Types of Bleeding Disorders

فهرست عناوین اصلی در این پاورپوینت

فهرست عناوین اصلی در این پاورپوینت

● The Student with Hemophilia
● What is Hemophilia?
● Clinical Characteristics
● Hemophilia Treatment Center Team Members
● Role of Hemophilia Treatment Center
● Services
● Types of Bleeding Disorders
● Incidence
● School Issues
● How Blood Clots
● Hemostasis
● Coagulation Cascade
● Bleeding in Hemophilia
● Inheritance
● Genetics
● Clinical Aspect
● Type and Severity
● First Bleed/Diagnosis
● Bleeding Pattern Mild
● Carriers
● Bleeding Pattern Moderate
● Bleeding Pattern Severe
● Types of Bleeds Treatment and Management
● Types of Bleeds
● Joint or Muscle Bleeding
● Treatment of Hemophilia
● Factor VIII Concentrate
● DDAVP (Desmopressin acetate)
● Stimate ®
● Factor IX Concentrate
● Minor Bleeding Episodes
● Major Bleeding Episodes
● Primary Prophylaxis
● Secondary Prophylaxis
● Morbidity of Chronic Disease
● Adjunctive Therapy
● Bleeding Episodes
● Life-Threatening Bleeding
● Joint Bleeds
● Advanced Joint Bleed
● Complications Joint Bleeds
● X-Ray of severe joint damage from recurrent hemarthrosis
● Muscle Bleeding
● Advanced joint and muscle bleed
● Complications Muscle Bleeds
● Other Common Bleeds
● School Issues
● Sports
● Responsibilities:Student
● Responsibility: Parent
● Responsibility: School
● School Issues
● IHP: Nursing Diagnosis
● IHP: Goals
● IHP: Nursing Interventions
● IHP Plan: Outcomes

نوع زبان: انگلیسی حجم: 0.68 مگا بایت
نوع فایل: اسلاید پاورپوینت تعداد اسلایدها: 60 صفحه
سطح مطلب: نامشخص پسوند فایل: ppt
گروه موضوعی: زمان استخراج مطلب: 2019/06/15 09:04:17

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عبارات مهم استفاده شده در این مطلب

عبارات مهم استفاده شده در این مطلب

bleed, bleeding, hemophilia, joint, factor, ., viii, ix, level, muscle, episode, unit,

توجه: این مطلب در تاریخ 2019/06/15 09:04:17 به صورت خودکار از فضای وب آشکار توسط موتور جستجوی پاورپوینت جمع آوری شده است و در صورت اعلام عدم رضایت تهیه کننده ی آن، طبق قوانین سایت از روی وب گاه حذف خواهد شد. این مطلب از وب سایت زیر استخراج شده است و مسئولیت انتشار آن با منبع اصلی است.

https://www.hemophilia.org/sites/default/files/document/files/The-Student-with-Hemophilia-Teaching-Strategies.ppt

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عبارات پرتکرار و مهم در این اسلاید عبارتند از: bleed, bleeding, hemophilia, joint, factor, ., viii, ix, level, muscle, episode, unit,

مشاهده محتوای متنیِ این اسلاید ppt

مشاهده محتوای متنیِ این اسلاید ppt

the student with hemophilia ellen white rn bsn yvette menga lsw what is hemophilia hemophilia is an inherited bleeding disorder in which there is a deficiency or lack of factor viii hemophilia a or factor ix hemophilia b clinical characteristics internal bleeding into joints muscles and major organs depending on the factor level bleeding can be spontaneous or caused by trauma bleeds longer not faster soft tissue bleeds hematomas hemophilia treatment center team members patient family hematologist pediatric adult nurse social worker physical therapist orthopedist primary care genetics home care company dental role of hemophilia treatment center state of the art medical treatment for persons with hemophilia through the life span education research outreach model of comprehensive care for chronic disease services medical nursing psychosocial physical therapy dental services diagnostic laboratory services genetic counseling and testing types of bleeding disorders hemophilia a factor viii deficiency hemophilia b factor ix deficiency incidence hemophilia a ۱ ۵ male births hemophilia b ۱ ۳ male births school issues frequent absences hard to catch up decreased peer support activity restrictions no contact sports immobilization during bleeding episodes pain chronic acute how blood clots blood vessels platelets plasma coagulation system proteolytic or fibrinolytic system hemostasis vasoconstriction platelet plug formation clotting cascade activated to form fibrin clot coagulation cascade hoffman et al. blood coagul fibrinolysis ۱۹۹۸ ۹ suppl ۱ s۶۱. tf bearing cell activated platelet platelet tf viiia va viiia va va viia tf viia xa x ii iia ix v va ii viii vwf viiia ii ixa x ix x ixa ixa viia xa iia iia xa bleeding in hemophilia vasoconstriction platelet plug formation the clotting cascade is not activated a fibrin clot does not form bleeding will continue inheritance hemophilia a and b are x linked recessive disorders hemophilia is typically expressed in males and carried by females severity level is consistent between family members ۳ of cases of hemophilia are new mutations affects all races and ethnic groups equally moderate mild deficiencies under diagnosed genetics affected males all daughters are carriers no sons are affected female carrier ۵ risk for carrier daughter ۵ risk for affected son clinical aspect type and severity normal factor viii or ix level ۵ ۱۵ mild hemophilia factor viii or ix level ۵ ۵ moderate hemophilia factor viii or ix level ۱ ۵ severe hemophilia factor viii or ix level ۱ first bleed diagnosis mild often has bleeds at an earlier age but not identified till later in life ۳ to ۱۴ years or older moderate usually before ۲ years severe within first year bleeding pattern mild once a year joint and muscle bleed unusual except with significant trauma trauma induced or contact sports significant hematomas internal deep bleeding only with significant trauma post op bleeding carriers carriers may have low factor levels carriers may experience bleeding symptoms seen in mild or moderate deficient states treat carriers as potential bleeders bleeding pattern moderate bleeds once a month minor trauma causes joint and muscle bleed may have target joints post surgical wound hematoma or oozing this patients do developed joints and muscle bleeds and can developed target joints. can have post circ bleeding ich are rare. post op wound hematomas and oozing rarely none. contact sports bleeding pattern severe bleeds once a week spontaneous joint and muscle bleed target joints patients with severe hemophilia a tend to bleed spontaneusly aprox ~ bleed a week the first bleed is withing the first year of life when they crawl ۳ bleed with circ. ۱to ۲ neonatal ich developed spontaneus joint and muscle bleeds developed target joints post op they bleed profuselly they bleed commomly with trauma and dental extractions they have ۱۵ ۲ prevalence if developing inhibitors. no responce to ddavp types of bleeds treatment and management types of bleeds joint bleeding hemarthrosis muscle hemorrhage soft tissue life threatening bleeding other common bleeding joint or muscle bleeding symptoms tingling or bubbling sensation stiffness warmth pain unusual limb position treatment of hemophilia replacement of missing clotting protein intravenous infusion on demand prophylaxis primary secondary factor viii concentrate intravenous infusion iv push dose varies depending on type of bleeding ranges from ۲ ۵ units kg. body weight half life ۸ ۱۲ hours each unit infused raises serum factor viii level by ۲ ddavp desmopressin acetate synthetic vasopressin method of action release of stores from endothelial cells raising factor viii and vwd serum levels administration intravenous subcutaneously nasally stimate stimate ® dosing every ۲۴ ۴۸ hours prn not to be used more than three days in a row ۵ kg. body weight ۱ spray ۱۵ mcg. ۵ kg. body weight ۲ sprays ۳ mcg. factor ix concentrate intravenous infusion iv push dose varies depending on type of bleeding ranges from ۲ ۱ units kg. body weight half life ۱۲ ۲۴ hours each unit infused raises serum factor ix level by ۱ minor bleeding episodes early joint bleeds soft tissue muscle bleeds nose gum bleeding not responding to local measures treatment of minor bleeding episodes ۴ ۵ correction fviii ۲ ۲۵ units kg fix ۴ ۵ units kg major bleeding episodes head neck injuries advanced soft tissue muscle bleeds abdominal bleeding advanced joint bleeding treatment of major bleeding episodes ۱ correction fviii ۵ units kg fix ۱ units kg primary prophylaxis scheduled infusion therapy at an early age before bleeding has regularly occurred to convert patient from severe deficient state to moderate deficient goal suppression of spontaneous bleeding episodes frequency ۲ to ۳ times weekly to keep trough factor viii or ix levels at ۲ ۳ use of ivad necessary in some patients secondary prophylaxis scheduled infusion therapy at any age after bleeding has regularly occurred or after injury to convert patient from severe deficient state to moderate deficient prior to sports activity goal suppression of spontaneous bleeding episodes or rebleeding frequency ۲ to ۳ times weekly to keep trough factor viii or ix levels at ۲ ۳ use of ivad necessary in some patients morbidity of chronic disease school absenteeism increased in children with severe hemophilia compared to normal population difficulty attending to task if in pain ability to achieve potential and find a productive appropriate place in work force number of bleeding episodes impacts ability to achieve potential prophylaxis decrease morbidity of chronic disease adjunctive therapy rice rest replacement ice immobilization compression elevation antifibrinolytic agents amicar ® aminocaproic acid used for mucocutaneous bleeding dosing ۵ mg. kg. q. ۶ hours po bleeding episodes life threatening bleeding head intracranial nausea vomiting headache drowsiness confusion visual changes loss of consciousness neck and throat pain swelling difficulty breathing swallowing abdominal gi pain tenderness swelling blood in the stools iliopsoas muscle back pain abdominal pain thigh tingling numbness decreased hip range of motion joint bleeds most common bleeding manifestation most common joint knees ankles elbows collection of blood in joint …

کلمات کلیدی پرکاربرد در این اسلاید پاورپوینت: bleed, bleeding, hemophilia, joint, factor, ., viii, ix, level, muscle, episode, unit,

این فایل پاورپوینت شامل 60 اسلاید و به زبان انگلیسی و حجم آن 0.68 مگا بایت است. نوع قالب فایل ppt بوده که با این لینک قابل دانلود است. این مطلب برگرفته از سایت زیر است و مسئولیت انتشار آن با منبع اصلی می باشد که در تاریخ 2019/06/15 09:04:17 استخراج شده است.

https://www.hemophilia.org/sites/default/files/document/files/The-Student-with-Hemophilia-Teaching-Strategies.ppt

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