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2013年9月24日星期二

Nebulizers Can Be Used for More Than Just Asthma or Emphysema



Our bodies are made of a series of interconnected organs and parts that make up a series of systems that help our bodies run like well tuned machines. One of the most important systems that we rely on to get through life is the respiratory system. The organs that help this system run work together to take oxygen that we breathe in and help it get into the blood and then is utilized by the rest of our body. The importance of oxygen in our bodies is.Nebulizer for Respiratory obvious however there are many ways for your respiratory system to be disrupted. Luckily, for those who suffer respiratory related ailments there are many treatment solutions out there, and affordable equipment available that help sufferers stay healthy and comfortable.


The most common and easy to use kinds of respiratory equipment on the market are nebulizers. A nebulizer comes in many different forms from pocket sized personal use nebulizers to jet nebulizers that have to be stored somewhere in a room. Nebulizers take compressed air and mix it with a prescribed medication to allow it to be breathed in as a gas. It is a mixture of gas and liquid that can be easily absorbed as you breathe it in. This allows for the medication to be sent directly into the lungs, offering almost instant relief.


The most common reason to use a nebulizer is to treat chronic bronchitis and emphysema. These conditions are usually treatable with a combination of treatments as well as oxygen therapy, all of which is possible through the use of a nebulizer. Asthma and acute bronchitis are commonly treated with nebulizers but these are just the tip of the iceberg. Just about any respiratory related problem a person typically has can be treated with a nebulizer.


Nebulizer for Respiratory Other respiratory equipment that is often used for respiratory conditions are an MDI, spacers or a compressor. A meter dose inhaler, or MDI, is probably the cheapest and the most convenient type of inhaler that is sold. While it is not used to treat many respiratory conditions it is still the most efficient one out there if you are a candidate, and available for a very affordable price. Spacers come in several varieties with the most popular one being the Aerochamber. Aerochamber’s are used in conjunction with other devices such as an MDI. Spacers maintain the aerosol content, eliminating the need for any real coordination when administering the medication, and controls the amount of aerosol delivered.


Compressors are a step up from an MDI and are only slightly more expensive. Compressors come in many different sizes and typically put out at least 8 to 9 liters a minute and the larger ones can put out much more and actually fill a room. Compressors are primarily used to fill a nebulizer or release the treatment into the air of the room.


Top quality respiratory equipment is essential when it comes to the care of yourself, your loved ones or your patients. Whether it’s portable or home use oxygen, nebulizers or CPAP equipment and supplies, you don’t want to cut corners when it comes to treating respiratory conditions.


About The Author:
Bob Nielsen is co-owner of RoSa Medical Supply an online retail store. His website offers some of the best high quality Durable Home Medical Equipment on the internet for your everyday home health care needs on a fixed budget. His products are always at cheap discount prices because he is an authorized online reseller of numerous major brand name manufacturers, thus cutting out the middle-man and passing the savings on to you. When you visit his respiratory page you can be assured of receiving FAST shipping direct to your door as well as 100% SAFE secure checkout.


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Source: http://www.rosasupply.com/2012/08/nebulizers-can-be-used-for-more-than-just-asthma-or-emphysema/


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2013年9月13日星期五

late-onset sepsis in premature infants of less than or equal to 32 weeks of gest - European Medicines Agency - Rare disease designations - EU/3/10/755



On 27 July 2010, orphan designation (EU/3/10/755) was granted by the European Commission to Schülke & Mayr GmbH, Germany, for octenidine dihydrochloride for the prevention of late-onset sepsis in premature infants of less than or equal to 32 weeks of gestational age.


What is late-onset sepsis?
Late-onset sepsis is a severe bacterial infection of the blood that occurs in newborn babies at least three days after birth. Premature babies born eight weeks or more too early (32 weeks of gestational age or less) have a higher risk of late-onset sepsis than other babies. This is because their immune system, skin and moist body surfaces are not yet fully developed, and because they need invasive procedures such as mechanical ventilation (using a machine to help them to breathe) or administration of medicines or feeding by injection, which can put them at risk of infections in neonatal intensive care units.
Late-onset sepsis is a life-threatening condition that is one of the causes of high mortality in premature babies born at 32 weeks of gestational age or less.


What is the estimated number of patients at risk of developing the condition?
At the time of designation, the number of premature babies born at 32 weeks of gestational age or less was estimated to be approximately 1.5 people in 10,000 in the European Union (EU)*. This is equivalent to a total of around 76,000 babies, and is below the threshold for orphan designation, which is 5 people in 10,000. This is based on the information provided by the sponsor and the knowledge of the Committee for Orphan Medicinal Products (COMP).
*Disclaimer: For the purpose of the designation, the number of patients affected by the condition is estimated and assessed on the basis of data from the European Union (EU 27), Norway, Iceland and Liechtenstein. This represents a population of 506,500,000 (Eurostat 2010).


What methods of prevention are available?
At the time of designation, no satisfactory methods were authorised in the EU for the prevention of late-onset sepsis in these babies. Common infection-control measures such as hand-washing were used to keep the infection rate as low as possible in neonatal intensive care units. In some cases, antibiotics and skin antiseptics were also used to prevent infection.


How is this medicine expected to work?
Octenidine dihydrochloride is an antiseptic that has been available in the EU since 1997 in two medicines, which also contain alcohol, for disinfecting the skin and moist body surfaces in children and adults. Octenidine dihydrochloride works by blocking the growth of bacteria, fungi and other organisms that can cause infection.
This medicine is an aqueous solution of octenidine dihydrochloride. The absence of alcohol is expected to make it suitable for use on the sensitive skin of premature babies.


What is the stage of development of this medicine?
The effects of octenidine dihydrochloride have been evaluated in experimental models.
At the time of submission of the application for orphan designation, no clinical trials with octenidine dihydrochloride in premature babies born at 32 weeks of gestational age or less had been started.
At the time of submission, octenidine dihydrochloride as single agent was not authorised anywhere in the EU for the prevention of late-onset sepsis in premature infants or designated as an orphan medicinal product elsewhere for this condition.
In accordance with Regulation (EC) No141/2000-of 16 December 1999, the COMP adopted a positive opinion on 8 April 2010 recommending the granting of this designation.


Opinions on orphan medicinal product designations are based on the following three criteriathe seriousness of the condition;the existence of alternative methods of diagnosis, prevention or treatment;either the rarity of the condition (affecting not more than 5 in 10,000 people in the EU) or insufficient returns on investment.Designated orphan medicinal products are products that are still under investigation and are considered for orphan designation on the basis of potential activity. An orphan designation is not a marketing authorisation. As a consequence, demonstration of quality, safety and efficacy is necessary before a product can be granted a marketing authorisation.


EU/3/10/755: Public summary of opinion on orphan designation: Octenidine dihydrochloride for the prevention of late-onset sepsis in premature infants of less than or equal to 32 weeks of gestational age
http://www.ema.europa.eu/docs/en_GB/document_library/Orphan_designation/2010/08/WC500095702.pdf


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European Medicines Agency – Rare disease designations – EU/3/10/755