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Institution

Lincoln Hospital

HealthcareNew York, New York, United States
About: Lincoln Hospital is a healthcare organization based out in New York, New York, United States. It is known for research contribution in the topics: Population & Emergency department. The organization has 1033 authors who have published 929 publications receiving 14486 citations. The organization is also known as: Lincoln Medical and Mental Health Center & Lincoln Hospital.


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11 Nov 2019
TL;DR: Breath holding spells might be a frightening experience for children and consequently for their parents, but these episodes may be prevented by distracting the child and by avoiding the triggers.
Abstract: Breath holding spells might be a frightening experience for children and consequently for their parents. Breath holding spells may occur in children who have a normal neurological exam and in children who meet age-appropriate developmental milestones, but normally breath-holding spells do not affect the subsequent neurological development of a child. Breath holding episodes usually follow an inciting event in which the patient is being disciplined, is angry, or is being irritated, etc. Then an episode of crying and breath holding episode may occur which may proceed to loss of consciousness. These episodes may be prevented by distracting the child and by avoiding the triggers.

1 citations

Journal ArticleDOI
TL;DR: A secundigravid patient with a history of a prior pregnancy affected by intrahepatic cholestasis who presented in the current pregnancy with elevated bile acid levels and severe pruritus not ameliorated is described.

1 citations

Journal ArticleDOI
TL;DR: A 16-year-old Hispanic boy with a history of intermittent asthma presents to the emergency department (ED) with recurrent unprovoked seizures and is discharged on oral oxcarbazepine with a diagnosis of idiopathic epilepsy.
Abstract: 1. Neha Gupta, MD* 2. Saurabh Talathi, MD, MPH* 3. Yenimar Ventura, MD* 4. Sergey Prokhorov, MD* 1. *Department of Pediatrics, Lincoln Medical Center, Bronx, NY A 16-year-old Hispanic boy with a history of intermittent asthma presents to the emergency department (ED) with recurrent unprovoked seizures. The first episode was 2 weeks before this visit and was characterized by generalized tonic-clonic seizures (GCTSs), with a postictal phase of 10 minutes. He was seen in the ED during that episode, with normal findings on examination and evaluation, including a complete blood cell count, chemistry, liver function tests, urine toxicology, and a computed tomographic (CT) scan. During the current visit, he presents with a history of 2 episodes of unprovoked GTCSs 4 hours apart. The first episode lasted 5 minutes, followed by a postictal phase of 5 minutes. In the ED, he has normal physical examination findings and is discharged on oral oxcarbazepine with a diagnosis of idiopathic epilepsy. Before starting the prescribed medication, he develops another episode of GCTSs, approximately 7 to 8 minutes, with no postictal phase. Each of these episodes were preceded by coughing spells lasting 10 to 20 minutes. He has no history of fever, head trauma, recent travel, drug intake, medication use, or sick contacts. In the ED, his vital signs are normal except for intermittent bradycardia (heart rate, 60 beats/min). Physical examination findings are normal except for bite marks on the right side of the tongue. Results of a complete blood cell count, chemistry, liver function tests, and urinalysis are within normal limits. Urine toxicology results are negative. Findings from electrocardiography (ECG), electroencephalography (EEG), and brain magnetic resonance imaging (MRI) are normal. The patient is started on divalproex. Primary generalized epilepsy is suspected by the ED physician for undocumented reasons, …

1 citations

Book ChapterDOI
01 Jan 2011
TL;DR: The purpose of this chapter is to review the diagnosis and management of challenging clinical situations in AOSD patients that are associated with significant morbidity and mortality and to provide the readers with information that could aid their decision-making process.
Abstract: Adult-onset Still’s disease (AOSD) is a rare systemic inflammatory disorder of unknown etiology, characterized by quotidian or double quotidian fever, a peri-febrile cutaneous eruption, polyarthritis, and multiorgan involvement. AOSD is a challenging disease with protean disease manifestations and rare, albeit potentially life-threatening, complications. In such cases, prompt diagnosis and treatment may prove life-saving.

1 citations

Journal ArticleDOI
Anna Rutgersson1
18 Mar 2022-Medicine
TL;DR: In this article , the authors characterize survivors of COVID-19 infection and acute kidney injury (AKI) that recover their renal function or progress to acute kidney disease (AKD) on discharge; and determine factors associated with progression to AKD during hospital stay.

1 citations


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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20231
20224
202178
202086
201984
201839