Ex Parte Kumar et alDownload PDFPatent Trial and Appeal BoardOct 22, 201211211489 (P.T.A.B. Oct. 22, 2012) Copy Citation UNITED STATES PATENT AND TRADEMARKOFFICE UNITED STATES DEPARTMENT OF COMMERCE United States Patent and Trademark Office Address: COMMISSIONER FOR PATENTS P.O. Box 1450 Alexandria, Virginia 22313-1450 www.uspto.gov APPLICATION NO. FILING DATE FIRST NAMED INVENTOR ATTORNEY DOCKET NO. CONFIRMATION NO. 11/211,489 08/26/2005 Atul Kumar A8130.0459/P459 6813 24998 7590 10/22/2012 DICKSTEIN SHAPIRO LLP 1825 EYE STREET NW Washington, DC 20006-5403 EXAMINER VU, QUYNH-NHU HOANG ART UNIT PAPER NUMBER 3763 MAIL DATE DELIVERY MODE 10/22/2012 PAPER Please find below and/or attached an Office communication concerning this application or proceeding. The time period for reply, if any, is set in the attached communication. PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE __________ BEFORE THE PATENT TRIAL AND APPEAL BOARD __________ Ex parte ATUL KUMAR and ALKA KUMAR __________ Appeal 2011-005662 Application 11/211,489 Technology Center 3700 __________ Before ERIC GRIMES, FRANCISCO C. PRATS, and JACQUELINE WRIGHT BONILLA, Administrative Patent Judges. BONILLA, Administrative Patent Judge. DECISION ON APPEAL This is an appeal under 35 U.S.C. § 134 involving claims directed to a system for distending body tissue cavities by fluid irrigation. The Examiner has rejected the claims as obvious. We have jurisdiction under 35 U.S.C. § 6(b). We affirm-in-part. Appeal 2011-005662 Application 11/211,489 2 STATEMENT OF THE CASE The Specification describes an apparatus for distending body tissue cavities in subjects using continuous flow irrigation during an endoscopic procedure (Spec. 1). Figure 2 in the Specification shows an embodiment: Figure 2 depicts a schematic diagram of a system for distending tissue cavities comprising a fluid source container (1), a fluid delivery tube (2), an inflow pump (3), an inflow tube (4) that carries pressurized irrigation fluid to tissue cavity (11), an outflow tube (12), a positive displacement pump (14), a waste fluid carrying tube (15), and a waste fluid collecting container (16) (id. at 17). The system also comprises a constriction site housing tube (7), which includes a constriction point (8) (id. at 18). Figure 1 in the Specification (not shown here) is similar to Figure 2, but also includes a pressure pulse dampening system (id. at 17). Claims 1, 3, 5-19, 22-25, and 27-31 are on appeal. Claims 1 and 30 are representative (emphasis added). 1. A system for distending body tissue cavities of subjects by continuous flow irrigation during endoscopic procedures the system comprising: Appeal 2011-005662 Application 11/211,489 3 a fluid source reservoir containing a non viscous physiologic fluid for continuous flow irrigation during an endoscopic procedure; a fluid delivery tube connecting the fluid source reservoir to an inlet end of an inflow dynamic pump an outlet end of the pump being connectable to a tissue cavity subjected to the endoscopic procedure through an inflow tube for pumping the fluid at a controlled flow rate into the cavity to obtain a distended cavity, the rate at which the fluid from the inflow tube enters into the tissue cavity being termed as the cavity inflow rate; a positive displacement outflow pump having an inlet end being connectable to the tissue cavity through an outflow tube for removing the fluid from the cavity at a controlled flow rate, the flow rate of the outflow pump being termed as the cavity outflow rate; an outlet end of the outflow pump connected to a waste fluid collecting container via a waste fluid carrying tube; and a tube having a fixed constriction site provided between the fluid source reservoir and the inflow tube such that the same by- passes the inflow pump, the constriction site having a fixed diameter, wherein the tube provides a route for any excess fluid being pumped by the inflow pump to bypass the inflow pump and return to the fluid supply tube or the fluid source reservoir. 30. The system as claimed in claim 1, further comprising an outflow pressure pulsation dampening means provided between the cavity and the positive displacement outflow pump, and connected to the outflow tube for dampening the pressure pulsations inside the cavity caused by the positive displacement outflow pump, wherein the pressure dampening means comprises a single outlet syringe mechanism, a piston of the same being coupled synchronously to the positive displacement outflow pump through coupling means and the single outlet end of the syringe mechanism being connected to the outflow tube. The claims stand rejected as follows: (I) claims 1-3, 5-16, 18-19, 22-25, 27-29, and 31 under 35 U.S.C. § 103(a) as obvious over Novak (U.S. Pat. No. 6,997,896, issued Feb. 14, Appeal 2011-005662 Application 11/211,489 4 2006) in view of Nowosielski et al. (U.S. Pat. No. 5,605,545, issued Feb. 25, 1997); and (II) claim 30 under 35 U.S.C. § 103(a) as being obvious over Novak in view of Nowosielski and further in view of Takamatsu et al. (U.S. Pat. No. 6,283,937, issued Sept. 1, 2001). I. Findings of Fact 1. Novak discloses an apparatus for controlling the introduction and removal of a fluid into a body cavity in order to facilitate a surgical procedure (Novak, col. 1, ll. 9-14). The apparatus “is used for the endoscopic irrigation of body cavities …” (id. at ll. 18-20). When using the apparatus, “the pressure and the flow rate can be controlled as independently from each other as possible” (id. at col. 2, ll. 15-17). 2. In Figure 1, Novak discloses the following embodiment: Appeal 2011-005662 Application 11/211,489 5 Figure 1 depicts a diagram of an apparatus for irrigating a body cavity (id. at col. 6, ll. 60-61). 3. As shown in Figure 1 above, “liquid is drawn from a liquid reservoir through conduit 118 in the direction of arrow 119” (id. at col. 7, ll. 26-27). The liquid flows into “an irrigation pump 114 connected to the body cavity 112 with irrigation conduit 116” (id. at ll. 24-26). Downstream from irrigation pump (114), a “flow transducer 121 is associated with the irrigation conduit 116, which is capable of determining the actual flow (f) of the liquid through the irrigation conduit 116” (id. at ll. 48-52). In addition, “pressure sensor 128 is associated with the irrigation conduit 116, which is capable of determining the actual pressure (p) in the irrigation conduit 116 or in the body cavity 112” (id. at ll. 45-49). Further downstream, a “first suction conduit 120 extends from the body cavity 112 to a suction pump 124.” At that point, “liquid is then drained off to a sump (not shown) via conduit 126 in the direction of arrow 127” (id. at ll. 42-45). 4. Novak teaches that an advantage of the disclosed apparatus over those disclosed in certain prior art is that “an obstruction in the suction conduit … may be drawn off by virtue of an automatically increasing higher suction power of the suction pump” (id. at col. 2, ll. 55-59). 5. Novak also teaches that “in case that the obstruction is such that it cannot be removed despite the increasing suction power, the power of the irrigation pump is decreased or even reduced to zero, in order to avoid an excessive pressure in the body cavity and thereby a risk for the patient” (id. at col. 3, ll. 28-34; see also ll. 34-36). Appeal 2011-005662 Application 11/211,489 6 6. Nowosielski discloses a “system and method for providing a pressurized fluid for irrigating or distending an internal body site or organ that is accessed … in conjunction with a laparoscope, endoscope, resectoscope or similar device used to perform a surgical procedure” (Nowosielski, col. 1, ll. 5-12). 7. Figures 4 and 5 in Nowosielski show the following: Figure 4 depicts a diagram of an irrigation system, including “by-pass 64” and “pinch valve 70’ (id. at col. 2, ll. 29-30, col. 4, ll. 15-20). Figure 5 depicts “a cross section of a by-pass section of an alternative embodiment” (id. at col. 2, ll. 31-32). 8. As taught in Nowosielski, “by-pass 64 provides a fluid path around the pump 16 to reduce the likelihood of high pressure in the tubing 50 and/or in the patient’s body” (id. at col. 3, ll. 42-47). The apparatus in Nowosielski endeavors to “avoid problems due to blockages and pressure irregularities” (id. at col. 1, ll. 60-63). 9. In relation to Figure 5, Nowosielski teaches that the “size of the orifice or restriction is selected based upon the known size and resistance in Appeal 2011-005662 Application 11/211,489 7 the second section of tubing 36 and the desired operating pressure” (id. at col. 3, l. 63 – col. 4, l. 2). To control operating pressure, “if there is an obstruction or if the physician turns off the flow at the tool, the amount of flow back through the by-pass will increase” (id. at col. 4, ll. 8-11). Principles of Law The Examiner bears the initial burden, on review of the prior art or on any other ground, of presenting a prima facie case of unpatentability. In re Oetiker, 977 F.2d 1443, 1445 (Fed. Cir. 1992). If the Examiner meets that initial burden, the burden of coming forward with evidence or argument shifts to the applicant. In re Rijckaert, 9 F.3d 1531, 1532 (Fed. Cir. 1993). After the applicant submits such evidence or argument, the PTO then determines patentability “on the totality of the record, by a preponderance of evidence with due consideration to persuasiveness of argument.” Oetiker, 977 F.2d at 1445. If the Examiner fails to establish a prima facie case of unpatentability in the first instance, however, the rejection is improper and must be reversed. Id.; Rijckaert, 9 F.3d at 1532. Analysis The Examiner rejects claims 1-3, 5-16, 18-19, 22-25, 27-29, and 31 as obvious over Novak in view of Nowosielski (Ans. 3). Appellants assert, and the Examiner acknowledges, that Novak does not disclose an apparatus comprising a tube with “a fixed constriction site” located between a fluid source reservoir and an inflow tube, as recited in claim 1 (App. Br. 5; Ans. 5). As noted by the Examiner, however, the by-pass tubing system presented in Nowosielski in relation to a similar device corresponds to “a Appeal 2011-005662 Application 11/211,489 8 tube having a fixed constriction site” provided between a fluid source reservoir and an inflow tube (Ans. 5, 8; FF 7, 9). Appellants argue that “Novak cannot function at all if a bypass tube (such as the bypass tube of Nowosielski) is installed in Novak, as the bypass tube jeopardizes patient’s safety” (App. Br. 5, 7). Appellants assert that the arrangement in Novak “works only if the entire fluid pumped by the inflow pump 114 enters into the body tissue cavity 112 via the inflow tube 116, which becomes impossible the moment the bypass tube of Nowosielski is installed into the system of Novak” (id. at 7). According to Appellants, because “a part of the fluid pumped by the inflow pump 114 constantly escapes at an unknown variable rate into the bypass,” “the fluid flow rate sensor 121 is never able to gauge the actual fluid pumped by the pump 114 and, thus, the system of Novak becomes erratic” (id.). We agree with the Examiner (Ans. 5) that it would have been obvious at the time the invention was made to a person having ordinary skill in the art to modify the device of Novak so that it included the by-pass tube of Nowosielski having a fixed constriction site (FF 7, 9). As stated by the Examiner, the by-pass tubing of Nowosielski would have provided “the benefit of providing pressure relief to the system so that pressure in the tubing will not build up distally of the location of the pump and regulating the flow by maintaining cavity pressure at a stable value” (Ans. 5). Novak teaches that in a case where “the obstruction is such that it cannot be removed despite the increasing suction power, the power of the irrigation pump is decreased or even reduced to zero, in order to avoid an excessive pressure in the body cavity and thereby a risk for the patient” (FF 5). In Appeal 2011-005662 Application 11/211,489 9 other words, Novak teaches avoiding exerting excessive pressure in the body cavity, which can harm a patient, even if increasing suction power might help remove an obstruction in certain situations. Based on teachings in both references, we also conclude that it would have been obvious to make an embodiment having one end of by-pass “tube 64” in Nowosielski (FF 7) upstream of irrigation pump (114) in Novak (FF 2), and the other end downstream of pump (114) but upstream of “flow transducer 121” (measuring flow) and “pressure sensor 128” (measuring pressure) (FF 3). Considering the purpose of the by-pass tube (to avoid excessive pressure and risk to the patient) (FF 5), it would have made sense to an ordinary artisan to measure flow and pressure at a point beyond the by- pass tube but before the liquid reaches the body cavity because, based on flow and pressure measurements, one would have been able to determine whether to turn off/down the apparatus, or to use an apparatus having a different sized “fixed constriction site” in the by-pass tube (FF 5, 8, 9). As noted by the Examiner, Appellants cite no evidence in support of the notion that Novak’s apparatus cannot function if one includes a bypass tube, as taught in Nowosielski (Ans. 9). Appellants have not provided any evidence that a by-pass tube in this embodiment would prevent one from controlling the irrigation pump of Novak as a function of a flow rate through a body cavity, or that a by-pass tube would cause “dangerous pressure fluctuations” inside a body cavity, as asserted by Appellants (App. Br. 7-8). Arguments of counsel cannot take the place of evidence in the record. In re Scarbrough, 500 F.2d 560, 566 (CCPA 1974). Appeal 2011-005662 Application 11/211,489 10 Appellants assert that one would not have been motivated combine the tube of Nowosielski with the apparatus of Novak, arguing, for example, that Nowosielski teaches a system for laparoscopy, not endoscopy, as recited in claim 1 (App. Br. 5; Reply Br. 3). As found by the Examiner, however, Nowosielski expressly discloses a system for distending an internal body site accessed in conjunction with an endoscope (Ans. 10; FF 6). We also disagree with Appellants that adding a by-pass tube to Novak’s device would “change the principle of operation” of the apparatus being modified (App. Br. 7). Contrary to Appellants’ assertions, the “crux of Novak” is not “removal of an obstruction/blockage” (id. at 8). Rather, Novak describes an apparatus where “the nominal pressure can be maintained in a particular exact manner in that the suction power of the suction pump is increased or reduced as a function of the acquired actual pressure in order to maintain the predetermined nominal pressure in the body cavity” (Novak, col. 3, ll. 32-37). As taught in Novak, in certain cases, one may wish to increase suction to help remove an obstruction, but in other cases an “obstruction is such that it cannot be removed despite the increasing suction power” (FF 5). In the latter situation, the “power of the irrigation pump [can be] decreased or even reduced to zero, in order to avoid an excessive pressure in the body cavity and thereby a risk for the patient,” as taught in Nowosielski (id.). Thus, the addition of a by-pass tube helps “avoid problems due to blockages and pressure irregularities” and ensure patient safety by preventing excessive pressure in a body cavity (FF 8). Appeal 2011-005662 Application 11/211,489 11 Appellants have not convinced us that the addition of such a by-pass tube would prevent appropriate pressure from building in the tubing, or prevent the suction pump from operating with increased power when appropriate (App. Br. 8-9), even if the by-pass tube could help avoid excessive pressure beyond that needed to safely remove an obstruction. The “resulting arrangement” would not prevent “the purposeful increase in the cavity pressure when a blockage occurs” (App. Br. 8), although it could prevent cavity pressure from going excessively high. For the reasons discussed above, we conclude that a preponderance of evidence supports the Examiner’s conclusion that independent claim 1 is obvious over Novak in view of Nowosielski. Because Appellants do not argue the claims separately, claims 2, 3, 5-16, 18-19, 22-25, 27-29, and 31 fall with claim 1. 37 C.F.R. § 41.37(c)(1)(vii). II. Additional Findings of Fact 10. Takamatsu teaches “an irrigation/aspiration apparatus which supplies an irrigation fluid to a surgical site and aspirates the irrigation fluid therefrom with residual tissue” (Takamatsu, col. 1, ll. 5-8). In this capacity, Takamatsu describes a “mechanism which is advantageous to damp out or absorb pulsations caused by a peristaltic suction pump” (id. at ll. 8-10). 11. Takamatsu discloses that “[i]n the field of ophthalmology, this kind of apparatus is used,” which includes “a peristaltic pump as a pump for effecting suction of the residual tissue” (id. at ll. 16-19). The peristaltic Appeal 2011-005662 Application 11/211,489 12 pump “causes pulsations which result in the disadvantage that the suction pressure varies” (id. at ll. 19-21). Analysis The Examiner rejects claim 30 as obvious over Novak in view of Nowosielski and further in view of Takamatsu (Ans. 6). As noted by Appellants, Takamatsu discusses its apparatus in the context of ophthalmic surgeries, while the “system of Novak is used in endoscopic surgery” (App. Br. 12). Consistently, Takamatsu does not describe cavity distension or endoscopy, but instead discloses an apparatus that “supplies an irrigation fluid to a surgical site and aspirates the irrigation fluid therefrom with residual tissue” (FF 10). When supplying fluid to the eye during cataract surgery, Takamatsu indicates that it is important to damp out or absorb pulsations caused by a peristaltic suction pump in the apparatus (FF 10, 11). By contrast, Novak and Nowosielski do not mention pulsations, or that pulsations might be problematic when irrigating a body cavity, especially in a situation where one might want to increase suction and pressure as a way to remove an obstruction during an endoscopic procedure. Moreover, we agree with Appellants that the “eye is a delicate organ and cannot withstand distension pressure like some other body cavities,” such as those subjected to endoscopy (App. Br. 12). Takamatsu provides an apparatus that carefully controls suction pressure, and prevents pulsations that might cause pressure to vary. Novak and Nowosielski do not suggest, on the other hand, that variations in suction pressure caused by pulsations Appeal 2011-005662 Application 11/211,489 13 generated by a suction pump present a disadvantage during endoscopy of a tissue cavity, or that damping out pulsations might provide an advantage. The Examiner cites no specific evidence indicating that an ordinary artisan would have been motivated to add the pulsation damping component of Takamatsu to the apparatus of Novak in view of Nowosielski. Thus, the Examiner has not established by a preponderance of the evidence that claim 30 is obvious over Novak in view of Nowosielski in further view of Takamatsu. SUMMARY We affirm the obviousness rejection of claims 1-3, 5-16, 18-19, 22-25, 27-29, and 31 over Novak in view of Nowosielski. We reverse the obviousness rejection of claim 30 over Novak in view of Nowosielski and further in view of Takamatsu. TIME PERIOD FOR RESPONSE No time period for taking any subsequent action in connection with this appeal may be extended under 37 C.F.R. § 1.136(a). AFFIRMED-IN-PART dm Copy with citationCopy as parenthetical citation