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1.
Am J Emerg Med ; 81: 130-135, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38728935

ABSTRACT

BACKGROUND: Gallbladder distention has been described in radiology literature but its value on point-of-care ultrasound (PoCUS) performed by emergency physicians is unclear. We sought to determine the test characteristics of gallbladder distention on PoCUS for cholecystitis (acute or chronic), and secondarily whether distention was associated with an obstructing stone-in-neck (SIN), acute cholecystitis on subsequent pathology report, and longer cholecystectomy operative times. METHODS: This was a dual-site retrospective cohort study of all Emergency Department (ED) patients that underwent diagnostic biliary PoCUS and were subsequently admitted from 11/1/2020 to 10/31/2022. Patients with pregnancy, liver failure, ascites, hepatobiliary cancer, prior cholecystectomy, or known cholecystitis were excluded. Gallbladder distention was defined as a width ≥4 cm or a length ≥10 cm. Saved ultrasound images were reviewed by three independent reviewers who obtained measurements during the review. Test characteristics, Cohen's kappa (κ), and strength of association between distention and our variables (acute cholecystitis on pathology report and SIN on PoCUS) were calculated using a Chi Square analysis, where intervention (cholecystectomy, percutaneous cholecystostomy, or intravenous antibiotics) was used as the reference standard for AC. A one-tail two sample t-test was calculated for mean operative times. RESULTS: Of 280 admitted patients who underwent ED biliary PoCUS, 53 were excluded, and 227 were analyzed. Of the 227 patients, 113 (49.8%) had cholecystitis according to our reference standard, and 68 (30.0%) had distention on PoCUS: 32 distended by both width and length, 16 distended by width alone, and 20 distended by length alone. Agreement between investigators was substantial for width (κ 0.630) and length (κ 0.676). Distention was 85.09% (95% CI 77.20-91.07%) specific and 45.1% (95% CI 35.8-54.8%) sensitive for cholecystitis. There was an association between distention and SIN; odds ratio (OR) 2.76 (95% CI 1.54-4.97). Distention of both length and width was associated with acute over chronic cholecystitis; OR 4.32 (95% CI 1.42-13.14). Among patients with acute cholecystitis, mean operative times were 114 min in patients with distention and 89 min in patients without distention (p = 0.03). CONCLUSION: Gallbladder distention on PoCUS was specific for cholecystitis (acute or chronic), and associated with SIN, acute cholecystitis on subsequent pathology report, and longer cholecystectomy operative times. Measurement of gallbladder dimensions as part of the assessment of cholecystitis may be advantageous.


Subject(s)
Cholecystitis, Acute , Ultrasonography , Humans , Cholecystitis, Acute/diagnostic imaging , Cholecystitis, Acute/diagnosis , Female , Retrospective Studies , Male , Middle Aged , Aged , Gallbladder/diagnostic imaging , Gallbladder/pathology , Emergency Service, Hospital , Adult , Cholecystectomy , Point-of-Care Systems , Operative Time
3.
Am J Emerg Med ; 51: 429.e3-429.e5, 2022 01.
Article in English | MEDLINE | ID: mdl-34325928

ABSTRACT

Acute flank pain associated with hematuria and unilateral hydronephrosis is a classic presentation for an obstructing ureteral stone. However, in the setting of hemorrhagic cystitis, blood can acutely obstruct the distal ureter and infrequently result in hydronephrosis. We present a case of an adult female patient with hemorrhagic cystitis who presented with acute right flank pain associated with unilateral hydronephrosis and perinephric fluid on point-of-care ultrasound (PoCUS) in the absence of renal or ureteral abnormality on CT scan hours earlier. Her symptoms resolved, urine cultures showed no growth, and her outpatient follow-up was unremarkable. We suspect given the acute onset of right obstructive uropathy, an unremarkable CT just hours earlier, and the brief nature of her symptoms, that blood obstructed her distal UVJ leading to acute and transient obstructive uropathy.


Subject(s)
Cystitis/diagnosis , Hemorrhage/etiology , Hydronephrosis/etiology , Ureteral Obstruction/diagnostic imaging , Acute Pain/etiology , Body Fluids/diagnostic imaging , Cystitis/complications , Female , Flank Pain/etiology , Humans , Hydronephrosis/diagnostic imaging , Middle Aged , Point-of-Care Systems , Tomography, X-Ray Computed , Ultrasonography , Ureteral Obstruction/complications
4.
Emerg Radiol ; 28(3): 469-476, 2021 Jun.
Article in English | MEDLINE | ID: mdl-33428043

ABSTRACT

OBJECTIVE: To investigate the incidence of thromboembolic events, specifically pulmonary embolism (PE), deep vein thrombosis (DVT), and cerebrovascular accidents (CVA), in patients who tested positive for COVID-19 through RT-PCR in a regional healthcare system in Connecticut. MATERIALS AND METHODS: All CT angiogram (CTA) and venous duplex extremity ultrasound (US) examinations performed on 192 consecutively documented cases of COVID-19 were retrospectively reviewed at a multi-centered healthcare system. Clinical characteristics and patient outcomes were evaluated and compared between two groups based on the presence or absence of acute thromboembolic events. RESULTS: Of the 16,264 patients tested for COVID-19, 3727 (23%) were positive. Out of those, 192 patients underwent 245 vascular imaging studies including chest CTA (86), venous duplex ultrasound (134), and CTA head and neck (25). Among those who underwent imaging, 49 (26%) demonstrated acute thromboembolic events which included 13/86 (15%) with PE, 34/134 (25%) with DVT, and 6/25 (24%) with CVA. One patient had positive results on all 3 examinations, and 2 patients had positive results on both chest CTA and venous duplex US. Males were more likely to have a thromboembolic event than females (33/103 (34%) vs. 14/89 (16%), p = 0.009). No significant difference was observed with respect to age, cardiopulmonary comorbidities, malignancy history, diabetes, or dialysis. CONCLUSION: Approximately 26% of COVID-19 patients with positive testing who underwent vascular imaging with CTA or venous duplex ultrasound had thromboembolic events including PE, DVT, and CVA. This indicates that COVID-19 patients are at increased risk for thromboembolic complications.


Subject(s)
COVID-19/complications , Computed Tomography Angiography/methods , Thromboembolism/diagnostic imaging , Thromboembolism/virology , Ultrasonography, Doppler, Duplex/methods , Aged , COVID-19/epidemiology , Connecticut/epidemiology , Female , Humans , Male , Middle Aged , Retrospective Studies , SARS-CoV-2 , Thromboembolism/epidemiology
5.
Emerg Radiol ; 25(3): 303-310, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29417357

ABSTRACT

PURPOSE: The purpose of the study was to assess the emergency department (ED) providers' interest and satisfaction with ED CT result reporting before and after the implementation of a standardized summary code for all CT scan reporting. MATERIALS AND METHODS: A summary code was provided at the end of all CTs ordered through the ED from August to October of 2016. A retrospective review was completed on all studies performed during this period. A pre- and post-survey was given to both ED and radiology providers. RESULTS: A total of 3980 CT scans excluding CTAs were ordered with 2240 CTs dedicated to the head and neck, 1685 CTs dedicated to the torso, and 55 CTs dedicated to the extremities. Approximately 74% CT scans were contrast enhanced. Of the 3980 ED CT examination ordered, 69% had a summary code assigned to it. Fifteen percent of the coded CTs had a critical or diagnostic positive result. CONCLUSIONS: The introduction of an ED CT summary code did not show a definitive improvement in communication. However, the ED providers are in consensus that radiology reports are crucial their patients' management. There is slightly increased satisfaction with the providers with less than 5 years of experience with the ED CT codes compared to more seasoned providers. The implementation of a user-friendly summary code may allow better analysis of results, practice improvement, and quality measurements in the future.


Subject(s)
Clinical Coding , Emergency Service, Hospital/statistics & numerical data , Tomography, X-Ray Computed , Humans , Retrospective Studies , Surveys and Questionnaires , United States
6.
AJR Am J Roentgenol ; 201(3): 550-4, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23971445

ABSTRACT

OBJECTIVE: We retrospectively reviewed the CT findings of lower respiratory tract infection (LRTI) due to parainfluenza virus (PIV) to determine the imaging features of PIV infection and to identify any differences compared with the CT appearances of LRTIs due to respiratory syncytial virus (RSV), adenovirus, and influenza virus. MATERIALS AND METHODS: The imaging features of LRTI from PIV over a 51-month period were retrospectively reviewed. The specific CT findings and overall pattern of infection in patients with LRTI due to PIV were recorded and were then compared with the CT appearances of RSV, adenovirus, and influenza LRTIs using data from a previous study. RESULTS: Twenty-four chest CT examinations of 24 patients with PIV infection were analyzed. Tree-in-bud opacities were the most common finding (13/24, 54%), and the airway-centric pattern of disease--characterized by combinations of bronchial wall thickening, tree-in-bud opacities, and peribronchiolar consolidation (bronchitis, bronchiolitis, and bronchopneumonia)--was the most common pattern (16/24, 67%). In comparison with previous data on RSV, adenovirus, and influenza virus, PIV showed tree-in-bud opacities and airway-centric patterns significantly more often than adenovirus or influenza virus. PIV and RSV showed similar CT findings and patterns of disease. CONCLUSION: Despite varying CT appearances of PIV LRTI, it most often shows airway-centric disease and is similar to the appearance of RSV infection, both of which are members of the Paramyxoviridae family of viruses.


Subject(s)
Paramyxoviridae Infections/diagnostic imaging , Respiratory Tract Infections/diagnostic imaging , Tomography, X-Ray Computed/methods , Adolescent , Adult , Aged , Aged, 80 and over , Contrast Media , Female , Humans , Iohexol , Iopamidol , Male , Middle Aged , Paramyxoviridae Infections/virology , Respiratory Tract Infections/virology , Retrospective Studies , Reverse Transcriptase Polymerase Chain Reaction , United States
7.
Blood Press Monit ; 8(3): 137-40, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12900592

ABSTRACT

BACKGROUND: Non-invasive blood pressure (BP) monitoring has become increasingly popular. To assure the accuracy of devices used for this purpose, these devices should be clinically validated using standard criteria such as those published by the Association for the Advancement of Medical Instrumentation (AAMI). The purpose of this study was to collect and assess non-invasive BP data using the Trimline BP cuffs (Branchburg, New Jersey, USA) with the Accutorr Plus Monitor (Datascope Corp., Mahwah, New Jersey, USA) in accordance with AAMI standards. METHODS: Blood pressure measurements taken employing this device were compared with the results obtained by two experienced observers using a mercury sphygmomanometer on 109 subjects (545 measurements). The limits of agreement were calculated for the device compared with the results of the two observers according to the AAMI standards. RESULTS: The agreement parameters between the two observers were -0.49+/-3.81 mmHg for systolic BP and 0.50+/-3.19 mmHg for diastolic BP. The agreement between the device and the observers was -0.13+/-7.51 and 2.54+/-5.21 mmHg for systolic and diastolic BP, respectively. The proportions of observer and device values agreeing within 5, 10, and 15 mmHg were 65, 87, and 94% for systolic BP and 72, 93, and 97% for diastolic BP. CONCLUSIONS: The Trimline BP cuffs in conjunction with the Accutorr Plus device demonstrated acceptable accuracy and precision in accordance with the AAMI criteria for a non-invasive BP monitoring device.


Subject(s)
Blood Pressure Determination/instrumentation , Blood Pressure Monitors/standards , Adult , Arm , Blood Pressure , Female , Humans , Male , Middle Aged , Observer Variation
8.
Blood Press Monit ; 7(5): 285-8, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12409889

ABSTRACT

BACKGROUND: Non-invasive blood pressure (BP) devices should be independently evaluated before being used in special populations. The objective of this study was to assess the accuracy of the Welch-Allyn transtelephonic home blood pressure monitor in adults with Parkinson's disease to evaluate the device for use in a large clinical trial involving the safety and efficacy of a monoamine oxidase inhibitor. METHODS: BP measurements taken with the device were compared with the results obtained by two experienced observers using a mercury sphygmomanometer in patients with Parkinson's disease. The limits of agreement were then calculated for the device and compared with the results of the two observers. RESULTS: The agreement parameters between the two observers were -0.5 +/- 2.6 mmHg for systolic BP and 0.1 +/- 2.2 mmHg for diastolic BP. The agreement between the Welch-Allyn transtelephonic device and the observers was -2.6 +/- 4.5 mmHg and -1.9 +/- 3.2 mmHg for systolic and diastolic BP respectively. Nearly 90% of the readings were within 10 mmHg of the observers for both systolic and diastolic BP. Mild tremor had a moderate effect on the validity of the device. CONCLUSIONS: The Welch-Allyn transtelephonic device demonstrated acceptable precision in this cohort of patients with Parkinson's disease and is considered valid for use in a clinical trial involving these patients.


Subject(s)
Blood Pressure Determination/instrumentation , Parkinson Disease/physiopathology , Adult , Aged , Aged, 80 and over , Blood Pressure , Female , Humans , Male , Middle Aged , Movement , Observer Variation , Oscillometry , Reproducibility of Results , Telecommunications/instrumentation
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