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1.
Int Forum Allergy Rhinol ; 8(10): 1162-1168, 2018 10.
Article in English | MEDLINE | ID: mdl-29856526

ABSTRACT

BACKGROUND: To better understand upper airway tissue regeneration, the exposed cartilage and bone at donor sites of tissue flaps may serve as in vivo "Petri dishes" for active wound healing. The pedicled nasoseptal flap (NSF) for skull-base reconstruction creates an exposed donor site within the nasal airway. The objective of this study is to evaluate whether grafting the donor site with a sinonasal repair cover graft is effective in promoting wound healing. METHODS: In this multicenter, prospective trial, subjects were randomized to intervention (graft) or control (no graft) intraoperatively after NSF elevation. Individuals were evaluated at 2, 6, and 12 weeks postintervention with endoscopic recordings. Videos were graded (Likert scale) by 3 otolaryngologists blinded to intervention on remucosalization, crusting, and edema. Scores were analyzed for interrater reliability and cohorts compared. Biopsy and immunohistochemistry at the leading edge of wound healing was performed in select cases. RESULTS: Twenty-one patients were randomized to intervention and 26 to control. Subjects receiving the graft had significantly greater overall remucosalization (p = 0.01) than controls over 12 weeks. Although crusting was less in the small intestine submucosa (SIS) group, this was not statistically significant (p = 0.08). There was no overall effect on nasal edema (p = 0.2). Immunohistochemistry demonstrated abundant upper airway basal cell progenitors in 2 intervention samples, suggesting that covering grafts may facilitate tissue proliferation via progenitor cell expansion. CONCLUSION: This prospective, randomized, controlled trial indicates that a porcine SIS graft placed on exposed cartilage and bone within the upper airway confers improved remucosalization compared to current practice standards.


Subject(s)
Intestinal Mucosa/transplantation , Nasal Septum/surgery , Rhinoplasty/methods , Skull Base/surgery , Stem Cells/cytology , Adult , Aged , Aged, 80 and over , Animals , Female , Humans , Male , Middle Aged , Nasal Septum/pathology , Prospective Studies , Skull Base/pathology , Stem Cells/metabolism , Surgical Flaps/pathology , Swine , Treatment Outcome , Wound Healing
2.
Psychiatry Res ; 203(2-3): 111-25, 2012.
Article in English | MEDLINE | ID: mdl-22981426

ABSTRACT

This meta-analysis evaluates alterations of neurometabolites in schizophrenia and bipolar disorder. PubMed was searched to find controlled studies evaluating N-acetylaspartate (NAA), Choline (Cho) and Creatine (Cr) assessed with ((1))H-MRS (proton magnetic resonance spectroscopy) in patients with schizophrenia and bipolar disorder up to September 2010. Random effects meta-analyses were conducted to estimate pooled standardized mean differences. The statistic was used to quantify inconsistencies. Subgroup analyses were conducted to explore potential explanations for inconsistencies. The systematic review included 146 studies with 5643 participants. NAA levels were affected in schizophrenia and bipolar disorder. Decreased levels in the basal ganglia and frontal lobe were the most consistent findings in schizophrenia; decreased levels in the basal ganglia were the most consistent findings in bipolar disorder. Cho and Cr levels were not altered in either disorder. Findings for Cr were most consistent in the thalamus, frontal lobe and dorsolateral prefrontal cortex in schizophrenia and the basal ganglia and frontal lobe in bipolar disorder. Findings for Cho were most consistent in the thalamus, frontal lobe and anterior cingulate cortex in schizophrenia and basal ganglia in bipolar disorder. Large, carefully designed studies are needed to better estimate the extent of alterations in neurometabolites.


Subject(s)
Aspartic Acid/analogs & derivatives , Bipolar Disorder/metabolism , Choline/metabolism , Creatine/metabolism , Magnetic Resonance Spectroscopy , Schizophrenia/metabolism , Schizophrenic Psychology , Aspartic Acid/metabolism , Basal Ganglia/metabolism , Bipolar Disorder/psychology , Gyrus Cinguli/metabolism , Humans , Prefrontal Cortex , Reference Values , Thalamus/metabolism
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