# US 10,869,802 B2 · Infant joint compression device and method > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 10,869,802 B2 - Document ID: US10869802B2 - Status: Granted - Kind: B2 - Application number: 15/454,970 - Filed: 2017-03-09 - Published: 2017-06-29 - Granted: 2020-12-22 - Earliest claimed: 2009-06-15 - Applicants: Barbara H. Kozol - Inventors: Barbara H. Kozol - Web page: https://patentgrep.com/patent/US10869802B2 ## CPC - A61H 1/006: {Apparatus for applying pressure or blows for compressive stressing of a part of the skeletal structure, e.g. for preventing or alleviating osteoporosis} - A61B 5/02438: {with portable devices, e.g. worn by the patient} - A61B 5/14542: {for measuring blood gases (A61B5/14551 takes precedence)} - A61B 5/6802: {Sensor mounted on worn items} - A61F 5/03: Corsets or bandages for abdomen, teat or breast support, with or without pads - A61F 5/3746: {Jacket-like sling} - A61B 2503/04: Babies, e.g. for SIDS detection - A61B 2503/045: Newborns, e.g. premature baby monitoring - A61H 2201/0221: Mechanism for heating or cooling - A61H 2201/165: Wearable interfaces - A61H 2201/169: Physical characteristics of the surface, e.g. material, relief, texture or indicia - A61H 2201/5082: Temperature sensors - A61H 2230/06: Heartbeat rate - A61H 2230/207: partial O2-value - A61H: PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY (electrotherapy, magnetotherapy, radiation therapy or ultrasound therapy A61N) - A61B: DIAGNOSIS; SURGERY; IDENTIFICATION (usefulness limited to only animals A61D) - A61F: FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS (dental prosthetics A61C) ## Abstract An infant joint compression device and methods of use including decreasing the length of stay in a neonatal intensive care unit and/or increasing bone density of a premature infant are disclosed. A device can include an elongated, generally cocoon-shaped device pod having a head pod end, a foot pod end and a pod interior extending between the head pod end and the foot pod end; a head opening at the head pod end and communicating with the pod interior; and a pod slit extending from the head opening toward the foot pod end and communicating with the pod interior. ## Claims ### Claim 1 A method for increasing bone density of a premature infant in a neonatal intensive care unit, comprising: positioning a premature infant joint compression device around the premature infant so that the premature infant is in a naturally flexed position and is capable of stretching and moving his or her arms and legs outwardly against an interior surface of the premature infant joint compression device with effort, the premature infant joint compression device comprising: an elongated, device pod including a stretchable material and having a head pod end, a foot pod end and a pod interior extending between the head pod end and the foot pod end, wherein the pod interior is sized for receiving the premature infant and the head pod end is configured for covering a back of a head and around a neck of the premature infant; a head opening at the head pod end configured to extend from an area directly above forehead of the premature infant down each side of a face of the premature infant and covering both ears to terminate at an area directly under a chin of the premature infant and communicating with the pod interior; a pod slit extending from the head opening toward the foot pod end and communicating with the pod interior; a series of fasteners positioned along an outer edge of the pod slit; a wire passage within the series of fasteners positioned along an outer edge of the pod slit for wire passage; and wherein the device is positioned only around the premature infant; fastening the series of fasteners along the outer edge of the pod slit of the premature infant joint compression device to create compression in the joints of the arms, legs and spine of the premature infant during normal movement patterns of the infant resulting in expansion and contraction of the stretchable material; and monitoring one or more vital signs of the premature infant, wherein monitoring one or more vital signs of the premature infant comprises connecting wiring from an instrumentation for vital sign monitoring to the premature infant via passing the wiring through the wire passage within the series of fasteners positioned along the outer edge of the pod slit; and increasing bone density of the premature infant as compared to bone density of a premature infant not treated with the premature infant joint compression device, by retaining the premature infant joint compression device around the premature infant to exert compression pressure against the bones and joints in the arms and legs of the premature infant until the infant is discharged or until they reach full gestational term which results in increasing bone density of the premature infant in the neonatal intensive care unit. ### Claim 2 (depends on 1) The method of claim 1, wherein the pod interior is sized for receiving a premature infant weighing up to 1000 grams. ### Claim 3 (depends on 1) The method of claim 1, wherein the pod interior is sized for receiving a premature infant weighing between 1000-1500 grams. ### Claim 4 (depends on 1) The method of claim 1, wherein the pod interior is sized for receiving a premature infant weighing between 1500-2000 grams. ### Claim 5 (depends on 1) The method of claim 1, wherein the pod interior is sized for receiving a premature infant weighing between 2000 to 2500 grams. ### Claim 6 (depends on 1) The method of claim 1, wherein monitoring one or more vital signs of the premature infant comprises monitoring at least heart rate and/or oxygen saturation of the premature infant. ### Claim 7 (depends on 1) The method of claim 1, wherein the method is performed from approximately 28 weeks to approximately 37 weeks of gestation. ### Claim 8 (depends on 1) The method of claim 1, wherein the device pod comprises 8-ounce polyester 4-way stretch fleece. ### Claim 9 (depends on 1) The method of claim 1, wherein the device pod is formed of a single piece of material with two seams. ### Claim 10 A method for decreasing a length of stay of a premature infant in a neonatal intensive care unit, comprising: positioning a premature infant joint compression device around the premature infant so that the premature infant is in a naturally flexed position and is capable of stretching and moving his or her arms and legs outwardly against an interior surface of the premature infant joint compression device with effort, the premature infant joint compression device comprising: an elongated, device pod including a stretchable material and having a head pod end, a foot pod end and a pod interior extending between the head pod end and the foot pod end, wherein the pod interior is sized for receiving the premature infant and the head pod end is configured for covering a back of a head and around a neck of the premature infant; a head opening at the head pod end configured to extend from an area directly above a forehead of the premature infant down each side of a face of the premature infant and covering both ears to terminate at an area directly under a chin of the premature infant and communicating with the pod interior; a pod slit extending from the head opening toward the foot pod end and communicating with the pod interior; a series of fasteners positioned along an outer edge of the pod slit; a wire passage within the series of fasteners positioned along an outer edge of the pod slit for wire passage; and wherein the device is positioned only around the premature infant; fastening the series of fasteners along the outer edge of the pod slit of the premature infant joint compression device to create compression in the joints of the arms, legs and spine of the premature infant during normal movement patterns of the premature infant resulting in expansion and contraction of the stretchable material; monitoring one or more vital signs of the premature infant, wherein monitoring one or more vital signs of the premature infant comprises connecting wiring from an instrumentation for vital sign monitoring to the infant via passing the wiring through the wire passage within the series of fasteners positioned along the outer edge of the pod slit; and retaining the premature infant joint compression device around the premature infant for substantially 2 to 6 weeks which decreases the length of stay of the premature infant in the neonatal intensive care unit. ### Claim 11 (depends on 10) The method of claim 10, wherein the pod interior is sized for receiving a premature infant weighing up to 1000 grams. ### Claim 12 (depends on 10) The method of claim 10, wherein the pod interior is sized for receiving a premature infant weighing between 1000-1500 grams. ### Claim 13 (depends on 10) The method of claim 10, wherein the pod interior is sized for receiving a premature infant weighing between 1500-2000 grams. ### Claim 14 (depends on 10) The method of claim 10, wherein the pod interior is sized for receiving a premature infant weighing between 2000 to 2500 grams. ### Claim 15 (depends on 10) The method of claim 10, wherein monitoring includes monitoring at least heart rate and/or oxygen saturation of the premature infant. ### Claim 16 (depends on 10) The method of claim 10, wherein the method is performed from approximately 28 weeks to approximately 37 weeks of gestation. ### Claim 17 (depends on 10) The method of claim 10, wherein the device pod comprises 8-ounce polyester 4-way stretch fleece. ### Claim 18 (depends on 10) The method of claim 10, wherein the device pod is formed of a single piece of material with two seams.