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1.
J Avian Med Surg ; 34(3): 268-273, 2020 Oct 20.
Article in English | MEDLINE | ID: mdl-33099980

ABSTRACT

Pressure-sensitive adhesive tapes are commonly used for the positioning of birds for radiography and securing bandages. The effect of 5 common tapes on feather structure was investigated with before-and-after comparisons. Each tape demonstrated a characteristic pattern of damage to the feather vane that involved separation of barbules and/or tearing of barbs. Tapes with rigid backing materials and strong adhesives were more likely to cause tearing and barbule separation, respectively, whereas flexible tapes with limited adhesion to feathers were more successful in securing feathers without causing irreparable damage. Consideration should be given to the appropriate selection of tape applied to the feathers of birds to prevent iatrogenic damage to their plumage.


Subject(s)
Adhesives , Birds/injuries , Feathers/injuries , Specimen Handling/veterinary , Adhesives/classification , Adhesives/standards , Animals
2.
Medicina (Kaunas) ; 55(7)2019 Jul 03.
Article in English | MEDLINE | ID: mdl-31277322

ABSTRACT

Gastric varices are less common than esophageal varices, and their treatment is quite challenging. Gastric varix bleedings (GVB) occur less frequently than esophageal varix (EV) bleedings and represent 10% to 30% of all variceal bleedings. They are; however, more severe and are associated with high mortality. Re-bleeding may occur in 35% to 90% of cases after spontaneous hemostasis. GV bleedings represent a serious clinical problem compared with esophageal varices due to their location. Sclerotherapy and band ligation, in particular, are less effective. Based on the anatomic site and location, treatment differs from EV and is categorized into two groups (i.e., endoscopic or radiologic treatment). Surgical management is used less frequently. Balloon-occluded retrograde transvenous obliteration (BRTO) and cyanoacrylate are safe but there is a high risk of re-bleeding. Portal pressure elevates following BRTO and leads to worsening of esophageal varix pressure. Other significant complications may include hemoglobinuria, abdominal pain, fever, and pleural effusion. Shock and atrial fibrillation are major complications. New and efficient treatment modalities will be possible in the future.


Subject(s)
Esophageal and Gastric Varices/surgery , Treatment Outcome , Adhesives/standards , Adhesives/therapeutic use , Balloon Occlusion/methods , Balloon Occlusion/standards , Esophageal and Gastric Varices/etiology , Humans , Liver Diseases/complications , Liver Diseases/surgery , Portasystemic Shunt, Transjugular Intrahepatic/methods , Portasystemic Shunt, Transjugular Intrahepatic/standards
3.
Philos Trans A Math Phys Eng Sci ; 377(2150): 20190131, 2019 Jul 29.
Article in English | MEDLINE | ID: mdl-31177956

ABSTRACT

Enlarged adhesive toe pads on the tip of each digit allow tree frogs to climb smooth vertical and overhanging surfaces, and are effective in generating reversible adhesion under both dry and wet conditions. In this review, we discuss the complexities of the structure of tree frog toe pads in relation to their function and review their biomimetic potential. Of particular importance are the (largely) hexagonal epithelial cells surrounded by deep channels that cover the surface of each toe pad and the array of nanopillars on their surface. Fluid secreted by the pads covers the surface of each pad, so the pads adhere by wet adhesion, involving both capillarity and viscosity-dependent forces. The fabrication and testing of toe pad mimics are challenging, but valuable both for testing hypotheses concerning tree frog toe pad function and for developing toe pad mimics. Initial mimics involved the fabrication of hexagonal pillars mimicking the toe pad epithelial structure. More recent ones additionally replicate the nanostructures on their surface. Finally we describe some of the biomimetic applications that have been developed from toe pad mimics, which include both bioinspired adhesives and friction-generating devices. This article is part of the theme issue 'Bioinspired materials and surfaces for green science and technology (part 2)'.


Subject(s)
Adhesives , Anura , Biomimetic Materials , Adhesiveness , Adhesives/chemistry , Adhesives/standards , Animals , Biomimetic Materials/chemistry , Surface Properties
4.
Acta Neurochir (Wien) ; 161(5): 865-870, 2019 05.
Article in English | MEDLINE | ID: mdl-30879130

ABSTRACT

OBJECT: In the past, the accuracy of surface matching has been shown to be disappointing. We aimed to determine whether this had improved over the years by assessing application accuracy of current navigation systems, using either surface matching or point-pair matching. METHODS: Eleven patients, scheduled for intracranial surgery, were included in this study after a power analysis had shown this small number to be sufficient. Prior to surgery, one additional fiducial marker was placed on the scalp, the "target marker," where the entry point of surgery was to be expected. Using one of three different navigation systems, two patient-to-image registration procedures were performed: one based on surface matching and one based on point-pair matching. Each registration procedure was followed by the digitization of the target marker's location, allowing calculation of the target registration error. If the system offered surface matching improvement, this was always used; and for the two systems that routinely offer an estimate of neuronavigation accuracy, this was also recorded. RESULTS: The error in localizing the target marker using point-pair matching or surface matching was respectively 2.49 mm and 5.35 mm, on average (p < 0.001). In those four cases where an attempt was made to improve the surface matching, the error increased to 6.35 mm, on average. For the seven cases where the system estimated accuracy, this estimate did not correlate with target registration error (R2 = 0.04, p = 0.67). CONCLUSION: The accuracy of navigation systems has not improved over the last decade, with surface matching consistently yielding errors that are twice as large as when point-pair matching with adhesive markers is used. These errors are not reliably reflected by the systems own prediction, when offered. These results are important to make an informed choice between image-to-patient registration strategies, depending on the type of surgery at hand.


Subject(s)
Adhesives/standards , Fiducial Markers/standards , Neuronavigation/standards , Humans , Neuronavigation/adverse effects , Neuronavigation/methods , Postoperative Complications/epidemiology , Postoperative Complications/prevention & control , Surgery, Computer-Assisted/methods
5.
Cochrane Database Syst Rev ; 10: CD004485, 2016 Oct 25.
Article in English | MEDLINE | ID: mdl-27779317

ABSTRACT

BACKGROUND: Orthodontic treatment involves using fixed or removable appliances (dental braces) to correct the positions of teeth. It has been shown that the quality of treatment result obtained with fixed appliances is much better than with removable appliances. Fixed appliances are, therefore, favoured by most orthodontists for treatment. The success of a fixed orthodontic appliance depends on the metal attachments (brackets and bands) being attached securely to the teeth so that they do not become loose during treatment. Brackets are usually attached to the front and side teeth, whereas bands (metal rings that go round the teeth) are more commonly used on the back teeth (molars). A number of adhesives are available to attach bands to teeth and it is important to understand which group of adhesives bond most reliably, as well as reducing or preventing dental decay during the treatment period. OBJECTIVES: To evaluate the effectiveness of the adhesives used to attach bands to teeth during fixed appliance treatment, in terms of:(1) how often the bands come off during treatment; and(2) whether they protect the banded teeth against decay during fixed appliance treatment. SEARCH METHODS: The following electronic databases were searched: Cochrane Oral Health's Trials Register (searched 2 June 2016), Cochrane Central Register of Controlled Trials (CENTRAL; 2016, Issue 5) in the Cochrane Library (searched 2 June 2016), MEDLINE Ovid (1946 to 2 June 2016) and EMBASE Ovid (1980 to 2 June 2016). We searched ClinicalTrials.gov and the World Health Organization International Clinical Trials Registry Platform for ongoing trials. No restrictions were placed on the language or date of publication when searching the electronic databases. SELECTION CRITERIA: Randomised and controlled clinical trials (RCTs and CCTs) (including split-mouth studies) of adhesives used to attach orthodontic bands to molar teeth were selected. Patients with full arch fixed orthodontic appliance(s) who had bands attached to molars were included. DATA COLLECTION AND ANALYSIS: All review authors were involved in study selection, validity assessment and data extraction without blinding to the authors, adhesives used or results obtained. All disagreements were resolved by discussion. MAIN RESULTS: Five RCTs and three CCTs were identified as meeting the review's inclusion criteria. All the included trials were of split-mouth design. Four trials compared chemically cured zinc phosphate and chemically cured glass ionomer; three trials compared chemically cured glass ionomer cement with light cured compomer; one trial compared chemically cured glass ionomer with a chemically cured glass phosphonate. Data analysis was often inappropriate within the studies meeting the inclusion criteria. AUTHORS' CONCLUSIONS: There is insufficient high quality evidence with regard to the most effective adhesive for attaching orthodontic bands to molar teeth. Further RCTs are required.


Subject(s)
Adhesives/standards , Dental Caries/prevention & control , Dental Cements/standards , Orthodontic Brackets , Orthodontics/standards , Adolescent , Clinical Trials as Topic , Dental Bonding , Female , Glass Ionomer Cements/standards , Humans , Male , Molar , Resin Cements/standards , Young Adult , Zinc Phosphate Cement/standards
6.
J Prosthet Dent ; 113(5): 391-397.e2, 2015 May.
Article in English | MEDLINE | ID: mdl-25749085

ABSTRACT

STATEMENT OF PROBLEM: Denture adhesives have been the objective of scientific research for over half a century. Although they are used by denture wearers worldwide, investigations of their effectiveness and biocompatibility have led to controversial conclusions. PURPOSE: The purpose of this study was to review the literature data with regard to the effectiveness and biocompatibility of denture adhesives as well as the attitudes of both patients and dental professionals toward these materials. MATERIAL AND METHODS: An electronic search of English peer-reviewed dental literature in the Medline database was conducted to evaluate the effectiveness and biocompatibility of denture adhesives. There was no limitation in publication year, so the search included all the available scientific evidence included in that particular database until March 2014. Specific inclusion criteria were used for the selection of the appropriate articles. A manual search of the citations of the obtained articles followed to extend the electronic search. RESULTS: A full text review was carried out for only 32 articles. Of the 32 articles, 21 examined the efficacy of denture adhesives in terms of retention and stability and masticatory performance, 6 evaluated the issue of the biocompatibility of denture adhesives, and 5 presented the attitudes of either professionals or patients toward these materials. CONCLUSIONS: The majority of clinical studies supported the fact that denture adhesives enhance the retention, stability, and masticatory performance of a removable prosthesis. In terms of biocompatibility, long-term in vivo studies to investigate potential harmful effects were lacking. Patients are satisfied with denture adhesives that meet their needs.


Subject(s)
Adhesives , Denture Retention , Adhesives/chemistry , Adhesives/standards , Attitude of Health Personnel , Attitude to Health , Biocompatible Materials/chemistry , Biocompatible Materials/standards , Denture, Complete , Denture, Partial, Removable , Humans , Mastication/physiology
7.
J Huazhong Univ Sci Technolog Med Sci ; 34(1): 108-113, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24496688

ABSTRACT

This study examined the adhesive strength of two self-adhesive methacrylate resin-based sealers (MetaSEAL and RealSeal SE) to root dentin and compared them with RealSeal and AH Plus in properties. A total of 48 extracted human single-rooted teeth were used to prepare the 0.9-mm thick longitudinal tooth slice (each per tooth). Standardized simulated canal spaces of uniform dimensions were prepared in the middle of radicular dentin. After treated with 5.25% sodium hypochlorite (NaOCl) and 17% EDTA, tooth slices were allocated randomly to four groups (n=12) in terms of different sealers used: MetaSEAL, RealSeal SE, RealSeal, and AH plus groups. The simulated canal spaces were obturated with different sealers in each group. There were 10 slabs with 20 simulated canal spaces (n=20) used in each group for push-out testing. The failure modes and the ultrastructures of fractured sealer-dentin interfaces were examined. The remaining 2 slabs in each group underwent partial demineralization for observation of the ultrastructure of resin tags. The results showed that the push-out bond strength was 12.01±4.66 MPa in MetaSEAL group, significantly higher than that in the other three groups (P<0.05). Moreover, no statistically significant differences were noted in the push-out bond strength between RealSeal SE (5.43±3.68 MPa) and AH Plus (7.34±2.83 MPa) groups and between RealSeal SE and RealSeal (2.93±1.76 MPa) groups (P>0.05). Mixed failures were predominant in the fractured sealer-dentin interfaces in MetaSEAL and AH Plus groups, while adhesive failures were frequently seen in RealSeal SE and RealSeal groups. In conclusion, after complete removal of the smear layer, MetaSEAL showed superior bond ability to root dentin. The RealSeal SE is applicable in clinical practice, with its adhesive strength similar to that of AH Plus. The self-adhesive methacrylate resin-based sealer holds promise for use in endodontic treatment.


Subject(s)
Adhesives/standards , Composite Resins/standards , Dentin-Bonding Agents/standards , Dentin , Methacrylates/standards , Tooth Root , Compressive Strength , Dental Bonding , Dental Pulp Cavity/ultrastructure , Dental Stress Analysis/methods , Epoxy Resins/standards , Humans , Materials Testing/methods , Microscopy, Electron, Scanning , Root Canal Filling Materials/standards , Root Canal Preparation
8.
J Nat Med ; 68(1): 181-5, 2014 Jan.
Article in English | MEDLINE | ID: mdl-23807625

ABSTRACT

Asini Corii Collas (ACC; donkey glue) is a crude drug used to promote hematopoiesis and arrest bleeding. Because adulteration of the drug with substances from other animals such as horses, cattle, and pigs has been found, we examined PCR methods based on the sequence of the cytochrome b gene for source species identification. Two strategies for extracting DNA from ACC were compared, and the ion-exchange resin procedure was revealed to be more suitable than the silica-based one. Using DNA extracted from ACC by the ion-exchange resin procedure, PCR methods for species-specific detection of donkey, horse, cattle, and pig substances were established. When these species-specific PCR methods were applied to ACC, amplicons were obtained only by the donkey-specific PCR. Cattle-specific PCR detected as little as 0.1% admixture of cattle glue in the ACC. These results suggest that the species-specific PCR methods established in this study would be useful for simple and easy detection of adulteration of ACC.


Subject(s)
Adhesives , Cytochromes b/genetics , DNA/analysis , Equidae/genetics , Species Specificity , Tissue Extracts/genetics , Adhesives/standards , Animals , Cattle , Chromatography, Ion Exchange , DNA Barcoding, Taxonomic , Drug Contamination , Equidae/metabolism , Horses , Polymerase Chain Reaction/methods , Quality Control , Swine , Tissue Extracts/metabolism , Tissue Extracts/standards
10.
Minim Invasive Neurosurg ; 51(1): 1-5, 2008 Feb.
Article in English | MEDLINE | ID: mdl-18306123

ABSTRACT

Carotid-cavernous fistulas (CCFs) are an uncommon pathology in current neurosurgical practice. Furthermore, they generally present a challenge to the neurosurgeon because of both their deep location and the major neurovascular structures that surround them. CCFs consist of a vascular anomaly in which blood flows from meningeal branches of the internal and external carotid arteries, or directly from the internal carotid artery, into the venous circulation around and in the cavernous sinus. Twelve patients with direct and indirect/dural CCFs who underwent examination and treatment between July 2003 and February 2006 are reported here. All patients of this retrospective evaluation were symptomatic at the time of diagnosis, which was confirmed by cerebral angiography. The patients were treated by endovascular approaches and the CCFs were occluded. From our evaluation, we concluded that the endovascular procedure is safe, effective and minimally invasive in patients with CCF.


Subject(s)
Carotid Artery, Internal/surgery , Carotid-Cavernous Sinus Fistula/surgery , Cavernous Sinus/surgery , Embolization, Therapeutic/methods , Vascular Surgical Procedures/methods , Adhesives/standards , Adhesives/therapeutic use , Adolescent , Adult , Aged , Carotid Artery, Internal/diagnostic imaging , Carotid Artery, Internal/pathology , Carotid-Cavernous Sinus Fistula/diagnostic imaging , Carotid-Cavernous Sinus Fistula/pathology , Catheterization/adverse effects , Catheterization/methods , Catheterization/standards , Cavernous Sinus/diagnostic imaging , Cavernous Sinus/pathology , Cerebral Angiography , Diagnostic Imaging , Embolization, Therapeutic/adverse effects , Embolization, Therapeutic/standards , Female , Humans , Male , Middle Aged , Patient Selection , Postoperative Complications , Prostheses and Implants/standards , Retrospective Studies , Treatment Outcome , Vascular Surgical Procedures/adverse effects , Vascular Surgical Procedures/standards
11.
J Wound Care ; Suppl: 3-31, 2008 Nov.
Article in English | MEDLINE | ID: mdl-19252457

ABSTRACT

Common causes of trauma and wound pain include: the removal of dressings that become stuck to the wound bed; skin stripping of peri-wound skin, as a result of the repeated application and removal of adhesive dressings; and tissue excoriation and maceration of the peri-wound skin, due to inadequate management of wound exudate. This supplement outlines how dressings with Safetac adhesive technology can help clinicians to avoid these problems. A review of the clinical and scientific evidence relating to dressings with Safetac clearly demonstrates that they can be used to prevent trauma and minimise pain on a wide range of wound types and skin injuries.


Subject(s)
Adhesives/adverse effects , Adhesives/standards , Bandages , Skin Care/instrumentation , Wounds and Injuries/therapy , Acute Disease , Adhesives/supply & distribution , Bandages/standards , Bandages/supply & distribution , Benchmarking , Chronic Disease , Evidence-Based Practice/organization & administration , Humans , Materials Testing , Pain/etiology , Pain/prevention & control , Randomized Controlled Trials as Topic , Research Design , Skin/injuries , Skin Care/adverse effects , Treatment Outcome , Wound Healing , Wounds and Injuries/etiology
12.
Cochrane Database Syst Rev ; (2): CD004485, 2007 Apr 18.
Article in English | MEDLINE | ID: mdl-17443548

ABSTRACT

BACKGROUND: Orthodontic treatment involves using fixed or removable appliances (dental braces) to correct the positions of teeth. It has been shown that the quality of treatment result obtained with fixed appliances is much better than with removable appliances. Fixed appliances are, therefore, favoured by most orthodontists for treatment. The success of a fixed orthodontic appliance depends on the metal attachments (brackets and bands) being attached securely to the teeth so that they do not become loose during treatment. Brackets are usually attached to the front and side teeth, whereas bands (metal rings that go round the teeth) are more commonly used on the back teeth (molars). A number of adhesives are available to attach bands to teeth and it is important to understand which group of adhesives bond most reliably, as well as reducing or preventing dental decay during the treatment period. OBJECTIVES: To evaluate the effectiveness of the adhesives used to attach bands to teeth during fixed appliance treatment, in terms of:(1) how often the bands come off during treatment; and(2) whether they protect the banded teeth against decay during fixed appliance treatment. SEARCH STRATEGY: Electronic databases were searched: the Cochrane Oral Health Group's Trials Register (29th January 2007), the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library 2007, Issue 1), MEDLINE (1966 to 29th January 2007) and EMBASE (1980 to 29th January 2007). A search of the internet was also undertaken. There was no restriction with regard to publication status or language of publication. SELECTION CRITERIA: Randomised and controlled clinical trials (RCTs and CCTs) (including split-mouth studies) of adhesives used to attach orthodontic bands to molar teeth were selected. Patients with full arch fixed orthodontic appliance(s) who had bands attached to molars were included. DATA COLLECTION AND ANALYSIS: All review authors were involved in study selection, validity assessment and data extraction without blinding to the authors, adhesives used or results obtained. All disagreements were resolved by discussion. MAIN RESULTS: Five RCTs and three CCTs were identified as meeting the review's inclusion criteria. All the included trials were of split-mouth design. Four trials compared chemically cured zinc phosphate and chemically cured glass ionomer; three trials compared chemically cured glass ionomer cement with light cured compomer; one trial compared chemically cured glass ionomer with a chemically cured glass phosphonate. Data analysis was often inappropriate within the studies meeting the inclusion criteria. AUTHORS' CONCLUSIONS: There is insufficient high quality evidence with regard to the most effective adhesive for attaching orthodontic bands to molar teeth. Further RCTs are required.


Subject(s)
Adhesives/standards , Dental Caries/prevention & control , Dental Cements/standards , Orthodontic Brackets , Orthodontics/standards , Clinical Trials as Topic , Dental Bonding , Glass Ionomer Cements/standards , Humans , Molar , Resin Cements/standards , Zinc Phosphate Cement/standards
13.
J Wound Ostomy Continence Nurs ; 33(5): 510-6; discussion 516-7, 2006.
Article in English | MEDLINE | ID: mdl-17133139

ABSTRACT

OBJECTIVE: We sought to develop a more effective method to evaluate the adhesive properties of skin barriers. DESIGN: The experimental design used was based on 3 principles: partial control, randomization, and repetition. Using these principles, the 180-degree peeling tests were conducted as specified in a standardized methodology (JIS Z0297) to the extent possible. However, the use of a stainless steel plate as a proxy for skin barrier application may result in the stretching and breaking of the skin barrier, making it impossible to obtain suitable measurements. INSTRUMENTS: Tests were conducted in constant temperature/ humidity chambers using a Tensilon Automatic Elongation Tester, where a sample was fixed on the side of a sample immobilization device, a sturdy metal (aluminum) box from which the air in the box was drawn off with a vacuum pump. METHODS: A fluorocarbon polymer film was applied to the adhesive surface of a sample skin barrier. The film was peeled off in the volte-face (180-degree) direction in order to measure adhesive strengths. RESULTS: The films exhibit such properties as (a) ease of removal from the adhesive surface, (b) no resistance to a 180-degree fold back due to the thinness and flexibility of the material, and (c) tolerance of elongation. The adhesive properties of skin barriers were measured by peeling the fluorocarbon polymers in a 180-degree direction. Twelve specimen skin barrier products were selected for measurement, providing results with satisfactory reproducibility. Results based on the conventional stainless steel plate-based testing method acted as a control. CONCLUSION: The newly developed testing method enables chronological measurement results for skin barriers applied to fluorocarbon polymer films after 24 hours, 48 hours, and longer period.


Subject(s)
Adhesives , Bandages , Fluorocarbon Polymers , Materials Testing/methods , Materials Testing/standards , Adhesiveness , Adhesives/standards , Elasticity , Fluorocarbon Polymers/standards , Humans , Humidity , Research Design , Temperature , Tensile Strength , Time Factors
14.
J Infus Nurs ; 29(4): 225-31, 2006.
Article in English | MEDLINE | ID: mdl-16858255

ABSTRACT

Inadequate catheter securement is an underrecognized patient safety issue that contributes significantly to catheter-related complications, including dislodgment, occlusion, infiltration, and infection. Pooled data from prospective product trials at 83 hospitals compared tape to a standard peripheral intravenous (PIV) securement method with a PIV-specific catheter-stabilizing device (StatLock). A 67% reduction (P<.001) in total patient complications was observed in the stabilizing device group, as compared with the tape group. Also, the need for unscheduled PIV restarts was reduced by 76% with the stabilizing device (P<.001). An annual cost savings of $18,000 per hospital on PIV materials and a combined savings of $277,000 on materials, complication costs, and nursing time were estimated on the basis of these reduced complications. Newer catheter-stabilizing technologies can help to reduce patient complications, for an overall cost savings, and consequently reduce needlestick exposures for healthcare providers by reducing restarts and prolonging dwell times.


Subject(s)
Adhesives/standards , Catheterization, Central Venous/instrumentation , Catheterization, Peripheral/instrumentation , Catheters, Indwelling , Accidents, Occupational/prevention & control , Adhesives/economics , Bandages , Benchmarking/organization & administration , Catheterization, Central Venous/adverse effects , Catheterization, Central Venous/economics , Catheterization, Central Venous/nursing , Catheterization, Peripheral/adverse effects , Catheterization, Peripheral/economics , Catheterization, Peripheral/nursing , Catheters, Indwelling/adverse effects , Clinical Nursing Research , Cost Savings , Equipment Design , Equipment Failure , Humans , Materials Testing , Needlestick Injuries/etiology , Needlestick Injuries/prevention & control , Phlebitis/epidemiology , Phlebitis/etiology , Prospective Studies , Safety Management , Time and Motion Studies , Workload
15.
Cochrane Database Syst Rev ; (3): CD004485, 2006 Jul 19.
Article in English | MEDLINE | ID: mdl-16856049

ABSTRACT

BACKGROUND: Orthodontic treatment involves using fixed or removable appliances (dental braces) to correct the positions of teeth. It has been shown that the quality of treatment result obtained with fixed appliances is much better than with removable appliances. Fixed appliances are, therefore, favoured by most orthodontists for treatment. The success of a fixed orthodontic appliance depends on the metal attachments (brackets and bands) being attached securely to the teeth so that they do not become loose during treatment. Brackets are usually attached to the front and side teeth, whereas bands (metal rings that go round the teeth) are more commonly used on the back teeth (molars). A number of adhesives are available to attach bands to teeth and it is important to understand which group of adhesives bond most reliably, as well as reducing or preventing dental decay during the treatment period. OBJECTIVES: To evaluate the effectiveness of the adhesives used to attach bands to teeth during fixed appliance treatment, in terms of:(1) how often the bands come off during treatment; and(2) whether they protect the banded teeth against decay during fixed appliance treatment. SEARCH STRATEGY: Electronic databases were searched: the Cochrane Oral Health Group's Trials Register (July 2005), the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library Issue 2, 2005), MEDLINE (1966 to July 2005) and EMBASE (1980 to July 2005). A search of the internet was also undertaken. There was no restriction with regard to publication status or language of publication. SELECTION CRITERIA: Randomised and controlled clinical trials (RCTs and CCTs) (including split-mouth studies) of adhesives used to attach orthodontic bands to molar teeth were selected. Patients with full arch fixed orthodontic appliance(s) who had bands attached to molars were included. DATA COLLECTION AND ANALYSIS: All review authors were involved in study selection, validity assessment and data extraction without blinding to the authors, adhesives used or results obtained. All disagreements were resolved by discussion. MAIN RESULTS: Five RCTs and three CCTs were identified as meeting the review's inclusion criteria. All the included trials were of split-mouth design. Four trials compared chemically cured zinc phosphate and chemically cured glass ionomer; three trials compared chemically cured glass ionomer cement with light cured compomer; one trial compared chemically cured glass ionomer with a chemically cured glass phosphonate. Data analysis was often inappropriate within the studies meeting the inclusion criteria. AUTHORS' CONCLUSIONS: There is insufficient high quality evidence with regard to the most effective adhesive for attaching orthodontic bands to molar teeth. Further RCTs are required.


Subject(s)
Adhesives/standards , Dental Caries/prevention & control , Dental Cements/standards , Orthodontic Brackets , Orthodontics/standards , Dental Bonding , Glass Ionomer Cements/standards , Humans , Molar , Resin Cements/standards , Zinc Phosphate Cement/standards
16.
J Infus Nurs ; 29(1): 14-7, 2006.
Article in English | MEDLINE | ID: mdl-16428996

ABSTRACT

A prospective, sequential clinical trial was undertaken to determine whether any of 3 methods of peripheral IV catheter (PIV) securement could extend the average survival time of such catheters sufficiently to allow the implementation of a 96-hour PIV change-protocol. Nonsterile tape, StatLock, and Hub-Guard were evaluated. The use of nonsterile tape securement resulted in an 8% PIV survival rate, HubGuard produced a 9% PIV survival rate, and Statlock produced a 52% PIV survival rate (P<.001). Although this study was not a randomized, controlled trial, it strongly suggests that a mechanical catheter securement device, as opposed to tape or die-cut tape, can render practicable the implementation of the 96-hour PIV change protocol that was sanctioned by the Centers for Disease Control and Prevention.


Subject(s)
Adhesives/standards , Catheterization, Peripheral/methods , Catheters, Indwelling , Adult , Catheterization, Peripheral/adverse effects , Catheterization, Peripheral/instrumentation , Catheterization, Peripheral/nursing , Catheters, Indwelling/adverse effects , Clinical Nursing Research , Clinical Protocols/standards , Equipment Design , Equipment Failure , Humans , Infection Control/methods , Infection Control/standards , Occlusive Dressings , Practice Guidelines as Topic , Prospective Studies , Skin Care/methods , Skin Care/nursing , Survival Rate , Time Factors
17.
J Infus Nurs ; 29(1): 34-8, 2006.
Article in English | MEDLINE | ID: mdl-16428999

ABSTRACT

This review focuses on available prospective data comparing standard methods of catheter securement with a securement device. The data demonstrate that the device, specifically engineered for catheter securement, significantly reduces overall catheter-associated complications. This appears to be the result of improved securement and reduced catheter motion. These studies make the authors question their current practice of securing catheters with tape and suture when better alternatives are available.


Subject(s)
Adhesives/standards , Catheterization, Central Venous/methods , Catheterization, Peripheral/methods , Catheters, Indwelling , Sutures/standards , Adhesives/adverse effects , Adult , Bandages , Catheterization, Central Venous/adverse effects , Catheterization, Central Venous/instrumentation , Catheterization, Central Venous/nursing , Catheterization, Peripheral/adverse effects , Catheterization, Peripheral/instrumentation , Catheterization, Peripheral/nursing , Catheters, Indwelling/adverse effects , Child , Clinical Nursing Research , Equipment Design , Equipment Failure , Humans , Nursing Evaluation Research , Outcome Assessment, Health Care , Prospective Studies , Randomized Controlled Trials as Topic , Research Design , Sutures/adverse effects , Time Factors
18.
J Biomed Mater Res B Appl Biomater ; 72(2): 339-44, 2005 Feb 15.
Article in English | MEDLINE | ID: mdl-15490482

ABSTRACT

The aim of this study was to determine the effect of 10% NaOCl gel and 10% NaOCl solution on dentin bond strengths of four adhesive systems. One hundred eighty bovine incisors were ground to achieve a flat polished surface, then divided into 12 groups: Gluma One Bond [G1-control; G2-NaOCl solution; G3-NaOCl gel]; Prime & Bond 2.1 [G4-control; G5-NaOCl solution; G6-NaOCl gel]; Single Bond [G7-control; G8-NaOCl solution; G9-NaOCl gel]; Prime & Bond NT [G10-control; G11-NaOCl solution; G12-NaOCl gel]. Dentin was etched, rinsed, and blot dried. For the experimental groups, after acid etching, 10% NaOCl solution or 10% NaOCl gel was applied for 60 s, rinsed, and blot dried. Composite resin was inserted and light cured. Shear bond strengths were tested with a crosshead speed of 0.5 mm/min. The mean values MPa (SD) were analyzed with two-way ANOVA and Tukey's tests (alpha < 0.01). Ten percent NaOCl solution significantly increased Gluma One Bond strength. No effect was observed for the other adhesives. The 10% NaOCl gel did not affect bond strengths. Ten percent NaOCl gel was less effective on collagen removal as compared to 10% NaOCl solution. The influence of collagen removal on bond strength is dependent on adhesive system, where both the solvent and the monomer can influence the results.


Subject(s)
Dentin-Bonding Agents/chemistry , Dentin-Bonding Agents/standards , Sodium Hypochlorite/chemistry , Adhesives/standards , Animals , Cattle , Collagen , Gels , Incisor , Materials Testing , Mechanics , Resin Cements/standards , Solutions
19.
J Wound Care ; 12(7): 260-2, 2003 Jul.
Article in English | MEDLINE | ID: mdl-12894697

ABSTRACT

OBJECTIVE: The study compared the level of discomfort experienced by healthy volunteers on the removal of a range of adhesive wounds. METHOD: This was an open, within subject comparative study of six adhesive dressings in 24 volunteers. The test site was the lower back. Allocation of test materials to the test sites was randomised. The peel force of removal was recorded after 24 hours of application using a device that removed the dressing at a constant speed and angle to the skin surface. The discomfort experienced at each removal was assessed by the subjects themselves using an electronic visual analogue scale. RESULTS: Overall, Mepilex Border was given a significantly lower discomfort score (p < or = 0.01) by the subjects than the other dressings. There were no clear differences between the five other products tested. Tielle and Allevyn Adhesive had significantly higher (p < or = 0.05) peel force than the other products. Mepilex Border caused less discomfort on removal than Duoderm Extra Thin, Biatain and Versiva, even though the peel force was similar. Tielle and Allevyn had higher peel force, but the levels of discomfort were not significantly higher for these products. CONCLUSION: It may be that the level of discomfort experienced by subjects on removal of an adhesive dressing is not entirely dependent on the peel force and that other aspects of the interaction of the skin surface and adhesive play a role.


Subject(s)
Adhesives/adverse effects , Bandages/adverse effects , Wounds and Injuries/therapy , Adhesives/standards , Adolescent , Adult , Bandages/standards , Female , Humans , Male , Middle Aged , Pain/etiology , Wounds and Injuries/nursing
20.
Zhonghua Kou Qiang Yi Xue Za Zhi ; 37(5): 346-8, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12425845

ABSTRACT

OBJECTIVE: To inspect the directionality of adhesive strength between composite resins and dental hard tissues. METHODS: Two kinds of composite resins were bonded with their luting kits to the enamel and dentin surfaces of bovine teeth separately. The dead load shear and impact shear testing were performed from both of root apex direction and cutting edge direction. RESULTS: The shear adhesive strength between the enamel and two kinds of composite resins was on the same behavior, that the shear adhesive strength of root apex direction was greater than that of cutting edge direction. In the dead load shear testing, the former was about two to three times of the latter (P < 0.05). In the impact shear testing, the former was about three to four times of the latter (P < 0.001). The effect of the direction of acting force was small on the shear adhesive strength between the dentin and two kinds of composite resins. In the both dead load shear testing and impact shear testing, there was no statistically significant difference between the datum of two directional loadings (P > 0.05, P > 0.5). CONCLUSION: The shear adhesive strength between the composite resins and enamel of bovine teeth is related to the acting direction of the shear force.


Subject(s)
Composite Resins/standards , Dental Enamel , Dentin , Resin Cements/standards , Adhesiveness , Adhesives/standards , Animals , Cattle , Dental Bonding , Dentin-Bonding Agents/standards , Materials Testing/methods , Shear Strength
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