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Last updated 12:33 AM on 4/20/26
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110 Terms

1
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RBC Physiology

-RBCs serve to transport

-Normal Hgb ____ serves as

-Left shift vs Right shift DOC

-Circulating RBCs, myeloid cells and lymphoid cells all originate from

-RBCs become enucleated during

<p></p>
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Next Step: If a patient presents with CO poisoning

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CO poisoning includes signs of

mental status changes

cherry red lips

hypoxia despire normal pulse ox readings

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Hgb-Ox disssociation curve

left shift

red shift

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Normal Hgb concentrations and Hct

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Micocytic anemia pneumonic

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Classification of Anemias

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Hemolytic Anemia

-defined by

-can be caused by

-SXS

-Workup

-Coombs Test

-Blood smear

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Mean RBC lifespan is

Consider IDA in elderly patients caused by

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IDA

-defined as

-results from

-SXS

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IDA

-Workup

-Blood Smear

-Tx

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Drug induced hemolytic anemia

-Pathophysiology

-Blood Smear

-Coombs Test

-Other Diagnostic Aids

-Treatment

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Auto-Immune Hemolytic Anemia (AIHA)

-Pathophysiology

-Blood Smear

-Coombs Test

-Other Diagnostic Aids

-Treatment

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Mechanical Hemolytic Anemia

-Pathophysiology

-Blood Smear

-Coombs Test

-Other Diagnostic Aids

-Treatment

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Hereditary spherocytosis hemolytic anemia

-Pathophysiology

-Blood Smear

-Coombs Test

-Other Diagnostic Aids

-Treatment

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G6PD hemolytic anemia

-Pathophysiology

-Blood Smear

-Coombs Test

-Other Diagnostic Aids

-Treatment

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Labs

  • Serum Iron

  • Ferritin

  • TIBC (transferrin)

  • Iron: TIBC Ratio

  • Blood smear

Type:

  • IDA

  • Chronic Dz

  • Lead poisioning

  • Sideroblastic

  • Thalassemia

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Lead Poisoning Anemia

-defined by

-similar presentation seen in

-SXS

-Workup

-Blood Smear

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Folate deficiency is most common cause of

megaloblastic anemia

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Folate Deficiency anemia

-SXS

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Inadequate folate intake is seen with _____ and in the ____ because of poor nutrition

alcoholism and in the elderly

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Vitamin B12 def anemia

-SXS

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Inadequate B12 intake is usually only seen in

strict vegetarians/ vegans

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Anemia of chronic disease

-defined by

-frequently assoicated with

-SXS

-Workup

-Blood smear

-TX

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___caused by inadequate dietary intake develops ___ vs ____from inadequate intake

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Aplastic Anemia

-Due to

-SXS

-Workup

-Tx

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Aplastic anemia in Sickle cell patient is classically caused by

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Sideroblastic anemia

-defined by

-can be a ___ or caused by ____

-Blood smear

-Tx

-Complications

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Patients with alpha thalsaeemia minima usually have a

normal MCV

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Thalassemia

-defined. by

-disease state arrises from

-normal Hgb

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Types of thalassemias and characteristics

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Alpha vs beta

-more prevalant in

-variants between

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Thalassemia

-Workup

-Blood smear

-Tx

-Complications

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Next Step: if microcytic anemia if found on blood smear

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Heterozygous carriers of sickle cell defect (sickle cell trait) are

Presence of fetal hgb in newborns delays presentation of

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Sickle cell disease

-___ cause Hgb S molecules to polymerize and distort RBCs into

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Sickle Cell Disease

-Radiology

-Blood Smear

Radiology:

  • Codfish vertebrae

  • Lung infiltrates if acute chest syndrome 

Blood smear: 

  • Target cells 

  • Nucleated RBCs

  • Deoxygenation of blood producing sickle cells 

<p><strong>Radiology:</strong></p><ul><li><p class="p1">Codfish vertebrae</p></li><li><p class="p1">Lung infiltrates if acute chest syndrome&nbsp;</p></li></ul><p class="p2"></p><p class="p1"><strong>Blood smear:&nbsp;</strong></p><ul><li><p class="p1">Target cells&nbsp;</p></li><li><p class="p1">Nucleated RBCs</p></li><li><p class="p1">Deoxygenation of blood producing sickle cells&nbsp;</p></li></ul><p></p>
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Sickle Cell Disease

-Crisis treatment

-To decrease frequency of crises

-Asplenia patients need

Sickle cell crisis treatment: 

- hydration 

-supplemental O2 

-analgesics 

To decrease frequency of crises 

-hydroxyurea 

Asplenic patients: 

-pneumococcal vaccine reduced risk of infection in asplenic patients 

-Give prophylactic penicillin until age 5 if no spleen 

<p><strong>Sickle cell crisis treatment:&nbsp;</strong></p><p class="p1">- hydration&nbsp;</p><p class="p1">-supplemental O2&nbsp;</p><p class="p1">-analgesics&nbsp;</p><p class="p2"></p><p class="p1"><strong>To decrease frequency of crises&nbsp;</strong></p><p class="p1">-hydroxyurea&nbsp;</p><p class="p2"></p><p class="p1"><strong>Asplenic patients:&nbsp;</strong></p><p class="p1">-pneumococcal vaccine reduced risk of infection in asplenic patients&nbsp;</p><p class="p1">-Give prophylactic penicillin until age 5 if no spleen&nbsp;</p>
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Patients with sickle cell disease are particularly susceptible to

Salmonella osteomyelitis 

Sepsis by NSH + klebsiella (encasuplated) 

<p>Salmonella osteomyelitis&nbsp;</p><p class="p1">Sepsis by NSH + klebsiella (encasuplated)&nbsp;</p>
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Lymphopenia without Immune deficiency

-Def

-SXS

-Workup

-Tx

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Eosinophilia

-Def

-SXS

-Workup

-Tx

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Neutropenia

-def

-SXS

-Workup

-Tx

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HSR reactions

-def

-Workup

-Tx

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Types of HSR table

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Anaphylaxsis

-Def

-SXS

-Workup

-Tx

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Normal Clotting Functions: Platelets

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Next Step: monitor heparin anticoagulation with

PTT

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LWMH do NOT require

monitoring by PTT

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Normal Clotting Function: Coagulation Cascade

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Common Anticoagulant Drugs

  • Mechanism

  • Role

  • Adverse Effects

Drugs:

  • ASA

  • Thienopyridines (ex.clopidogrel, ticlopidine)

  • GP3b/2b inhibitors (abciximab, tirofiban, eptifibatide)

  • Adenosine reuptake inhibitors (dipyridamole)

  • Heparin

  • LWMH/ enoxaparin/dalteparin

  • Direct Thrombin inhibitors (apixaban, rivaroxaban)

  • Direct XA inhibitors (-ban)

  • Warfarin

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Antithrombic drugs are used to ____; can affect ______

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Next Step: Monitor warfarin anticoagulation with

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Do not start warfarin therapy for _____ until _____ because _____

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Thrombocytopenia

-Defined as

-may be caused by

-SXS

-Workup

-Blood smear

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Causes of thrombocytopenia

  • pathology

  • Dx

  • Tx

  1. Impaired production

  • drugs

  • infection

  • aplastic anemia

  • folate/vitamin B 12 def

  • alcohol

  • cirrhosis

  1. abnormal pooling

  2. HIT

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Causes of thrombocytopenia

  • pathology

  • Dx

  • Tx

  1. ITP

  2. TTP-HUS

  3. Antiphospholipid Syndrome

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Causes of thrombocytopenia

  • pathology

  • Dx

  • Tx

HELLP syndrome

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vWD

-def

-SXS
-workup

-Tx

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Administration of FFP is indicated in patients with

VWF and Factor8 are the only clotting factors not synthesized eclusively by

patients using warfarin can present with clinical picture similar to that of

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60
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Vitamin K deficiency

-definition

-Vitamin K is required in

-SXS

-Workup

-Tx

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Hemophilia

-definition of

-SXS

-Workup

-Tx

-Complications

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Hemophiliacs tend not to develop significant bleeds unless they have

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DIC

-def and pathophysiology

-SXS

Workup

-Blood smear

-Treatment

-Complications

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Bleeding in DIC occurs because

bleeding in other clotting disorders occurs because

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Sepsis

-Defined by

-Dx criteria for SIRS

-Common community acquired pathogens include

-Common nosocomial pathogens include

-SXS

-Workup

-Radiology

-Staph aureus is most common cause of sepsis in

-Tx

-Complication

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Sepsis: Next Step: Do not start abx until after

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Malaria

-def

-SXS

-workup

-blood smear

-tx

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although rare in US, malaria is common in ___

travers should take _____

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Infectious mononucleosis

-def

-transmitted by

-SXS

-Workup

-Blood smear

-Tx

-Complications

<p></p>
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Symptoms of mono do not appear until

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HIV infection has greatest prevlance in

transmission typically through

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HIV

-defined by

-Viruses use

-Transmitted via

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HIV

-Following acute infection, patients enter

-Late SXS

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Next Step: although rate of HIV transmission through needle sticks is very low, prophylactic ______ should be started immediately if there is an appreciable risk of transmission

_____ tests should be performed _____ after exposure to determine if transmission occured

-Tx should be continued for ____

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Opportunistic infections, Neoplasms and Complications seen in AIDS:

  • CD4 level when seen

  • SXS

  • Dx

  • Tx

HSV

Kaposi Sarcoma

Parasitic Diarrhea (isopora, strongyloides, cryptosporidum)

Wasting syndrome

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Opportunistic infections, Neoplasms and Complications seen in AIDS:

  • CD4 level when seen

  • SXS

  • Dx

  • Tx

Coccidiodomycosis

AIDS dementia

Bacterial PNA (S. PNA, H.flu, Nocardia)

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Opportunistic infections, Neoplasms and Complications seen in AIDS:

  • CD4 level when seen

  • SXS

  • Dx

  • Tx

Candida esophagitis

Cervical Cancer

PJP

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Opportunistic infections, Neoplasms and Complications seen in AIDS:

  • CD4 level when seen

  • SXS

  • Dx

  • Tx

TB

Histo

Cerebral Toxo

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Opportunistic infections, Neoplasms and Complications seen in AIDS:

  • CD4 level when seen

  • SXS

  • Dx

  • Tx

Lymphoma (CNS or non Hodgkin)

PML/JC virus

Cryptococcal meningitis

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Opportunistic infections, Neoplasms and Complications seen in AIDS:

  • CD4 level when seen

  • SXS

  • Dx

  • Tx

CMV

Mycobacterium avium complex

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HIV

-W/U

1. ELIZA 

2. Repeat ELIZA if positive 

3. Western blot to r/o false positive 

4. Viral load and  CD4 count to track extent of disease progression 

<p>1. ELIZA&nbsp;</p><p class="p1">2. Repeat ELIZA if positive&nbsp;</p><p class="p1">3. Western blot to r/o false positive&nbsp;</p><p class="p1">4. Viral load and&nbsp; CD4 count to track extent of disease progression&nbsp;</p>
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It may take up to _____ for HIV abs to appear in the serum

6 months

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Serologic profile of HIV

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HIV

-Treatment

  • ART should be initated for all HIV infected patients, regardless of

  • Utility of starting ART in acute infection is

  • Common initial HAART regimens

  • Compliance with therapy is

  • Indications for changing ART include

  • Abx prophylaxis for opportunistic infections

  • close following of serology is important for

  • Pregnant mothers with HIV

-Complications

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Mother to infant transmission of HIV is

rare when viral load <1000

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ART for HIV

-Examples of drug

-Mechanism

-Adverse effects

  • NRTIs

  • NNRTis

  • Protease Inhibitors

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ART for HIV

-Examples of drug

-Mechanism

-Adverse effects

  • INSTIs

  • Fusion Inhibitor

  • CCR5 antagonist

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HIV positive mothers should NOT

DO NOT breastfeed their infants

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Polycythemia Vera

-def

-tends to occur after age

-SXS
-Workup

-Tx

-Complications

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The most common cause of increased RBC production is

chronic hypoxia

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Multiple Myeloma

-defined by

-abnormal monoclonal protein ___ produced by

-SXS

-Radiology

-Tx

-Complications

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Lymphoma

-def

-categorized as

ALL is the

Most ALL originates in

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Hodgkin lymphoma vs Non Hodgkin Lymphoma

  • cells of origin

  • classification low to higher grade

  • RF, patient population

  • SXS

  • Labs

  • Tx

    • Prognosis

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Leukemia

-defined as

-acute leukemia tends to involve

-Bone marrow involvement can cause

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ALL

-epidemiology

-def

-SXS

-Workup

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ALL

-Blood smear

-Tx

-Complications

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AML

-def

-SXS

-Workup

Blood smear

-Tx

-Complications

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CLL

-def

-SXS

-Workup

-Blood Smear

-Tx

Complications

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term image

lymphoma

<p>lymphoma</p>
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term image

ALL