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Association of Perioperative Registered Nurses

NonprofitDenver, Colorado, United States
About: Association of Perioperative Registered Nurses is a nonprofit organization based out in Denver, Colorado, United States. It is known for research contribution in the topics: Guideline & Perioperative. The organization has 19 authors who have published 29 publications receiving 1839 citations.

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Journal ArticleDOI
TL;DR: Joint Practice Guideline for Sterile Technique during Vascular and Interventional Radiology Procedures: From the Society of Interventional radiology, Association of periOperative Registered Nurses, and Association for Radiologic and Imaging Nursing.

38 citations

Journal ArticleDOI
TL;DR: The updated Guideline for the Prevention of SSI from the Centers for Disease Control and Prevention (CDC) and the Healthcare Infection Control Practices Advisory Committee (HICPAC) is introduced.
Abstract: Surgical site infection (SSI) is a common type of health-care-associated infection (HAI) and adds considerably to the individual, social, and economic costs of surgical treatment This document serves to introduce the updated Guideline for the Prevention of SSI from the Centers for Disease Control and Prevention (CDC) and the Healthcare Infection Control Practices Advisory Committee (HICPAC) The Core section of the guideline addresses issues relevant to multiple surgical specialties and procedures The second procedure-specific section focuses on a high-volume, high-burden procedure: Prosthetic joint arthroplasty While many elements of the 1999 guideline remain current, others warrant updating to incorporate new knowledge and changes in the patient population, operative techniques, emerging pathogens, and guideline development methodology

33 citations

Journal ArticleDOI
TL;DR: The toolkit is designed to encourage providers to decrease the morbidity and mortality of CRC and other cancers and is useful to facilitate efforts of office‐based clinicians to reduce disparities by applying screening guidelines on a universal basis to the age‐appropriate population.
Abstract: Purpose: The purpose of this project was to increase colorectal cancer screening (CRC) rates in the state of Nevada Research has shown that there are several interventions for providers to use to increase CRC screening rates in practice The Nevada Colon Cancer Partnership (NCCP) has created a toolkit to assist providers to implement these interventions in practice Data Sources: Research has repeatedly shown that CRC screening has a great impact on the morbidity and mortality of CRC Studies have shown that a fecal occult blood test can detect 60–85% of CRCs and a colonoscopy with polyp removal can reduce mortality by 60–90% Multiple studies have shown that a provider's recommendation is the most consistently influential factor in cancer screening Furthermore, offering patients a choice and encouraging active participation in health care decision making has proven to increase CRC screening rates Conclusions: The NCCP has collaborated with the American Cancer Society to create a web based toolkit for use by providers to change practice and screen all eligible patients for CRC The toolkit is designed to encourage providers to decrease the morbidity and mortality of CRC and other cancers The toolkit is useful to facilitate efforts of office-based clinicians to reduce disparities by applying screening guidelines on a universal basis to the age-appropriate population A team approach to screening is encouraged to promote an opportunistic or global approach to assure all eligible patients are reached Implications for Practice: As healthcare reform continues to evolve, Nurse Practitioners (NPs) will assume much of the primary care needs of our country A preventive care model is an important aspect of the future of healthcare NPs are in a perfect position to change the health of patients in a global way The strategies and tools presented in this toolkit are designed to improve preventive care and assist the NP in assuring that every eligible patient receives the screening tests they need

24 citations

Journal ArticleDOI
01 Apr 2020
TL;DR: This trial master protocol describes 2 multicenter pragmatic cluster randomized crossover trials, Aqueous-PREP and PREPARE, which seek to compare the effectiveness of iodophor and chlorhexidine surgical skin preparation solutions at reducing surgical site infections and unplanned fracture-related reoperations.
Abstract: Importance The risk of developing a surgical site infection after extremity fracture repair is nearly 5 times greater than in most elective orthopedic surgical procedures. For all surgical procedures, it is standard practice to prepare the operative site with an antiseptic solution; however, there is limited evidence to guide the choice of solution used for orthopedic fracture repair. Objective To compare the effectiveness of iodophor vs chlorhexidine solutions to reduce surgical site infections and unplanned fracture-related reoperations for patients who underwent fracture repair. Design, Setting, and Participants The PREP-IT (Program of Randomized Trials to Evaluate Pre-operative Antiseptic Skin Solutions in Orthopaedic Trauma) master protocol will be followed to conduct 2 multicenter pragmatic cluster randomized crossover trials, Aqueous-PREP (Pragmatic Randomized Trial Evaluating Pre-Operative Aqueous Antiseptic Skin Solution in Open Fractures) and PREPARE (Pragmatic Randomized Trial Evaluating Pre-Operative Alcohol Skin Solutions in Fractured Extremities). The Aqueous-PREP trial will compare 4% aqueous chlorhexidine vs 10% povidone-iodine for patients with open extremity fractures. The PREPARE trial will compare 2% chlorhexidine in 70% isopropyl alcohol vs 0.7% iodine povacrylex in 74% isopropyl alcohol for patients with open extremity fractures and patients with closed lower extremity or pelvic fractures. Both trials will share key aspects of study design and trial infrastructure. The studies will follow a pragmatic cluster randomized crossover design with alternating treatment periods of approximately 2 months. The primary outcome will be surgical site infection and the secondary outcome will be unplanned fracture-related reoperations within 12 months. The Aqueous-PREP trial will enroll a minimum of 1540 patients with open extremity fractures from at least 12 hospitals; PREPARE will enroll a minimum of 1540 patients with open extremity fractures and 6280 patients with closed lower extremity and pelvic fractures from at least 18 hospitals. The primary analyses will adhere to the intention-to-treat principle and account for potential between-cluster and between-period variability. The patient-centered design, implementation, and dissemination of results are guided by a multidisciplinary team that includes 3 patients and other relevant stakeholders. Discussion The PREP-IT master protocol increases efficiency through shared trial infrastructure and study design components. Because prophylactic skin antisepsis is used prior to all surgical procedures and the application, cost, and availability of all study solutions are similar, the results of the PREP-IT trials are poised to inform clinical guidelines and bring about an immediate change in clinical practice. Trial Registration ClinicalTrials.gov Identifiers:NCT03385304andNCT03523962

23 citations

Journal ArticleDOI
TL;DR: The possibility of PAA to effectively control tumor progression and serve as an adjunct to standard of care PDA chemotherapy regimens is illustrated in a patient with poorly differentiated stage IV PDA as an exclusive chemotherapeutic regimen.
Abstract: Pancreatic ductal adenocarcinoma (PDA) has a dismal prognosis and is often discovered at an advanced stage with few therapeutic options. Current conventional regimens for PDA are associated with significant morbidity, decreased quality of life, and a considerable financial burden. As a result, some patients turn to integrative medicine therapies as an alternate option after a diagnosis of PDA. Intravenous pharmacologic ascorbic acid (PAA) is one such treatment. The use of PAA has been passionately debated for many years, but more recent rigorous scientific research has shown that there are significant blood concentration differences when ascorbic acid is given parenterally when compared to oral dosing. This pharmacologic difference appears to be critical for its role in oncology. Here, we report the use of PAA in a patient with poorly differentiated stage IV PDA as an exclusive chemotherapeutic regimen. The patient survived nearly 4 years after diagnosis, with PAA as his sole treatment, and he achieved objective regression of his disease. He died from sepsis and organ failure from a bowel perforation event. This case illustrates the possibility of PAA to effectively control tumor progression and serve as an adjunct to standard of care PDA chemotherapy regimens. Our patient's experience with PAA should be taken into consideration, along with previous research in cell, animal, and clinical experiments to design future treatment trials.

19 citations


Authors
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20222
20214
20205
20191
20181
20175