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Artificial heart

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An AbioCor artificial heart

An artificial heart is a prosthetic device that is implanted into the body to replace the biological heart. It is distinct from a cardiopulmonary bypass machine (CPB), which is an external device used to provide the functions of both the heart and the lungs. The CPB oxygenates the blood, so does not need to be connected to both blood circuits. Also, a CPB is suitable only for a few hours use, while artificial hearts have been used for periods longer than a year (as of 2007).

Artificial Heart Important Distinction

Total Artificial Heart (TAH) implantation involves the removal of the native heart. It is a surgical procedure similar to heart transplantation with a human donor heart.
The assist devices are completely different. The patient’s heart is not removed when it is implanted either a Left Ventricular Assist Device (LVAD) or a Right Ventricular Assist Device (RVAD) or both. The assist device takes only a part of the cardiac output of the patient’s heart.

Origins

A synthetic replacement for the heart remains one of the long-sought holy grails of modern medicine. The obvious benefit of a functional artificial heart would be to lower the need for heart transplants, because the demand for donor hearts (as it is for all organs) always greatly exceeds supply.

Although the heart is conceptually simple (basically a muscle that functions as a pump), it embodies subtleties that defy straightforward emulation with synthetic materials and power supplies. Consequences of these issues include severe foreign-body rejection and external batteries that limit patient mobility. These complications limited the lifespan of early human recipients to hours or days.

Early designs

A heart-lung machine was used in 1953 during the first successful open heart surgery. Dr. John Heysham Gibbon performed the operation and developed the heart-lung substitute himself. Whether this device could be considered as an artificial heart is a subject of debate.

The scientific interest for the development of a solution for heart disease developed in different research groups worldwide.

Early Designs of Total Artificial Hearts

In Russia in 1937 V.P. Demichov implanted TAH in dogs. Motor roller types TAH (inside the chest) with the driver shaft of which carried through the sternum.
In 1957 Tet Akutsu and Willem Kolff initiated their extended TAH research at the Cleveland Clinic.
In 1958 Domingo Liotta started the studies of TAH replacement at Lyon, France and in 1959-60 at the National University of Cordoba, Argentina. He presented his work at the meeting of the American Society for Artificial Internal Organs meeting held in Atlantic City in March 1961. On that meeting Dr Liotta described the implantation of three types of orthotopic (inside the pericardial sac) TAH in dogs, each of which used a different source of external energy: an implantable electric motor, an implantable rotating pump with an external electric motor and a pneumatic pump.

Early Clinical Application of Assisted Circulation and Total Artificial Heart The Left Ventricular Assist Device (LVAD) system was created by Domingo Liotta at Baylor University College of Medicine in Houston in 1962.
First Clinical Application of an Intrathoracic Pump: In the evening of July 19,1963 E. Stanley Crawford and Domingo Liotta implanted the first clinical LVAD at the Methodist Hospital in Houston, Texas in a patient who had a cardiac arrest after surgery. The patient survived for 4 days under mechanical support but didn't recover from the complications of the cardiac arrest, finally the pump was discontinued and the patient died.
First Clinical Application of a Paracorporeal Pump: In the afternoon of April 21,1966 Michael DeBakey and Domingo Liotta implanted the first clinical LVAD in a paracorporeal position (the external pump rests at the side of the patient) at the Methodist Hospital in Houston in a patient with cardiogenic shock after heart surgery. The patient developed neurological and pulmonary complications and died after few days of LVAD mechanical support. In October 1966 Michael E. DeBakey and Domingo Liotta implanted the paracorporeal Liotta-DeBakey LVAD in a new patient who recovered well, and was discharged from hospital after 10 days of mechanical support. thus constituting the first successful use of an LVAD for postcardiotomy shock.

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April 21st. 1966 Dr. Michael E. DeBakey and at his right Dr. Domingo Liotta, during the clinical implantation of a Para corporeal Assisted Cardiocirculatory Device, at the Methodist Hospital, Houston, Texas, USA

First Clinical Implantation of a Total Artificial Heart: In the afternoon of April 4, 1969 Denton A. Cooley and Domingo Liotta replaced a dying man’s heart with a mechanical heart inside the chest at the Texas Heart Institute in Houston as a bridge for a transplant. The patient woke up and recovered well. After 64 hours the pneumatic powered artificial heart was removed and replaced by a donor heart. However, thirty-two hours after transplantation the patient died of what was later proved to be an acute pulmonary infection, extended to both lungs, caused by fungi. Most likely caused by a immunosuppressive drugs complication.

File:Cooley-LiottaTAH.jpg


Historical Operation, the first in medical history. Total heart Replacement with an Artificial Heart (orthotopic position, inside the pericardial sac). On the left, Dr. Liotta; in the center of the picture, the empty pericardial sac of the patient, Mr. H. Karp. On the right, the hands of Dr. Cooley holding Mr. Karp’s heart and the artificial heart just before implantation. Texas Heart Institute, Houston (April 4, 1969).


The original prototype of Liotta-Cooley artificial heart used in this historic operation is prominently displayed in The Smithsonian Museum Treasures of American History in Washington, DC.


The first patented artificial heart was invented by Paul Winchell in 1963. Winchell subsequently assigned the patent to the University of Utah, where Robert Jarvik ultimately used it as the model for his Jarvik-7. Jarvik's designs improved the device, but his patients succumbed after brief trials. His first Jarvik-7 patient, 61-year-old retired dentist Barney Clark, survived for 112 days after it was implanted at the University of Utah on December 2, 1982. One of the innovations of the Jarvik-7 was the inner coating of rough material, developed by David Gernes. This coating helped the blood to clot and coat the inside of the device, enabling a more natural blood flow.

After about 90 people received the Jarvik device, the implantation of artificial hearts was banned for permanent use in patients with heart failure, because most of the recipients could not live more than half a year. However, it is used temporarily for some heart transplantation candidates who cannot find a natural heart immediately but urgently need an efficiently working heart.

Hiroaki Harasaki of the Cleveland Clinic developed two important improvements for the artificial heart and projected future artificial organs. The two patented inventions solved major obstacles for any fully implanted artificial organs and materials. The first was a non-clotting surface material which significantly reduces the risk of rejection of the organ by the patient's immune system. The second development, which required the collaboration of many disciplines, was an implantable power source which does not create tissue-damaging heat.

Recent developments

On July 2, 2001, Robert Tools received the AbioCor Implantable Replacement Heart produced by the AbioMed company of Danvers, Massachusetts. It was the first completely self-contained artificial heart transplant. The surgery was done by University of Louisville doctors at Jewish Hospital in Louisville, Kentucky. Tom Christerson survived for 17 months after another AbioCor transplant. On September 6, 2006 the AbioCor device became the first fully implantable artificial heart to be approved under 'Humanitarian Use Device' rules.[1]

The 'CardioWest' temporary Total Artificial Heart (TAH‑t) was developed from the Jarvik-7 by University of Arizona researchers and approved for use in 2004.[2] It is the first implantable artificial heart to be approved by the U.S. Food and Drug Administration, and has also been approved by the CE. The TAH-t is used only in patients with end stage biventricular failure as a way to improve life expectancy while they are waiting for a heart transplant. In a pivotal clinical study, these patients were successfully transplanted 79% of the time;[3], One-year and five-year survival rates after heart transplant among these patients were 86 and 64 percent. The longest TAH‑t implantation so far went 620 days (20.4 months).[4] There are several medical centers where this device can be implanted:

United States: [5]

- University Medical Center (Tucson, AZ) [1]

- Cleveland Clinic (Cleveland, OH) [2]

- Virginia Commonwealth University Health System (Richmond, VA) [3]

- Aurora St. Luke's (Milwaukee, WI) [4]

- University of Michigan Health System (Ann Arbor, MI) [5]

- Penn State Hershey Medical Center (Hershey, PA) [6]

- Ohio State University Medical Center (Columbus, OH) [7]

- Hospital of the University of Pennsylvania (Philadelphia, PA) [8]

- Barnes Jewish Hospital (St. Louis, MO) [9]

Canada:

- Montreal Heart Institute (Quebec, Canada) [10]

Europe:

- Groupe Hospitalier La Pitié-Salpêtrière (Paris, France) [11]

- Hôpital Guillaume et René Laennec (Nantes, France) [12]

- Deutsches Herzzentrum Berlin / German Heart Institute Berlin (Berlin, Germany) [13]

- Herz-und Diabeteszentrum Nordrhein Westfalen / Heart and Diabetes Center (Bad Oeynhausen, Germany) [14]

- Herzzentrum Leipzig GmbH Universitaetsklinik (Leipzig, Germany) [15]

- Universitäts Klinikum Freiburg (Freiburg, Germany) [16]

- Universitätsklinikum Münster (Munster, Germany) [17]

- Herzzentrum Köln (Cologne, Germany) [18]

- University Hospital Munich (Munich, Germany) [19]

- Friedrich-Alexander University Hospital (Nuremberg, Germany) [20]

In August 2006, an artificial heart was implanted into a 15-year old girl at the Stollery Children's Hospital in Edmonton, Alberta, Canada. It was intended to act as a temporary fixture until a donor heart could be found. Instead, the artificial heart (called a Berlin Heart) allowed for natural processes to occur and her heart healed on its own. After 146 days the Berlin Heart was removed and the girl's heart was able to function properly on its own.[6].

With increased understanding of the heart and continuing improvements in prosthetics engineering, computer science, electronics, battery technology, and fuel cells, a practical artificial heart may be a reality in the 21st century.

Heart assist devices

Patients who have some remaining heart function but who can no longer live normally may be candidates for ventricular assist devices which do not replace the heart, but boost its output. The first heart assist device was FDA approved in 1994, and two more received approval in 1998.[7] While the original assist devices emulated the pulsating heart newer versions, such as the Heartmate II,[8] developed by the Texas Heart Institute of Houston, Texas, provide continuous flow. These pumps (which may be cetrifugal or axial flow) are smaller and potentially more durable and long-lasting than the current generation of total heart replacement pumps. Several continuous flow ventricular assist devices have been approved for use in the European Union and as at August 2007 were undergoing clinical trials for FDA approval.

In fiction

The earliest example of a fictional artificial heart is the French pulp hero the Nyctalope.

In the fictional Star Trek universe, Captain Jean-Luc Picard had an artificial heart implanted in 2328, which was later replaced twice. Joseph Sisko, father of Benjamin Sisko, had several artificial organs, including a new aorta he received in 2372.

The British science fiction series Space: 1999 had a character, Victor Bergman (portrayed by Barry Morse), with an artificial heart. He was able to modify its rate of operation with a wrist-worn device.

The novels of Philip K. Dick feature the use of 'artiforgs' or artificial organs.

In the 1981 movie Threshold, it is stated from IMDB, that "The celebrated heart surgeon Dr. Vrain supports the research of the offbeat scientist Aldo Gehring, who is inventing an artificial heart. Dr. Vrain performs the first artificial human heart transplant against the advice of the Ethics Committee." This movie, which stars Donald Sutherland and Mare Winningham, is a study in artificial heart transplant, though it is fictional.

The German heavy metal band Accept wrote about artificial hearts in their album "Metal Heart" (1985).

In the 1987 movie Robocop, there is a commercial for an artificial heart clinic called "The Family Heart Center" where surgeons operate on persons and implant artificial hearts from "the complete line of hearts by Jensen and Yamaha," encouraging its customers "You pick the heart!" These hearts come with extended warranties, financing, and qualify for "health tax credit."

The computer game Syndicate (by Bullfrog) features humans agents the player can modify bionically, including replacing the heart with more and more advanced technology.

References

  1. ^ FDA Approves First Totally Implanted Permanent Artificial Heart for Humanitarian Uses at FDA.gov
  2. ^ Home Page at CardioWest
  3. ^ Cardiac replacement with a total artificial heart as a bridge to transplantation at the National Institutes of Health
  4. ^ Current status of the total artificial heart at Elsevier.com
  5. ^ "CardioWest temporary Total Artificial Heart" (Press release). SynCardia Systems, Inc. 2007-01-18. Retrieved 2007-04-26. {{cite press release}}: Check date values in: |date= (help)
  6. ^ Capital Health: One year later: Berlin Heart bridges patient back to health
  7. ^ FDA APPROVES TWO PORTABLE HEART-ASSIST DEVICES at FDA.gov
  8. ^ An Artificial Heart That Doesn't Beat at TechnologyReview.com

George B. Griffenhagen and Calvin H. Hughes. The History of the Mechanical Heart. Smithsonian Report for 1955, (Pub. 4241): 339-356, 1956.