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CHAPTER 4

HEMATOLOGY
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INTRODUCTION

Since it is generally agreed that a depression in the formed elements of the peripheral
blood is the most useful practical clinical index of the degree of exposure to jioniziny radiation,
4 systematic study of the leukocytes and platelets was relied upon as a major aid in evaluating
the clinical status, severity of the radiation injury, and prognosis of the exposed individuals.
Animal experimentation had previously shown that the rate of development and magnitude of
the depression were equaliy important in evaluating the severity of radiation injury. Since
there had been no previous exposure of human beings to significant amounts of fallout radiation,

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no hematological data known to be strictly applicable* were available for use as a guide in the.

evaluation of the exposed Americans and Marshallese. Accordingly emphasis was placed on a

systematic serial studies, utilizing a few highly standardized hematologic determinations to

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insure that individual and group trends would have maximum validity. Since it was known that
the Utirik group had received a very small dose of radiation compared to the other exposure
roups, less extensive determinations were carried out on these people.

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GENERAL METHODS

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Hematological examinations included total leukocyte, neutrophile, lymphocyte and platelet
counts, and hematocrit determinations. Whenever possible an entire exposure group was
studied in a single day. Occasionally two days were required to complete the larger groups.
Capillary blood was used, usually obtained from the finger but occasionally from the heel
or ear, Two pipettes each for total leukocyte and platelet counts were filled. From each pipette
- a single hemocytometer chamber wasfilled. All pipettes were rotated for 10 minutes, and the
cells were allowed to settle for 10 minutes in the hemocytometer chamber before counting. A
3 per cent acetic acid diluting fluid was used for total leukocyte counts. The blood was diluted
with 1 per cent ammonium oxalate for platelet counts and counted in flat bottom hemocytometers using a dark phase contrast microscope.** Two blood smears were made with each ex-

amination, using a beveled end glass slide for spreading. One blood smear was fixed in methyl
‘alcohol. The other was stained by Wright’s method, from which a 100 cell differentia! count
was made. Hematocrits were performed using heparinized capillary tubes. One end of the
capillary tube was heat seated and the tube was centrifuged in an ALOE centrifuge at 12,500
rpm for 5 minutes.

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— “A large literature on the hematologic effects of radiation exists; however, these data were
not relied upon for direct comparison nnd evaluation of the exposed individuals for reasonsthat
will be indicated later in the discussion.

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