ABSTRACT
Burn and blast injuries are frequently complicated by invasive infections, which lead to poor wound healing, delay in treatment, disability, or death. Traditional approach centers on early debridement, fluid resuscitation, and adjunct intravenous antibiotics. These modalities often prove inadequate in burns, where compromised local vasculature limits the tissue penetration of systemic antibiotics. Here, we demonstrate the treatment of infected burns with topical delivery of ultrahigh concentrations of antibiotics. Standardized burns were inoculated with Staphylococcus aureus or Pseudomonas aeruginosa. After debridement, burns were treated with either gentamicin (2 mg/mL) or minocycline (1 mg/mL) at concentrations greater than 1,000 times the minimum inhibitory concentration. Amount of bacteria was quantified in tissue biopsies and wound fluid following treatment. After six days of gentamicin or minocycline treatment, S. aureus counts decreased from 4.2 to 0.31 and 0.72 log CFU/g in tissue, respectively. Similarly, P. aeruginosa counts decreased from 2.5 to 0.0 and 1.5 log CFU/g in tissue, respectively. Counts of both S. aureus and P. aeruginosa remained at a baseline of 0.0 log CFU/mL in wound fluid for both treatment groups. The findings here demonstrate that super-therapeutic concentrations of antibiotics delivered topically can rapidly reduce bacterial counts in infected full-thickness porcine burns. This treatment approach may aid wound bed preparation and accelerate time to grafting.
Subject(s)
Anti-Bacterial Agents/administration & dosage , Anti-Bacterial Agents/pharmacology , Burns/drug therapy , Burns/microbiology , Pseudomonas Infections/drug therapy , Staphylococcal Infections/drug therapy , Wound Infection/drug therapy , Administration, Topical , Animals , Burns/pathology , Debridement , Disease Models, Animal , Female , Gentamicins/administration & dosage , Gentamicins/pharmacology , Minocycline/administration & dosage , Minocycline/pharmacology , Pseudomonas Infections/microbiology , Pseudomonas Infections/pathology , Pseudomonas aeruginosa/drug effects , Staphylococcal Infections/microbiology , Staphylococcal Infections/pathology , Staphylococcus aureus/drug effects , Swine , Wound Healing/drug effects , Wound Infection/microbiology , Wound Infection/pathologyABSTRACT
Within-session habituation and extinction learning co-occur as do subsequent consolidation of habituation (i.e., between-session habituation) and extinction memory. We sought to determine whether, as we predicted: (1) between-session habituation is greater across a night of sleep versus a day awake; (2) time-of-day accounts for differences; (3) between-session habituation predicts consolidation of extinction memory; (4) sleep predicts between-session habituation and/or extinction memory. Participants (N = 28) completed 4-5 sessions alternating between mornings and evenings over 3 successive days (2 nights) with session 1 in either the morning (N = 13) or evening (N = 15). Twelve participants underwent laboratory polysomnography. During 4 sessions, participants completed a loud-tone habituation protocol, while skin conductance response (SCR), blink startle electromyography (EMG), heart-rate acceleration and heart-rate deceleration (HRD) were recorded. For sessions 1 and 2, between-session habituation of EMG, SCR and HRD was greater across sleep. SCR and HRD were generally lower in the morning. Between-session habituation of SCR for sessions 1 and 2 was positively related to intervening (first night) slow wave sleep. In the evening before night 2, participants also underwent fear conditioning and extinction learning phases of a second protocol. Extinction recall was tested the following morning. Extinction recall was predicted only by between-session habituation of SCR across the same night (second night) and by intervening REM. We conclude that: (1) sleep augments between-session habituation, as does morning testing; (2) extinction recall is predicted by concurrent between-session habituation; and (3) both phenomena may be influenced by sleep.
Subject(s)
Circadian Rhythm/physiology , Extinction, Psychological/physiology , Habituation, Psychophysiologic/physiology , Memory/physiology , Sleep/physiology , Wakefulness/physiology , Adult , Analysis of Variance , Conditioning, Psychological , Electromyography , Fear/physiology , Galvanic Skin Response , Heart Rate , Humans , Male , Polysomnography , Self Report , Time Factors , Young AdultABSTRACT
Occult submucous cleft palate is a congenital deformity characterized by deficient union of the muscles that normally cross the velum and aid in elevation of the soft palate. Despite this insufficient muscle coverage, occult submucous cleft palate by definition lacks clear external anatomic landmarks. This absence of anatomic signs makes diagnosis of occult submucous cleft less obvious, more dependent on ancillary tests, and potentially missed entirely. Current diagnostic methodologies are limited and often are unrevealing in the presurgical patient; however, a missed diagnosis of occult submucous cleft palate can result in velopharyngeal insufficiency and major functional impairment in patients after surgery on the oropharynx. By accurately and easily diagnosing occult submucous cleft palate, it is possible to defer or modify pharyngeal surgical intervention that may further impair velopharyngeal function in susceptible patients. In this report, we introduce transillumination of the soft palate using a transnasal or transoral flexible endoscope as an inexpensive and simple technique for identification of submucous cleft palate. The use of transillumination of an occult submucous cleft palate is illustrated in a patient case and is compared to other current diagnostic methodologies.
Subject(s)
Cleft Palate/diagnosis , Transillumination/methods , Adult , Cineradiography/methods , Cleft Palate/diagnostic imaging , Female , Humans , Laryngoscopes , Laryngoscopy/methods , Magnetic Resonance Imaging/methods , Oropharynx/surgery , Palatal Muscles/abnormalities , Palatal Muscles/diagnostic imaging , Palate, Soft/abnormalities , Palate, Soft/diagnostic imaging , Peritonsillar Abscess/surgery , Tonsillectomy/adverse effects , Ultrasonography , Velopharyngeal Insufficiency/etiology , Video Recording/methodsABSTRACT
UNLABELLED: Mucocele formation is a very rare complication of rhinoplasty surgery, with only 26 incidences documented in the medical literature. Postrhinoplasty nasal mucoceles are believed to result from the growth of ectopic nasal respiratory epithelium displaced during the rhinoplasty procedure. Although most cases of nasal mucocele present within weeks of rhinoplasty surgery, exceptional accounts describe nasal mucoceles presenting years after rhinoplasty. This case report describes an extremely delayed case of dorsal nasal mucocele that presented 21 years after the patient underwent a septorhinoplasty. The aesthetically bothersome mucocele was successfully removed with an open rhinoplasty approach, and the histopathologic analysis was consistent with a simple benign mucous retention cyst. The history, etiology, and prevention of mucocele formation in rhinoplasty surgery also are discussed. LEVEL OF EVIDENCE V: This journal requires that authors assign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266 .
Subject(s)
Mucocele/etiology , Nose Diseases/etiology , Rhinoplasty/adverse effects , Humans , Male , Middle Aged , Time FactorsSubject(s)
Choledochal Cyst/diagnosis , Choledochal Cyst/therapy , Drainage , Female , Humans , Jejunostomy , Tomography, X-Ray Computed , Treatment Outcome , Young AdultABSTRACT
Significance: Fibroblasts play a critical role in normal wound healing. Various extracellular matrix (ECM) components, including collagens, fibrin, fibronectin, proteoglycans, glycosaminoglycans, and matricellular proteins, can be considered potent protagonists of fibroblast survival, migration, and metabolism. Recent Advances: Advances in tissue culture, tissue engineering, and ex vivo models have made the examination and precise measurements of ECM components in wound healing possible. Likewise, the development of specific transgenic animal models has created the opportunity to characterize the role of various ECM molecules in healing wounds. In addition, the recent characterization of new ECM molecules, including matricellular proteins, dermatopontin, and FACIT collagens (Fibril-Associated Collagens with Interrupted Triple helices), further demonstrates our cursory knowledge of the ECM in coordinated wound healing. Critical Issues: The manipulation and augmentation of ECM components in the healing wound is emerging in patient care, as demonstrated by the use of acellular dermal matrices, tissue scaffolds, and wound dressings or topical products bearing ECM proteins such as collagen, hyaluronan (HA), or elastin. Once thought of as neutral structural proteins, these molecules are now known to directly influence many aspects of cellular wound healing. Future Directions: The role that ECM molecules, such as CCN2, osteopontin, and secreted protein, acidic and rich in cysteine, play in signaling homing of fibroblast progenitor cells to sites of injury invites future research as we continue investigating the heterotopic origin of certain populations of fibroblasts in a healing wound. Likewise, research into differently sized fragments of the same polymeric ECM molecule is warranted as we learn that fragments of molecules such as HA and tenascin-C can have opposing effects on dermal fibroblasts.
ABSTRACT
Poor ability to remember the extinction of conditioned fear, elevated trait anxiety, and delayed or disrupted nocturnal sleep are reported in anxiety disorders. The current study examines the interrelationship of these factors in healthy young-adult males. Skin-conductance response was conditioned to two differently colored lamps. One color but not the other was then extinguished. After varying delays, both colors were presented to determine extinction recall and generalization. Questionnaires measured sleep quality, morningness-eveningness, neuroticism and trait anxiety. A subset produced a mean 7.0 nights of actigraphy and sleep diaries. Median split of mean sleep midpoint defined early- and late-"sleep timers". Extinction was more rapidly learned in the morning than evening only in early timers who also better generalized extinction recall. Extinction recall was greater with higher sleep efficiency. Sleep efficiency and morningness were negatively associated with neuroticism and anxiety. However, neuroticism and anxiety did not predict extinction learning, recall or generalization. Therefore, neuroticism/anxiety and deficient fear extinction, although both associated with poor quality and late timing of sleep, are not directly associated with each other. Elevated trait anxiety, in addition to predisposing directly to anxiety disorders, may thus also indirectly promote such disorders by impairing sleep and, consequently, extinction memory.
Subject(s)
Emotions/physiology , Memory/physiology , Mental Recall/physiology , Sleep/physiology , Adolescent , Adult , Anxiety/physiopathology , Anxiety Disorders/physiopathology , Extinction, Psychological/physiology , Fear/physiology , Galvanic Skin Response , Healthy Volunteers , Humans , Learning/physiology , Male , Neuroticism , Surveys and Questionnaires , Young AdultABSTRACT
BACKGROUND: Injury to the skin can predispose individuals to invasive infection. The standard of care for infected wounds is treatment with intravenous antibiotics. However, antibiotics delivered intravenously may have poor tissue penetration and be dose limited by systemic side effects. Topical delivery of antibiotics reduces systemic complications and delivers increased drug concentrations directly to the wound. METHODS: Porcine full-thickness wounds infected with Staphylococcus aureus were treated with ultrahigh concentrations (over 1000 times the minimum inhibitory concentration) of gentamicin using an incubator-like wound healing platform. The aim of the present study was to evaluate clearance of infection and reduction in inflammation following treatment. Gentamicin cytotoxicity was evaluated by in vitro assays. RESULTS: Application of 2000 µg/ml gentamicin decreased bacterial counts in wound tissue from 7.2 ± 0.3 log colony-forming units/g to 2.6 ± 0.6 log colony-forming units/g in 6 hours, with no reduction observed in saline controls (p < 0.005). Bacterial counts in wound fluid decreased from 5.7 ± 0.9 log colony-forming units/ml to 0.0 ± 0 log colony-forming units/ml in 1 hour, with no reduction observed in saline controls (p < 0.005). Levels of interleukin-1ß were significantly reduced in gentamicin-treated wounds compared with saline controls (p < 0.005). In vitro, keratinocyte migration and proliferation were reduced at gentamicin concentrations between 100 and 1000 µg/ml. CONCLUSIONS: Topical delivery of ultrahigh concentrations of gentamicin rapidly decontaminates acutely infected wounds and maintains safe systemic levels. Treatment of infected wounds using the proposed methodology protects the wound and establishes a favorable baseline for subsequent treatment.
Subject(s)
Anti-Bacterial Agents/administration & dosage , Gentamicins/administration & dosage , Staphylococcal Infections/drug therapy , Wound Infection/drug therapy , Administration, Topical , Animals , Female , SwineABSTRACT
INTRODUCTION: Electromechanical reshaping (EMR) involves the application of an electrical current to mechanically deformed cartilage to create sustained tissue shape change. Although EMR may evolve to become an inexpensive and reliable way of producing shape change in cartilage during reconstructive surgery, the precise mechanism of EMR is unknown. We aim to examine the isolated effect of protonation (pH) on shape change in cartilage. METHODS: Nasal septal cartilages of rabbits were mechanically deformed and placed in a rigid jig. The deformed cartilages were submerged in isotonic phosphate buffered saline baths (osm = 290 mmol/Kg) with a pH of 3 (N = 51), pH of 7 (N = 51), and a pH of 11 (N = 51) for 15 minutes. Following re-equilibration, specimens were removed from their jig and the angle change from baseline was measured using digital micrometry. RESULTS: Significant shape change was noted in all specimens, with an angle change of 33.6°, 33.3°, and 32.0° experienced by the pH of 3, 7, and 11 groups, respectively. Despite a trend toward increased shape change in the acidic treatment, there was no significant difference between groups. CONCLUSIONS: Although current evidence indicates that dynamic oxidation-reduction reactions within the extracellular matrix of cartilage may be implicated in EMR-induced shape change, when pH was isolated as a single variable it was not sufficient to produce cartilage shape change.
ABSTRACT
Microcapsules containing subfemtoliter volumes of n-hexadecane (HD) within a 4-40 nm thick shell of poly(alkyl methacrylates) were prepared. The size of the HD drop was varied between 50 and 140 nm. The alkyl substituents on the methacrylate monomer were varied to alter the surface tension between the HD and the polymer shell in order to investigate the effects of surface tension on the freezing point of the HD. The size dependence of the supercooling as predicted by the G-T equation was not observed in our systems. An effect on the magnitude of supercooling with variation in the side chains was observed, where freezing the HD in capsules with bulkier side chains requires a greater magnitude of supercooling. This is in agreement with the increased hydrophobic character of the polymers and also correlates with the decrease in glass transition temperature of the polymer. We also observed aging of the capsules, which could be accelerated by heating.