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Dive into the research topics where Dennis L. Murray is active.

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Featured researches published by Dennis L. Murray.


Pediatrics | 1998

Prevention of respiratory syncytial virus infections: Indications for the use of palivizumab and update on the use of RSV-IGIV

Neal A. Halsey; Jon S. Abramson; P. Joan Chesney; Margaret C. Fisher; Michael A. Gerber; S. Michael Marcy; Dennis L. Murray; Gary D. Overturf; Charles G. Prober; Thomas N. Saari; Leonard B. Weiner; Richard J. Whitley; R. Breiman; M. Carolyn Hardegree; A. Hirsch; Richard F. Jacobs; N. E. MacDonald; Walter A. Orenstein; N. Regina Rabinovich; B. Schwartz; Georges Peter; Carol J. Baker; Larry K. Pickering; H. Cody Meissner; James A. Lemons; Lillian R. Blackmon; William P. Kanto; Hugh MacDonald; Carol Miller; Lu Ann Papile

The Food and Drug Administration recently approved the use of palivizumab (palē-vizhū-mäb), an intramuscularly administered monoclonal antibody preparation. Recommendations for its use are based on a large, randomized study demonstrating a 55% reduction in the risk of hospitalization attributable to respiratory syncytial virus (RSV) infections in high-risk pediatric patients. Infants and children with chronic lung disease (CLD), formerly designated bronchopulmonary dysplasia, as well as prematurely born infants without CLD experienced a reduced number of hospitalizations while receiving palivizumab compared with a placebo. Both palivizumab and respiratory syncytial virus immune globulin intravenous (RSV-IGIV) are available for protecting high-risk children against serious complications from RSV infections. Palivizumab is preferred for most high-risk children because of ease of administration (intramuscular), lack of interference with measles–mumps–rubella vaccine and varicella vaccine, and lack of complications associated with intravenous administration of human immune globulin products. RSV-IGIV, however, provides additional protection against other respiratory viral illnesses and may be preferred for selected high-risk children including those receiving replacement intravenous immune globulin because of underlying immune deficiency or human immuno-deficiency virus infection. For premature infants about to be discharged from hospitals during the RSV season, physicians could consider administering RSV-IGIV for the first month of prophylaxis. Most of the guidelines from the American Academy of Pediatrics for the selection of infants and children to receive RSV-prophylaxis remain unchanged. Palivizumab has been shown to provide benefit for infants who were 32 to 35 weeks of gestation at birth. RSV-IGIV is contraindicated and palivizumab is not recommended for children with cyanotic congenital heart disease. The number of patients with adverse events judged to be related to palivizumab was similar to that of the placebo group (11% vs 10%, respectively); discontinuation of injections for adverse events related to palivizumab was rare.


Pediatrics | 2014

Updated Guidance for Palivizumab Prophylaxis Among Infants and Young Children at Increased Risk of Hospitalization for Respiratory Syncytial Virus Infection

Michael T. Brady; Carrie L. Byington; H. Dele Davies; Kathryn M. Edwards; Mary Anne Jackson; Yvonne Maldonado; Dennis L. Murray; Walter A. Orenstein; Mobeen H. Rathore; Mark H. Sawyer; Gordon E. Schutze; Rodney E. Willoughby; Theoklis E. Zaoutis; Henry H. Bernstein; David W. Kimberlin; Sarah S. Long; H. Cody Meissner; Marc A. Fischer; Bruce G. Gellin; Richard L. Gorman; Lucia H. Lee; R. Douglas Pratt; Jennifer S. Read; Joan Robinson; Marco Aurelio Palazzi Safadi; Jane F. Seward; Jeffrey R. Starke; Geoffrey R. Simon; Tina Q. Tan; Joseph A. Bocchini

Palivizumab was licensed in June 1998 by the Food and Drug Administration for the reduction of serious lower respiratory tract infection caused by respiratory syncytial virus (RSV) in children at increased risk of severe disease. Since that time, the American Academy of Pediatrics has updated its guidance for the use of palivizumab 4 times as additional data became available to provide a better understanding of infants and young children at greatest risk of hospitalization attributable to RSV infection. The updated recommendations in this policy statement reflect new information regarding the seasonality of RSV circulation, palivizumab pharmacokinetics, the changing incidence of bronchiolitis hospitalizations, the effect of gestational age and other risk factors on RSV hospitalization rates, the mortality of children hospitalized with RSV infection, the effect of prophylaxis on wheezing, and palivizumab-resistant RSV isolates. This policy statement updates and replaces the recommendations found in the 2012 Red Book.


Pediatrics | 2013

Clostridium difficile Infection in Infants and Children

Gordon E. Schutze; Rodney E. Willoughby; Michael T. Brady; Carrie L. Byington; H. Dele Davies; Kathryn M. Edwards; Mary P. Glode; Mary Anne Jackson; Harry L. Keyserling; Yvonne Maldonado; Dennis L. Murray; Walter A. Orenstein; Theoklis E. Zaoutis

Infections caused by Clostridium difficile in hospitalized children are increasing. The recent publication of clinical practice guidelines for C difficile infection in adults did not address issues that are specific to children. The purpose of this policy statement is to provide the pediatrician with updated information and recommendations about C difficile infections affecting pediatric patients.


Pediatrics | 2012

Recommendations for Prevention and Control of Influenza in Children, 2012–2013

Michael T. Brady; Carrie L. Byington; H. Dele Davies; Kathryn M. Edwards; Mary P. Glode; Mary Anne Jackson; Harry L. Keyserling; Yvonne Maldonado; Dennis L. Murray; Walter A. Orenstein; Gordon E. Schutze; Rodney E. Willoughby; Theoklis E. Zaoutis

The purpose of this statement is to update recommendations for routine use of trivalent seasonal influenza vaccine and antiviral medications for the prevention and treatment of influenza in children. The key points for the upcoming 2012–2013 season are: (1) this year’s trivalent influenza vaccine contains A/California/7/2009 (H1N1)–like antigen (derived from influenza A [H1N1] pdm09 [pH1N1] virus); A/Victoria/361/2011 (H3N2)–like antigen; and B/Wisconsin/1/2010–like antigen (the influenza A [H3N2] and B antigens differ from those contained in the 2010–2011 and 2011–2012 seasonal vaccines); (2) annual universal influenza immunization is indicated; and (3) an updated dosing algorithm for administration of influenza vaccine to children 6 months through 8 years of age has been created. Pediatricians, nurses, and all health care personnel should promote influenza vaccine use and infection control measures. In addition, pediatricians should promptly identify influenza infections to enable rapid treatment, when indicated, to reduce morbidity and mortality.


Pediatrics | 2000

Varicella vaccine update

Neal A. Halsey; Jon S. Abramson; P. J. Chesney; Margaret C. Fisher; Michael A. Gerber; S. M. Marcy; Dennis L. Murray; Gary D. Overturf; Charles G. Prober; Thomas N. Saari; Leonard B. Weiner; Richard J. Whitley; G. Peter; L. K. Pickering; Carol J. Baker; A. Hirsch; Richard F. Jacobs; N. E. MacDonald; B. Schwartz; Walter A. Orenstein; P. A. Patriarca; N. R. Rabinovich; R. Breiman; Jane F. Seward; Anne A. Gershon

Recommendations for routine varicella vaccination were published by the American Academy of Pediatrics in May 1995, but many eligible children remain unimmunized. This update provides additional information on the varicella disease burden before the availability of varicella vaccine, potential barriers to immunization, efforts to increase the level of coverage, new safety data, and new recommendations for use of the varicella vaccine after exposure and in children with human immunodeficiency virus infections. Pediatricians are strongly encouraged to support public health officials in the development and implementation of varicella immunization requirements for child care and school entry.


Pediatrics | 1998

Hepatitis C virus infection

Neal A. Halsey; Jon S. Abramson; P. J. Chesney; Margaret C. Fisher; Michael A. Gerber; D. S. Gromisch; S. Kohl; S. M. Marcy; Dennis L. Murray; Gary D. Overturf; Richard J. Whitley; R. Yogev

Hepatitis C virus (HCV) has become the most significant cause of chronic liver disease of infectious etiology in the United States. The recognition that HCV can be transmitted perinatally or through blood transfusions warrants particular attention by the pediatrician. The American Academy of Pediatrics recommends screening infants born to HCV-infected mothers and persons with risk factors for HCV infection such as injection drug use, transfusion of ≥1 U of blood or blood products before 1992, or hemodialysis should be screened for anti-HCV. Also, persons who received clotting factor concentrates before 1987, when effective inactivation procedures were introduced, also should be screened. Guidelines for counseling families of HCV-infected children are provided.


Pediatrics | 1998

Severe invasive group a streptococcal infections: A subject review

Neal A. Halsey; Jon S. Abramson; P. J. Chesney; Margaret C. Fisher; Michael A. Gerber; D. S. Gromisch; S. Kohl; S. M. Marcy; Dennis L. Murray; Gary D. Overturf; Richard J. Whitley; R. Yogev; G. Peter; C. B. Hall; B. Schwartz; R. Breiman; M. C. Hardegree; Richard F. Jacobs; N. E. MacDonald; Walter A. Orenstein; N. R. Rabinovich

The course of severe invasive group A β-hemolytic streptococcal (GABHS) infections is often precipitous, requiring prompt diagnosis and rapid initiation of appropriate therapy. Therefore, physicians must have a high index of suspicion of this disease, particularly in patients at increased risk (eg, those with varicella or diabetes mellitus). Although a relationship between the use of nonsteroidal antiinflammatory drugs and severe invasive GABHS infections has been suggested, at present data on which to base a clinical decision about the use or restriction of nonsteroidal antiinflammatory drugs in children with varicella are insufficient. When necrotizing fasciitis is suspected, prompt surgical drainage, debridement, fasciotomy, or amputation often is necessary. Many experts recommend intravenously administered penicillin G and clindamycin for the treatment of invasive GABHS infections on the basis of animal studies. Some evidence exists that intravenous immunoglobulin given in addition to appropriate antimicrobial and surgical therapy may be beneficial. Although chemoprophylaxis for household contacts of persons with invasive GABHS infections has been considered by some experts, the limited available data indicate that the risk of secondary cases is low (2.9 per 1000) and data about the effectiveness of any drug are insufficient to make recommendations. Because of the low risk of secondary cases of invasive GABHS infections in schools or child care facilities, chemoprophylaxis is not indicated in these settings. Routine immunization of all healthy children against varicella is recommended and is an effective means to decrease the risk of invasive GABHS infections.


Pediatrics | 2012

Strategies for Prevention of Health Care-Associated Infections in the NICU

Richard A. Polin; Susan E. Denson; Michael T. Brady; Lu Ann Papile; Jill E. Baley; Waldemar A. Carlo; James J. Cummings; Praveen Kumar; Rosemarie C. Tan; Kristi L. Watterberg; Carrie L. Byington; H. Dele Davies; Kathryn M. Edwards; Mary P. Glode; Mary Anne Jackson; Harry L. Keyserling; Yvonne Maldonado; Dennis L. Murray; Walter A. Orenstein; Gordon E. Schutze; Rodney E. Willoughby; Theoklis E. Zaoutis

Health care–associated infections in the NICU result in increased morbidity and mortality, prolonged lengths of stay, and increased medical costs. Neonates are at high risk of acquiring health care–associated infections because of impaired host-defense mechanisms, limited amounts of protective endogenous flora on skin and mucosal surfaces at time of birth, reduced barrier function of their skin, use of invasive procedures and devices, and frequent exposure to broad-spectrum antibiotic agents. This clinical report reviews management and prevention of health care–associated infections in newborn infants.


Pediatrics | 2012

HPV Vaccine Recommendations

Michael T. Brady; Carrie L. Byington; H. Dele Davies; Kathryn M. Edwards; Mary P. Glode; Mary Anne Jackson; Harry L. Keyserling; Yvonne Maldonado; Dennis L. Murray; Walter A. Orenstein; Gordon E. Schutze; Rodney E. Willoughby; Theoklis E. Zaoutis

On October 25, 2011, the Advisory Committee on Immunization Practices of the Centers for Disease Control and Prevention recommended that the quadrivalent human papillomavirus vaccine (Gardasil; Merck & Co, Inc, Whitehouse Station, NJ) be used routinely in males. The American Academy of Pediatrics has reviewed updated data provided by the Advisory Committee on Immunization Practices on vaccine efficacy, safety, and cost-effectiveness as well as programmatic considerations and supports this recommendation. This revised statement updates recommendations for human papillomavirus immunization of both males and females.


Human Vaccines & Immunotherapeutics | 2013

Impact of a physician recommendation and parental immunization attitudes on receipt or intention to receive adolescent vaccines

Lisa M. Gargano; Natasha L. Herbert; Julia E. Painter; Jessica M. Sales; Christopher Morfaw; Kimberly J. Rask; Dennis L. Murray; Ralph J. DiClemente; James M. Hughes

Four vaccines are recommended by the Centers for Disease Control and Prevention’s Advisory Committee on Immunization Practices for adolescents. Parental attitudes may play a key role in vaccination uptake in this age group. In 2011, we conducted a cross-sectional survey among parents of adolescents in one county in Georgia to identify parental attitudes toward adolescent vaccination, reasons for vaccine acceptance or refusal, and impact of a physician recommendation for vaccination. Physician recommendation was reported as one of the top reasons for receipt or intent to receive any of the vaccines. Physician recommendation of any of the four vaccines was associated with receipt of Tdap (p < 0.001), MCV4 (p < 0.001), and HPV (p = 0.03) and intent to receive Tdap (p = 0.05), MCV4 (p = 0.005), and HPV (p = 0.05). Compared with parents who did not intend to have their adolescent vaccinated with any of the vaccines, parents who did intend reported higher perceived susceptibility (3.12 vs. 2.63, p = 0.03) and severity of disease (3.89 vs. 3.70, p = 0.02) and higher perceived benefit of vaccination (8.48 vs. 7.74, p = 0.02). These findings suggest that future vaccination efforts geared toward parents may benefit from addressing the advantages of vaccination and enhancing social norms. Physicians can play a key role by providing information on the benefits of adolescent vaccination.

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Richard J. Whitley

University of Alabama at Birmingham

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Michael A. Gerber

Cincinnati Children's Hospital Medical Center

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Gary D. Overturf

University of Southern California

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