Page 711 - Clinical Hematology_ Theory _ Procedures ( PDFDrive )
P. 711

CHAPTER 32  ■  Laboratory Manual: Manual Procedures in Hematology                                         695







                             COAGULATION PROCEDURES (continued)





                        Tis proce  ure, in CLSI  ormat, is provi  e   on this book’s                                           Quality Control

                   companion Web site at http://thepoint.lww.com/  urgeon6e.                                                   A normal patient plasma shoul   be teste   at the same time as


                                                                                                                               that o  the unknown patient.
                   BLEEDING TIME: STANDARDIZED IVY METHOD


                   Principle                                                                                                   Procedure

                   Te blee  ing time test is an in vivo measurement o  plate-                                                  1.  Using  resh plasma, prepare the  ollowing   ilutions:

                   let a  hesion an   aggregation on locally injure   vascular                                                 2.  Incubate  the control an   patient specimens an    mix-

                   suben  othelium. T is test provi  es an estimate o  the integ-                                                   tures at 37°C an   per orm an AP     or P   assay on each

                   rity o  the platelet plug an   thereby measures the interac-                                                     plasma, control, an   plasma-control mixture a  er 10, 30,

                   tion between the capillaries an   platelets. T e blee  ing time                                                  an   60 minutes.

                   re  ects this aspect o  platelet  unction by measuring the

                   length o  time two stan  ar  ize   punctures o  the ventral                                                 Reporting Results

                    orearm take to stop blee  ing. Clinically, the blee  ing time                                              I  the abnormality is that o  a   ef ciency, a normal plasma

                   is prolonge   in thrombocytopenia, qualitative platelet   isor-                                             sample will correct the assay results to a re erence value. I  the

                     ers such as von Willebran  ’s   isease, aspirin ingestion, or                                             abnormality is cause   by a circulating anticoagulant (inhibi-

                   the presence o  vascular problems.                                                                          tor), a greater correction is   emonstrate   as the ratio o  nor-

                        T is proce  ure, in CLSI  ormat, is provi  e   on this book’s                                          mal plasma increases in the mixture.

                   companion Web site at http://thepoint.lww.com/  urgeon6e.

                                                                                                                                   Patient             Normal                De  ciency                Inhibitor

                   CIRCULATING ANTICOAGULANTS

                   Principle                                                                                                       9 parts             1 part                Signi  cant               No signi  cant

                   Some coagulation   ef ciencies are cause   by inhibitors to                                                                                               correction                correction


                   specif c  actors rather than the lack o  a  actor. T ese inhibi-                                                5 parts             5 parts               Signi  cant               Some
                   tors are sometimes re erre   to as circulating anticoagulants.                                                                                            correction                correction


                    o   etect a circulating anticoagulant, the AP     an   the P                                                   1 part              9 parts               Signi  cant               More
                   that were originally abnormal are repeate   using various                                                                                                 correction                correction


                    ilutions o  patient plasma an  normal plasma. T e   ilu-                                                       Note: It is important to incubate the test specimens for 60 minutes because
                   tions are incubate   at 37°C an   teste   a  er 10, 30, 60, an                                                  some inhibitors act progressively, and it may take time for the APTT and/


                   120 minutes o  incubation. I  the abnormality is a   ef ciency,                                                 or PT results of the patient plasma and patient plasma-normal control mix-
                   10% normal plasma will correct the test result to be close to                                                   tures to show the effects of the inhibitor (a prolonged clotting time). To inter-


                   the normal range, as will the a    ition o  50% normal plasma.                                                  pret the results, the end point of the normal control has to be compared to
                   I  the abnormality is cause   by a circulating anticoagulant,                                                   the patient-normal plasma mixtures. As the specimens incubate, a slight
                                                                                                                                   increase in the end points will be observed because of the loss of labile clot-
                   more correction will usually be shown as the ratio o  nor-                                                      ting factors. The degree of prolongation in the patient and patient-control
                   mal plasma increases in the mixture. T e   etection o  an                                                       mixtures must be greater than the normal control plasma.


                   inhibitor may show up imme  iately or may require incuba-
                   tion o  the normal plasma in the presence o  the inhibitor.


                   Di  erentiation between a coagulation  actor   ef ciency an                                                     Factor           Disorder
                   a circulating anticoagulant is important in the correct treat-


                   ment o  a patient.                                                                                              II               Myeloma, systemic lupus erythematosus (SLE)
                                                                                                                                   V                Streptomycin administration, idiopathic



                       Patient Plasma                                Normal Plasma                                                 VIII             SLE, rheumatoid arthritis, drug reaction,
                                                                                                                                                    asthma, in  ammatory bowel disease,

                       9 parts                                       1 part                                                                         postpartum

                       5 parts                                       5 parts                                                       VIII, IX         Following replacement therapy for hereditary


                       1 part                                        9 parts                                                                        de  ciency

                                                                                                                                   IX               SLE—rare
                   Specimen


                   Re er to the AP     proce  ure  or treatment o  the original                                                    X                Amyloidosis
                   specimen.                                                                                                       X, V             SLE—common


                   Reagents, Supplies, and Equipment                                                                               XI               SLE—very rare


                   Re er to the AP     proce  ure.                                                                                 XIII             Isoniazid administration, idiopathic






                                                                                                                                                                                                                    (continued)
   706   707   708   709   710   711   712   713   714   715   716