degree of burns

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    Degree of Burns

    First Degree Burns: First degree burns affect

    only the skin surface, also known as the

    epidermis. The burn site often is red, painful

    and dry. Sunburn is a good example of a first

    degree burn

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    Second Degree Burns: Second Degree Burns

    penetrate the skin surface and involve the

    next lawyer of skin tissue known as the

    dermis. The urn site is often red, blistered,

    swollen and painful. These burns are

    frequently caused by scalding injuries from

    hot fluids, flames and brief skin contact with ahot object.

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    Third Degree Burns: Third Degree Burns are deepburns that destroy the outer and inner skinprotections. In these burns the epidermis anddermis tissue is destroyed. Often times in a third

    degree burn in addition to skin damage, bones,tendons and muscles are also injured. The skinappears to be white or charred. In a third degreeburn nerve tissue is also damaged causing varying

    amounts of pain. Like second degree burns, thirddegree burns are frequently caused by a scaldingliquid, skin that comes into contact with a hotobject, flames and electrical or chemical contact.

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    Siklus toxoplasma gondii

    Siklus hidup toxoplasma ada dua fase, yaitu

    fase intestinal dan ekstraintestinal. Fase

    intestinal hanya terjadi dalam intestinum

    kucing. Enzim pencernaan dihasilkan

    toxoplasma untuk menembus dinding

    intestinum.

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    Reproduksi parasit menghasilkan berjuta-juta

    oocyst yang tidak infeksius, yang akan

    diekskresikan bersama feses. Di luar tubuh

    kucing, oocyst mengalami sporulasi

    (sporogony) yang terjadi paling lama 21 hari,

    dan menghasilkan oocyst infeksius.

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    Pada daerah dengan suhu panas dankelembaban tinggi, oocyst dapat tahan hidupsampai satu tahun. Fase ekstraintestinal dapat

    terjadi pada semua hewan atau manusia yangterinfeksi. Pada fase ini, bentuk tachyzoite(trophozoite) dapat menyebar ke berbagaiorgan melalui sirkulasi. Dalam jaringan akan

    berubah menjadi zoithocyste (bradyzoite)yang dapat menjadi persisten selama hidup,menjadi bentuk infeksi khornik atau laten.

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    DIABETES MELLITUS

    Insulin Dependent Diabetes(Tipe I)

    Kurangnya insulin dalam jumlah besarkarena hancurnya sel beta.

    Perkembangannya cepat.

    Biasanya terjadi pada usia 35 tahun&kebanyakan terjadi antara usia 10-16tahun.(oleh karena juvenile diabetes).

    Catatan laporan diabetik sekitar 10%.

    Non Insulin DependentDiabetes(Tipe II)

    Sela beta tidak menghasilkan

    cukup insulin / insulin yangdihasilkan menjadi kurangefektif.

    Perkembangan secaraberangsur-angsur.

    Biasanya terjadi pada usia > 40tahun (oleh karena faktor usia)

    Catatan laporan diabetik sekitar90%.

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    ANTI DIABETIK ORAL

    GOLONGAN ANTI DIABETIK ORAL

    1. SULFONILUREA Golongan obat ini bekerja dengan cara menstimulasi

    sel-sel beta di pulau langerhans pankreas untukmeningkatkan sekresi insulin.

    Contoh : klorpropamid, tolbutamid, tolazamid, glimepirid,glibenklamid, glipizid, gliklazid.

    2. BIGUANID

    Mekanisme kerja obat ini belum diketahui dengan pasti,kemungkinan adalah dengan penghambatan glukoneogenesis

    di hati & peningkatan penyerapan glukosa di jaringan perifer.

    Contoh : metformin, fenformin dan buformin.

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    3. ANALOG MEGLITINID

    Bekerja dengan cara mengikat reseptor sulfonilurea &

    menutup ATP-sensitive potassium chanal

    Contoh : Repaglinid

    4. ALFA GLUKOSIDASE INHIBITOR

    obat ini bekerja dengan cara inhibisi enzim alfa glukosidase

    di mukosa duodenum sehingga penguraian di/polisakaridamenjadi monosakarida dihambat.

    contoh : akarbose, miglitol

    5. THIAZOLIDINDION

    obat ini bekerja dengan cara meningkatkan sensitivitasjaringan perifer terhadap insulin, sehingga mendorongpankreas untuk meningkatkan pelepasan insulin.

    contoh : rosiglitazon, pioglitazon

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    Significant implications of the UKPDS

    findings include the following:

    Glycemic control has minimal effect on

    macrovascular disease risk; excess

    macrovascular risk appears to be related to

    conventional risk factors such as dyslipidemiaand hypertension

    Sulfonylureas and insulin therapy do not

    increase macrovascular disease risk

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    Metformin reduces macrovascular risk in

    patients who are obese[

    Vigorous blood pressure control reduces

    microvascular and macrovascular events; beta

    blockers and angiotensin-converting enzyme

    (ACE) inhibitors appear to be equally effective

    in this regard

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    Conventional oral hypoglycemic agents, such assulfonylurea (SU), are not suitable due to the riskof prolonged hypoglycemia; furthermore,

    metformin is contraindicated for moderate toadvanced CKD

    The National Kidney Foundation Kidney DiseaseOutcomes Quality Initiative guidelines

    recommended that alpha-glucosidase inhibitorsshould be avoided in patients with advancedstage CKD and on dialysis

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    Cardioversion

    The most common indications for

    synchronized cardioversion are unstable atrial

    fibrillation, atrial flutter, atrial tachycardia, and

    supraventricular tachycardias.