Page 442 - Equine Clinical Medicine, Surgery and Reproduction, 2nd Edition
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Reproductive system: 2.1 The female reproductive tr act                    417



  VetBooks.ir  speculum or manual vaginal examination (Fig. 2.16).   should  be considered as  potentially  pathogenic:
          Use of a sterile double-guarded swab passed directly
                                                         beta-hemolytic streptococci; haemolytic  Escherichia
          into the uterine lumen is the best way of avoiding
                                                         types); Candida spp.; certain Staphylococcus spp.
          commensal contamination. It is important that the   coli; Pseudomonas spp.; Klebsiella spp. (certain capsule
          perineum of the mare is washed and dried, and an
          aseptic vaginal examination carried out either man-  Uterine cytology
          ually or by vaginoscopy. The collection of samples   Uterine cytology is a simple but effective method
          for cytological examination can be carried out at the   of detecting signs of uterine inflammation, and
          same time. Cultures are best taken in early oestrus   complements uterine bacteriological sampling. The
          since the cervix is relaxing, there are increased secre-  presence of neutrophils in uterine cytological speci-
          tions from the uterus and there is less risk of false   mens indicates an active inflammatory process. The
          results or introducing an infection. Swabs, however,   sample should be collected in early to mid-oestrus
          can be taken at any time. As the swab is dry, it should   using the same basic technique as for uterine cul-
          be either plated out immediately or transported in   ture. Cytological samples can be obtained in two
          a suitable transport medium. The swabs are plated   different ways:
          on blood agar and a selective gram-negative medium
          (McConkey) and incubated at 37°C (98.6°F) both     • A small-volume uterine flush: 60 ml of sterile
          aerobically and microaerophilically.             isotonic saline is flushed into the uterus and then
            In general, pure cultures and heavy growths    aspirated. This is then centrifuged and placed
          are  more likely to  be significant than  light mixed   onto a slide.
          growths, which are often contaminants. The inter-    • A double-guarded swab or a swab taken through
          pretation of culture results is helped by correlating   a vaginal speculum, which is then ‘rolled’ onto a
          them with the cytological and/or ultrasound find-  microscope slide. The swab can also be used for
          ings. For example, if the culture is positive (moderate   endometrial culture if the slide is sterile.
          to light growth) but the cytology results are negative
          for inflammatory cells (particularly neutrophils), the   The collected smears are stained (pre-stained
          culture is likely to be a contaminant. Where cyto-  slides may be used) using, for example, Diff-Quik
                                                                                                    ®
          logical findings are persistently positive with nega-  and examined for the presence of endometrial epi-
          tive cultures, the cause of the inflammatory response   thelial cells and polymorphonuclear neutrophils
          should be explored further. The following bacte-  (Fig. 2.18). It is also possible to have an indication
          rial organisms, if cultured in significant numbers,   as to whether the mare is anovulatory, transitional


                                             2.18











          Fig. 2.18  An endometrial smear
          from an oestrous mare with large
          numbers of polymorphonuclear
          neutrophils present suggesting
          the presence of inflammation and
          possible infection. (Photo courtesy
          Graham Munroe).
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