Pacemaker Effect With Closed Loop Sensor in Neuromodulated Syncope Refractory to Medical Therapy

Overview

Vasovagal syncope is an entity frequently in the emergency services, its treatment includes pharmacological and non-pharmacological measures, and in some severe cases, requires the implantation of cardiac stimulation devices, specifically, those pacemakers that have closed-loop sensors (CLS). This research is an intervention study, multi-institutional, randomized and double blind that will be carried out in patients older than 18 years, with a diagnosis of neurally mediated type 1, 2A or 2B syncope documented in a tilting table test, who have had at least 2 syncope in the last year and that significantly affects the quality of life despite the use of pharmacological and non-pharmacological non-interventionist therapy. This study aims to evaluate the effect of cardiac pacing therapy with CLS pacemakers on quality of life, recurrence of syncope and pre-syncopal symptoms in patients with a diagnosis of neurally mediated syncope in this group of patients.

Syncope is defined as a loss of consciousness with inability to maintain the postural tone, with subsequent spontaneous recovery and without neurological sequelae. This occurs due to cerebral hypoperfusion by two mechanisms: 1) decreased cardiac output, usually due to bradycardia, and 2) hypotension due to decreased peripheral vascular resistance. An incidence of 6.2 per 1000 persons / year has been calculated, constitutes 2% of the reasons for consultation by emergency department and is found in 40% of the hospitalized participants. Its prevalence increases with age and is clearly influenced by the presence or absence of heart disease. The most frequent etiology is vasovagal, which has a benign course, with a mortality that does not exceed the expected for the general population. However, up to 21.6% have recurrences, which affects the quality of life and can generate physical injuries, especially in the geriatric population. The pathophysiology is not completely clear, it is thought that orthostasis has an important mechanism by decreasing the venous return, therefore, this leads to a vigorous contraction of the myocardium in the presence of a little filled heart chamber, it can stimulate the mechanoreceptors and thus precipitate the Bezold Jarisch reflex, which results in paradoxical hypotension and bradycardia. The management can be variable, and will depend on the patient's response, from conservative strategies such as changes in lifestyle, avoiding triggers, abortive maneuvers in the case of prodromes, and some drugs (fludrocortisone) to cardiac stimulation devices such as pacemakers. Cardiac stimulation has been studied in participants with cardioinhibitory response in the Tilt test with divergent results, especially with the use of conventional pacemakers that monitor the fall in heart rate. Interestingly, an other type of pacemakers, those with closed handle sensor (CLS), that measures the impedance through each beat, which is related to myocardial contractility, in this way it could detect changes in the contractility that precede the cardioinhibitory response, and thus guarantee a good cardiac output and avoid syncope. The use of cardiac stimulation therapy has been proposed as an effective strategy in participants with recurrent syncope and refractory to pharmacological and non-pharmacological measures, a special group are those with a cardioinhibitory response with asystole greater than 6 seconds, however, this benefit it could be extrapolated to those of mixed commitment. In the world, there is no definitive consensus on the level of recommendation for the implantation of pacemakers with CLS in this disease, however, based on the pathophysiology, studies of the disease and technical elements on the functioning of these devices, they have come implanting in Colombia and in the world with apparent good results in the quality of life of the participants, syncope-free event rate, longer time to the first syncope and improvement in hemodynamic parameters in the Tilt Test. In Colombia, more research is needed to confirm or reject this assertion. General objective: Evaluate the effect of cardiac pacing therapy with CLS pacemakers on quality of life, recurrence of syncope and pre-syncopal symptoms of participants with a diagnosis of neurally mediated syncope (with mixed response or inhibitory cardio) refractory to pharmacological and non-pharmacological management, in six health care centers in the city of Medellín. Specific objectives * Sociodemographically and clinically characterize the study population. * Evaluate the impact on quality of life, pre and post implant. * Measure the occurrence of episodes of syncope, pre and post implant. * Assess the reduction of pre-syncopal symptoms. * Evaluate if the mode and programming functions influence the appearance of syncopes and recurrences. * Determine the average time that elapses from the implantation of the CLS pacemaker until the first episode of syncope. Interventions of participants * A: participants who will be activated the CLS function one month after implantation of the pacemaker. They will be reevaluated after 4 months and will be changed to DDD-R mode for another 4 months, when the results will be analyzed to define the final form of reprogramming. * B: patient to whom, one month after the implantation of the pacemaker, the R function will be activated. They will be reevaluated after 4 months and will be switched to DDD-CLS mode for another 4 months, when they will be evaluated again and the results will be analyzed for define final form of reprogramming. Participants will be contacted through the electrophysiology service of "CES Cardiology" in Medellín, Colombia. The calculation of the sample size was carried out probabilistically with the following parameters and based on the previous studies: Power 80%, confidence: 95%, expected proportion of group 1: 72%, expected proportion group2: 99% What gave the following results: intervention A: 26 participants, intervention B: 26 participants. Total sample: 52 participants. Selection of participants All participants will be recruited and who meet all the inclusion criteria and none of the exclusion criteria will be selected by one of the members of the research team previously trained on the Plan of Clinical Research and that has been designated to perform this type of tasks. Estimated time to include participants The inclusion of all participants requires approximately 6 months. The anticipated duration of this study is 27 months. This will depend on the inclusion rate. Informed consent process: It will be prepared by the principal investigator, with the information indicated in article 15 of resolution 8430. * It will be reviewed by the Human Research Ethics Committee of the CES University and can only be signed by the patient, researchers and witnesses when it is approved. * Indicate the names and contact forms of the principal investigators and who should be contacted in case of any difficulty or adverse event. * It must be signed by two witnesses and by the research subject or his legal representative. If the research subject does not know how to sign, he will print his fingerprint and in his name he will sign another person that he designates. * It will be prepared in duplicate, leaving a copy in the possession of the research subject or his legal representative. Blinding of the study: The programming modes of the intracardiac devices can only be known through the use of specific reprogramming equipment provided by each generating company of the device. In the case of pacemakers with CLS, their only manufacturer is Biotronik, so they provide a device that connects with the device that the patient has implanted. Unless the reprogramming card is delivered, neither the patient nor another person will be able to establish the programming mode. In this way the people who will be in contact with the programming of the device will be: Electrophysiologist in charge of implanting the device: it could be any of the members of the CES Cardiology group with this training, it will implant the device and leave it in DDD-CLS mode to start the first month or washing time. This electrophysiologist will not make any scheduled visits or reprogram the device in any of his visits. Electrophysiologist commissioned the visit by electrophysiology within each of the visits scheduled and listed above: professional in charge of programming the devices as established by the paper envelopes generated in the random assignment. It will be the only person who will know the way of programming during the 8 months of intervention and will not disclose this information to the patient or their relatives. Main co-investigators: they will not know the way of programming the device nor will they attend the part of the visit that performs electrophysiology. In another office and before or after the program, they will evaluate the patient clinically and ask the questions included in the scales of quality of life used. The person who will analyze the information: will know the process. The patient: He will not know the programming mode of his device, that is, he will not know if he is in DDD - CLS or DDD - R. This study will be double blind. Random assignment Through computer-based randomization programs, 26 participants will be assigned to the group of participants who, in the month of implantation, will be programmed in DDD-CLS mode and 26 participants who will be programmed in DDD-R mode one month after implantation. The randomization will be known by the investigating epidemiologist who will activate the randomization program and the electrophysiologist who will program the patient. Initial randomized programming modes will be delivered in sealed envelopes to the electrophysiologist who will program the patient. Procedures The clinical trial will be conducted in accordance with the Clinical Research Plan. All those who participate in the conduct of the clinical study will be qualified by training, training or experience to carry out their tasks and this training should be documented in an appropriate manner. The clinical study will not begin until it receives written approval from the Ethics Committee and the relevant regulatory authorities and all necessary documentation has been collected. Procedures during the time of intervention. Once the patient enters the health center with criteria to participate in the study, as long as it does not meet any of the exclusion criteria and has signed the informed consent (the participant or a legal representative in case this is not in conditions to sign). Starting point: Prior to implanting the device. Between the day of implantation and the first month (at which time the initial visit will take place) will be the washing or "wash out" process in which the device will be left in DDD-CLS mode until the start visit. Start visit: One month after implanting the device. It includes two parts: Evaluation by electrophysiology and Clinical evaluation. Visit # 1: It will happen 4 months after the start visit. It includes two parts: Evaluation by electrophysiology and Clinical evaluation. Visit # 2: Finally, a final check (visit # 2) will be made 8 months after the start visit and 4 months after the visit # 1. It includes two parts: Evaluation by electrophysiology and Clinical evaluation. Procedures during the time following the end of the intervention: At the end of the 8 months in which the information on the mode of reprogramming was recorded and these modes were reversed, the follow-up will continue for 12 more months counted from visit # 2 as follows: * Visit # 3: It will take place 6 months after the visit # 2 and 14 months after the initial visit. The patient will be evaluated clinically (without pacemaker programming) by one of the researchers who will apply the SFSQ and SF-36 quality of life scales. * Visit # 4: It will take place 12 months after the visit # 2 and 20 months after the initial visit. The patient will be evaluated clinically (without pacemaker programming) by one of the researchers who will apply the SFSQ and SF-36 quality of life scales. After this the study ends. Procedures in case of Adverse Events: In the event of any adverse event related or not to the implant or use of the device or any condition of the patient, the patient must notify the group of researchers in the contact telephone numbers that are delivered and according to the severity and needs of the event will be cited in an additional visit for clinical evaluation and / or electrophysiology or will be redirected to the CES Clinic if the event or situation requires management in the emergency department or intrahospital service. Each of these adverse events must be reported on a form and a communication sent within 72 hours after the group of researchers had knowledge of the Human Research Ethics Committee of the CES University, making the event known to all. the details.