Section: Special Hematology
Duration: 1 month
Goals & Objectives
The goal of these rotations is to provide residents with the opportunity to increase their knowledge base and skills in the interpretation of a wide range of hematologic abnormalities. Through regularly scheduled sign-out sessions with the attending pathologists, the residents should gain a great deal of practical experience in how to approach potential diagnoses of hematologic malignancies, systemic disorders affecting bone marrow, lymph nodes and other organs; bleeding abnormalities and thrombotic conditions; hemoglobinopathies, thalassemias, anemias; and a varied array of other hematologic abnormalities presenting in both the inpatient and outpatient populations. A major goal of the rotation is that the resident gain sophistication in the appropriate choice of laboratory tests for a given clinical situation. While the achievement of technical proficiency in laboratory procedures is not a specific objective of this rotation, sufficient familiarity is required such that the resident can appreciate the intrinsic limitations of the procedures, as well as recognize unlikely individual test results that might reflect technical artifact. During this rotation, the resident should also learn how quality control is maintained for hematologic procedures. In order to maximize achievement of these objectives, residents on this rotation are strongly advised to establish close working relationships with technologists and supervisors in the laboratories - a number of whom are truly expert in the field.
Duties & Responsiblities
- Become credentialed to take histories on all referral patients for hemostatic workups. Select studies most appropri-ate to evalu-ate the patient's disorder. Before the patient leaves, review the history and proposed tests with the attend-ing pathologist.
- Sign out:
- Hemostasis evaluations: Work with the technologists and attending pathologist to determine the appropriate tests to be performed. Sign out interpretation with attend-ing pathologist and contact referring physician to discuss future diagnostic and follow-up testing and proper thera-py.
- Hemoglobin/thalassemia evaluations: Work with the tech-nologists to determine the appropriate tests to be performed. Check the Wright-stained blood films. Procure further clinical information as indicated. Write interpretation and sign out with the attending pathologist.
- Osmotic fragility determinations: Work with the technologists to determine the appropriateness of an osmotic fragility determination, in consideration of the clinical history and, if available, the peripheral blood film. Write interpretation and sign-out with the attending pathologist.
- Evaluate requests for bleeding time determinations in the following circumstances: · If the request is received during the second or third shifts when the laboratory staffing is decreased. · If the technologist has a question about the appropriate-ness of the ordered bleeding time. · Become familiar with all procedures. These include instrument checks, calibration and quality control. During the month that this rotation is combined with the rotation in Clinical Chemistry, the resident will spend one week focusing not only upon testing performed in the special testing section, but also upon testing performed with high volume and more automated instrumentation.
Instrumentation (principles and maintenance)
- The microscope
- Microscope illumination
- Blood diluting procedures
- Abbott Cell-Dyne 4000
- Diabnostica Stago. STA Coagulation Instrument
- Hemoglobinometry
- Calibration
- Maintenance of spectrophotometers
- Phase microscopy and patelet counting
- Centrifuges
- Standard
- Microhematocrit
- Platelet lumi-aggregometer and whole blood aggregometer
- Bechman and Sebia electrophoresis apparati
- Isoelectric focusing apparatus
- Bio variant HPLC apparatus
Preparation of reagents
- Wright's stain
- Cytochemical methods
- Blood-diluting fluids
- Use of anticoagulants: Citrate, Heparin, EDTA
- Buffer solutions
Quantitative evaluation of laboratory data
- Quality Control statistics
- Factor assays, inhibitor assays, etc.
Economics and administration of hematologic laboratory Hematologic procedures
- Obtaining blood: Capillary, Venous, Various sites
- Counting of erythrocytes: Abbott Cell Dyne
- Preparation of blood films: slide, coverslip
- Staining of blood films: Wright's stain, Special stains
- Reticulocyte counts
- Platelet counts: Phase-microscopy, Abbott Cell Dyne
- Hematocrit: micro, Abbott Cell Dyne
- Red cell indices
- Review, interpret blood cell histograms from Abbott Cell Dyne
- Westergren Sedimentation rates (ESR)
- Automated erythrocyte sedimentation rate (Vesmatic)
- Eosinophil counts
- Osmotic fragility of erythrocytes
- Autohemolysis
- Sickling determinations
- Hemoglobin electrophoresis - alkaline electrophoresis, acid electrophoresis, isoelectric focusing
- Sucrose hemolysis test
- Acid serum hemolysis test
- G-6PD screening tests and assay
- Unstable hemoglobin: heat denaturation; isopropanol solubility
- Hemoglobin A2 assay (this is a part of the HPLC method - no manual method
- Acid elution (fetal hemoglobin)
- Heinz body preparation
- Hemoglobin H Preparation (brilliant cresyl blue)
Coagulation and Platelet Procedures.
- Obtaining blood (special techniques, such as two syringe tech-nique)
- Bleeding time - Simplate II
- Partial thromboplastin time, Thrombin time, One-stage prothrom-bin time
- Platelet aggregation and release reaction studies; imped-ance aggregometry
- Clot retraction
- Platelet count
- Procoagulant factor assays
- Fibrinolysis - Euglobulin lysis time
- Screening Test for fibrin degradation products: D dimer tests
- Fibrinogen assay
- Circulating inhibitors - Lupus-like inhibitor test battery - Factor VIII inhibitor (Bethesda) - PFA-100
- von Willebrand Factor Antigen, Activated Protein C resistance
- Ristocetin cofactor
- Factor XIII screening test (urea solubility)
- Platelet-associated immunoglobulin, anti-platelet antibodies
- Chromogenic assays - Protein C activity, Antithrombin III activity Heparin levels, etc.
Hematology, Abnormal Results Standard Operating Procedure
The Hematology technical staff will call the patient's physician immediately to report any of the following:
- Hematocrit < 25 or > 55% WBC < 2 x 103/?L or > 30 x 103/?L
- Platelet < 50 x 103/?L or > 1000 x 103/?L
- Prothrombin time > 30 sec
- Partial Thromboplastin time > 90 sec
- Thrombin Time > 40 sec
- Bleeding Time > 12.0 min.
Unexpected differential findings, including blasts in a new patient or leukemic patient in supposed remission will also be called. These findings will be confirmed with the Hematology Supervisor, the Clinical Pathology Bone Marrow Resident (or resident on-call), or the Attending Pathologist.
In the case of a clinically important unexpected finding (such as blast cells in a new patient suggesting the diagnosis of leukemia), the Hematology Supervisor will consult the Clinical Pathology Bone Marrow resident. The resident will confirm the finding, checking with the hematopathology fellow or attending pathologist as necessary, and call the clinical physician to report the finding and inform the clinician of its implications.
Evaluation
Global Rating of Live or Recorded Performance: A rater judges general categories of ability (patient care skills, medical knowledge, interpersonal and communication skills) and the ratings are completed retrospectively based on general impressions collected over a period of time (end of rotation) derived from multiple sources of information (direct observations or interactions); input from other faculty, lab technicians and residents and review of work products or written materials. Evaluations will be based on the above objectives.
Recommended Reading
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