ofthe total while blooel cent (coefficien! of Correlation of 0.9).

count were due to changes ib the neatrophiie count.
ape proups.,

Thas (lacethuctasatais wo total

This was true of both the older ined younger

Tecan be seen from Table 4.2 that (he neutrophtle count’ was cousistently preater

than the lymphocyte count in the older age group.

In the younger groups, differences in the neu.

frophile and lymphocyte count were less marked and on six occastons the lyinphoeyvie count wies

older are proups were Approximately 70 per cent of the control group (Fig. 4.4).

Following this,

the platelet count fell reaching a low of approximately 35 per cent of control value during the
fourth week. The platelet count rose during the 5th week and reached the value noted for the
initial counts on the 40th day. A second decrease in the platelet count (P< 0,01) developed dur ing the 7th and 8th weeks, and values remained at approximately 70 per cent of the control
troup during the remainder of the observation period. The pattern of platelet counts in the below 15-year group was remarkably similar to that noted in the older age groups. Differences
between the age groups were jess apparent if the platelet counts were expressed as per cent of
the control group.
4.6

cote ee ewe ay
ee ee ete

grevler than the neutrophile count.
Platelets were first counted _10 days after exposure, at which lime platelet values of the

AILINGINAE GROUP
in this proup there wore only three individuals below age 5, For this reason, remarks will

be confined essentially to the older aye proup.

The absolute neutrophife count fluctuated around the control value for the first six weeks
of observation (Table 4.3), At this time the counts began to fall, and a value approximately 75
per cent of the control count was reached and maintained throughout the duration of the obser-

i

vation period. The lymphocytes in this group fell to a value of 55 per cent of normal during the
first week. The counts then Siuctuated around this value throughout the period of observatic n,

and no definite upward trend of the lymphocyte count was noted during the period of observa- _
tion.
.
AS was noted in the Rongelap group the lymphocyte counts remained at an essentially constant low level throughout the period of observation. The total leukocyte count in this grour
also reflected changes in the neutrophile count.
7
The platelet counts in the Ailinginae group were low, approximately 75 per cent of normal,

when first enumerated on post-exposure day 10. The counts remained at this level during the
second and third week;
a low value 45 per cent
value approximatcly 70
the observation period.

4.7

however, a definite fall in count was noted during the fourth week when
of control was attained. The counts returned during the fifth week toa
per cent of the control level, where they remained for the duration of
A secondary fall, as observed in the Rongelap group was not detected.

UTIRIK GROUP

In the ¢reater than 5 age group the total white blogd cell and neutrophile counts were depressed slightly below control values during the first and second weeks (Table 4.4). The
lymphocyte counts were below control levels consistently, and the total white count equal to

the control value obtained on day 29 was due to a neutrophilic leukocytosis.
Platelet counts on the 29th day were significantly lower than on the 19th day and were
lower than control values. The 29th day coincides with the time of maximum depression for
the more heavily exposed groups.

4.8

RONGERIK GROUP (AMERICANS)
The neutrophile count in generai reflected the time course of the total leukocyte count

(Fig. 4.5). Neutrophiles accounted almost entirely for the marked rise in total count on postexposure day one, and the values for absolute neutrophile count fluctuated near the contro}

80

'

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