Ear Surgery in Fairfield CA


The surgery called otoplasty and it is targeted to correct protruding or large outer ears. It is usually done in children ages 4-14. The ear reaches it's final size around ages 4-6 and therefore it is better to perform the surgery at a younger age to avoid unnecessary suffering. Additional conditions which can be corrected are "lop ear" in which the upper ear is folded and leans forward, "cupped ear" in which the outer ears are unusually small and "shell ear" in which there is flattening of the folds resulting in a shell like ear. Long, short or torn ear lobes also can be fixed. This operation can repair congenital ear defects and make reconstruction of the outer ear after trauma.

The operation usually lasts between 1-3 hours; more complex procedures may last even longer. A cut is made behind the ear, making it invisible, to allow excess to ear cartilage. Then the surgeon will design the cartilage using cuts and sutures to get the desired shape. Sometimes non-absorbable stitches are used in order to create fold, those stitches will be under the skin and there is no need to remove them. A few surgeons prefer to make the cut in front of the ear and hide the scar behind the skin folds. In most of the cases the scar fades with time and is hardly seen. Both ears can be corrected in the same operation.

For younger children general anesthesia is preferred, for cooperative adults it can be done using local anesthetics and sedative drugs. Every operation has its risk. There is risk of blood clots under the scar area which usually absorb after few days; otherwise there is a need to drain then. There is a risk of infection involving the ear cartilage which can leave a scar. Those infection can be treated successfully with antibiotics in most of the cases and rarely require surgical drainage.

After the surgery a majority of the adults can return to their homes, young children usually left overnight for observation. The ears are bandaged with a bandage around the head to prevent bleeding and preserve the final shape. The ears will be swollen and painful for a couple of days. It is advised to avoid any activities that can harm the ears for about a month. Children should pay extra attention while playing. You shouldn't sleep on the repaired ear for about 7-10 days

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    Best Western Cordelia Inn, 4373 Central Place, ? +1 707 864-2029 (toll free: +1 800 422-7575, fax: +1 707 864-5834), [1].
    Courtyard Fairfield Napa Valley Area, 1350 Holiday Lane, ? +1 707 422-4111 (fax: +1 707 428-3452), [2].


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  • The Committee for Medicinal Products for Human Use (CHMP) of the EMEA has adopted a negative opinion, recommending the refusal of the marketing authorisation for the medicinal product Lenalidomide Celgene Europe, intended for the treatment of anaemia due to myelodysplastic syndromes (MDS). Lenalidomide, under the brand name Revlimid®, is currently approved in the UK for the treatment of multiple myeloma. Lenalidomide Celgene Europe was expected to be used to treat anaemia caused by MDS (associated with deletion of part of chromosome number 5), in patients who were dependent on blood transfusions and who had a low to intermediate risk of progressing to leukaemia or death. According to the Question and Answers document, the CHMP was of the opinion that the benefits of Lenalidomide – Celgene Europe in the treatment of this condition did not outweigh its potential risks. There were some concerns expressed over the main study, including its design and the recording of results (please see the link above for further details).

  • The European Medicines Agency (EMEA) has recommended the approval of Thalidomide Pharmion (thalidomide) for the treatment of multiple myeloma, a rare cancer of the bone marrow. The Agency’s Committee for Medicinal Products for Human Use (CHMP) has concluded that the benefits of Thalidomide Pharmion® in combination with melphalan and prednisone outweigh its risks for the first-line treatment of multiple myeloma for patients over 65 years of age or who cannot be treated with high-dose chemotherapy. Thalidomide is teratogenic and because of this, the CHMP has consulted representatives of thalidomide victims and myeloma patient groups from across the European Union to develop measures that can effectively minimise the risk of foetal exposure to thalidomide. The CHMP has approved a risk management plan that includes a number of actions intended to prevent pregnancies in women being treated with thalidomide and exposure of unborn children to the medicine. For example, all women of child-bearing potential who are treated with Thalidomide Pharmion must undergo pregnancy tests before, during and after treatment, in addition to using selected and effective contraception. Subject to the granting of a marketing authorisation by the European Commission, Thalidomide Pharmion will only be available by prescription, and treatment will be initiated and monitored by a doctor who has experience in the treatment of multiple myeloma. A clear warning will be printed on the boxes containing the medicine, indicating that Thalidomide Pharmion causes birth defects and foetal death. Educational materials will be provided to healthcare professionals and patients by Pharmion Ltd prior to the launch of Thalidomide Pharmion in each Member State to ensure the safe use of the product.

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