In Re: Kayyali ( 2016 )


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  •        NOTE: This disposition is nonprecedential.
    United States Court of Appeals
    for the Federal Circuit
    ______________________
    IN RE: HANI KAYYALI, CRAIG A. FREDERICK,
    CHRISTIAN MARTIN, ROBERT N. SCHMIDT,
    BRIAN M. KOLKOWSKI,
    Appellants
    ______________________
    2016-1081
    ______________________
    Appeal from the United States Patent and Trademark
    Office, Patent Trial and Appeal Board in No. 11/811,156.
    ______________________
    Decided: June 14, 2016
    ______________________
    BRIAN M. KOLKOWSKI, Flocel Inc., Cleveland, OH, for
    appellants. Also represented by MARK PENNINGTON,
    NeuroWave Systems Inc., Cleveland Heights, OH.
    THOMAS W. KRAUSE, Office of the Solicitor, United
    States Patent and Trademark Office, Alexandria, VA, for
    appellee Michelle K. Lee. Also represented by BENJAMIN
    T. HICKMAN, FRANCES LYNCH.
    ______________________
    Before TARANTO, CLEVENGER, and CHEN, Circuit Judges.
    PER CURIAM.
    2                                            IN RE: KAYYALI
    Hani Kayyali, Craig A. Frederick, Christian Martin,
    Robert N. Schmidt, and Brian M. Kolkowski (collectively,
    Kayyali) filed an application for a patent on methods of
    conducting an at-home sleep analysis. As relevant here,
    an examiner rejected Kayyali’s claims for obviousness
    based on the prior-art reference Westbrook, either alone
    or in combination with another prior-art reference, Fey.
    The Patent Trial and Appeal Board affirmed.
    Kayyali appeals, arguing that an ordinarily skilled ar-
    tisan would not have been motivated to modify West-
    brook, that Westbrook actually teaches away from the
    modification, that Fey is not analogous art, and that an
    ordinarily skilled artisan would not have been motivated
    to combine Westbrook and Fey. We reject those argu-
    ments and therefore affirm.
    BACKGROUND
    Kayyali’s patent application describes “a method of
    conducting a sleep analysis by collecting physiologic and
    kinetic data from a subject, preferably via a wireless in-
    home data acquisition system, while the subject attempts
    to sleep at home.” J.A. 69. The in-home sleep test “pro-
    vides more accurate data for the sleep diagnosis” than
    would a sleep test conducted in a laboratory, subjects
    being “generally more comfortable sleeping at home.” J.A.
    73. Kayyali describes applying at least two sensors to the
    subject to collect physiological, kinetic, or environmental
    signals. For example, electrodes may be placed on the
    subject’s scalp to measure brain waves or on the subject’s
    torso to measure electrical currents generated by the
    heart. The application also calls for a pulse oximeter to
    measure respiration and oxygenation of the subject’s
    blood. The various sensors are connected to a data acqui-
    sition system, which is preferably light-weight, easily
    transported, and capable of collecting and transmitting
    data from the sensors. Sleep-test data is transmitted,
    IN RE: KAYYALI                                             3
    preferably in real time, to allow for a sleep-trained techni-
    cian to monitor and analyze the test results remotely.
    Pending claims 1–7 and 34–47 are at issue in this ap-
    peal. Claims 1 and 7 are illustrative for present purposes:
    1. A method of conducting an at-home sleep
    analysis comprising the steps of:
    applying at least two sensors and a pulse oxime-
    ter to a subject,
    connecting the at least two sensors and the
    pulse oximeter before or after application to
    the subject to a data acquisition system includ-
    ing a patient interface box with wireless radio
    frequency transmission capability, the patient
    interface box being capable of receiving signals
    from the at least two sensors and the pulse ox-
    imeter, digitizing the signals, and retransmit-
    ting the digitized signals, or transmitting
    another digitized signal based at least in part
    on at least one of the sensor signals by bidirec-
    tional wireless radio frequency transmission,
    collecting and digitizing the signals from the at
    least two sensors and the pulse oximeter ap-
    plied to the subject while the subject is sleep-
    ing at home with the patient interface box,
    transmitting the digitized signals or transmit-
    ting the other digitized signal based at least in
    part on the sensor signals to a remote location,
    at least in part by wirelessly transmitting the
    digitized signals utilizing a bidirectional radio
    frequency signal transmission, and
    analyzing the retransmitted digitized signals or
    the transmitted other digitized signal by a
    sleep trained individual to diagnose whether
    the subject has a sleeping disorder.
    4                                              IN RE: KAYYALI
    J.A. 4.
    7. The method in claim 1, including the further
    steps of having the subject visit a physician’s or
    clinician’s office or place of business;
    providing the subject at the physician’s or clini-
    cian’s office or place of business with the port-
    able patient interface and three sensors;
    providing the subject or the subject’s care pro-
    vider with direct face-to[-]face demonstration
    with instruction and guidance regarding use
    and application of the portable patient inter-
    face box and the three sensors;
    sending the subject home or to another location
    remote from the physician’s or clinician’s office
    or place of business with the portable patient
    interface box and the three sensors and having
    the subject or the subject’s care provider use
    the instruction and guidance to apply and con-
    nect the sensors and to use the patient inter-
    face box;
    analyzing the transmitted data at a location re-
    mote from both the physician’s or clinician’s of-
    fice or place of business and the subject’s home
    or other remote location to make the diagnosis
    of whether the subject has the sleep disorder;
    sending the diagnosis of the collected data to the
    physician or clinician;
    and determining a treatment if required for the
    subject.
    J.A. 5. Claim 38 further requires the subject to “return
    the portable patient interface box and the sensors . . .
    after the data is collected.” J.A. 7.
    IN RE: KAYYALI                                             5
    The examiner rejected claims 1–7 and 34–47 for obvi-
    ousness: claims 1–3, 6, 34, and 41 over Westbrook; claim 4
    over Westbrook in view of Thompson; claim 5 over West-
    brook in view of Auphan; and claims 7, 35–40, and 42–47
    over Westbrook in view of Fey. Only Westbrook and Fey
    are now pertinent, because Kayyali has not independently
    challenged the rejection of claims 4 and 5.
    U.S. Patent Application Publication No. 2005/0027207
    to Westbrook et al. describes a monitoring system for
    collecting and analyzing physiological signals to detect
    sleep apnea. The system includes a small, light-weight
    device that is attached to the subject’s forehead and
    contains several sensors, including a pulse oximeter. The
    system collects data, which “may be directly transmitted
    to an offsite facility for processing and report generation.”
    Westbrook, ¶ 78. Although Westbrook recognizes that
    “[t]he current ‘gold standard’ for the diagnosis of [sleep
    apnea] is an . . . overnight sleep study . . . administered
    and analyzed by a trained technician,” id. ¶ 8, the de-
    scribed system automatically generates a report based on
    the sleep data that can include “a full-disclosure presenta-
    tion of the physiological recordings from the entire ses-
    sion” for physicians to analyze, id. ¶ 156.
    U.S. Patent Application Publication No. 2007/0143151
    to Fey et al. describes a system to manage and analyze
    electronic medical records. After undergoing medical
    testing, a patient receives a smart drive that contains test
    results and other information. The patient can plug the
    smart drive into her computer to input data and to inter-
    act with data already stored on the device. “[T]he user-
    inputted information can be transmitted to the central-
    ized system and one or more health care professionals for
    evaluation and feedback,” allowing health plans to be
    revised and updated. Fey, ¶ 40.
    Kayyali appealed the rejection of claims 1–7 and 34–
    47 to the Board. Kayyali argued that the examiner did
    6                                            IN RE: KAYYALI
    not identify any motivation a relevant skilled artisan
    would have had to modify Westbrook to have a remotely
    located sleep-trained technician analyze sleep data and
    that Westbrook teaches away from using a sleep-trained
    individual altogether. Kayyali further argued that Fey is
    not analogous art because, contrary to the examiner’s
    finding, it does not describe an “ambulatory physiological
    monitor.”
    The Board affirmed the examiner’s rejection of claims
    1–7 and 34–47. The Board adopted the factual findings
    and analysis of the examiner’s answer, which concluded
    that “[i]t would have been obvious to one of ordinary skill
    in the art to substitute one known method for another to
    achieve the expected results of diagnosing sleep disorders,
    such as using a board-certified clinician to analyze col-
    lected data as taught by Westbrook in place of the com-
    puterized analysis used in the invention of Westbrook.”
    J.A. 619. In denying Kayyali’s request for rehearing, the
    Board elaborated: “it was well known at the time of the
    invention to use sleep trained individuals to review sleep
    data and additionally well known that sleep data could be
    forwarded to a remote location in view of Westbrook, to
    have sleep trained individuals to review sleep data at a
    remote location.” J.A. 688–89.
    Kayyali appealed to this court, and because the Board
    did not address Kayyali’s arguments regarding Fey, this
    court granted the Director’s motion to remand the case for
    further proceedings. On remand, the Board again af-
    firmed the examiner’s rejection of claims 1–7 and 34–47.
    The Board repeated its analysis that it would have been
    obvious to use a sleep-trained individual to analyze the
    sleep data generated in Westbrook. With respect to Fey,
    the Board explained that Fey shows “the well-known
    rudimentary business practice of examining a patient in a
    medical center, providing the patient with a medical
    recording device, returning home to use the device, and
    returning the device to the physician.” J.A. 24. The
    IN RE: KAYYALI                                            7
    Board found that Fey is both within the field of the inven-
    tor’s endeavor—“ambulatory physiological monitoring”—
    and reasonably pertinent to solving the inventor’s prob-
    lem.
    Kayyali appeals under 
    35 U.S.C. § 141
    (a), challenging
    the Board’s rejection of claims 1–7 and 34–47 for obvious-
    ness.      We have jurisdiction under 
    28 U.S.C. § 1295
    (a)(4)(A).
    DISCUSSION
    We review the Board’s ultimate determinations of ob-
    viousness de novo. Randall Mfg. v. Rea, 
    733 F.3d 1355
    ,
    1362 (Fed. Cir. 2013). Underlying factual findings, in-
    cluding findings as to whether a reference is analogous
    art and the presence or absence of a motivation to com-
    bine or modify with a reasonable expectation of success,
    are reviewed for substantial evidence. Id.; In re Bigio,
    
    381 F.3d 1320
    , 1324 (Fed. Cir. 2004).
    Kayyali first challenges the Board’s rejection of claims
    1–3, 6, 34, and 41 for obviousness over Westbrook; in so
    doing, Kayyali treats claim 1 as representative. Kayyali
    argues that a relevant skilled artisan would not have
    been motivated to modify the computer-automated analy-
    sis described in Westbrook to allow a sleep-trained indi-
    vidual to perform the diagnosis. But Westbrook explicitly
    states that diagnosis by a sleep-trained clinician is the
    current “gold standard,” thus confirming that a skilled
    artisan would have a motivation to replace computer-
    automated diagnosis with diagnosis by a specialist (at
    least some of the time) to achieve better diagnosis of the
    patient.
    Kayyali also argues that Westbrook teaches away
    from the modification because it disparages the use of a
    sleep-trained individual. Westbrook suggests that an
    overnight sleep study conducted by a sleep-trained clini-
    cian is expensive and that detection can vary by clinician
    8                                           IN RE: KAYYALI
    because professional organizations have provided limited
    guidelines. At most, those suggestions indicate some
    advantages for computer analysis that may make such
    analysis preferable in many circumstances. That is not
    enough to teach skilled artisans away from the alterna-
    tive that Westbrook identifies and calls the “gold stand-
    ard.” See In re Fulton, 
    391 F.3d 1195
    , 1201 (Fed. Cir.
    2004); DePuy Spine, Inc. v. Medtronic Sofamor Danek,
    Inc., 
    567 F.3d 1314
    , 1327 (Fed. Cir. 2009). The Board,
    therefore, did not err in finding that Westbrook does not
    teach away from using sleep-trained individuals.
    In addition, Kayyali challenges the Board’s rejection
    of claims 7, 35–40, and 42–47 on the ground that Fey is
    not analogous art; in so doing, Kayyali treats claim 7 as
    representative. To be analogous art, a prior-art reference
    must (1) be reasonably pertinent to the particular prob-
    lem with which the inventor is involved or (2) be from the
    same field of endeavor. See Innovention Toys, LLC v.
    MGA Entm’t, Inc., 
    637 F.3d 1314
    , 1321 (Fed. Cir. 2011).
    The Board found that Fey qualifies under both of the
    alternatives. Kayyali argues that Fey qualifies under
    neither.
    The Board properly found that Fey is reasonably per-
    tinent to the problem at hand, as “Fey would logically
    have commended itself to an inventor’s attention in
    considering the problem of medical device portability,
    data transfer and ambulatory physiological monitoring.”
    J.A. 26. Fey discloses a device that the patient can take
    home to “input and manage information pertaining to one
    or more health/intervention plans” and that can “include
    a plan revision component for updating the one or more
    health plans based upon the user-inputted information.”
    Fey, ¶ 40. The device allows both the patient and physi-
    cian to observe and review the patient’s physiological
    health data. Therefore, as the Board found, Fey is rea-
    sonably pertinent to the problem faced by Kayyali—
    providing a patient with a medical device, sending the
    IN RE: KAYYALI                                           9
    device home for the patient to use, and returning the
    device after use. Because substantial evidence supports
    the Board’s finding that Fey is reasonably pertinent to the
    particular problem of the claimed invention, and therefore
    analogous art, we need not reach Kayyali’s argument that
    Fey is not in the same field of endeavor.
    Finally, Kayyali contends that a relevant skilled arti-
    san would not have been motivated to combine the in-
    home sleep-test device of Westbrook with the teachings of
    Fey. The Board found that “Fey solves the known prob-
    lem of providing patient care using an ambulatory medi-
    cal device by giving the patient the portable device in
    person, and sending [the patient] home to use the device,
    and later returning the device.” J.A. 29. The Board
    determined that Fey’s method itself provides a motivation
    to combine Fey with Westbrook—to achieve the benefits
    of “providing patient care using an ambulatory medical
    device.” J.A. 27. The Board did not err in reaching this
    conclusion.
    CONCLUSION
    For the foregoing reasons, we affirm the Board’s rejec-
    tion of the claims at issue.
    AFFIRMED
    

Document Info

Docket Number: 2016-1081

Judges: Taranto, Clevenger, Chen

Filed Date: 6/14/2016

Precedential Status: Non-Precedential

Modified Date: 11/6/2024