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BioVac® direct suction device
BioVac® Case Report Series • Report 1


“The procedure would have been aborted and
patient referred for angiography as the patient
was bleeding significantly, but because the
BioVac® [device] was used coagulated                                Procedure	                                                   Indications
blood was easily suctioned. The BioVac®                             • Colonscopy with injection therapy and coagulation	         • Rectal bleeding
[device] facilitated safe and quick
advancement of the endoscope.”                                      Findings
                                                                    • Excessive red and maroon blood in the entire colon
Daniel S. Mishkin, MD,CM, FRCP(C)                                   • Red and maroon blood in the entire stomach
Boston University Medical Center
Granite Medical Group                                               Direct endoscopic suction
                                                                    Upon endoscope insertion, an excessive amount of red blood immediately obscured the field of view.
                                                                    In order to identify the source of the bleeding, the BioVac® direct suction device was utilized for quick
                                                                    evacuation, resulting in the removal of 250cc of maroon/red coagulated blood from the colon. The
                                                                    BioVac® device’s remote irrigation line facilitated easy, intraprocedural water lavage. With the majority of
                                                                    blood removed, the endoscope was safely and quickly advanced to identify an actively bleeding, nipple-
                                                                    like projection in the ascending colon. The site, the result of a recent polypectomy, was easily identified
                                                                    due to the sharp transition of blood at its location; it was actively oozing. The post polypectomy bleed
                                                                    was injected and then cauterized with a bipolar probe. There was no active bleeding noted at the
                                                                    completion of the procedure.




                                        1. Excessive amount of blood in     2. Colon after evacuation with          3. Active bleeding site.               4. Bleed site after injection and 	
                                        the colon.                          the BioVac® device.                                                            	 cauterization.
BioVac® direct suction device
BioVac® Case Report Series • Report 2


“The BioVac® [device] easily suctioned the retained
blood inside the stomach, expediting the
procedure and time to make a diagnosis.
Without this device, the procedure would            Procedure	                                                                                   Indications
have most likely been aborted, and the              • Upper GI endoscopy	                                                                        • Hematemesis
patient would have continued to
bleed.”                                             Findings
                                                                 • Mallory-Weiss tear
D
 aniel S. Mishkin, MD,CM, FRCP(C)                               • Red and maroon blood in the entire stomach
Boston University Medical
Center                                                           BioVac® Direct Suction
Granite Medical Group                                            An upper endoscopy was performed for significant upper GI bleeding. Upon scope intubation, there was obvious
                                                                 red blood in the distal esophagus and a large volume of blood in the stomach. No source of bleeding was
                                                                 immediately identified. The BioVac® direct suction device was utilized to evacuate the retained blood from the
                                                                 gastric fundus. Approximately 200cc of blood was efficiently removed. An actively oozing Mallory-Weiss tear with
                                                                 stigmata of recent bleeding was identified. The tear extended from the GE junction to approximately 3cm down
                                                                 the greater curvature. A combination of injection therapy and electrocautery was successful. The stomach and
                                                                 duodenum were examined. After thorough lavage, no ulcers or other bleeding lesions were found; the stomach
                                                                 and duodenum were normal.




                                                                 1. Large volume of blood in the                       2. Stomach after evacuation with                      3. Actively oozing Mallory-Weiss tear.
                                                                 	 stomach.                                            	 the BioVac® device.

                                                                       “When blood is evacuated with the BioVac® [device] it flows in a
                                                                          string-like manner, continually suctioning blood in a line
                                                                               so little movement of the scope is necessary.”
                                                  This case report is not intended to provide device or clinical instruction or intended to be a substitute for the Instructions For Use (IFU)
                                                  which are packaged with the device. Please consult the IFU prior to using the BioVac® device.
                                                  Listening…and delivering solutions®, the US Endoscopy listening…and delivering solutions design, and all marks denoted with ® or ™                     760510 Rev. B
                                                  are registered with the U.S. Patent and Trademark Office, or trademarks owned by US Endoscopy

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760510b biovac mishkin case report web.pdf

  • 1. BioVac® direct suction device BioVac® Case Report Series • Report 1 “The procedure would have been aborted and patient referred for angiography as the patient was bleeding significantly, but because the BioVac® [device] was used coagulated Procedure Indications blood was easily suctioned. The BioVac® • Colonscopy with injection therapy and coagulation • Rectal bleeding [device] facilitated safe and quick advancement of the endoscope.” Findings • Excessive red and maroon blood in the entire colon Daniel S. Mishkin, MD,CM, FRCP(C) • Red and maroon blood in the entire stomach Boston University Medical Center Granite Medical Group Direct endoscopic suction Upon endoscope insertion, an excessive amount of red blood immediately obscured the field of view. In order to identify the source of the bleeding, the BioVac® direct suction device was utilized for quick evacuation, resulting in the removal of 250cc of maroon/red coagulated blood from the colon. The BioVac® device’s remote irrigation line facilitated easy, intraprocedural water lavage. With the majority of blood removed, the endoscope was safely and quickly advanced to identify an actively bleeding, nipple- like projection in the ascending colon. The site, the result of a recent polypectomy, was easily identified due to the sharp transition of blood at its location; it was actively oozing. The post polypectomy bleed was injected and then cauterized with a bipolar probe. There was no active bleeding noted at the completion of the procedure. 1. Excessive amount of blood in 2. Colon after evacuation with 3. Active bleeding site. 4. Bleed site after injection and the colon. the BioVac® device. cauterization.
  • 2. BioVac® direct suction device BioVac® Case Report Series • Report 2 “The BioVac® [device] easily suctioned the retained blood inside the stomach, expediting the procedure and time to make a diagnosis. Without this device, the procedure would Procedure Indications have most likely been aborted, and the • Upper GI endoscopy • Hematemesis patient would have continued to bleed.” Findings • Mallory-Weiss tear D aniel S. Mishkin, MD,CM, FRCP(C) • Red and maroon blood in the entire stomach Boston University Medical Center BioVac® Direct Suction Granite Medical Group An upper endoscopy was performed for significant upper GI bleeding. Upon scope intubation, there was obvious red blood in the distal esophagus and a large volume of blood in the stomach. No source of bleeding was immediately identified. The BioVac® direct suction device was utilized to evacuate the retained blood from the gastric fundus. Approximately 200cc of blood was efficiently removed. An actively oozing Mallory-Weiss tear with stigmata of recent bleeding was identified. The tear extended from the GE junction to approximately 3cm down the greater curvature. A combination of injection therapy and electrocautery was successful. The stomach and duodenum were examined. After thorough lavage, no ulcers or other bleeding lesions were found; the stomach and duodenum were normal. 1. Large volume of blood in the 2. Stomach after evacuation with 3. Actively oozing Mallory-Weiss tear. stomach. the BioVac® device. “When blood is evacuated with the BioVac® [device] it flows in a string-like manner, continually suctioning blood in a line so little movement of the scope is necessary.” This case report is not intended to provide device or clinical instruction or intended to be a substitute for the Instructions For Use (IFU) which are packaged with the device. Please consult the IFU prior to using the BioVac® device. Listening…and delivering solutions®, the US Endoscopy listening…and delivering solutions design, and all marks denoted with ® or ™ 760510 Rev. B are registered with the U.S. Patent and Trademark Office, or trademarks owned by US Endoscopy