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Occlusive Dressing

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41. Semi-occlusive dressing for the treatment of fingertip amputations with exposed bone: quantity and quality of soft-tissue regeneration. (PubMed)

Semi-occlusive dressing for the treatment of fingertip amputations with exposed bone: quantity and quality of soft-tissue regeneration. Nineteen fingertip amputations with exposed bone were treated with a semi-occlusive dressing. The quantity and quality of the regenerated soft tissue was examined. In all 19 fingers there was sufficient uncomplicated healing such that secondary surgical procedures were not needed. At follow-up 6-18 months after the injury, soft tissue thickness around the bone

2013 Journal of Hand Surgery - European

42. Oxyzyme and Iodozyme 2-layer hydrogel wound dressings with iodine for treating chronic wounds

(Kerr 2007a) it was noted at the 3-week assessment that the dressing had been incorrectly applied, with the primary dressing applied on top of the secondary dressing. In another case report (Kerr 2007b) it was noted that an occlusive secondary dressing had been used instead of an air-permeable dressing as specified in the manufacturer's instructions for use. Randomised controlled trial Randomised controlled trial Moffatt et al. 2014: Oxyzyme and Iodozyme Moffatt et al. 2014: Oxyzyme and Iodozyme (...) Oxyzyme and Iodozyme 2-layer hydrogel wound dressings with iodine for treating chronic wounds Oxyzyme and Iodozyme 2-la Oxyzyme and Iodozyme 2-lay yer h er hy ydrogel wound drogel wound dressings with iodine for treating chronic wounds dressings with iodine for treating chronic wounds Medtech innovation briefing Published: 19 November 2014 nice.org.uk/guidance/mib11 pathways Summary Summary Oxyzyme and Iodozyme are chronic wound dressings that release iodine and oxygen onto the wound surface

2014 National Institute for Health and Clinical Excellence - Advice

43. Occlusive drainage system for split-thickness skin graft: A prospective randomized controlled trial. (PubMed)

: alberto.mangano@gmail.com. Marciano Laura L University Center of Statistics for the Biomedical Sciences, Vita-Salute San Raffaele University, Milan, Italy. eng Letter Comment 2017 10 09 Netherlands Burns 8913178 0305-4179 IM Burns. 2017 Mar;43(2):379-387 28341261 Burns surgery Drainage Humans Occlusive Dressings Prospective Studies Skin Transplantation 2017 05 09 2017 05 10 2017 10 17 6 0 2018 11 27 6 0 2017 10 17 6 0 ppublish 29032967 S0305-4179(17)30478-3 10.1016/j.burns.2017.05.028 (...) Occlusive drainage system for split-thickness skin graft: A prospective randomized controlled trial. 29032967 2018 11 26 2018 11 26 1879-1409 43 8 2017 12 Burns : journal of the International Society for Burn Injuries Burns Occlusive drainage system for split-thickness skin graft: A prospective randomized controlled trial. 1817 S0305-4179(17)30478-3 10.1016/j.burns.2017.05.028 Mangano Alberto A Board Certified in General Surgery, Private Practice, Lake Como, Italy. Electronic address

2018 Burns : journal of the International Society for Burn Injuries

44. Low dose ketamine versus morphine for acute severe vaso occlusive pain in children: a randomized controlled trial. (PubMed)

Low dose ketamine versus morphine for acute severe vaso occlusive pain in children: a randomized controlled trial. Acute pain episodes associated with sickle cell disease (SCD) are very difficult to manage effectively. Opioid tolerance and side effects have been major roadblocks in our ability to provide these patients with adequate pain relief. Ketamine is cheap, widely safe, readily available drug, with analgesic effects at sub-anesthetic doses and has been used in wide range of surgeries (...) , pediatric burns dressing change and cancer related pain however, literature concerning its use in sickle cell crises is still limited in our setting. This study aimed to establish if 1 mg/kg of intravenous ketamine is non inferior to intravenous morphine 0.1 mg/kg in severe SCD-associated pain.We performed an institutional review board-approved randomized, prospective, double-blinded, active-control, non-inferiority trial at the national referral sickle cell center. Children between 7 and 18 years

2018 Scandinavian journal of pain

45. Delayed Surgical Debridement and Use of Semiocclusive Dressings for Salvage of Fingers After Purpura Fulminans (PubMed)

and successfully treated with semi-occlusive dressing without complications. Conclusion: Early recognition of infectious PF and timely supportive management are important pillars of its treatment. Delayed surgical debridement allows for less aggressive resection and good functional outcome. (...) Delayed Surgical Debridement and Use of Semiocclusive Dressings for Salvage of Fingers After Purpura Fulminans Background: Purpura fulminans is a condition characterized by rapidly evolving skin necrosis and disseminated intravascular coagulation. Early recognition and aggressive supportive management has led to a decrease in its mortality rate, but most of these patients must undergo extensive soft tissue debridement and partial or total limb amputation. There is controversial evidence about

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2016 Hand (New York, N.Y.)

46. Maggot Debridement Therapy Versus Conventional Dressing Therapy to Treat Diabetic Foot Ulcers

heal completely, when wounds assessed. Other Names: MDT Maggot Therapy Larvae Therapy Active Comparator: Conventional Dressing Therapy(CDT) Participant will be disinfected by iodophor and dressed by gauze 3 days until the wound heal completely, when wounds assessed. Procedure: Conventional Dressing Therapy Participant will be disinfected by iodophor and dressed by gauze 3 days until the wound heal completely, when wounds assessed. Other Names: CDT Occlusive Dressings Dressing Therapy Outcome (...) Verified: June 2016 Individual Participant Data (IPD) Sharing Statement: Plan to Share IPD: Undecided Keywords provided by The First Affiliated Hospital of Dalian Medical University: Diabetic Foot Wound Healing Larva Occlusive Dressings Additional relevant MeSH terms: Layout table for MeSH terms Ulcer Diabetic Foot Foot Ulcer Pathologic Processes Diabetic Angiopathies Vascular Diseases Cardiovascular Diseases Leg Ulcer Skin Ulcer Skin Diseases Diabetes Complications Diabetes Mellitus Endocrine System

2016 Clinical Trials

47. VAC Dressings for Colorectal Resections

by coverage of the incision, Mepitel, and foam with an occlusive Tegederm ™ dressing to establish an airtight seal. Negative pressure will then be applied using a SensaT.R.A.C. Pad ™ to a setting of 100 mmHg continuous suction. Dressings shall remain in place and will be removed by the surgical team on the morning of the third post-operative day and left open to air thereafter. Any loss of seal of the dressing shall be reinforced using occlusive dressings. Device: Incisional Negative Pressure Wound (...) VAC Dressings for Colorectal Resections VAC Dressings for Colorectal Resections - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. VAC Dressings for Colorectal Resections (VACCRR) The safety and scientific

2016 Clinical Trials

48. Assessing Current Peripheral Nerve Block Catheter Fixation and Dressing Strategies: An Equivalence Study

of gum mastic liquid adhesive to nerve catheter dressing Other Name: Mastisol Liquid Adhesive Outcome Measures Go to Primary Outcome Measures : nerve block catheter dislodgement [ Time Frame: duration of catheter use, up to but not longer than, 1 week ] presence or absence of catheter dislodgement (catheter out or no longer in a clinically effective position) Secondary Outcome Measures : nerve block catheter occlusion [ Time Frame: duration of catheter use, up to but not longer than, 1 week (...) ] presence or absence of catheter occlusion nerve block catheter leakage [ Time Frame: duration of catheter use, up to but not longer than, 1 week ] presence or absence of catheter leakage (presence of local anesthetic under occlusive dressing) skin irritation at site of nerve block catheter skin entry [ Time Frame: duration of catheter use, up to but not longer than, 1 week ] presence or absence of skin irritation (presence of hyperemic cutaneous reaction not present at dressing placement) catheter site

2016 Clinical Trials

49. Central venous Access device SeCurement And Dressing Effectiveness (CASCADE) in paediatrics: protocol for pilot randomised controlled trials. (PubMed)

Central venous Access device SeCurement And Dressing Effectiveness (CASCADE) in paediatrics: protocol for pilot randomised controlled trials. Paediatric central venous access devices (CVADs) are associated with a 25% incidence of failure. Securement and dressing are strategies used to reduce failure and complication; however, innovative technologies have not been evaluated for their effectiveness across device types. The primary aim of this research is to evaluate the feasibility of launching (...) a full-scale randomised controlled efficacy trial across three CVAD types regarding CVAD securement and dressing, using predefined feasibility criteria.Three feasibility randomised, controlled trials are to be undertaken at the Royal Children's Hospital and the Lady Cilento Children's Hospital, Brisbane, Australia. CVAD securement and dressing interventions under examination compare current practice with sutureless securement devices, integrated securement dressings and tissue adhesive. In total, 328

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2016 BMJ open

50. WITHDRAWN: Gauze and tape and transparent polyurethane dressings for central venous catheters.

, Central Venous adverse effects Catheters, Indwelling adverse effects Child Humans Occlusive Dressings Polyurethanes therapeutic use Randomized Controlled Trials as Topic 2016 5 5 6 0 2016 5 5 6 0 2016 7 29 6 0 epublish 27144903 10.1002/14651858.CD003827.pub3 (...) WITHDRAWN: Gauze and tape and transparent polyurethane dressings for central venous catheters. 27144903 2016 07 28 2018 12 21 1469-493X 5 2016 May 04 The Cochrane database of systematic reviews Cochrane Database Syst Rev WITHDRAWN: Gauze and tape and transparent polyurethane dressings for central venous catheters. CD003827 10.1002/14651858.CD003827.pub3 Webster Joan J Centre for Clinical Nursing, Royal Brisbane and Women's Hospital, Level 2, Building 34, Butterfield Street, Brisbane, Queensland

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2016 The Cochrane database of systematic reviews

51. Hydrocolloid Dressing

Dressing Aka: Hydrocolloid Dressing , Carrasmart , Combiderm , Comfeel , Cutinova Range , Dermafilm , Duoderm , Exuderm , Hyperion , Nuderm , Primacol , RepliCare , Restore , Tegasorb , Sorbex , Ultec II. Category First-line, cost effective Wafers, pastes and powders composed of gelatin or pectin III. Characteristics Absorptive Occlusive or semipermeable Adhesive Moisture retentive IV. Indications Light to moderately edudative wounds Type 2 to 4 s (some dressings may be used in Type I sores) Dry (...) Hydrocolloid Dressing Hydrocolloid Dressing Toggle navigation Brain Head & Neck Chest Endocrine Abdomen Musculoskeletal Skin Infectious Disease Hematology & Oncology Cohorts Diagnostics Emergency Findings Procedures Prevention & Management Pharmacy Resuscitation Trauma Emergency Procedures Ultrasound Cardiovascular Emergencies Lung Emergencies Infectious Disease Pediatrics Neurologic Emergencies Skin Exposure Miscellaneous Abuse Cancer Administration 4 Hydrocolloid Dressing Hydrocolloid

2018 FP Notebook

52. Alginate Dressing

to 4 s V. Contraindications Avoid in non-exudative, dry wounds Avoid in sinus tracts VI. Technique Rinse wound residue with each bandage change Change dressing daily to every 3 days VII. Advantages Requires less care than other dressings Designed to be occlusive Designed to absorb large exudates (up to 20 times its own weight) Fills dead space Conforms to wound shape VIII. Efficacy Improves healing time Used before See for sample protocol IX. Disadvantages No trial data on effectiveness in s (...) Alginate Dressing Alginate Dressing Toggle navigation Brain Head & Neck Chest Endocrine Abdomen Musculoskeletal Skin Infectious Disease Hematology & Oncology Cohorts Diagnostics Emergency Findings Procedures Prevention & Management Pharmacy Resuscitation Trauma Emergency Procedures Ultrasound Cardiovascular Emergencies Lung Emergencies Infectious Disease Pediatrics Neurologic Emergencies Skin Exposure Miscellaneous Abuse Cancer Administration 4 Alginate Dressing Alginate Dressing Aka: Alginate

2018 FP Notebook

53. A Deadly Digital Dressing: A Case of Surgical Decompression for Finger Ischemia Due to Circumferential Finger Dressing. (PubMed)

a novel technique successfully salvaged the finger. Operative intervention for this complication has previously been unreported.It is important that circumferential digital dressings are applied correctly. Vascular insufficiency from an occlusive dressing is an iatrogenic and avoidable complication. Successful operative decompression may be indicated to minimize tissue loss and improve circulation.Copyright © 2014 Elsevier Inc. All rights reserved. (...) A Deadly Digital Dressing: A Case of Surgical Decompression for Finger Ischemia Due to Circumferential Finger Dressing. Tubular gauze dressings are commonly used, but have potential to cause iatrogenic finger ischemia.To inform health care providers of an avoidable complication and to discuss appropriate methods of prevention and treatment.We discuss a teenage female's finger that narrowly avoided amputation after a tubular gauze dressing caused iatrogenic ischemia. Surgical decompression using

2014 Journal of Emergency Medicine

54. A pilot trial of bordered polyurethane dressings, tissue adhesive and sutureless devices compared with standard polyurethane dressings for securing short-term arterial catheters. (PubMed)

2012.Standard polyurethane (SPU) dressing (controls); bordered polyurethane (BPU) + SPU dressing; tissue adhesive (TA) + SPU dressing; and sutureless securement device (SSD) + SPU dressing (no sutures used).AC failure, ie, complete dislodgement, occlusion (monitor failure, inability to infuse or fluid leaking), pain or infection (local or blood).Median AC dwell time was 26.2 hours and was comparable between groups. AC failure occurred in 26/195 patients (13%). AC failure was significantly worse (...) A pilot trial of bordered polyurethane dressings, tissue adhesive and sutureless devices compared with standard polyurethane dressings for securing short-term arterial catheters. To improve arterial catheter (AC) securement and reduce AC failure; to assess feasibility of a large randomised controlled trial.A four-arm, parallel, randomised, controlled, non-blinded pilot trial with 195 intensive care patients taking part, in a tertiary referral hospital in Brisbane, Australia from May to November

2014 Critical care and resuscitation : journal of the Australasian Academy of Critical Care Medicine

55. A Trial Comparing the Efficacy and Safety of Open Dressing With Petrolatum Jelly vs. Standard Gauze Dressing With Silver Sulfadiazine

insufficient evidence to support or refute such antimicrobial prophylaxis. Another review compared silver sulfadiazine dressings with other occlusive and non-antimicrobial dressings and found insufficient evidence to guide practice. Other research has suggested that dressings with petrolatum gel are as effective as silver sulfadiazine. This trial sought to compare the effectiveness of conventional silver sulfadiazine dressings with treatment with petrolatum gel alone. Condition or disease Intervention (...) A Trial Comparing the Efficacy and Safety of Open Dressing With Petrolatum Jelly vs. Standard Gauze Dressing With Silver Sulfadiazine A Trial Comparing the Efficacy and Safety of Open Dressing With Petrolatum Jelly vs. Standard Gauze Dressing With Silver Sulfadiazine - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You

2014 Clinical Trials

56. Occlusive Dressing

Occlusive Dressing Occlusive Dressing Toggle navigation Brain Head & Neck Chest Endocrine Abdomen Musculoskeletal Skin Infectious Disease Hematology & Oncology Cohorts Diagnostics Emergency Findings Procedures Prevention & Management Pharmacy Resuscitation Trauma Emergency Procedures Ultrasound Cardiovascular Emergencies Lung Emergencies Infectious Disease Pediatrics Neurologic Emergencies Skin Exposure Miscellaneous Abuse Cancer Administration 4 Occlusive Dressing Occlusive Dressing Aka (...) : Occlusive Dressing , Occlusion From Related Chapters II. Indications Increased potency of topical medication May be used in combination with all s III. Contraindications Avoid use on face Avoid use in intertriginous areas (risk of maceration and ) IV. Adverse Effects Skin maceration Rapidly spreading infection V. Mechanism Increases topical medication (e.g. ) penetration into skin Increases potency of topical medication VI. Preparations Simple plastic wrap (from kitchen) Steroid impregnated dressing

2015 FP Notebook

57. Occlusive drainage system for split-thickness skin graft: A prospective randomized controlled trial. (PubMed)

Occlusive drainage system for split-thickness skin graft: A prospective randomized controlled trial. Split-thickness skin grafts are widely used in reconstruction of large area defects. Conventional postoperative recipient site care includes saline-moistened gauze with a protective layer of petroleum gauze and splints for immobilization. This method causes pain while changing the dressing. We designed a better occlusive drainage system for split-thickness skin grafts. We compared the treatment (...) effect and subjective evaluation of our occlusive drainage system with that of the conventional method for coverage of split-thickness skin grafts.A randomized controlled trial was carried out in patients who received split-thickness skin grafts. Patients aged 24-76 years were randomly assigned to the occlusive drainage system or the conventional indirect wet dressing method. The status of graft take, pain, and subjective evaluations were compared.Twenty-eight participants were enrolled, with 14

2017 Burns : journal of the International Society for Burn Injuries

58. Prevention of Radial Artery Occlusion After Transradial Access Using Nitroglycerin

Prevention of Radial Artery Occlusion After Transradial Access Using Nitroglycerin Prevention of Radial Artery Occlusion After Transradial Access Using Nitroglycerin - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before (...) adding more. Prevention of Radial Artery Occlusion After Transradial Access Using Nitroglycerin (Patens) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03158532 Recruitment Status : Recruiting First Posted : May 18, 2017

2017 Clinical Trials

59. Evaluation of Efficacy, Duration of Remission and Safety of a Light and Occlusive Patch Therapy for Plaque Psoriasis

. ClinicalTrials.gov Identifier: NCT03180866 Recruitment Status : Recruiting First Posted : June 8, 2017 Last Update Posted : June 8, 2017 See Sponsor: Illumicure Inc Information provided by (Responsible Party): Illumicure Inc Study Details Study Description Go to Brief Summary: This is a proof of concept, investigator blinded study to evaluate the efficacy and safety of a novel combination of a home narrow band ultraviolet B (NBUVB) lamp with an occlusive dressing in adult subjects with mild to moderate psoriasis (...) vulgaris. Two interpatient arms will be used to compare the efficacy of combination of NBUVB with an occlusive dressing (active) to no treatment (control). 32 patients will be enrolled in this 30 week study. Condition or disease Intervention/treatment Phase Psoriasis Device: Luma Light System Not Applicable Detailed Description: This is a multi-center, investigator blinded, randomized study designed to assess the efficacy, duration of effect, safety and tolerability of Luma Light System for plaque

2017 Clinical Trials

60. Efficacy of a total occlusive ionic silver-containing dressing combination in decreasing risk of surgical site infection: an RCT. (PubMed)

Efficacy of a total occlusive ionic silver-containing dressing combination in decreasing risk of surgical site infection: an RCT. To perform a comparative assessment of the efficacy of total occlusive ionic silver-containing dressing (TOISD) combination vs no dressing after colorectal surgery.The surgical sites from both groups were swabbed and sent for culture and sensitivity upon wound closure (superficial incisional skin surface) in the operating theatre, as a baseline for bacterial (...) colonisation. The patients' surgical wounds in the study group were dressed with TOISD combination and the patient's surgical wounds in the control group received the conventional method of no dressing. A second swab was taken from the superficial incisional skin surface for culture and sensitivity investigation between the fifth to seventh postoperative day for comparison of the bacterial colonisation in the two groups.One-hundred and sixty-six patients were recruited. Six patients dropped out before

2011 Journal of wound care

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