Cricoid cartilage

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    of the throat. If nothing is found then you look at the teeth to see if anything is broken or missing. Also, checking to see if there is any blood found that could cause clotting or any other form of obstruction. When you're checking the nose you need to take a light source and pug nose the patient. This way you can look and see things effectively. Looking for any swelling, bleeding, and/or any signs for inhalation burns When the problem has been identified it needs to be determined if the patient needs a Cricothyrotomy. Before the Cricothyrotomy can be performed the cricothyroid membrane must be found. Finding the Cricothyroid membrane is found by palpating the trachea just above the Sternal notch until the cricoid cartilage is identified. After the cricothyroid cartilage is found it is time to get the tools you need. So, a scalpel, ET tube, trachea hook, syringe, BVM, and alcohol prep pads. Now everything has been accounted for the cricothyroid membrane needs to be found again. After the membrane has been found again place one hand on the trachea. Being sure that you are as gentle but firm as possible. Gently clean the site with alcohol wipes. Cleaning in a circular motion from the inside out. Never going over the same area twice. Grab the scalpel and steady your hand with your pinky on the patient’s chest. The first incision must be done vertically about an inch and a half long. Only cutting the skin. While still holding the trachea takes the scalpel and turn it…

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    What Is Achondroplasia?

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    most cases it streams from having a mutation randomly occur in the FGFR3 gene later in life. FGFR3 protein has many versions, which are found in different areas of the body. Many of these proteins are found in the cells that forms bone. FGFR3 is believed to regulate bone growth. Age can effects the mutation, therefore someone who develops achondroplasia later in life could pass a less severe case to their children. “Achondroplasia means without cartilage formation”(3), and is a Greek word.…

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    Osteogenesis Imperfecta (OI) is a genetic disorder that affects the formation of bones. The term Osteogenesis Imperfecta literally means imperfect bone formation. People with OI have bones that break easily, usually caused by a mild trauma or no cause at all. Multiple fractures are common with this disease since bones are weak. Although, in severe cases fracture of bones can occur before birth. This disease is caused by defective connective tissue and the lack of Type One Collagen. There are…

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    Osteoarthritis Osteoarthritis is a degenerative condition of the joint cartilage, the smooth cushion of gristle found in all of our normal joints (Porter, 277). Inflammation does not occur but bare bone ends begin to rub against each other. The British call it osteoarthrosis, because of the fact it is not an inflammatory condition. The most common type of arthritis next to rheumatoid arthritis. This arthritis tends to occur in the hand joints, spine, hips, knees, and great toes. The lifetime…

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    Osteogenesis imperfecta (OI) is a genetic disorder that affects the skeletal system. The disorder affects the bones, it makes them fragile and easy to break. OI has many different types; type I one being the most common and mildest, and type II is the most severe. The first case of OI was found in a partially mummified infant's skeleton found from ancient Egypt. In 1835, Jean Lobstein made the term for osteogenesis imperfecta and was the first to correctly understand the causes of the disorder. …

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    The most common disease also referred to as common joint disease (OA) is what occurs when one or more synovial joints fail. This failure of the joint causes the top layer of cartilage to break down and the affected bones slowly become bigger. Aside from this joint breakdown and bone growth, cartilage wearing causes rubbing to occur which then leads to sharp pain. This disease affects 80% of people over the age of 75 and it is highly prevalent among those over 60. Women experience OA more than…

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    As the body age’s, different ailments and diseases seem to creep in and attach itself to joints, ligaments, and bones. One such disease is osteoarthritis. Osteoarthritis is a degeneration of joint and cartilage and the underlying bone. This is more common in the middle age onward. This disease causes pain and stiffness in the joint if affects. The joints it affects is the hip, knee, and thumb joints (USA.GOV, 2015). Therefore, “Evidence-based clinical guidelines: A New System to Better Determine…

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    Osteoarthritis (OA) is a degenerative condition of articular cartilage in joints commonly affecting the knees (Sinusas 2012) and slowly develops over many years resulting from mechanical stress (Kisner and Colby 2003). Unfortunately, the risk of developing OA increases with several factors including genetics, increasing age, obesity and female gender (Sinusas 2012). OA causes pain and stiffness in the joints however it is an incurable disease and therefore physiotherapy treatment should focus on…

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    However, it wasn’t until 2006 that it was discovered that the gene ACVR 1 in chromosome 2 was the main cause of FOP (Kaplan, Nassau, & Shore, 2014). This gene is responsible for providing instructions to a protein that assists the development and replacement of bone in the human body. What happens, is that the gene mutation that occurs in ACVR 1 alters stem cells ability to differentiate into the specific types of tissues or cells that are needed to repair injuries and replace cells (Kaplan,…

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    her knees and fingers. The physician diagnosed the woman with osteoarthritis (OA). Osteoarthritis, or degenerative joint disease, is considered one of the most globally prevalent rheumatoid disorders (Mayo Foundation for Medical Education and Research, 2014a). This specific type of arthritis is an asymmetric, metabolic disorder of the synovial joints and articular cartilage. According to Porth (2015), clients diagnosed with osteoarthritis will manifest symptoms such as restricted range of…

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