What is the difference between a temporary and permanent pacemaker




















A pacemaker can also help correct a wide variety of other abnormal heart rhythms arrhythmias. More than , Americans are living with artificial pacemakers, and the number is steadily rising.

If you have a temporary problem with heart rhythm a common condition for patients recovering from a heart attack , you may need just a temporary pacemaker. Your doctor can attach a small device to your skin that sends an electronic signal to your heart. Most pacemakers, however, are implanted in the body. Each implantable pacemaker has two main parts, a "pulse generator" that emits the electrical signal and one or two "leads," or wires that carry the electricity to the heart.

The pulse generator, about the size of three stacked poker chips, usually sits below the collarbone. The leads are threaded through large veins until they reach the heart.

Early pacemakers produced the same unwavering rhythm at all times, but thanks to computer technology, today's pacemakers are much more flexible and adaptable.

For instance, some devices turn on only when your heart rate drops below a certain level. These are called demand pacemakers. Other devices, known as rate-adaptive pacemakers, automatically increase your heart rate when you exercise and slow down when you rest -- just like a healthy heart does. A study by researchers from Johns Hopkins University suggests that the newer pacemakers can make a real difference for heart failure patients. In a review of studies involving over 1, patients who used the latest model pacemakers, the researchers found that the patients' risk of death from heart failure decreased by 51 percent, while hospitalizations decreased by 29 percent.

It's a simple procedure -- nothing even close to the trauma of open-heart surgery. Your doctor will probably give you a local anesthetic, which means you'll be awake for the whole procedure. She'll first make a small cut underneath your collarbone. Then, with the help of an x-ray machine, your doctor will guide the lead or leads through your veins to the appropriate place on your heart. Two patients with atrioventricular block did not return to a normal heart rate.

However, the patient with type II second degree AV block recovered normal cardiac rhythm in the early period. Actuarial survival curves are given in table I.

During the surgical procedure used for orthotopic cardiac transplantation, the posterior portions of donor preserved right and left donor atria are left in situ with the sinus node and its neural connections undisturbed The transplant recipient thus has two sinus nodes with electrical activity and eletrocardiography expression totally independent of the surface eletrocardiogram.

The donor sinus node is responsible for electrical stimulation despite its anatomical and functional denervation 3,13, Normal sinus node function is dependent on a complex balance between intrinsic sinus node electrophysiologic properties, sinoatrial conduction properties and a number of extrinsic factors, the most important of which is the autonomic nervous system Although reinnervation after cardiac transplant has been observed in animal models, complete restoration of normal myocardial innervation in human transplantation has not been observed, although evidence of partial recovery does exist 17, Cardiac frequency in a denervated heart is regulated according to venous return, atrial receptor stimulation, atrial stretching and circulating catecholamine levels Donor sinus node dysfunction is the most common cause of bradyarrhythmia reported after transplantation 4,9,10, Some authors believe that the presence of sinus node dysfunction may be seen as evidence of a worse prognosis after transplantation.

These data are similar to ours. Hemodynamic dysfunction, myocardial damage and rejection may contribute to this prognosis. In an attempt to control bradyarrhythmias, we may use drugs such as isoprenaline, dopamine, dobutamine, terbutaline, theophylline.

Artificial cardiac stimulation is indicated if no response to drugs occurs 3, Indications for permanent pacing are: sinus node dysfunction mainly , type II second degree atrioventricular block, and total atrioventricular block. Our data confirmed these findings 4,5,8,12,21, The etiology of permanent sinus node dysfunction is multifactorial, and rejection, sinus node ischemia during transplant organ transport, surgical maneuvers, anomalies in the sinus node artery, prolonged ischemia time in the perioperative period, sinus node dysfunction prior to thesurgical act, and myocardial fibrosis after cyclosporine.

Local trauma to the superior vena cava, donor age, inadequate denervated heart response to vasoactive amines and previous use of antiarrhythmic drugs, especially amiodarone , may be involved 4,5,8,9,11,12,13,17, The optimum timing of permanent pacing is still controversial and must reflect the compromise between the advantages of early pacemaker implantation and the risks of delaying this procedure. According to some authors epicardial pacing wires are usually removed on day 21 afterthe operation, and a decision regarding permanent pacing is made at this point 3.

As part of the routine, an epicardial pacemaker is implanted in the postoperative period of cardiac surgery. At the end of the operation, an epicardial electrode is implanted in order to guarantee temporary stimulation in case of bradyarrhythmias soon after surgery.

However, epicardial pacing in recipients may present difficulties due to rejection, fibrosis after rejection and myocyte fibrosis after cyclosporine 8. Studies in retransplantation or necropsy have shown that cardiac conduction tissue is a specific target related to allograft rejection The arteries to sinoatrial and atrioventricular tissue are frequently involved in both an acute cellular reaction and in the chronic intimal fibro-cellular rejection reaction, causing sinus node dysfunction The beneficial hemodynamic effects of atrial contribution must be considered when deciding the optimal mode of pacing of patients undergoing cardiac transplantation, although some authors advocate only ventricular stimulation 3.

Implantation of rate responsive pacemakers is based on the observation of chronotropic incompetence noticed after cardiac transplantation 9, Chronotropic response to exercise is abnormal in transplanted patients due to autonomic denervation 8, Stimulation must be individualized using an atrioventricular pacemaker whenever it is possible, and a rate responsive pacemaker in patients who have chronotropic incompetence 25, In our series we used a dual chamber pacemaker in 4 patients with permanent pacing, a rate responsive pacemaker being necessary in only one of them.

At first, you may feel the weight of the pacemaker in your chest. However, over time, most people become accustomed to the pacemaker. The generator is very small, about the size of two silver dollars stacked on top of each other, and weighs about an ounce or less, depending on the make and model of the device. Our highly skilled electrophysiologists provide expert care for people with all types of arrhythmias.

We are at the forefront of research, studying the most advanced devices and techniques for managing heart rate and rhythm. Share on Facebook.

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New to MyHealth? Manage Your Care From Anywhere. Activate Account. Create a New Account. Forgot Username or Password? Types Our Approach for Pacemakers If your heart rate is too slow, you may need a pacemaker.

What is the difference between a dual chamber pacemaker and a single chamber pacemaker? Make an Appointment. Find a Clinic. Nationally recognized expertise in pacemaker programming and device management to tailor treatment to your specific needs. Remote device monitoring by our device nurses, who can monitor your pacemaker and address any issues as soon as they arise—meaning fewer office visits.

One convenient location with our device clinic, catheterization lab, and other care areas for all your care—from evaluation to procedure to follow-up—in one place. Support services for all aspects of your care , including device management, support groups, and individual counseling for people living with a pacemaker. Thought leadership by Stanford doctors who publish articles and textbooks to train other electrophysiologists in the latest pacemaker advances. Make An Appointment.

What is a Pacemaker? Conditions Treated. Types of Pacemakers. Single-chamber pacemaker This type of pacemaker has one lead that connects the pulse generator to one chamber of your heart. Dual-chamber pacemaker With two leads, this device connects to both chambers on the right side of your heart, the right atrium and the right ventricle. Biventricular pacemaker This pacemaker, also known as a cardiac resynchronization therapy CRT device, has three leads connected to the right atrium and both ventricles.

Previous Section Next Section. What to Expect. Before During After. Before the Procedure. You won't be allowed to eat or drink for eight hours prior to the procedure. We will instruct you if you need to stop any medications before the procedure. During the Procedure. Patients will receive some sedation intravenously to help with relaxation during the procedure.

Pacemaker Insertion Process Generally, a pacemaker insertion follows this process: Patients will be asked to remove any jewelry or other objects that may interfere with the procedure Patients will be asked to remove clothing and will be given a gown to wear Patients will be asked to empty their bladder prior to the procedure An intravenous IV line will be started in the hand or arm prior to the procedure for injection of medication and to administer IV fluids, if needed Patients will be placed in a supine on back position on the procedure table Patients will be connected to an electrocardiogram ECG or EKG monitor that records the electrical activity of the heart and monitors the heart during the procedure using small, adhesive electrodes.

Vital signs heart rate, blood pressure, breathing rate, and oxygenation level will be monitored during the procedure Large electrode pads will be placed on the front and back of the chest Patients will receive a sedative medication in IV before the procedure to help patients relax. However, patients will likely remain awake during the procedure The pacemaker insertion site will be cleansed with antiseptic soap Sterile towels and a sheet will be placed around this area A local anesthetic will be injected into the skin at the insertion site Once the anesthetic has taken effect, the doctor will make a small incision at the insertion site A sheath, or introducer, is inserted into a blood vessel, usually under the collarbone.

The sheath is a plastic tube through which the pacemaker lead wire will be inserted into the blood vessel and advanced into the heart It will be very important for patients to remain still during the procedure so that the placement will not be disturbed and to prevent damage to the insertion site The lead wire will be inserted through the introducer into the blood vessel.

The doctor will advance the lead wire through the blood vessel into the heart Once the lead wire is inside the heart, it will be tested to verify proper location and that it works. Fluoroscopy, a special type of X-ray that will be displayed on a TV monitor , may be used to assist in testing the location of the leads Once the lead wire has been tested, an incision will be made close to the location of the catheter insertion just under the collarbone.

Patients will receive local anesthetic medication before the incision is made The pacemaker generator will be slipped under the skin through the incision after the lead wire is attached to the generator.

Generally, the generator will be placed on the non-dominant side. If patients are right-handed, the device will be placed in the upper left chest. After the Procedure. Wound Care Change the dressing over the PM incision site daily: Remember to wash your hands before and after changing the dressing Remove the dressing from your incision and look at it carefully in a mirror If you have steri-strips, do not remove them the steri-strips will be removed at your two-week incision check-up Replace the dressing with a clean dressing dressing materials should be provided to you before your discharge Notify the Stanford Cardiac Arrhythmia Service at for the following: Infection - swelling, redness, or warmth around the incision; significant pain when touched; yellowish, greenish, or bloody discharges on your dressing or on the incision; foul smell Bleeding - blood oozing from the incision or PM site has become swollen or enlarged and feels tense bleeding beneath the skin Fever - if you are feeling excessively warm or have chills and your temperature is greater than F Sponge bath only for the first 5 days following the PM implantation.

Showers can be done after the fifth day, unless otherwise instructed by your doctor The incision site can get wet; do not cover the incision with plastic wrap while showering Do not rub directly over the incision site or use a wash cloth, but let the water or soapy water flow Do not submerge your incision site in the tub, pool, hot tub or lake until it is well healed at least 7 days Avoid using deodorants, powders, creams, lotions, etc. Do not rub while drying.

Activity Activity on the side of the pacemaker should be limited for week six weeks recommended for biventricular pacemaker as follows: Do not lift the elbow that is on the side of your pacemaker above the shoulder. Movement of the large shoulder muscle could cause the lead inside of the heart to move out of position. Repositioning of the leads will require another surgical procedure.

Cao Q, Zhang J, Xu G ; Hemodynamic changes and baroreflex sensitivity associated with carotid endarterectomy and carotid artery stenting. Interv Neurol. Epub Jun Temporary Cardiac Pacing ; University of Ottowa, Hi, I recently had a limb lead test for my arms and legs. Leads 2 and 3 were both healthy and normal but lead 1 had a regularity. It was a slow weak signal. Naturally I'm going to be talking with my Disclaimer: This article is for information only and should not be used for the diagnosis or treatment of medical conditions.

Egton Medical Information Systems Limited has used all reasonable care in compiling the information but make no warranty as to its accuracy. Consult a doctor or other health care professional for diagnosis and treatment of medical conditions. For details see our conditions.



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