Research Spotlight

Posted October 15th 2021

Extracorporeal membrane oxygenation for patients with pulmonary embolism undergoing thrombolysis.

John J. Squiers, M.D.

John J. Squiers, M.D.

Kluis, A., J. Eisenga, J. Squiers, J. M. Dimaio, D. Gable, J. Kedora, W. Shutze and T. George (2021). “Extracorporeal membrane oxygenation for patients with pulmonary embolism undergoing thrombolysis.” Ann Thorac Surg.

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Patients with massive pulmonary embolism undergoing catheter-directed therapy are at high risk for cardiopulmonary arrest in the periprocedural period due to severe right ventricular dysfunction. We report the outcomes of three patients with massive pulmonary embolism treated successfully with catheter-directed thrombolytic therapy and veno-arterial extracorporeal membrane oxygenation.


Posted October 15th 2021

Orthognathic Surgery of the Mandible.

Likith V. Reddy, M.D.

Likith V. Reddy, M.D.

Bahmanyar, S., A. W. Namin, R. O. Weiss, 2nd, A. G. Vincent, A. M. Read-Fuller and L. V. Reddy (2021). “Orthognathic Surgery of the Mandible.” Facial Plast Surg.

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Orthognathic surgery performed in conjunction with orthodontic treatment is commonly performed to correct skeletal irregularities and realign the maxillomandibular relationship to improve occlusal function and facial esthetics. A thorough understanding of soft tissue esthetics, skeletal and occlusal relationships, and surgical techniques is required to obtain successful results. Surgical techniques have evolved greatly throughout history, as technological advances such as virtual surgical planning have become available and widely used to obtain predictable movements with minimized complications. The aim of this article is to review the orthognathic surgical procedures of the mandible, with particular attention to the indications, contraindications, preoperative assessment, surgical technique, and possible complications encountered.


Posted October 12th 2021

Early versus late awake prone positioning in non-intubated patients with COVID-19.

Idrees Mogri, M.D.

Idrees Mogri, M.D.

Kaur, R., D. L. Vines, S. Mirza, A. Elshafei, J. A. Jackson, L. J. Harnois, T. Weiss, J. B. Scott, M. W. Trump, I. Mogri, F. Cerda, A. A. Alolaiwat, A. R. Miller, A. M. Klein, T. W. Oetting, L. Morris, S. Heckart, L. Capouch, H. He and J. Li (2021). “Early versus late awake prone positioning in non-intubated patients with COVID-19.” Crit Care 25(1): 340.

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BACKGROUND: Awake prone positioning (APP) is widely used in the management of patients with coronavirus disease (COVID-19). The primary objective of this study was to compare the outcome of COVID-19 patients who received early versus late APP. METHODS: Post hoc analysis of data collected for a randomized controlled trial (ClinicalTrials.gov NCT04325906). Adult patients with acute hypoxemic respiratory failure secondary to COVID-19 who received APP for at least one hour were included. Early prone positioning was defined as APP initiated within 24 h of high-flow nasal cannula (HFNC) start. Primary outcomes were 28-day mortality and intubation rate. RESULTS: We included 125 patients (79 male) with a mean age of 62 years. Of them, 92 (73.6%) received early APP and 33 (26.4%) received late APP. Median time from HFNC initiation to APP was 2.25 (0.8-12.82) vs 36.35 (30.2-75.23) hours in the early and late APP group (p < 0.0001), respectively. Average APP duration was 5.07 (2.0-9.05) and 3.0 (1.09-5.64) hours per day in early and late APP group (p < 0.0001), respectively. The early APP group had lower mortality compared to the late APP group (26% vs 45%, p = 0.039), but no difference was found in intubation rate. Advanced age (OR 1.12 [95% CI 1.0-1.95], p = 0.001), intubation (OR 10.65 [95% CI 2.77-40.91], p = 0.001), longer time to initiate APP (OR 1.02 [95% CI 1.0-1.04], p = 0.047) and hydrocortisone use (OR 6.2 [95% CI 1.23-31.1], p = 0.027) were associated with increased mortality. CONCLUSIONS: Early initiation (< 24 h of HFNC use) of APP in acute hypoxemic respiratory failure secondary to COVID-19 improves 28-day survival. Trial registration ClinicalTrials.gov NCT04325906.


Posted October 12th 2021

Improving the safety of outpatient parenteral antimicrobial therapy for patients with solid tumors.

Emma Dishner M.D.

Emma Dishner M.D.

Robins, A., E. Dishner, P. McDaneld, M. Rowan, J. Bartek, Y. Jiang, J. Adachi and N. J. M. Dailey Garnes (2021). “Improving the safety of outpatient parenteral antimicrobial therapy for patients with solid tumors.” Support Care Cancer.

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BACKGROUND AND OBJECTIVES: Outpatient parenteral antimicrobial therapy (OPAT) for infections has been in use for nearly 40 years, and although it has been found safe and efficacious, its use has been studied primarily among otherwise healthy patients. We aimed to develop and evaluate an OPAT program for patients with cancer, particularly solid tumors. METHODS: We implemented multiple quality improvement interventions between June 2018 and January 2020. We retrospectively and prospectively collected data on demographics, the completeness of infectious diseases (ID) physician consultation notes, rates of laboratory test result monitoring, ID clinic follow-up, and 30-day outcomes, including unplanned OPAT-related readmissions, OPAT-related emergency center visits, and deaths. RESULTS: Completeness of ID provider notes improved from a baseline of 77 to 100% (p < .0001) for antimicrobial recommendations, 75 to 97% (p < .0001) for follow-up recommendations, and 19 to 98% (p < .0001) for laboratory test result monitoring recommendations. Completion of laboratory tests increased from a baseline rate of 24 to 56% (p = .027). Thirty-day unplanned OPAT-related readmission, ID clinic follow-up, 30-day emergency center visit, and death rates improved without reaching statistical significance. CONCLUSIONS: Sustained efforts, multiple interventions, and multidisciplinary engagement can improve laboratory test result monitoring among solid tumor patients discharged with OPAT. Although demonstrating a decrease in unplanned readmissions through institution of a formal OPAT program among patients with solid malignancies may be more difficult compared with the general population, the program may still result in improved safety.


Posted September 16th 2021

How different time intervals between repeated applications of CPP-ACP fluoride varnish effect smooth surface enamel demineralization?

Peter H. Buschang, Ph.D.

Peter H. Buschang, Ph.D.

Abufarwa, M., A. Noureldin, P. M. Campbell and P. H. Buschang (2021). “How different time intervals between repeated applications of CPP-ACP fluoride varnish effect smooth surface enamel demineralization?” J Dent 112: 103742.

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OBJECTIVES: To evaluate the preventive effects of different time intervals between repeated applications of the CPP-ACP fluoride varnish on enamel demineralization. METHODS: Human teeth were sectioned and randomly allocated to three groups: 4-week, 6-week, and 12-week (N = 22/group). Baseline images of the enamel surfaces were obtained using the FluoreCam recording the area, intensity, and impact of baseline enamel demineralization. All groups received fluoride varnish applications at the beginning of the experiment. The varnish was reapplied every 4 or 6 weeks in the 4-week and 6-week groups, respectively. Following each application, the groups underwent thermo-cycling, tooth brushing and pH cycling to simulate the time effect. After 12 weeks, the enamel surfaces were reimaged using the FluoreCam. Within and between-group differences in the area, intensity and impact of demineralization were evaluated. RESULTS: At baseline, there were no significant between-group differences for area, intensity, or impact. Statistically significant (p<0.001) enamel demineralization occurred over time within each group. There were significant between-group differences in the changes that occurred in area (P = 0.004), impact (P = 0.022), but not intensity. The 12-week had significantly larger areas of demineralization than the 6-week (P = 0.041) and 4-week (P = 0.001) groups. Changes in impact was significantly (P = 0.007) greater in the 12-week group than 4-week group, but not greater than the 6-week group. There were no statistically significant differences between 4- and 6-week groups in the changes of area, intensity, or impact. CONCLUSION: Reapplication of the CPP-ACP fluoride varnish every 4-6 weeks, is more effective in reducing enamel demineralization compared to every 12 weeks.