Page 133 - Clinical Manual of Small Animal Endosurgery
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Diagnostic Laparoscopy  121

























                                  Fig. 4.13  Margin of liver after removal of two biopsies. Note that almost
                                  no bleeding has occurred.


                                  therefore small samples taken at the edge of the lobes may not reflect
                                  deeper lesions.
                                    The biopsy forceps are inserted through the operating port, directed
                                  toward the area to be sampled, and the tissue is grasped. The forceps
                                  are kept in position for 15–30 s, and then the tissue is gently twisted and
                                  pulled to retrieve the sample. In this way haemostasis is produced, dimin-
                                  ishing the haemorrhage from the biopsy site. The area is closely moni-
                                  tored  until  haemorrhage  stops  (Fig.  4.13).  This  usually  occurs  within
                                  2–3 min; if bleeding is more than expected, pressure can be applied to
                                  the biopsy site using the palpation probe or the tip of the laparoscope.
                                  If the haemorrhage persists, a haemostatic agent such as absorbable gela-
                                  tine felt can be applied into the tissue defect and pressure applied for
                                  approximately 1 min.
                                    Using a pre-tied loop ligature or extracorporeally assembled loop liga-
                                  ture to obtain biopsy samples is recommended in case haemorrhage is
                                  anticipated, such as in patients with coagulopathies, severe hepatic failure
                                  or highly vascular lesions. This technique requires one additional operat-
                                  ing port for introducing the loop, which is manipulated around the biopsy
                                  site (usually the tip of a lobe). With a blunt probe or grasping forceps the
                                  liver  lobe  is  elevated,  so  the  loop  can  be  positioned  and  tightened.
                                  The friable liver parenchyma is crushed, and the knot securely ligates
                                  the blood vessels and bile ducts, thus allowing the sample to be collected
                                  with laparoscopic scissors from the liver tissue distal to the loop.
                                    A needle-core biopsy technique can also be used to obtain samples of
                                  the liver, but due to the restricted amount of tissue obtained this method
                                  is most often used to obtain samples of focal vascular liver masses. The
                                  biopsy needle can be inserted percutaneously through a small puncture just
                                  lateral to the xiphoid cartilage and manipulated under direct visualisation.
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