Kirk Reichard
Kirk Reichard has a total of 19 co-authors. Here are the top co-authors by number of shared publications:
Alicia Olivant Fisher
Nemours Biomedical Research, Wilmington, USA
1 shared publication- Charles D. Vinocur
Nemours - Alfred I DuPont Hospital for Children, Wilmington, DE; Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA
1 shared publication Douglas A Katz
Department of Surgery, Nemours/Alfred I. duPont Hospital for Children, Wilmington, USA
1 shared publication- Frances L. Morales
Massachusetts General Hospital, Department of Surgery
1 shared publication Kirk W Dabney
Department of Orthopedic Surgery, Nemours/Alfred I. duPont Hospital for Children, Wilmington, USA
1 shared publication- Loren Berman
Department of Surgery, Nemours Children's Health, Delaware Valley, 1600 Rockland Road, Wilmington, DE 19803, USA
1 shared publication
Latest Publications
- 22 June 2026
- Published by Springer Nature
- p. 707-718
Pediatric Metabolic and Bariatric Surgery
- 1 August 2020
- Published by Elsevier in Journal of Pediatric Surgery
- Vol. 55 (8) , 1470-1474
The safety and efficacy of using negative pressure incisional wound VACs in pediatric and neonatal patients
- 1 August 2020
- Published by Elsevier in Journal of Pediatric Surgery
- Vol. 55 (8) , 1470-1474
The safety and efficacy of using negative pressure incisional wound VACs in pediatric and neonatal patients
- Open Access
- 2 January 2015
- Published by Wiley in Pediatric Anesthesia
- Vol. 25 (6) , 587-594
Prophylactic methylprednisolone to reduce inflammation and improve outcomes from one lung ventilation in children: a randomized clinical trial
Background: One lung ventilation (OLV) results in inflammatory and mechanical injury, leading to intraoperative and postoperative complications in children. No interventions have been studied in children to minimize such injury.Objective: We hypothesized that a single 2‐mg·kg−1 dose of methylprednisolone given 45–60 min prior to lung collapse would minimize injury from OLV and improve physiological stability.Methods: Twenty‐eight children scheduled to undergo OLV were randomly assigned to receive 2 mg·kg−1 methylprednisolone (MP) or normal saline (placebo group) prior to OLV. Anesthetic management was standardized, and data were collected for physiological stability (bronchospasm, respiratory resistance, and compliance). Plasma was assayed for inflammatory markers related to lung injury at timed intervals related to administration of methylprednisolone.Results: Three children in the placebo group experienced clinically significant intraoperative and postoperative respiratory complications. Respiratory resistance was lower (P = 0.04) in the methylprednisolone group. Pro‐inflammatory cytokine IL‐6 was lower (P = 0.01), and anti‐inflammatory cytokine IL‐10 was higher (P = 0.001) in the methylprednisolone group. Tryptase, measured before and after OLV, was lower (P = 0.03) in the methylprednisolone group while increased levels of tryptase were seen in placebo group after OLV (did not achieve significance). There were no side effects observed that could be attributed to methylprednisolone in this study.Conclusions: Methylprednisolone at 2 mg·kg−1 given as a single dose prior to OLV provides physiological stability to children undergoing OLV. In addition, methylprednisolone results in lower pro‐inflammatory markers and higher anti‐inflammatory markers in the children's plasma.
- 2 January 2015
- Published by Wiley in Pediatric Anesthesia
- Vol. 25 (6) , 587-594
Open AccessProphylactic methylprednisolone to reduce inflammation and improve outcomes from one lung ventilation in children: a randomized clinical trial
Background: One lung ventilation (OLV) results in inflammatory and mechanical injury, leading to intraoperative and postoperative complications in children. No interventions have been studied in children to minimize such injury.Objective: We hypothesized that a single 2‐mg·kg−1 dose of methylprednisolone given 45–60 min prior to lung collapse would minimize injury from OLV and improve physiological stability.Methods: Twenty‐eight children scheduled to undergo OLV were randomly assigned to receive 2 mg·kg−1 methylprednisolone (MP) or normal saline (placebo group) prior to OLV. Anesthetic management was standardized, and data were collected for physiological stability (bronchospasm, respiratory resistance, and compliance). Plasma was assayed for inflammatory markers related to lung injury at timed intervals related to administration of methylprednisolone.Results: Three children in the placebo group experienced clinically significant intraoperative and postoperative respiratory complications. Respiratory resistance was lower (P = 0.04) in the methylprednisolone group. Pro‐inflammatory cytokine IL‐6 was lower (P = 0.01), and anti‐inflammatory cytokine IL‐10 was higher (P = 0.001) in the methylprednisolone group. Tryptase, measured before and after OLV, was lower (P = 0.03) in the methylprednisolone group while increased levels of tryptase were seen in placebo group after OLV (did not achieve significance). There were no side effects observed that could be attributed to methylprednisolone in this study.Conclusions: Methylprednisolone at 2 mg·kg−1 given as a single dose prior to OLV provides physiological stability to children undergoing OLV. In addition, methylprednisolone results in lower pro‐inflammatory markers and higher anti‐inflammatory markers in the children's plasma.