Clinical Apps Final Flashcards
Preferred diagnostic test for DVT?
Venous Duplex Ultrasonography
its a non-invasive ultrasound to assess the flow of blood through the veins of arms and legs
Management / Interventions for DVT
Bed-rest w/ legs elevated Gradual ambulation as tolerated by pt Change positions often Compression hose SCDs Leg exercises Adequate hydration
Patient education for DVT
Elevate legs when in bed or chair
Wear knee or thigh high compression stockings
Teach pt and family about anti-coagulation therapy
Avoid potentially traumatic events
DO NOT MASSAGE THE AFFECTED EXTREMITY- to prevent thrombus from dislodging and becoming an embolisms
Deep Vein Thrombosis (DVT)
- Most common type of thrombophlebitis. Presents greater risk for PE.
- With PE, a dislodged blood clot travels to the pulmonary artery
Where does DVT mainly occur
more common in lower extremities
can occur in upper arms from increased use of central venous devices
Classic S/S of DVT
calf or groin tenderness and pain and sudden onset of unilateral swelling of the leg
How will you assess a patient with DVT?
- Assess cap refill
- Assess skin –> color and temp will be red and warm
- Peripheral pulses may be decreased or absent (doppler may be needed)
- GENTLY palpate the site, observing for induction (hardening along the blood vessels and for warmth and edema)
- Monitor for signs of PE –> dyspnea, chest pain, tachypnea, cough, temp, syncope
Other test that may be ordered for a patient with DVT?
- MRI
- Impedence Plethysmography -> measures change in blood flow through veins
- D-dimmer test –> neg test can exclude a DVT without an ultrasound
How will DVT be treated?
*IV Anticoagulants (usually IV heparin and LMWH) typically followed by oral anti-coagulation with Warfarin (Coumadin)
Labs needed before starting DVT patient on IV unfractionated heparin.
- aPTT
- PT
- INR
- CBC
- Platelet count
- Urinalysis
- Stool for occult blood
- Creatinine
Management/Prevention of DVT
Bed-rest w/ legs elevated Gradual ambulation as tolerated by pt Change positions often Compression hose SCDs
Patient education for DVT
Elevate legs when in bed or chair
Wear knee or thigh high compression stockings
DO NOT MASSAGE THE AFFECTED EXTREMITY- to prevent thrombus from dislodging and becoming an embolisms
DVT risk factors
Smoking
Immobility
Oral contraceptives
Surgery
Autoimmune Thrombocytopenic Purpura
aka: Idiopathic Thrombocytopenia Purpura (ITP)
where the # of circulating platelets is greatly reduced, even though platelet production is normal.
pt with this makes an antibody against the surface of their own platelets
What causes ITP
cause unknown, viral infection suspected
Patients with ITP are at great risk for what
BLEEDING!
ITP is most common in who
Women ages 20-50 and people with autoimmune disorders
S/S in patients with ITP
**Symptoms first seen in the skin and mucous membrane
Large ecchymoses (bruises)
Petechial rash on arms, legs, upper chest, and neck
Mucosal bleeding occurs easily
What to assess in ITP patients?
ecchymoses (bruises)
petechial rashes
mucosa for bleeding
What test will be ordered for ITP patient?
Platelet count- will be low
Megakaryocytes in bone marrow- increased
Hct and HgB- will be low if bleeding episode occurs
Drugs to treat ITP
Drugs that suppress the immune function
Corticosteroids!
azathiprine (Imuran)
eltromopag
rituximab (Rituxan)
Treatment options for ITP patients
Drugs that suppress the immune function
Platelet transfusion- if platelet count is less than 10,000/mm3
Surgery: Splenectomy- for pts who do not respond to drug therapy
Patient education for ITP
Use electric razer
Use soft bristle toothbrush
Don’t floss
Don’t eat hard food/candy (ex: tortilla ships)
Have safe environment to protect from bleeding
Sickle Cell Disease (sickle cell anemia)
genetic hemoglobin disorder that results in chronic anemia, pain, disability, organ damage, increased risk for infection, and early death as a result of poor blood perfusion.
gets worse over time in adults
What do sickled cells do
they become rigid and clump together, causing RBCs to become “sticky” and fragile.
SCD results in formation of abnormal hemoglobin chains
Sickle cell crisis occurs from
occurs in response to conditions that cause local system Hypoxemia.
Examples:
- Stress
- Dehydration
- Pregnancy
- High altitudes
- Smoking
Most common symptom of SCD crisis
PAIN!!
Cardiovascular changes in SCD
*Risk of high output heart failure r/t anemia
JVD
Murmurs
Respiratory changes in SCD
occurs over time, many SCD pts develop pulmonary hypertension and all are at risk for recurrent pneumonia
Skin changes in SCD
pallor
cyanosis
jaundice
Abdominal changes in SCD
damage to the spleen and liver
(which often occurs early from many episodes of hypoxia and ischemia
Kidney and Urinary changes in SCD
poor perfusion can lead to CKD
Musculoskeletal changes in SCD
joints may be damaged from hypoxic episodes
Central Nervous System (CNS) changes
assess for a “pronator drift” a bilateral hand grasps strength, gait, and coordination
How is SCD diagnosed
based on percentage of Hemoglobin S (HgS) on electrophoresis
Tests ordered for SCD patient
- Percentage of HgS
- Hematocrit- low
- Reticulocyte count- high, indicating anemia of long duration
- Total bilirubin level- may be high
- Total WBC count- usually high
- ECG- can show any heart damage
Drug therapy for SCD
Drug therapy for pts in crisis often starts with at least 48hrs of IV analgesics
- morphine - hydromorphone (Diladid)
hydroxyurea (Droxia)- may reduce # of sickling and pain episodes by stimulating fetal hemoglobin (HbF) production.