scholarly journals Inpatient dental consultations at a pediatric hospital: A single center 1‐year review

2020 ◽  
Author(s):  
Kyler B. Hayes ◽  
Barbara Sheller ◽  
Bryan J. Williams ◽  
Shervin S. Churchill
2019 ◽  
Vol 09 (01) ◽  
pp. 045-050
Author(s):  
Alicia May Lim ◽  
Siew Le Chong ◽  
Yong Hong Ng ◽  
Yoke Hwee Chan ◽  
Jan Hau Lee

AbstractMost children who present with hypertensive crisis have a secondary cause for hypertension. This study describes the epidemiology and management of children with hypertensive crisis. A retrospective cohort study was done in a tertiary pediatric hospital from 2009 to 2015. Thirty-seven patients were treated for hypertensive crisis. Twelve (32.4%) patients were treated for hypertensive emergency. The majority of our patients (33 [89.1%]) had a secondary cause of hypertension. The most common identifiable cause of hypertension was a renal pathology (18/37 [48.6%]). Oral nifedipine (23 [62.1%]) was the most frequently used antihypertensive, followed by intravenous labetalol (8 [21.6%]). There were no mortalities or morbidities. Hypertensive crisis in children is likely secondary in nature. Oral nifedipine and intravenous labetalol are both effective treatments.


2013 ◽  
Vol 131 (2) ◽  
pp. AB87
Author(s):  
Rushani W. Saltzman ◽  
Mary E. Kelleher ◽  
Jonathan M. Spergel

2020 ◽  
Vol 36 (11) ◽  
pp. 2789-2799 ◽  
Author(s):  
Alberto Balestrino ◽  
Gianluca Piatelli ◽  
Alessandro Consales ◽  
Armando Cama ◽  
Andrea Rossi ◽  
...  

2021 ◽  
pp. 105566562110537
Author(s):  
Erin E. Anstadt ◽  
Madeleine K. Bruce ◽  
Matthew Ford ◽  
Noel Jabbour ◽  
Miles J. Pfaff ◽  
...  

Purpose Persistent velopharyngeal insufficiency (VPI) following primary palatoplasty remains a difficult problem to treat. This study evaluates speech outcomes following revision palatoplasty with tissue augmentation using buccal myomucosal flaps (BMF) as an alternative to pharyngoplasty for patients with VPI. Methods A retrospective single-center review of revision palatoplasty with tissue augmentation at a tertiary pediatric hospital Cleft-Craniofacial Center between January 2017 and March 2021 was conducted. Patients with a history of previous palatoplasty, a diagnosis of persistent or recurrent VPI, and comprehensive pre- and postoperative speech evaluations who underwent revision palatoplasty with BMF were included. Results Twenty patients met inclusion criteria (35% female, 20% syndromic). Mean age at the time of revision palatoplasty with BMF was 9.7 years. Preoperatively, all patients had stigmatizing speech and received the recommendation for speech surgery; the mean Pittsburgh Weighted Speech Score (PWSS) was 14.3 ± 4.9. The mean postoperative PWSS at the most recent assessment was 4.2 ± 2.3, representing a statistically significant improvement from preoperative scores ( P < .001). Mean follow-up time was 8.9 months. Following revision palatoplasty with BMF, only one patient has received the recommendation for further speech surgery. No complications were noted. Conclusion In patients with VPI following primary palatoplasty, revision palatoplasty with tissue augmentation offers an alternative to pharyngoplasty. This approach preserves dynamic velopharyngeal function, improves speech outcomes, and should be considered an option when treating patients with post-primary palatoplasty VPI.


2018 ◽  
Vol 8 (4) ◽  
pp. 232-235
Author(s):  
F. Eduardo Martinez ◽  
Erin Kelty ◽  
Samantha Barr ◽  
Monique McLeod ◽  
Nathan Smalley

2020 ◽  
Author(s):  
Christopher S Thom ◽  
Emily Echevarria ◽  
Ashley D Osborne ◽  
Leah Carr ◽  
Kathryn Rubey ◽  
...  

Extreme thrombocytosis (ET, platelet count >1000 × 103/ul) is an uncommon clinical finding 1. Primary ET is associated with myeloproliferative disorders, such as essential thrombocythemia 2. Secondary ET is more common and occurs in reaction to infection, inflammation, or iron deficiency. Bleeding and thrombotic complications more frequently arise in primary ET cases 1, but have been reported with secondary ET in adults 3. Etiologies and complications associated with ET in children are less well-defined, as prior pediatric studies have been relatively small or restricted to specialized patient populations 4,5. We aimed to characterize ET in a large, single-center pediatric cohort.


2007 ◽  
Vol 177 (4S) ◽  
pp. 549-549
Author(s):  
Hannes Steiner ◽  
Thomas Akkad ◽  
Christian Gozzi ◽  
Brigitte Springer-Stoehr ◽  
Georg Bartsch

2007 ◽  
Vol 177 (4S) ◽  
pp. 17-17
Author(s):  
Monish Aron ◽  
Georges-Pascal Haber ◽  
Jose R. Colombo ◽  
Troy R. Gianduzzo ◽  
Jason M. Hafron ◽  
...  

2007 ◽  
Vol 177 (4S) ◽  
pp. 55-55
Author(s):  
Christian Schwentner ◽  
Andreas Lunacek ◽  
Alexandre E. Pelzer ◽  
Richard Neururer ◽  
Wolfgang Horninger ◽  
...  

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