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1.
Cureus ; 13(5): e15014, 2021 May 13.
Article in English | MEDLINE | ID: mdl-34150377

ABSTRACT

Calciphylaxis is a rare syndrome of calcific microvascular occlusion, whereas non-uremic calciphylaxis (NUC) is a subset of this disease in which renal impairment is not observed. Recombinant human parathyroid hormone (rhPTH) (1-84) is a medication approved for the management of hypocalcemia in patients with hypoparathyroidism. We present a case report of a 38-year-old woman with postoperative hypoparathyroidism treated with rhPTH who subsequently developed calciphylactic lesions on her abdomen. Multidisciplinary interventions included intravenous and intralesional sodium thiosulfate therapy, laboratory monitoring, dermatological wound care, and pain management. Calciphylaxis can rarely be precipitated by rhPTH due to its effect on calcium and phosphorus balance even in the setting of normal renal function. The use of calcium and calcitriol supplementation, complicated by factors such as female sex and obesity, may have contributed in this patient's case. Hence, regular follow-up with tapering off of calcium and calcitriol supplementation is important in patients receiving rhPTH.

2.
Am J Health Syst Pharm ; 78(18): 1674-1680, 2021 Sep 07.
Article in English | MEDLINE | ID: mdl-33948625

ABSTRACT

PURPOSE: The case of a transgender female who developed gallstone pancreatitis in the context of estrogen use for gender-affirming hormone therapy is reported. SUMMARY: A 24-year-old Caucasian transgender female presented to the emergency department for abdominal pain and vomiting after referral from urgent care for suspected pancreatitis. Her home medications included estradiol, medroxyprogesterone, and spironolactone for gender-affirming hormone therapy and omeprazole for reflux. The patient reported minimal alcohol intake, presented with mildly elevated triglyceride levels, and did not have a family history of pancreatitis or gallstone disease. She underwent a laparoscopic cholecystectomy on hospital day 4 and was given a postoperative diagnosis of chronic cholecystitis, cholelithiasis, and pancreatitis. Given her history and the present illness, the use of estrogen therapy is a likely risk factor for the development of gallstone pancreatitis. CONCLUSION: Estrogen is a cornerstone of gender-affirming hormone therapy used by transgender women; however, in addition to its role in gender identity confirmation, estrogen can result in drug-induced pancreatitis.


Subject(s)
Gallstones , Pancreatitis , Transgender Persons , Adult , Estrogens/adverse effects , Female , Gallstones/diagnosis , Gallstones/diagnostic imaging , Gender Identity , Humans , Male , Pancreatitis/chemically induced , Pancreatitis/diagnosis , Young Adult
3.
Int J Obes (Lond) ; 44(6): 1210-1226, 2020 06.
Article in English | MEDLINE | ID: mdl-32066824

ABSTRACT

As the prevalence of obesity continues to grow worldwide, the health and financial burden of obesity-related comorbidities grows too. Cardiovascular disease (CVD) is clearly associated with increased adiposity. Importantly, women are at higher risk of CVD when obese and insulin resistant, in particular at higher risk of developing heart failure with preserved ejection fraction and ischemic heart disease. Increased aldosterone and mineralocorticoid receptor activation, aberrant estrogenic signaling and elevated levels of androgens are among some of the proposed mechanisms explaining the heightened CVD risk. In addition to traditional cardiovascular risk factors, understanding nontraditional risk factors specific to women, like excess weight gain during pregnancy, preeclampsia, gestational diabetes, and menopause are central to designing personalized interventions aimed to curb the epidemic of CVD. In the present review, we examine the available evidence supporting a differential cardiovascular impact of increased adiposity in women compared with men and the proposed pathophysiological mechanisms behind these differences. We also discuss women-specific cardiovascular risk factors associated with obesity and insulin resistance.


Subject(s)
Cardiovascular Diseases/epidemiology , Obesity/epidemiology , Comorbidity , Diabetes, Gestational , Female , Heart Disease Risk Factors , Humans , Insulin Resistance , Menopause , Pre-Eclampsia , Pregnancy , Prevalence , Weight Gain
4.
Curr Diab Rep ; 19(12): 161, 2019 12 11.
Article in English | MEDLINE | ID: mdl-31828525

ABSTRACT

PURPOSE OF REVIEW: Cardiovascular disease (CVD) is the leading cause of mortality in people with diabetes. Our aim was to review the pathophysiology of CVD in diabetes, review related landmark trials, and discuss the cardiovascular benefit of glucose-lowering agents. We have also discussed the role of controversial anti-platelet therapy. RECENT FINDINGS: Recent studies have shown the impact of glucose-lowering agents on CVD in people with diabetes. Statins are now recommended for all patients with diabetes over the age of 40 regardless of the LDL level given the cardiovascular benefit of these drugs. Current recommendations suggest a blood pressure < 130/80 for individuals with high cardiovascular risk. Cardiovascular risk reduction should be an important part of the management of diabetes. Focusing solely on glycemic control may not be the best therapeutic strategy. Multifactorial risk reduction should be taken into account. Lipid-lowering agents and anti-hypertensives should be a corner stone of treatment of diabetes. With currently available data, glucose-lowering agents with cardiovascular benefit should be started early in the disease process.


Subject(s)
Cardiovascular Diseases/physiopathology , Diabetes Complications/physiopathology , Blood Glucose/analysis , Cardiovascular Diseases/etiology , Cardiovascular Diseases/therapy , Diabetes Complications/complications , Diabetes Complications/prevention & control , Humans , Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use , Hypertension/etiology , Hypertension/therapy , Hypolipidemic Agents/therapeutic use , Risk Factors
5.
Am J Trop Med Hyg ; 94(6): 1376-9, 2016 Jun 01.
Article in English | MEDLINE | ID: mdl-27001756

ABSTRACT

Human rabies is a fatal disease, transmitted by saliva of infected animals, and the diagnosis requires a high index of suspicion. Very few cases are reported annually in the United States. We present a case of human rabies without a clear exposure history that masqueraded as serotonin syndrome.


Subject(s)
Rabies virus/classification , Rabies/virology , Serotonin Syndrome/etiology , Animals , Diagnosis, Differential , Fatal Outcome , Genome, Viral , Humans , Male , Middle Aged , Rabies/pathology , Rabies virus/genetics , Serotonin Syndrome/pathology
6.
Article in English | MEDLINE | ID: mdl-26126820

ABSTRACT

Several new oral anticoagulants (NOAC) have been recently studied and approved for the prevention and treatment of venous thromboembolism (VTE) which includes deep vein thrombosis and pulmonary embolism. Although, NOACs possess several advantages when compared to traditional therapy each has its own limitations; especially in the elderly and in patients with low body weight, renal impairment and in those with high risk of bleeding. Apixaban is a factor Xa inhibitor recently approved for the treatment and prevention of VTE in the United States. The purpose of this manuscript is to review describes the pharmacological properties of NAOC's and to discuss clinical trial results and clinical applications of these agents in the prevention and treatment of VTE with special emphasis on the role of apixaban.


Subject(s)
Anticoagulants/therapeutic use , Blood Coagulation/drug effects , Drug Discovery , Pyrazoles/therapeutic use , Pyridones/therapeutic use , Venous Thromboembolism/prevention & control , Administration, Oral , Anticoagulants/administration & dosage , Anticoagulants/adverse effects , Clinical Trials as Topic , Humans , Orthopedic Procedures/adverse effects , Pyrazoles/administration & dosage , Pyrazoles/adverse effects , Pyridones/administration & dosage , Pyridones/adverse effects , Secondary Prevention , Treatment Outcome , Venous Thromboembolism/blood , Venous Thromboembolism/etiology
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