Nitric oxide does not relieve pain in patients with sickle-cell disease, a new study finds.
Patients in the study treated with nitric oxide for pain fared no better in terms of the length of their pain episodes than those who inhaled a placebo, the study found.
Inhaling the gas also did not shorten patients’ hospital stays, or the amount of pain medication they took.
Patients with sickle-cell disease suffer pain when misshapen blood cells clog their blood vessels. Nitric oxide relaxes blood vessels and improves blood flow. Previously, two smaller studies suggested breathing nitric oxide reduced pain and medication use in sickle-cell patients.
But the new findings take nitric oxide off the table as a therapeutic drug for pain for sickle-cell disease, said study researcher Dr. Gregory Kato, head of National Heart, Lung and Blood Institute’s Sickle Cell Vascular Disease Section. However, the drug might still be useful for other complications of the disease, such as high blood pressure in the arteries to the lungs, Kato said. Developing new treatments is critical because only one drug, called hydroxyurea, has been approved by the U.S. Food and Drug Administration to mollify patients’ pain, and not all patients respond to it.
The researchers are not discouraged by their results.
“All of my collaborators on this study are not disheartened, but are dedicated to advancing the treatment of sickle-cell disease and will go on to test additional treatments in the future,” Kato said.
The new study will be published tomorrow (March 2) in the Journal of the American Medical Association.
Sickle-cell disease and pain crises
Sickle-cell disease is a hereditary condition in which the shape of red blood cells become distorted — they are sometimes C-shaped instead of their normal doughnut shape. The misshapen cells can block blood vessels, leading topain, organ and nerve damage and stroke. Episodes of intense pain, which doctors call pain crises, are common — an average patient has two per year, though the number can vary widely — and require hospitalization, the researchers said.
People with sickle-cell disease may have sickle-cell anemia, the most severe form of the disease, or sickle-cell trait, a less-severe form. In the United States, 70,000 to 100,000 African-Americans are estimated to have sickle-cell anemia, according to the Centers for Disease Control and Prevention.
Kato and his colleagues examined the effectiveness of nitric oxide in reducing pain in 150 patients with sickle-cell disease between October 2004 and December 2008. Upon hospitalization, patients were randomly assigned to receive nitric oxide or a nitrogen gas placebo. Patients inhaled the gas for up to 72 hours.
The nitric oxide treatment was safe, but did not treat the pain. The pain crises of patients given nitric oxide lasted 73 hours, whereas they lasted 65.5 hours in those who received the placebo. Patients were considered recovered once they had not taken pain medication for 5 hours, rated their pain level as 6 or lower on a scale of 0 to 10, and decided, along with their family and physician, that their pain could be managed at home.
The researchers also found that patients who received nitric oxide were hospitalized for an average of 4.1 days, while those who received the placebo were hospitalized for 3.1 days.
Why doesn’t it work?
The researchers don’t know why nitric oxide treatment showed benefits in earlier studies, but not in the new study. It’s possible that the previous findings in smaller studies were due to chance, Kato said.
The new study provides a framework for how new drugs should be tested for the treatment of sickle-cell disease, Kato said.
“It’s time for us to look for additional new treatments that are being developed in the drug pipeline ,” Kato said.
Pass it on: Inhaling nitric oxide does not appear to provide a therapeutic benefit for patients with sickle-cell disease.
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