ASKEP THALASEMIA PDF

Askep Thalasemia Ela – Download as Word Doc .doc /.docx), PDF File .pdf), Text File .txt) or read online. The PDF file you selected should load here if your Web browser has a PDF reader plug-in installed (for example, a recent version of Adobe Acrobat Reader). Thalassemias are inherited blood disorders characterized by abnormal hemoglobin production. Symptoms depend on the type and can vary from none to severe.

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Warna kulit pucat kekuningan, jika anak telah sering mendapat transfusi warna kulit akan menjadi kelabu seperti besi.

Hal ini terjadi karena adanya penumpukan zat besi dalam jaringan kulit hemosiderosis. Williams Hematology 9e ed. Dokumentasikan gambaran keperawatan 1 x 24 jam, tidak terjadi perkembangan kulit setiap hari kerusakan pada integritas kulit: Berikan perlindungan pada kulit seperti krim pelembab atau penyerap cairan, untuk mengatasi basah berlebih 5. Brother’s blood is boon of life Archived 22 September at the Wayback Machine.

Askep Teori Thalasemia Nic Noc – PDF Free Download

Department of Medical Sciences. Analysis of clinical evidences and their relations. Using this InsP4 receptor, an assay for measuring tissue content of InsP4 was developed. SITE To ensure the functioning of the site, we use cookies. All articles with dead external links Articles with dead external links from May Articles with permanently dead external links Wikipedia articles needing page number citations from June CS1 Thai-language sources th Webarchive template wayback links Infobox medical condition new All articles with unsourced statements Articles with unsourced statements from June Articles with unsourced statements from March Articles with Curlie links Use dmy dates from September RTT.

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The best results are with very young people. Kulit dan mulai dari hari pertama dirawat Setelah NOC dilakukan Membran Mukosa – Perfusi jaringan tidak terganggu – Integritas kulit tidak – terganggu Tidak ada lesi pada kulit Tidak ada pigmentasi abnormal 2.

Thalassemias are inherited blood disorders characterized by abnormal hemoglobin production. Archived from the original on 15 September In the same tissue samples the amount of Ins 1,4,5 P3 was determined in parallel with a similar assay using a binding protein preparation from beef liver. Archived from the original on 28 July Nowadays, it is found in populations living in Africa, the Americas, and in Tharu people in the Terai region of Nepal and India.

The child was born from an embryo screened to be free of the disease before implantation with aske; vitro fertilization. Current Opinion in Obstetrics and Gynecology. Goljan, Pathology, 2nd ed. Pasang bantalan pada siku dan tumit jika dibutuhkan 8. Implementasi Implementasi yang dilakukan sesuai intervensi keperawatan E.

The situation of both alleles determines the clinical picture:. The iron overload related to thalassemia may be treated by chelation therapy with the medications deferoxaminedeferiproneor thalasrmia.

Berikan informasi mengenai zskep pengurangan – nyamanan nyeri nyeri yang terkontrol nyeri, seperti penyebab nyeri, berapa lama nyeri akan dirasakan, dan antisipasi dari ketidak nyamanan akibat prosedur 5. Perbaikan perfusi jaringan dengan tanda-tanda vital yang stabil.

The baby’s supply of immunologically compatible cord blood was saved for transplantation to his brother. Tentukan status gizi pasien dan kemampuan untuk memenuhi kebutuhan gizi 2. Enter the email address you signed up with and we’ll email you a reset link. Deferoxamine is only effective via daily injections which makes its long-term use more difficult. For the autosomal recessive forms of the disease, thhalasemia parents must be carriers for a child to be affected. qskep

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As askeppthalassemia occurs in about million people, with abouthaving severe disease. Pantau alat-alat yang dapat menimbulkan gesekan dan tekanan 7. Retrieved 6 September Monitor efektifitas terapi oksigen dengan tepat 6.

Pertumbuhan dan Perkembangan Adanya kecenderungan gangguan tumbuh kembang sejak anak masih bayi, karena adanya pengaruh hipoksia jaringan yang bersifat kronik. Multiple blood transfusions can result in iron overload. Risiko kerusakan integritas kulit 3.

The American College of Obstetricians and Gynecologists recommends all people thinking of becoming pregnant be tested to see if they have thalassemia. Intruksikan pasien mengenai kebutuhan nutrisi 5.

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We share information about your activities on the site with our partners and Google partners: Beta thalassemias are due to mutations in the HBB gene on chromosome 11, [24] also inherited in an autosomal, recessive fashion. The beta form of thalassemia is particularly prevalent among Mediterranean peoples, and this geographical association is responsible for its original name. Mata dan konjungtiva pucat dan kekuningan d.

Rhalasemia jumlah kalori dan jenis nutrisi yang thalaemia untuk memenuhi persyaratan gizi 2. Pada inspeksi terlihat dada kiri menonjol karena adanya pembesaran jantung dan disebabkan oleh anemia kronik. Hereditary spherocytosis Minkowski—Chauffard syndrome Hereditary elliptocytosis Southeast Asian ovalocytosis Hereditary stomatocytosis.