Cathy Grisby
Cincinnati Children's Hospital Medical Center
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Featured researches published by Cathy Grisby.
The New England Journal of Medicine | 2008
Brenda H. Morris; William Oh; Jon E. Tyson; David K. Stevenson; Dale L. Phelps; T. Michael O'Shea; Georgia E. McDavid; Rebecca Perritt; Krisa P. Van Meurs; Betty R. Vohr; Cathy Grisby; Qing Yao; Claudia Pedroza; Abhik Das; W. Kenneth Poole; Waldemar A. Carlo; Shahnaz Duara; Abbot R. Laptook; Walid A. Salhab; Seetha Shankaran; Brenda B. Poindexter; Avroy A. Fanaroff; Michele C. Walsh; Maynard R. Rasmussen; Barbara J. Stoll; C. Michael Cotten; Edward F. Donovan; Richard A. Ehrenkranz; Ronnie Guillet; Rosemary D. Higgins
BACKGROUND It is unclear whether aggressive phototherapy to prevent neurotoxic effects of bilirubin benefits or harms infants with extremely low birth weight (1000 g or less). METHODS We randomly assigned 1974 infants with extremely low birth weight at 12 to 36 hours of age to undergo either aggressive or conservative phototherapy. The primary outcome was a composite of death or neurodevelopmental impairment determined for 91% of the infants by investigators who were unaware of the treatment assignments. RESULTS Aggressive phototherapy, as compared with conservative phototherapy, significantly reduced the mean peak serum bilirubin level (7.0 vs. 9.8 mg per deciliter [120 vs. 168 micromol per liter], P<0.01) but not the rate of the primary outcome (52% vs. 55%; relative risk, 0.94; 95% confidence interval [CI], 0.87 to 1.02; P=0.15). Aggressive phototherapy did reduce rates of neurodevelopmental impairment (26%, vs. 30% for conservative phototherapy; relative risk, 0.86; 95% CI, 0.74 to 0.99). Rates of death in the aggressive-phototherapy and conservative-phototherapy groups were 24% and 23%, respectively (relative risk, 1.05; 95% CI, 0.90 to 1.22). In preplanned subgroup analyses, the rates of death were 13% with aggressive phototherapy and 14% with conservative phototherapy for infants with a birth weight of 751 to 1000 g and 39% and 34%, respectively (relative risk, 1.13; 95% CI, 0.96 to 1.34), for infants with a birth weight of 501 to 750 g. CONCLUSIONS Aggressive phototherapy did not significantly reduce the rate of death or neurodevelopmental impairment. The rate of neurodevelopmental impairment alone was significantly reduced with aggressive phototherapy. This reduction may be offset by an increase in mortality among infants weighing 501 to 750 g at birth. (ClinicalTrials.gov number, NCT00114543.)
Journal of Perinatology | 2012
Jon E. Tyson; Claudia Pedroza; John Langer; Charles E. Green; B Morris; Daniel Stevenson; Kp Van Meurs; William Oh; Dale L. Phelps; Michael O'Shea; Georgia E. McDavid; Cathy Grisby; Rosemary D. Higgins
Objective:Aggressive phototherapy (AgPT) is widely used and assumed to be safe and effective for even the most immature infants. We assessed whether the benefits and hazards for the smallest and sickest infants differed from those for other extremely low-birth-weight (ELBW; ⩽1000 g) infants in our Neonatal Research Network trial, the only large trial of AgPT.Study Design:ELBW infants (n=1974) were randomized to AgPT or conservative phototherapy at age 12 to 36 h. The effect of AgPT on outcomes (death, impairment, profound impairment, death or impairment (primary outcome), and death or profound impairment) at 18 to 22 months of corrected age was related to BW stratum (501 to 750 g; 751 to 1000 g) and baseline severity of illness using multilevel regression equations. The probability of benefit and of harm was directly assessed with Bayesian analyses.Result:Baseline illness severity was well characterized using mechanical ventilation and FiO2 at 24 h age. Among mechanically ventilated infants ⩽750 g BW (n=684), a reduction in impairment and in profound impairment was offset by higher mortality (P for interaction <0.05) with no significant effect on composite outcomes. Conservative Bayesian analyses of this subgroup identified a 99% (posterior) probability that AgPT increased mortality, a 97% probability that AgPT reduced impairment, and a 99% probability that AgPT reduced profound impairment.Conclusion:Findings from the only large trial of AgPT suggest that AgPT may increase mortality while reducing impairment and profound impairment among the smallest and sickest infants. New approaches to reduce their serum bilirubin need development and rigorous testing.
Pediatrics | 2014
Nansi S. Boghossian; Nellie I. Hansen; Edward F. Bell; Barbara J. Stoll; Jeffrey C. Murray; John C. Carey; Ira Adams-Chapman; Seetha Shankaran; Michele C. Walsh; Abbot R. Laptook; Roger G. Faix; Nancy S. Newman; Ellen C. Hale; Abhik Das; Leslie D. Wilson; Angelita M. Hensman; Cathy Grisby; Monica V. Collins; Diana M. Vasil; Joanne Finkle; Deanna Maffett; M. Bethany Ball; Conra Backstrom Lacy; Rebecca Bara; Rosemary D. Higgins
OBJECTIVE: Little is known about how very low birth weight (VLBW) affects survival and morbidities among infants with trisomy 13 (T13) or trisomy 18 (T18). We examined the care plans for VLBW infants with T13 or T18 and compared their risks of mortality and neonatal morbidities with VLBW infants with trisomy 21 and VLBW infants without birth defects. METHODS: Infants with birth weight 401 to 1500 g born or cared for at a participating center of the Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network during the period 1994–2009 were studied. Poisson regression models were used to examine risk of death and neonatal morbidities among infants with T13 or T18. RESULTS: Of 52 262 VLBW infants, 38 (0.07%) had T13 and 128 (0.24%) had T18. Intensity of care in the delivery room varied depending on whether the trisomy was diagnosed before or after birth. The plan for subsequent care for the majority of the infants was to withdraw care or to provide comfort care. Eleven percent of infants with T13 and 9% of infants with T18 survived to hospital discharge. Survivors with T13 or T18 had significantly increased risk of patent ductus arteriosus and respiratory distress syndrome compared with infants without birth defects. No infant with T13 or T18 developed necrotizing enterocolitis. CONCLUSIONS: In this cohort of liveborn VLBW infants with T13 or T18, the timing of trisomy diagnosis affected the plan for care, survival was poor, and death usually occurred early.
Journal of Perinatology | 2013
Brenda H. Morris; Jon E. Tyson; David K. Stevenson; William Oh; Dale L. Phelps; Thomas M. O'Shea; Georgia E. McDavid; Kp Van Meurs; Betty R. Vohr; Cathy Grisby; Qing Yao; Sarah Kandefer; Dennis Wallace; Rosemary D. Higgins
Objective:Evaluate the efficacy of phototherapy (PT) devices and the outcomes of extremely premature infants treated with those devices.Study Design:This substudy of the National Institute of Child Health and Human Development Neonatal Research Network PT trial included 1404 infants treated with a single type of PT device during the first 24±12 h of treatment. The absolute (primary outcome) and relative decrease in total serum bilirubin (TSB) and other measures were evaluated. For infants treated with one PT type during the 2-week intervention period (n=1223), adjusted outcomes at discharge and 18 to 22 months corrected age were determined.Result:In the first 24 h, the adjusted absolute (mean (±s.d.)) and relative (%) decrease in TSB (mg dl−1) were: light-emitting diodes (LEDs) −2.2 (±3), −22%; Spotlights −1.7 (±2), −19%; Banks −1.3 (±3), −8%; Blankets −0.8 (±3), −1%; (P<0.0002). Some findings at 18 to 22 months differed between groups.Conclusion:LEDs achieved the greatest initial absolute reduction in TSB but were similar to Spots in the other performance measures. Long-term effects of PT devices in extremely premature infants deserve rigorous evaluation.
Acta Paediatrica | 2011
Susan R. Hintz; David K. Stevenson; Qing Yao; Ronald J. Wong; Abhik Das; Krisa P. Van Meurs; Brenda H. Morris; Jon E. Tyson; William Oh; W. Kenneth Poole; Dale L. Phelps; Georgia E. McDavid; Cathy Grisby; Rosemary D. Higgins
Aim: To compare risk‐adjusted outcomes at 18‐ to 22‐month‐corrected age for extremely low birth weight (ELBW) infants who never received phototherapy (NoPTx) to those who received any phototherapy (PTx) in the NICHD Neonatal Research Network randomized trial of Aggressive vs. Conservative Phototherapy.
Pediatrics | 2004
Michele C. Walsh; Qing Yao; Patricia Gettner; Ellen C. Hale; Monica Collins; Angelita Hensman; Ruth Everette; Nancy Peters; Nancy A. Miller; Gerry Muran; Kathy J. Auten; Nancy S. Newman; Gina Rowan; Cathy Grisby; Kathy Arnell; Lucy Miller; Bethany Ball; Georgia E. McDavid
The Journal of Pediatrics | 2016
Carl T. D'Angio; Namasivayam Ambalavanan; Waldemar A. Carlo; Scott A. McDonald; Kristin Skogstrand; David M. Hougaard; Seetha Shankaran; Ronald N. Goldberg; Richard A. Ehrenkranz; Jon E. Tyson; Barbara J. Stoll; Abhik Das; Rosemary D. Higgins; Alan H. Jobe; Abbot R. Laptook; William Oh; Lewis P. Rubin; Angelita M. Hensman; Avroy A. Fanaroff; Michele C. Walsh; Nancy S. Newman; Bonnie S. Siner; Edward F. Donovan; Vivek Narendran; Barbara D. Alexander; Cathy Grisby; Jody Hessling; Marcia Worley Mersmann; Holly L. Mincey; C. Michael Cotten
Publisher | 2017
Seetha Shankaran; Abbot R. Laptook; Athina Pappas; Scott A. McDonald; Abhik Das; Jon E. Tyson; Brenda B. Poindexter; Kurt Schibler; Edward F. Bell; Roy J. Heyne; Claudia Pedroza; Rebecca Bara; Krisa P. Van Meurs; Carolyn M. Petrie Huitema; Cathy Grisby; Uday Devaskar; Richard A. Ehrenkranz; Heidi M. Harmon; Lina F. Chalak; Sara B. DeMauro; Meena Garg; Michelle Hartley-McAndrew; Amir M. Khan; Michele C. Walsh; Namasivayam Ambalavanan; Jane E. Brumbaugh; Kristi L. Watterberg; Edward G. Shepherd; Shannon E. G. Hamrick; John Barks
Obstetrical & Gynecological Survey | 2015
Seetha Shankaran; Abbot R. Laptook; Athina Pappas; Scott A. McDonald; Abhik Das; Jon E. Tyson; Brenda B. Poindexter; Kurt Schibler; Edward F. Bell; Roy J. Heyne; Claudia Pedroza; Rebecca Bara; Krisa P. Van Meurs; Cathy Grisby; Carolyn M. Petrie Huitema; Meena Garg; Richard A. Ehrenkranz; Edward G. Shepherd; Lina F. Chalak; Shannon E. G. Hamrick; Amir M. Khan; Anne Marie Reynolds; Matthew M. Laughon; William E. Truog; Kevin Dysart; Waldemar A. Carlo; Michele C. Walsh; Kristi L. Watterberg; Rosemary D. Higgins
PMC | 2014
Seetha Shankaran; Abbot R. Laptook; Athina Pappas; Scott A. McDonald; Abhik Das; Jon E. Tyson; Brenda B. Poindexter; Kurt Schibler; Edward F. Bell; Roy J. Heyne; Claudia Pedroza; Rebecca Bara; Krisa P. Van Meurs; Cathy Grisby; Carolyn M. Petrie Huitema; Meena Garg; Richard A. Ehrenkranz; Edward G. Shepherd; Lina F. Chalak; Shannon E. G. Hamrick; Amir M. Khan; Anne Marie Reynolds; Matthew M. Laughon; William E. Truog; Kevin Dysart; Waldemar A. Carlo; Michele C. Walsh; Kristi L. Watterberg; Rosemary D. Higgins