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1.
Learn Health Syst ; 5(3): e10281, 2021 Jul.
Article in English | MEDLINE | ID: mdl-34277946

ABSTRACT

INTRODUCTION: Learning health systems (LHSs) are usually created and maintained by single institutions or healthcare systems. The Indiana Learning Health System Initiative (ILHSI) is a new multi-institutional, collaborative regional LHS initiative led by the Regenstrief Institute (RI) and developed in partnership with five additional organizations: two Indiana-based health systems, two schools at Indiana University, and our state-wide health information exchange. We report our experiences and lessons learned during the initial 2-year phase of developing and implementing the ILHSI. METHODS: The initial goals of the ILHSI were to instantiate the concept, establish partnerships, and perform LHS pilot projects to inform expansion. We established shared governance and technical capabilities, conducted a literature review-based and regional environmental scan, and convened key stakeholders to iteratively identify focus areas, and select and implement six initial joint projects. RESULTS: The ILHSI successfully collaborated with its partner organizations to establish a foundational governance structure, set goals and strategies, and prioritize projects and training activities. We developed and deployed strategies to effectively use health system and regional HIE infrastructure and minimize information silos, a frequent challenge for multi-organizational LHSs. Successful projects were diverse and included deploying a Fast Healthcare Interoperability Standards (FHIR)-based tool across emergency departments state-wide, analyzing free-text elements of cross-hospital surveys, and developing models to provide clinical decision support based on clinical and social determinants of health. We also experienced organizational challenges, including changes in key leadership personnel and varying levels of engagement with health system partners, which impacted initial ILHSI efforts and structures. Reflecting on these early experiences, we identified lessons learned and next steps. CONCLUSIONS: Multi-organizational LHSs can be challenging to develop but present the opportunity to leverage learning across multiple organizations and systems to benefit the general population. Attention to governance decisions, shared goal setting and monitoring, and careful selection of projects are important for early success.

2.
J Craniofac Surg ; 30(4): 1228-1230, 2019 Jun.
Article in English | MEDLINE | ID: mdl-30817510

ABSTRACT

BACKGROUND: To propose a reconstructive protocol based on surgical management experience of polymorphous low-grade adenocarcinoma (PLGA) and the location of the primary lesion. METHODS: Data on the surgical management and the reconstructive technique of 14 histologically conformed patients with PLGA, all treated by the same surgeon, were analyzed and evaluated. RESULTS: Mean follow-up period in our series was 6.2 years. Mean age at diagnosis was 55.5 years and female to male ratio was 2.2:1. The most common presenting sign was a nonpainful lump or mass in an intraoral location. Most patients were managed by wide local excision and reconstruction method varied from primary closure to the use of radial forearm graft. Recurrence appeared in one of the patients in this series, while 2 required further radiation therapy. A protocol for reconstruction of intraoral patients with PLGA is suggested based on our analysis. CONCLUSION: Surgical management is the gold standard for PLGA treatment. Neck dissection is recommended only in patients with presurgery fine-needle aspiration confirmed lymph node involvement. The reconstruction depends mainly on location and size of the primary lesion.


Subject(s)
Adenocarcinoma , Oral Surgical Procedures , Salivary Gland Neoplasms , Adenocarcinoma/mortality , Adenocarcinoma/pathology , Adenocarcinoma/surgery , Aged , Biopsy, Fine-Needle/methods , Female , Humans , Israel , Male , Middle Aged , Neoplasm Grading , Neoplasm Recurrence, Local/pathology , Neoplasm Staging , Oral Surgical Procedures/adverse effects , Oral Surgical Procedures/methods , Oral Surgical Procedures/mortality , Prognosis , Salivary Gland Neoplasms/pathology , Salivary Gland Neoplasms/surgery , Salivary Glands/pathology , Survival Rate , Treatment Outcome
3.
J Emerg Med ; 50(3): 458-61, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26482828

ABSTRACT

BACKGROUND: Point-of-care ultrasound is emerging as an important imaging modality for characterizing soft-tissue infections and provides advantages over physical examination and magnetic resonance imaging (MRI). CASE REPORT: A 30-year-old man presented to the emergency department with extensive left upper extremity cellulitis. Magnetic resonance imaging of the left arm was preliminarily interpreted as soft-tissue swelling without evidence of deep-space infection. Point-of-care ultrasound revealed pockets of fluid with sonographic fluctuance tracking along the tendon sheath that were concerning for deep abscesses. Based on the ultrasound findings, the patient was taken emergently to the operating room, where multiple left hand and wrist loculated deep-space abscesses were decompressed. WHY SHOULD AN EMERGENCY PHYSICIAN BE AWARE OF THIS?: This case report highlights the significant advantages and easy-to-learn findings present in point-of-care ultrasound of musculoskeletal infections.


Subject(s)
Hand/diagnostic imaging , Point-of-Care Systems , Soft Tissue Infections/diagnostic imaging , Ultrasonography/methods , Abscess/diagnostic imaging , Adult , Humans , Male
4.
J Healthc Qual ; 38(3): e10-8, 2016.
Article in English | MEDLINE | ID: mdl-26042762

ABSTRACT

In 2006, the U.S. Centers for Disease Control and Prevention released revised recommendations for routinization of HIV testing in healthcare settings. Health professionals have been challenged to incorporate these guidelines. In March 2013, a routine HIV testing initiative was launched at a large urban academic medical center in a high prevalence region. The goal was to routinize HIV testing by achieving a 75% offer and 75% acceptance rate and promoting linkage to care in the inpatient setting. A systematic six-step organizational change process included stakeholder buy-in, identification of an interdisciplinary leadership team, infrastructure development, staff education, implementation, and continuous quality improvement. Success was measured by monitoring the percentage of offered and accepted HIV tests from March to December 2013. The targeted offer rate was exceeded consistently once nurses became part of the consent process (September 2013). Fifteen persons were newly diagnosed with HIV. Seventy-eight persons were identified as previously diagnosed with HIV, but not engaged in care. Through this process, patients who may have remained undiagnosed or out-of-care were identified and linked to care. The authors propose that this process can be replicated in other settings. Increasing identification and treatment will improve the individual patient's health and reduce community disease burden.


Subject(s)
HIV Infections/diagnosis , Inpatients , Mass Screening/organization & administration , Diagnostic Tests, Routine , Humans , Organizational Innovation , United States
5.
JBJS Case Connect ; 6(1): e12, 2016.
Article in English | MEDLINE | ID: mdl-29252718

ABSTRACT

CASE: A sixty-one-year-old man underwent anterior cervical discectomy and fusion (ACDF) from C4 to C7 for the treatment of cervical spondylosis. Postoperatively, the patient experienced paroxysmal surges in blood pressure with associated diaphoresis and anxiety that were difficult to control. He had additional episodes after discharge, requiring a second hospital admission. He was ultimately diagnosed with baroreflex failure syndrome and was managed with a three-drug regimen. He gradually improved and was symptom-free at seven months. CONCLUSION: Baroreflex failure syndrome should be considered in the setting of volatile hypertension following ACDF. Prompt recognition of this condition can lead to early referral to a specialist and may reduce patient morbidity.

6.
Clin Neurol Neurosurg ; 138: 165-8, 2015 Nov.
Article in English | MEDLINE | ID: mdl-26342438

ABSTRACT

BACKGROUND: The efficacy of expansile cervical laminoplasty for cervical spondylotic myelopathy has been validated in the literature. To date, however, the majority of large, long-term data in the literature have originated in Japan. Few studies have originated from North America that include follow up greater than one year, and none of these includes a single surgeon's experience. This paper presents the retrospective results of a single surgeon with an average follow up of 47 months in a large population of North American patients. METHODS: A single surgeon's series of 80 consecutive patients who underwent expansile open-door laminoplasty for cervical myelopathy was reviewed. The severity of disability was graded using the Nurick Functional Disability Score and the Miami Upper Extremity Function (MUEF) score. Patients were evaluated preoperatively, six months postoperatively, and at a minimum of 24 months postoperatively. All examinations were performed by a single physician. MRI scans of the cervical spine were obtained at four months postoperatively in all patients. Radiographs were used to evaluate postoperative lordosis. RESULTS: Average length of follow up was 47 months. Nurick scores improved from an average of 2.3 preoperatively to postoperative scores of 1.5 (p>.05) at six months and 1.4 (p>.05) at two years. MUEF scores also improved at both the six month and two year intervals. All patients had improved canal diameter on post-operative MRI scan evaluation obtained four months post-operatively. CONCLUSION: This study confirms that laminoplasty is a safe and effective treatment of cervical spondylotic myelopathy in the North American population. LEVEL OF EVIDENCE: Case Series Level IV.


Subject(s)
Cervical Vertebrae/surgery , Laminoplasty/methods , Spinal Cord Diseases/surgery , Spinal Stenosis/surgery , Spondylosis/surgery , Adult , Aged , Aged, 80 and over , Follow-Up Studies , Humans , Magnetic Resonance Imaging , Middle Aged , Neck/surgery , North America , Retrospective Studies , Tomography, X-Ray Computed , Treatment Outcome
7.
Spine (Phila Pa 1976) ; 40(12): E719-28, 2015 Jun 15.
Article in English | MEDLINE | ID: mdl-25816141

ABSTRACT

STUDY DESIGN: Review of the literature. OBJECTIVE: To retrospectively examine the frequency of published fungal infections by species and the treatment algorithms used to eradicate the disease. SUMMARY OF BACKGROUND DATA: Fungal infections of the spine present unique challenges to the modern multispecialty treatment team. Although rare in comparison with bacterial infections, fungal infections have been increasing in incidence over the past several decades. Evidences-based practice is limited to referencing smaller case series. METHODS: MEDLINE, Scopus, and EMBASE searches were carried out by one of the authors as well as by the research desk at the University of Miami/Calder Memorial Library. We included peer-reviewed articles published between 1948 and September 2010; case reports, series, and reviews were all examined and compiled into a database. RESULTS: A total of 130 articles, representing 157 cases, were included in the review. Aspergillus (60 cases, 38.2% of the total) and Candida species (36 cases, 22.9% of the total) were the 2 most common organisms. Surgery was associated with a greater survival rate than medical management alone in patients with Aspergillus (26.9% mortality in surgical patients; 60% in medically treated patients) and Candida (0% vs. 28.6%). Overall mortality was 19.3%. The overall recurrence rate was 7.4%. Amphotericin use was associated with a higher mortality rate than azoles. CONCLUSION: Aspergillus is the most common published pathogen in fungal infections of the spine. Recent publications depicting the use of newer antifungal medications such as azoles report higher survival rates. Surgically treated patients in combination with antifungal therapy showed highest frequencies of patient survival in Aspergillus and Candida infections. LEVEL OF EVIDENCE: 3.


Subject(s)
Antifungal Agents/therapeutic use , Mycoses/therapy , Orthopedic Procedures , Osteomyelitis/therapy , Spinal Diseases/therapy , Algorithms , Combined Modality Therapy , Critical Pathways , Humans , Incidence , Microbial Sensitivity Tests , Mycoses/diagnosis , Mycoses/microbiology , Mycoses/mortality , Osteomyelitis/diagnosis , Osteomyelitis/microbiology , Osteomyelitis/mortality , Practice Guidelines as Topic , Predictive Value of Tests , Recurrence , Risk Factors , Spinal Diseases/diagnosis , Spinal Diseases/microbiology , Spinal Diseases/mortality , Treatment Outcome
8.
Am J Surg ; 198(2): 270-6, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19362289

ABSTRACT

BACKGROUND: Surgical peer review might be characterized by assessment heterogeneity. METHODS: We performed a prospective, anonymous, peer review of surgeon and system performance during a morbidity and mortality conference. RESULTS: Twenty-two cases were reviewed by a mean of 48.9 respondents each, including attendings, fellows, and residents. A mean of 50% (standard deviation, 23%) of respondents identified some quality issue in each case, reflecting high heterogeneity. The mean percentage in identifying a system issue was 27%, and in identifying a physician issue was 37%. When identifying a physician issue, physician care was judged as appropriate by 72%, as controversial by 26%, or as inappropriate by 2%. Residents were more likely than attendings to identify system issues (odds ratio, 2.23) and physician issues (odds ratio, 3.58), but attendings were more likely to rate care controversial or inappropriate (odds ratio, 2.53). CONCLUSIONS: Surgical peer reviews, even after group discussion, display substantial heterogeneity. Review methods should account for this heterogeneity.


Subject(s)
Congresses as Topic , Morbidity , Mortality , Peer Review , Quality Assurance, Health Care , Clinical Competence , General Surgery , Humans , Internship and Residency , Medical Staff, Hospital , Missouri , Prospective Studies
9.
J Thromb Thrombolysis ; 28(2): 124-31, 2009 Aug.
Article in English | MEDLINE | ID: mdl-18839278

ABSTRACT

BACKGROUND: Subtle decreases in platelet count may impede timely recognition of heparin-induced thrombocytopenia (HIT), placing the patient at increased risk of thrombotic events. OBJECTIVE: A clinical decision support system (CDSS) was developed to alert physicians using computerized provider order entry when a patient with an active order for heparin experienced platelet count decreases consistent with HIT. METHODS: Comparisons for timeliness of HIT identification and treatment were evaluated for the year preceding and year following implementation of the CDSS in patients with laboratory confirmation of HIT. RESULTS: During the intervention time period, the CDSS alert occurred 41,922 times identifying 2,036 patients who had 2,338 inpatient admissions. The CDSS had no significant impact on time from fall in platelet count to HIT laboratory testing (control 2.3 days vs intervention 3.0 days P = 0.30) and therapy (control 19.3 days vs intervention 15.0 days P = 0.45), and appeared to delay discontinuation of heparin products (control 1.3 days vs. intervention 2.9 days P = 0.04). However, discontinuation of heparin following shorter exposure duration and after smaller decrease in platelet count occurred during the intervention period. The HIT CDSS sensitivity and specificity were each 87% with a negative predictive value of 99.9% and positive predictive value of 2.3%. CONCLUSIONS: Implementation of a CDSS did not appear to improve the ability to detect and respond to potential HIT, but resulted in increased laboratory testing and changes in clinician reactions to decreasing platelet counts that deserve further study.


Subject(s)
Decision Support Systems, Clinical , Heparin/adverse effects , Thrombocytopenia/chemically induced , Thrombocytopenia/diagnosis , Aged , Female , Humans , Male , Middle Aged , Retrospective Studies , Thrombocytopenia/drug therapy , Thrombosis/prevention & control
10.
J Hosp Med ; 2(4): 234-40, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17702035

ABSTRACT

OBJECTIVE: To determine the incidence and manifestations of hypoglycemia in hospitalized patients receiving antihyperglycemic therapy. RESEARCH DESIGN AND METHODS: The study was a 3-month prospective review of consecutive medical records of all adult, nonpregnant hospitalized patients at a 675-bed university hospital who experienced at least 1 blood glucose (BG)

Subject(s)
Hypoglycemia/etiology , Hypoglycemic Agents/adverse effects , Adult , Adverse Drug Reaction Reporting Systems , Aged , Aged, 80 and over , Blood Glucose/analysis , Chi-Square Distribution , Female , Glycemic Index , Humans , Hypoglycemia/epidemiology , Incidence , Male , Middle Aged , Philadelphia/epidemiology , Prospective Studies , Risk Factors , Treatment Outcome
11.
JPEN J Parenter Enteral Nutr ; 30(5): 440-5, 2006.
Article in English | MEDLINE | ID: mdl-16931614

ABSTRACT

BACKGROUND: An intervention to reduce complications from insertion of small-bore nasogastric feeding tubes was performed. METHODS: This was a Performance Improvement project with the Plan, Do, Study, Act (PDSA) format; interventions occurred in July 2003. Electronic searches of risk management and radiology databases identified feeding-tube malpositions and complications from January 1, 2001, through December 31, 2004. Chart abstraction and a pre- and postintervention comparison were performed. Interventions were adoption of a more compliant feeding tube, direct supervision of residents, technology-guided insertion, and implementation of explicit policies and procedures. RESULTS: Of all small-bore nasogastric feeding-tube placements, 1.3%-2.4% resulted in 50 documented cases of feeding-tube malpositions during 4 years. Over half of the 50 patients were mechanically ventilated, and only 2 had a normal mental status. There were 13 complications (26% of malpositions), including 2 deaths, which were directly attributed to the feeding-tube malposition. Only 2 of the 13 complications and none of the misplacements had been recorded in the risk management database; most cases were identified from the search of radiology reports. In the 15-month postintervention period, no complications were identified. The control chart showed that after the intervention, there was a significant increase in the "number between" tube insertions without complications, confirming the effectiveness of the performance improvement (PI) project. CONCLUSIONS: Unassisted feeding tube insertion carries significant risk in vulnerable patients, which can be mitigated. Voluntary reporting appears inadequate to capture complications from feeding tube insertion.


Subject(s)
Enteral Nutrition , Intubation, Gastrointestinal/standards , Patient Care/standards , Quality Assurance, Health Care , Safety , Enteral Nutrition/instrumentation , Enteral Nutrition/methods , Enteral Nutrition/standards , Humans , Intubation, Gastrointestinal/adverse effects , Patient Care/instrumentation , Patient Care/methods , Retrospective Studies , Treatment Outcome
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