33. Mansour M, Ruskin J, Keane D. Initiation of atrial fibrillation by ectopic beats originating from the ostium of the inferior vena cava. J Cardiovasc Electrophysiol. 2002;13(12):1292‐1295. [DOI] [PubMed] [Google Scholar]
- 34. Goya M, Ouyang F, Ernst S, Volkmer M, Antz M, Kuck KH. Electroanatomic mapping and catheter ablation of breakthroughs from the right atrium to the superior vena cava in patients with atrial fibrillation. Circulation. 2002;106(11):1317‐1320. [DOI] [PubMed] [Google Scholar]
- 35. Vandecasteele T, van den Broeck W, Tay H, Couck L, van Loon G, Cornillie P. 3D reconstruction of the porcine and equine pulmonary veins, supplemented with the identification of telocytes in the horse. Anat Histol Embryol. 2018;47(2):145‐152. [DOI] [PubMed] [Google Scholar]
- 36. Linz D, Hesselkilde E, Kutieleh R, Jespersen T, Buhl R, Sanders P. Pulmonary vein firing initiating atrial fibrillation in the horse: oversized dimensions but similar mechanisms. J Cardiovasc Electrophysiol. 2020;31(5):1211‐1212. [DOI] [PubMed] [Google Scholar]
- 37. Ibrahim L, Vanhove C, Descamps B, van Loon G, Cornillie P. Morphology of myocardial sleeves in the caudal vena cava of the horse heart. 33rd EAVA Congress, Ghent University: Ghent Belgium; 2021. [Google Scholar]
- 38. Dong J, Zrenner B, Schreieck J, et al. Catheter ablation of left atrial focal tachycardia guided by electroanatomic mapping and new insights into interatrial electrical conduction. Heart Rhythm. 2005;2(6):578‐591. [DOI] [PubMed] [Google Scholar]
- 39. Cosío FG. Atrial flutter, typical and atypical: a review. Arrhythm Electrophysiol Rev. 2017;6:55‐62. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40. Bai R, Di BL, Mohanty P, et al. Ablation of perimitral flutter following catheter ablation of atrial fibrillation: impact on outcomes from a randomized study (PROPOSE). J Cardiovasc Electrophysiol. 2012;23(2):137‐144. [DOI] [PubMed] [Google Scholar]
- 41. Aktas MK, Khan MN, Di Biase L, et al. Higher rate of recurrent atrial flutter and atrial fibrillation following atrial flutter ablation after cardiac surgery. J Cardiovasc Electrophysiol. 2010;21(7):760‐765. [DOI] [PubMed] [Google Scholar]
- 42. Kuniss M, Vogtmann T, Ventura R, et al. Prospective randomized comparison of durability of bidirectional conduction block in the cavotricuspid isthmus in patients after ablation of common atrial flutter using cryothermy and radiofrequency energy: the CRYOTIP study. Heart Rhythm. 2009;6(12):1699‐1705. [DOI] [PubMed] [Google Scholar]
- 43. Das M, Loveday JJ, Wynn GJ, et al. Ablation index, a novel marker of ablation lesion quality: prediction of pulmonary vein reconnection at repeat electrophysiology study and regional differences in target values. Europace. 2017;19(5):775‐783. [DOI] [PubMed] [Google Scholar]
- 44. Markowitz SM, Lerman BB. Ablation of nonisthmus‐dependent flutters and atrial macroreentry. Catheter Ablation of Cardiac Arrhythmias. Elsevier ‐ Health Sciences Division: Amsterdam, The Netherlands; 2019:187‐204. [Google Scholar]
- 45. Ertuğrul İ, Karagöz T, Aykan HH. A rare complication of radiofrequency ablation: skin burn. Cardiol Young. 2014;25(7):1385‐1386. [DOI] [PubMed] [Google Scholar]
- 46. Shah RU, Freeman JV, Shilane D, Wang PJ, Go AS, Hlatky MA. Procedural complications, rehospitalizations, and repeat procedures after catheter ablation for atrial fibrillation. J Am Coll Cardiol. 2012;59(2):143‐149. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47. Vernemmen I, Vera L, Van Steenkiste G, van Loon G, Decloedt A. Reference values for 2‐dimensional and M‐mode echocardiography in Friesian and Warmblood horses. J Vet Intern Med. 2020;34(6):2701‐2709. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48. Decloedt A, Verheyen T, Van Der Vekens N, Sys S, De Clercq D, van Loon G. Long‐term follow‐up of atrial function after cardioversion of atrial fibrillation in horses. Vet J. 2013;197:583‐588. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.