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Drug Hypersensitivity due to Azathioprine with Elevated Procalcitonin
Ahuja, Tania; Chung, Frank R; Ruiz-Maya, Tania
We present a case of azathioprine hypersensitivity presenting as sepsis with elevated procalcitonin in a 68-year-old man with myasthenia gravis. The patient presented with fever, chills, nausea, vomiting, and headache. He developed numerous 1 cm erythematous papules over his upper torso. Infectious workup including bacteriological tests and microbial cultures was negative and a skin biopsy was performed which revealed suppurative folliculitis with eosinophils, consistent with drug hypersensitivity. Notably, acute phase reactants including C-reactive protein and procalcitonin were elevated upon presentation, likely secondary to drug hypersensitivity.
PMCID:6015696
PMID: 29984007
ISSN: 2090-6463
CID: 3192212
Phenibut (beta-Phenyl-gamma-aminobutyric Acid) Dependence and Management of Withdrawal: Emerging Nootropics of Abuse
Ahuja, Tania; Mgbako, Ofole; Katzman, Caroline; Grossman, Allison
This case report describes the development of withdrawal from phenibut, a gamma-aminobutyric acid-receptor type B agonist. Although phenibut is not an FDA-approved medication, it is available through online retailers as a nootropic supplement. There are reports of dependence in patients that misuse phenibut. We report a case in which a patient experienced withdrawal symptoms from phenibut and was successfully treated with a baclofen taper. This case report highlights the development of phenibut use disorder with coingestion of alcohol and potential management for phenibut withdrawal. We believe clinicians must be aware of how phenibut dependence may present and how to manage the withdrawal syndrome.
PMCID:5952553
PMID: 29854531
ISSN: 2090-682x
CID: 3136422
Acquired Coagulopathy and Hemorrhage Secondary to Subcutaneous Heparin Prophylaxis
Sunseri, Maria; Ahuja, Tania; Wilcox, Tanya; Green, David
Unfractionated heparin and low-molecular-weight heparins are commonly used as thromboprophylaxis for hospitalized patients. Though generally considered safe at prophylactic doses, cases of catastrophic hemorrhage have been reported. The proposed mechanism involves bioaccumulation of heparin through saturation of the rapid-elimination pathway in its metabolism. We present an unusual case of an average-weight man with metastatic melanoma who suffered hemorrhage with syncope and end-organ damage while on prophylactic three times daily unfractionated heparin. Coagulation studies were consistent with heparin toxicity. Despite administration of protamine, the clearance of heparin was remarkably delayed, as demonstrated by serial coagulation studies. We review the suspected risk factors for heparin bioaccumulation and the emerging understanding of this unusual adverse event involving a nearly ubiquitous medication.
PMCID:5818886
PMID: 29545958
ISSN: 2090-6560
CID: 2993982
EVALUATING ANTI-XA AND APTT MONITORING OF HEPARIN IN PATIENTS WITH AN IMPELLA DEVICE [Meeting Abstract]
Musallam, Nadine; Altshuler, Diana; Ahuja, Tania; Aberle, Caitlin; Papadopoulos, John
ISI:000388910200178
ISSN: 0090-3493
CID: 5333312
HIGH-DOSE FOUR-FACTOR PROTHROMBIN COMPLEX CONCENTRATE FOR WARFARIN-INDUCED INTRACEREBRAL HEMORRHAGE [Meeting Abstract]
Merchan, Cristian; Raco, Veronica; Ahuja, Tania; Lewis, Ariane
ISI:000388910201008
ISSN: 0090-3493
CID: 5333322
Extended-Infusion versus Standard-Infusion Piperacillin-Tazobactam for Sepsis Syndromes at a Tertiary Medical Center
Cutro, Scott R; Holzman, Robert; Dubrovskaya, Yanina; Chen, Xian Jie Cindy; Ahuja, Tania; Scipione, Marco R; Chen, Donald; Papadopoulos, John; Phillips, Michael S; Mehta, Sapna A
Piperacillin-tazobactam (PTZ) is frequently used as empirical and targeted therapy for Gram-negative sepsis. Time-dependent killing properties of PTZ support the use of extended-infusion (EI) dosing; however, studies have shown inconsistent benefits of EI PTZ treatment on clinical outcomes. We performed a retrospective cohort study of adult patients who received EI PTZ treatment and historical controls who received standard-infusion (SI) PTZ treatment for presumed sepsis syndromes. Data on mortality rates, clinical outcomes, length of stay (LOS), and disease severity were obtained. A total of 843 patients (662 with EI treatment and 181 with SI treatment) were available for analysis. Baseline characteristics of the two groups were similar, except for fewer female patients receiving EI treatment. No significant differences between the EI and SI groups in inpatient mortality rates (10.9% versus 13.8%; P = 0.282), overall LOS (10 versus 12 days; P = 0.171), intensive care unit (ICU) LOS (7 versus 6 days; P = 0.061), or clinical failure rates (18.4% versus 19.9%; P = 0.756) were observed. However, the duration of PTZ therapy was shorter in the EI group (5 versus 6 days; P < 0.001). Among ICU patients, no significant differences in outcomes between the EI and SI groups were observed. Patients with urinary or intra-abdominal infections had lower mortality and clinical failure rates when receiving EI PTZ treatment. We did not observe significant differences in inpatient mortality rates, overall LOS, ICU LOS, or clinical failure rates between patients receiving EI PTZ treatment and patients receiving SI PTZ treatment. Patients receiving EI PTZ treatment had a shorter duration of PTZ therapy than did patients receiving SI treatment, and EI dosing may provide cost savings to hospitals.
PMCID:4136013
PMID: 24867975
ISSN: 0066-4804
CID: 1102662