Search
Powered By HealthLine
Special Offers
Health Tools
 Heart Healthy Diet
 Ideal Body Weight Calculator
 Diet Reviews
 Fitness and Family
 Quiz: Test Your Fitness IQ
 Exercise and Fitness Guide
 Eat Out Smart
 Healthy Cooking
 BMI Calculator
Featured Conditions
 Diet & Exercise
 Stop Smoking
 Food & Fitness
 High Blood Pressure
 Cholesterol
 Heart
Resources
Healthscout News
3D Health Animations
Health Videos
Quizzes & Tools
Health Encyclopedia
In-Depth Reports
Library & Communities
News Archive
Drug Library
Find a Therapist
Enter City or Zip Code:
Powered by Psychology Today
PR Newswire
 Read latest







Channels
Home |  Today | Women| Men| Kids| Seniors| Diseases| Addictions| Sex & Relationships| Diet, Fitness, Looks| Alternative Medicine| Drug Checker
 Printer Friendly  Send to a Friend

Bone Marrow Transplants May Cure Sickle Cell in Adults

Previously, only children could get transplants because adults were thought to be too sick to handle the procedure

By Jennifer Thomas
HealthDay Reporter


Related Encyclopedia
 border=
Acne
Alagille Syndrome
Aneurysms
Angina Pectoris
More...

Related Healthscout Videos
 border=
New Improved Metal Hearts
Two for One Heart Repair
Fixing Foot Drop
Seeing Clearly with an Iris Implant
More...

Related Animations
 border=
Angioplasty
Coronary Bypass Surgery
Dental Cavities
What is a Heart Attack?
More...

Related Drug Information
 border=
Accupril
Adderal XR
Altace
Avapro
More...

Related News Articles
 border=
Rugby Headgear Not Enough to Stop Head, Spine Trauma
Common Epilepsy Drug Taken During Pregnancy Might Raise Spina Bifida Risk
Health Tip: Recognizing a Bleeding Disorder
New Piece of Alzheimer's Puzzle Identified
More...

WEDNESDAY, Dec. 9 (HealthDay News) -- Researchers say that a new method of bone marrow transplantation cured nine out of 10 adult patients with sickle cell disease, an inherited condition that causes bouts of severe pain, organ damage and sharply limits life expectancy.

Adults have typically not been candidates because they were thought to be too sick to handle the high doses of chemotherapy and radiation necessary to prep the body for the procedure, explained senior study author Dr. John Tisdale, a senior investigator in the molecular and clinical hematology branch at the U.S. National Institutes of Health.

Text Continues Below



Until now, transplantation was generally reserved for more resilient children, whose bodies had not yet suffered as much damage from sickle cell disease.

But the new method allows for a less grueling pre-transplantation routine, one that even adults with severe sickle cell can tolerate.

More than 70,000 Americans suffer from sickle cell disease, and it is especially common among blacks. People with the disease have abnormal, crescent-shaped hemoglobin. The abnormal cells have difficulty passing through small blood vessels, causing blockages and damaging tissues. Over time, the damage can lead to stroke and severe bouts of pain in the chest, arms, legs, chest and abdomen. Sickle cell disease also damages the kidneys, liver and spleen, leaving people, especially children, more susceptible to infection, said Dr. Lanetta Jordan, chief medical officer for the Sickle Cell Disease Association of America.

Treatments include prophylactic antibiotics to fight infections, blood transfusions and hydroxyurea, the only drug U.S. Food and Drug Administration-approved drug for treating sickle cell, Jordan said.

In the new study, Tisdale and his colleagues gave 10 patients ages 16 to 45 with severe sickle cell disease alemtuzumab, a drug used to suppress immune system T-cells; relatively low doses of radiation; and sirolimus, an immune suppressant to fight rejection. Marrow donors were siblings with matched HLA (human leukocyte antigen) markers in their blood.

Page:  1 | 2 | 3 | Next >>

Copyright © 2009 ScoutNews, LLC. All rights reserved.
Last updated 12/9/2009

Related Links
 border=
From Healthscout's partner site on breast cancer, MyBreastCancerNetwork.com
VIDEO: Chemo booster cuts treatment time by two months
SYMPTOMS: Learn what to look for and what the symptoms mean
PROGNOSIS: Early detection and new treatments improve survival rates





SOURCES: John Tisdale, M.D., senior investigator, molecular and clinical hematology branch, U.S. National Heart, Lung, and Blood Institute and U.S. National Institute of Diabetes and Digestive and Kidney Diseases, U.S. National Institutes of Health, Bethesda, MD; Lanetta Jordan, M.D., M.P.H., chief medical officer, Sickle Cell Disease Association of America, Baltimore; Miguel Abboud, M.D., professor of pediatrics, American University of Beirut Medical Center, Beirut, Lebanon; Lakshmanan Krishnamurti, M.D., pediatric hematologist/oncologist, University of Pittsburgh and director, Sickle Cell Program at Children's Hospital, Pittsburgh, Pa.; Dec. 10, 2009, New England Journal of Medicine


HealthScout is a part of HealthCentral
About Us   Our Blog   Contact Us   Privacy Policy   Terms of Use   Site Map  
Copyright © 2001-2010. The HealthCentralNetwork, Inc. All rights reserved.
Advertising Policy   Editorial Policy Advertise With Us   Anti-Spam Policy   PR Newswire