Statistical modelling
for clinical mastitis
501
structural variables for mastitis risk from
the modelling process [37]. Consequently,
such explanatory designed models intend to
decrease the confounding problems. With
such models, the dependence between suc-
cessive cases within a lactation can explic-
itly be considered by these models [36]. In
the future, the modelling could be signifi-
cantly improved by performing the
study at
the quarter level since quarter bacteriolog-
ical status could be determined. Through
this design, it would be possible to combine
the two explanatory models already pub-
lished [1, 2, 36, 37]. Such explanatory mod-
els could also help to define optimum
criteria for incidence
rate definition at the
herd level, even to justify the time lag in
order to eliminate successive reoccurrences
within a lactation. The model developed
from the survival functions [36, 37] only
considers the first CMAST occurrence in a
lactation, or builds the
analysis on a dichot-
omous response at the lactation level (in the
absence of recurrence parameters, more
than one clinical mastitis case per lactation
in the epidemiological context of the exper-
imental studied herds could not occur).
But explanatory modelling techniques
require more scientific investment than the
generalist exploratory models. Neverthe-
less, they allow to add to the
modelling, as
published through a dynamic discrete event
stochastic simulation model [1, 2], the
main epidemiological and experimental
knowledge concerning the CMAST risk.
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