The diagnostics and treatment of tropical diseasesStitt, E. R. (Edward Rhodes)
Science
The diagnostics and treatment of tropical diseases
Stitt, E. R. (Edward Rhodes)
Tropical medicine
Ritchie has recently tested the sera of 792 normal persons and found
that 30% of these individuals agglutinated Shiga bacilli in 1 to 32,
while with Flexner strains 41% agglutinated in 1 to 64 and 30% in 1
to 128. For comparison Ritchie’s results with typhoid showed that
only 6% agglutinated such bacilli in 1 to 16. There is some evidence
that typhoid vaccination increases the agglutinating power of the
serum against dysentery organisms. These findings are remarkable, as
the usual advice is to consider an agglutination of 1 to 30 as fairly
specific for Shiga infections and 1 to 100 for Flexner ones.
Willmore and Savage tried heating serum to 56°C. for thirty
minutes, but found that such a procedure was of no practical
value with dysentery, thus differing from Malta fever serum where
such a procedure is of value in destroying coagglutinins and thus
increasing the specific action. The work of Ohno would indicate
that we should trust to the acid-producing effect on mannite
for differentiating Flexner and Shiga strains rather than on
agglutination because it was found that agglutinins for an acid
strain were not always more specific for such strains than for
nonacid ones.
At the same time it is the rule for a Flexner type bacillus to
show specificity for its serum and the Shiga type for the serum of
the more toxic, nonacid-fast Shiga strain cases. The statement of
Willmore and Savage that the differentiation of bacillary dysentery
infections is a refinement of technique seems a proper view because
with a polyvalent serum for treatment one only needs to know that
the case is one of bacillary dysentery for proper treatment. Of
course with a monovalent serum, effective only for the Shiga
bacillus, one would have to determine whether the organism
producing the dysentery was of that strain.
As a matter of fact it takes considerable time and laboratory skill
to carry out reliable cultural and serological tests.
From a practical standpoint we can use the therapeutic polyvalent
serum for agglutination and any organism recovered on the plate
made from the faeces which agglutinates in 1 to 50 or 1 to 100
may be considered as diagnostic of bacillary as against amoebic
dysentery. Often one does not see a case of dysentery until late
in the disease and then, provided the condition is serious and the
diagnosis points to a bacillary infection it would be better to
inject the curative serum rather than await laboratory confirmation.
PROPHYLAXIS AND TREATMENT
=Prophylaxis.=—The ease with which water-closet seats may be
contaminated should make us pay great attention to their disinfection
during an outbreak of bacillary dysentery. The same applies to the
bedclothes of such patients sent out for laundering.
Public-domain text, read in full here on John Shaqi.
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