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C-Section and Asthma Relation April 14, 2009

Posted by healthandsurvival in Asthma, Women's Health.
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(NaturalNews) Children delivered by cesarean section (c-section) are significantly more likely to develop asthma and allergies later in life than children delivered through natural, vaginal birth, according to a study conducted by researchers from National Institute for Public Health and the Environment in Bilthoven, the Netherlands.

A c-section is a procedure in which a child is surgically removed through a mother’s abdomen, rather than emerging naturally through the vaginal opening. It is medically recommended only in cases where vaginal delivery would seriously endanger the life of infant or mother, but is becoming more common as many women’s preferred method of childbirth.

Researchers compared the rates of asthma and allergies among 2,917 eight-year-olds, comparing the rates between those who had been delivered vaginally and those who had been delivered by c-section. They found that the risk of asthma was 79 percent higher in those delivered by c-section compared with those delivered vaginally. The correlation between c-section and asthma risk was even higher among children born to one or more parents with allergies.

“Our results emphasize the importance of gene-environment interactions on the development of asthma in children,” the researchers wrote. “The increased rate of cesarean section is partly due to maternal demand without medical reason. In this situation, the mother should be informed of the risk of asthma for her child, especially when the parents have a history of allergy or asthma.”…read more here…

Risky Asthma Drugs December 7, 2008

Posted by healthandsurvival in Asthma, Children's Health, Drugs.
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December 6, 2008

Warning Given on Use of 4 Popular Asthma Drugs, but Debate Remains

WASHINGTON — Two federal drug officials have concluded that asthma sufferers risk death if they continue to use four hugely popular asthma drugs — Advair, Symbicort, Serevent and Foradil. But the officials’ views are not universally shared within the government.

The two officials, who work in the safety division of the Food and Drug Administration, wrote in an assessment on the agency’s Web site on Friday that asthma sufferers of all ages should no longer take the medicines. A third drug-safety official concluded that Advair and Symbicort could be used by adults but that all four drugs should no longer be used by people age 17 and under.

Dr. Badrul A. Chowdhury, director of the division of pulmonary and allergy products at the agency, cautioned in his own assessment that the risk of death associated with the drugs was small and that banning their use “would be an extreme approach” that could lead asthmatics to rely on other risky medications.

Once unheard of, public disagreements among agency experts have occurred on occasion in recent years. The agency is convening a committee of experts on Wednesday and Thursday to sort out the disagreement, which has divided not only the F.D.A. but also clinicians and experts for more than a decade.

Sudden deaths among asthmatics still clutching their inhalers have fed the debate. But trying to determine whether the deaths were caused by patients’ breathing problems or the inhalers has proved difficult.

The stakes for drug makers are high. Advair sales last year were $6.9 billion and may approach $8 billion this year, making the medication GlaxoSmithKline’s biggest seller and one of the biggest-selling drugs in the world. Glaxo also sells Serevent, which had $538 million in sales last year. Symbicort is made by AstraZeneca and Foradil by Novartis.

Whatever the committee’s decision, the drugs will almost certainly remain on the market because even the agency’s drug-safety officials concluded that they were useful in patients suffering from chronic obstructive pulmonary disease, nearly all of whom are elderly.

Dr. Katharine Knobil, global clinical vice president for Glaxo, dismissed the conclusions of the agency’s drug-safety division as “not supported by their own data.” Dr. Knobil said that Advair was safe and that Serevent was safe when used with a steroid.

Michele Meeker, a spokeswoman for AstraZeneca, said that the F.D.A.’s safety division improperly excluded most studies of Symbicort in its analysis, and that a review of all of the information shows that the drug does not increase the risks of death or hospitalization.

Dr. Daniel Frattarelli, a Detroit pediatrician and member of the American Academy of Pediatrics’s committee on drugs, said that he was treating children with Advair and that his committee had recently discussed the safety of the medicines.

“Most of us felt these were pretty good drugs,” Dr. Frattarelli said. “I’m really looking forward to hearing what the F.D.A. committee decides.”

About 9 percent of Advair’s prescriptions go to those age 17 and under, according to Glaxo. Ms. Meeker could not provide similar figures for Symbicort.

In 1994, Serevent was approved for sale, and the F.D.A. began receiving reports of deaths. A letter to the New England Journal of Medicine described two elderly patients who died holding Serevent inhalers. Glaxo warned patients that the medicine, unlike albuterol, does not work instantly and should not be used during an attack.

In 1996, Glaxo began a study of Serevent’s safety, but the company refused for years to report the results publicly. In 2001, the company introduced Advair, whose sales quickly cannibalized those of Serevent and then far surpassed them.

Finally in 2003, Glaxo reported the results of its Serevent study, which showed that those given the medicine were more likely to die than those given placebo inhalers. Glaxo said problems with the trial made its results impossible to interpret.

Asthma is caused when airways within the lungs spasm and swell, restricting the supply of oxygen. The two primary treatments are steroids, which reduce swelling, and beta agonists, which treat spasms. Rescue inhalers usually contain albuterol, which is a beta agonist with limited duration. Serevent and Foradil are both beta agonists but have a longer duration than albuterol and were intended to be taken daily to prevent attacks.

Advair contains Serevent and a steroid. Symbicort, introduced last year, contains Foradil and a steroid. In the first nine months of this year, Symbicort had $209 million in sales.

The problem with albuterol is that it seems to make patients’ lungs more vulnerable to severe attacks, which is why asthmatics are advised to use their rescue inhalers only when needed. The long-acting beta agonists may have the same risks.

But drug makers say this risk disappears when long-acting beta agonists are paired with steroids. The labels that accompany Serevent and Foradil instruct doctors to pair the medicines with an inhaled steroid.

Ozone-Depleting Inhalers Being Phased Out June 1, 2008

Posted by healthandsurvival in Allergies, Asthma, Diseases, Drugs, Global Warming, Politics and Medicine, Society, economy, environment, medicine.
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Surprisingly  the alternative to these medications are newly patented devices with the same “generic medicine” inside them. The result is patients will have to pay more money for the basic asthma rescue medicine, albuterol.  My personal opinion is that this has more to do with money and little to do with a hole in the ozone layer.

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Ozone-Depleting Inhalers Being Phased Out

By Steven Reinberg
HealthDay Reporter

 

FRIDAY, May 30 (HealthDay News) — Asthma inhalers that contain the drug albuterol to relax the airways also contain chemicals that harm the ozone layer. And these inhalers won’t be available after this year, so U.S. health officials are urging patients to switch to alternative inhalers now.

Chlorofluorocarbons, or CFCs, are widely used to propel inhaled drugs into the lungs. However, products containing CFCs are being phased out, because the chemicals damage the Earth’s protective ozone layer. CFC inhalers are being replaced by inhalers powered by HFAs, or hydrofluoroalkanes, which are ozone-friendly.

The change to HFA-powered inhalers has been in the works for several years, but the FDA issued an advisory on Friday, urging patients still using CFC inhalers to switch now. Inhalers containing CFCs will not be available after Dec. 31.

FDA officials said people with respiratory problems, such as asthma and chronic obstructive pulmonary disease, may need some time to acclimate to HFA-based inhalers.

“There are 52 million prescriptions written for albuterol inhalers each year in the United States,” Dr. Badrul Chowdhury, director of the U.S. Food and Drug Administration’s Division of Pulmonary and Allergy Products, said during a teleconference. Albuterol is used to treat shortness of breath in people with asthma and chronic obstructive pulmonary disease, he noted.

Chowdhury said that approximately 65 percent of inhaler users have already switched to HFA inhalers.

“These new handlers may taste and feel different than the current CFC inhalers,” he said. “In addition, HFA inhalers may feel softer than CFC inhalers.”

Also, patients using HFA inhalers will have to prime and clean them to prevent the buildup of albuterol in the inhalers’ nozzle. This buildup could block the medicine from reaching the lungs, Chowdhury said.

Each HFA inhaler has a different priming mechanism and cleaning and drying instructions. So, users should carefully read the instructions before using the inhaler. And HFA inhalers may cost more, because there’s no generic HFA inhaler available yet, Chowdhury said.

Three HFA-propelled albuterol inhalers have been approved by the FDA: Proair HFA Inhalation Aerosol; Proventil HFA Inhalation Aerosol; and Ventolin HFA Inhalation Aerosol. Also, an HFA-propelled inhaler containing levalbuterol, a medicine similar to albuterol, is available as Xopenex HFA Inhalation Aerosol, the agency said.

Dr. Ira Finegold, chief of the Division of Allergy and Clinical Immunology at St. Luke’s-Roosevelt Hospital Center in New York City, doesn’t see much difference in the effectiveness of the two types of inhalers. “The end result — if you need it, does it open up your lungs? Yes, it does,” he said.

However, the changeover will involve some patient education, he said. “The old medication, CFC albuterol, was really a very nice product, because the propellant got in your body and came out of your body — it wasn’t absorbed. And remarkably, it is a cleaning agent, so the device was self-cleaning.”

The new HFA propellant is safe in the body but can clog the inhaler, Feingold said. “So, after use, these inhalers need to be rinsed out or they are not going to work correctly,” he said.

“In addition,” Feingold added, “each of the four new inhalers on the market is different in the number of times you have to prime it. There is also a little difference in feel and taste.”

The discontinuation of CFC-propelled inhalers is the result of the U.S. Clean Air Act and an international treaty known as the Montreal Protocol on Substances That Deplete the Ozone Layer.

Under provisions of this treaty, the United States agreed to stop the production and importation of substances that damage the ozone layer, including CFCs, according to the FDA.

More information

For more on inhalers, visit the U.S. Food and Drug Administration.

SOURCES: May 30, 2008, teleconference with Badrul Chowdhury, M.D., Ph.D., director, Division of Pulmonary and Allergy Products, Center for Drug Evaluation and Research, U.S. Food and Drug Administration; Ira Finegold, M.D., chief, Division of Allergy and Clinical Immunology, Department of Medicine at St. Luke’s-Roosevelt Hospital Center, New York City

Common Allergy and Asthma Triggers- May 27, 2008

Posted by healthandsurvival in Allergies, Asthma, Children's Health, Diseases, Society, Wellness, environment, health, medicine.
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Allergies and Asthma  are conditions that are usually triggered by “trigger factors” that can be found both indoor and outdoor environments.  Prevention of an asthma attack or allergy exacerbation can be controlled by controlling exposure to the below triggers.  If avoidance is not possible, minimizing exposure is vital.

Common triggers include:

  • tobacco
  • smoke
  • perfumes
  • dust
  • dust mites
  • pet dander
  • pet hair
  • chemicals (lysol and other household cleaning chemicals)
  • paints
  • new carpets and the glues that they admit
  • cold viruses

 

For in home allergy prevention, HEPA filters, non HEPA air cleaners and home allergy cleaning supplies can all be helpfulAustin Air HEPA filters and Blue Air HEPA filter  units are among the industry leaders when it comes to indoor air HEPA filters. These units are doctor recommended for those with allergies and asthma. 

 

Cause Of Allergies Discovered? January 27, 2008

Posted by healthandsurvival in Allergies, Asthma, Diseases, medicine.
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bees.jpg  How Allergic Reactions Are Triggered

ScienceDaily (2008-01-17) — In demonstrating that a group of calcium ion channels play a crucial role in triggering inflammatory responses, researchers have not only solved a longstanding molecular mystery regarding the onset of asthma and allergy symptoms, but have also provided a fundamental discovery regarding the functioning of mast cells.

A group of immune cells found in tissues throughout the body, mast cells were once exclusively known for their role in allergic reactions, according to the study’s lead author Monika Vig, PhD, an investigator in the Department of Pathology at BIDMC and Instructor of Medicine at Harvard Medical School. “Mast cells store inflammatory cytokines and compounds [including histamine and heparin] in sacs called granules,” she explains. “When the mast cells encounter an allergen — pollen, for example — they ‘degranuate,’ releasing their contents and triggering allergic reactions.”

But, she adds, in recent years, scientists have uncovered numerous other roles for mast cells, suggesting they are key to a number of biological processes and are involved in diseases ranging from multiple sclerosis and rheumatoid arthritis to cancer and atherosclerosis. … > read full article

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