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Dural augmentation approaches and complication rates after posterior fossa decompression for Chiari I malformation and syringomyelia: a Park-Reeves Syringomyelia Research Consortium study.
Yahanda, Alexander T; Adelson, P David; Akbari, S Hassan A; Albert, Gregory W; Aldana, Philipp R; Alden, Tord D; Anderson, Richard C E; Bauer, David F; Bethel-Anderson, Tammy; Brockmeyer, Douglas L; Chern, Joshua J; Couture, Daniel E; Daniels, David J; Dlouhy, Brian J; Durham, Susan R; Ellenbogen, Richard G; Eskandari, Ramin; George, Timothy M; Grant, Gerald A; Graupman, Patrick C; Greene, Stephanie; Greenfield, Jeffrey P; Gross, Naina L; Guillaume, Daniel J; Hankinson, Todd C; Heuer, Gregory G; Iantosca, Mark; Iskandar, Bermans J; Jackson, Eric M; Johnston, James M; Keating, Robert F; Krieger, Mark D; Leonard, Jeffrey R; Maher, Cormac O; Mangano, Francesco T; McComb, J Gordon; McEvoy, Sean D; Meehan, Thanda; Menezes, Arnold H; O'Neill, Brent R; Olavarria, Greg; Ragheb, John; Selden, Nathan R; Shah, Manish N; Shannon, Chevis N; Shimony, Joshua S; Smyth, Matthew D; Stone, Scellig S D; Strahle, Jennifer M; Torner, James C.
Affiliation
  • Yahanda AT; 1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, MO.
  • Adelson PD; 2Division of Pediatric Neurosurgery, Barrow Neurological Institute at Phoenix Children's Hospital, Phoenix, AZ.
  • Akbari SHA; 3Division of Pediatric Neurosurgery, University of Alabama at Birmingham, AL.
  • Albert GW; 4Division of Neurosurgery, Arkansas Children's Hospital, Little Rock, AR.
  • Aldana PR; 5Division of Pediatric Neurosurgery, University of Florida College of Medicine, Jacksonville, FL.
  • Alden TD; 6Division of Pediatric Neurosurgery, Ann and Robert H. Lurie Children's Hospital of Chicago, IL.
  • Anderson RCE; 7Division of Pediatric Neurosurgery, Department of Neurological Surgery, Children's Hospital of New York, Columbia-Presbyterian, New York, NY.
  • Bauer DF; 8Department of Neurosurgery, Dartmouth-Hitchcock Medical Center, Lebanon, NH.
  • Bethel-Anderson T; 1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, MO.
  • Brockmeyer DL; 9Division of Pediatric Neurosurgery, Primary Children's Hospital, Salt Lake City, UT.
  • Chern JJ; 10Division of Pediatric Neurosurgery, Children's Healthcare of Atlanta, GA.
  • Couture DE; 11Department of Neurological Surgery, Wake Forest University School of Medicine, Winston-Salem, NC.
  • Daniels DJ; 12Department of Neurosurgery, Mayo Clinic, Rochester, MN.
  • Dlouhy BJ; 13Department of Neurosurgery, University of Iowa Hospitals and Clinics, Iowa City, IA.
  • Durham SR; 14Department of Neurosurgery, University of Vermont, Burlington, VT.
  • Ellenbogen RG; 15Division of Pediatric Neurosurgery, Seattle Children's Hospital, Seattle, WA.
  • Eskandari R; 16Department of Neurosurgery, Medical University of South Carolina, Charleston, SC.
  • George TM; 17Division of Pediatric Neurosurgery, Dell Children's Medical Center, Austin, TX.
  • Grant GA; 18Division of Pediatric Neurosurgery, Lucile Packard Children's Hospital, Palo Alto, CA.
  • Graupman PC; 19Division of Pediatric Neurosurgery, Gillette Children's Hospital, St. Paul, MN.
  • Greene S; 20Division of Pediatric Neurosurgery, Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh, PA.
  • Greenfield JP; 21Department of Neurological Surgery, Weill Cornell Medical College, NewYork-Presbyterian Hospital, New York, NY.
  • Gross NL; 22Department of Neurosurgery, University of Oklahoma, Oklahoma City, OK.
  • Guillaume DJ; 23Department of Neurosurgery, University of Minnesota Medical School, Minneapolis, MN.
  • Hankinson TC; 24Department of Neurosurgery, Children's Hospital Colorado, Aurora, CO.
  • Heuer GG; 25Division of Pediatric Neurosurgery, Children's Hospital of Pennsylvania, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Iantosca M; 26Department of Neurosurgery, Penn State Milton S. Hershey Medical Center, Hershey, PA.
  • Iskandar BJ; 27Department of Neurological Surgery, University of Wisconsin at Madison, WI.
  • Jackson EM; 28Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Johnston JM; 3Division of Pediatric Neurosurgery, University of Alabama at Birmingham, AL.
  • Keating RF; 29Department of Neurosurgery, Children's National Medical Center, Washington, DC.
  • Krieger MD; 30Division of Pediatric Neurosurgery, Children's Hospital of Los Angeles, CA.
  • Leonard JR; 31Division of Pediatric Neurosurgery, Nationwide Children's Hospital, Columbus, OH.
  • Maher CO; 32Department of Neurosurgery, University of Michigan, Ann Arbor, MI.
  • Mangano FT; 33Division of Pediatric Neurosurgery, Cincinnati Children's Medical Center, Cincinnati, OH.
  • McComb JG; 30Division of Pediatric Neurosurgery, Children's Hospital of Los Angeles, CA.
  • McEvoy SD; 1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, MO.
  • Meehan T; 1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, MO.
  • Menezes AH; 13Department of Neurosurgery, University of Iowa Hospitals and Clinics, Iowa City, IA.
  • O'Neill BR; 24Department of Neurosurgery, Children's Hospital Colorado, Aurora, CO.
  • Olavarria G; 34Division of Pediatric Neurosurgery, Arnold Palmer Hospital for Children, Orlando, FL.
  • Ragheb J; 35Department of Neurological Surgery, University of Miami School of Medicine, Miami, FL.
  • Selden NR; 36Department of Neurological Surgery and Doernbecher Children's Hospital, Oregon Health & Science University, Portland, OR.
  • Shah MN; 37Division of Pediatric Neurosurgery, McGovern Medical School, Houston, TX.
  • Shannon CN; 38Division of Pediatric Neurosurgery, Monroe Carell Jr. Children's Hospital of Vanderbilt University, Nashville, TN.
  • Shimony JS; 39Department of Radiology, Washington University School of Medicine, St. Louis, MO.
  • Smyth MD; 1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, MO.
  • Stone SSD; 40Division of Pediatric Neurosurgery, Boston Children's Hospital, Boston, MA.
  • Strahle JM; 1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, MO.
  • Torner JC; 13Department of Neurosurgery, University of Iowa Hospitals and Clinics, Iowa City, IA.
J Neurosurg Pediatr ; 27(4): 459-468, 2021 Feb 12.
Article in En | MEDLINE | ID: mdl-33578390
ABSTRACT

OBJECTIVE:

Posterior fossa decompression with duraplasty (PFDD) is commonly performed for Chiari I malformation (CM-I) with syringomyelia (SM). However, complication rates associated with various dural graft types are not well established. The objective of this study was to elucidate complication rates within 6 months of surgery among autograft and commonly used nonautologous grafts for pediatric patients who underwent PFDD for CM-I/SM.

METHODS:

The Park-Reeves Syringomyelia Research Consortium database was queried for pediatric patients who had undergone PFDD for CM-I with SM. All patients had tonsillar ectopia ≥ 5 mm, syrinx diameter ≥ 3 mm, and ≥ 6 months of postoperative follow-up after PFDD. Complications (e.g., pseudomeningocele, CSF leak, meningitis, and hydrocephalus) and postoperative changes in syrinx size, headaches, and neck pain were compared for autograft versus nonautologous graft.

RESULTS:

A total of 781 PFDD cases were analyzed (359 autograft, 422 nonautologous graft). Nonautologous grafts included bovine pericardium (n = 63), bovine collagen (n = 225), synthetic (n = 99), and human cadaveric allograft (n = 35). Autograft (103/359, 28.7%) had a similar overall complication rate compared to nonautologous graft (143/422, 33.9%) (p = 0.12). However, nonautologous graft was associated with significantly higher rates of pseudomeningocele (p = 0.04) and meningitis (p < 0.001). The higher rate of meningitis was influenced particularly by the higher rate of chemical meningitis (p = 0.002) versus infectious meningitis (p = 0.132). Among 4 types of nonautologous grafts, there were differences in complication rates (p = 0.02), including chemical meningitis (p = 0.01) and postoperative nausea/vomiting (p = 0.03). Allograft demonstrated the lowest complication rates overall (14.3%) and yielded significantly fewer complications compared to bovine collagen (p = 0.02) and synthetic (p = 0.003) grafts. Synthetic graft yielded higher complication rates than autograft (p = 0.01). Autograft and nonautologous graft resulted in equal improvements in syrinx size (p < 0.0001). No differences were found for postoperative changes in headaches or neck pain.

CONCLUSIONS:

In the largest multicenter cohort to date, complication rates for dural autograft and nonautologous graft are similar after PFDD for CM-I/SM, although nonautologous graft results in higher rates of pseudomeningocele and meningitis. Rates of meningitis differ among nonautologous graft types. Autograft and nonautologous graft are equivalent for reducing syrinx size, headaches, and neck pain.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arnold-Chiari Malformation / Postoperative Complications / Syringomyelia / Neurosurgical Procedures / Dura Mater Type of study: Clinical_trials Limits: Adolescent / Child / Female / Humans / Male Language: En Journal: J Neurosurg Pediatr Journal subject: NEUROCIRURGIA / PEDIATRIA Year: 2021 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arnold-Chiari Malformation / Postoperative Complications / Syringomyelia / Neurosurgical Procedures / Dura Mater Type of study: Clinical_trials Limits: Adolescent / Child / Female / Humans / Male Language: En Journal: J Neurosurg Pediatr Journal subject: NEUROCIRURGIA / PEDIATRIA Year: 2021 Document type: Article Affiliation country: