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1.
J Emerg Med ; 52(2): 223-226, 2017 Feb.
Article in English | MEDLINE | ID: mdl-27717592

ABSTRACT

BACKGROUND: Sodium-glucose cotransporter-2 (SGLT2) inhibitor medications are a class of antihyperglycemic agents that increase urinary glucose excretion by interfering with the reabsorption of glucose in the proximal renal tubules. In May of 2015, the U.S. Food and Drug Administration released a warning concerning a potential increased risk of ketoacidosis and ketosis in patients taking these medications. CASE REPORT: We present a case of a 57-year-old woman with type 2 diabetes mellitus taking a combination of canagliflozin and metformin who presented with progressive altered mental status over the previous 2 days. Her work-up demonstrated a metabolic acidosis with an anion gap of 38 and a venous serum pH of 7.08. The serum glucose was 168 mg/dL. The urinalysis showed glucose > 500 mg/dL and ketones of 80 mg/dL. Further evaluation demonstrated an elevated serum osmolality of 319 mOsm/kg and an acetone concentration of 93 mg/dL. She was treated with intravenous insulin and fluids, and the metabolic abnormalities and her altered mental status resolved within 36 h. This was the first episode of diabetic ketoacidosis (DKA) for this patient. WHY SHOULD AN EMERGENCY PHYSICIAN BE AWARE OF THIS?: Diabetic patients on SGLT2 inhibitor medications are at risk for ketoacidosis. Due to the renal glucose-wasting properties of these drugs, they may present with ketoacidosis with only mild elevations in serum glucose, potentially complicating the diagnosis. Acetone is one of the three main ketone bodies formed during DKA and it may be present at considerable concentrations, contributing to the serum osmolality.


Subject(s)
Acetone/analysis , Diabetic Ketoacidosis/diagnosis , Sodium-Glucose Transporter 2/agonists , Acetone/blood , Antihypertensive Agents/adverse effects , Antihypertensive Agents/therapeutic use , Blood Glucose/analysis , Canagliflozin/adverse effects , Canagliflozin/therapeutic use , Diabetes Complications , Female , Humans , Insulin/pharmacology , Insulin/therapeutic use , Metformin/pharmacology , Metformin/therapeutic use , Middle Aged , Sodium-Glucose Transporter 2/therapeutic use
2.
Obstet Gynecol Surv ; 70(10): 633-43, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26490163

ABSTRACT

IMPORTANCE: When a major burn is suffered during pregnancy, the obstetric provider is challenged to respond on an evidence basis because personal experience usually is lacking. Currently, there is a paucity of publications to inform the obstetrician, guide practice, and impact early critical decision making. OBJECTIVE: The aims of this study were to summarize the available information on early management of burns during pregnancy and to identify components of best practices for optimal outcome. EVIDENCE ACQUISITION: The PubMed database was searched for relevant titles and abstracts involving pregnant patients suffering from second-/third-degree burns. Among these studies, the bibliographies were investigated for further relevant literature. A total of 114 studies were identified during the initial search, and only studies published in English and French were included for a total of 42. Variable data were available for 1141 patients, with complete data for 139 cases. Mediation and regression analysis were used for available data. Insufficient data were available to undertake a systematic review. RESULTS: Total body surface area of burns (TBSAB) was positively associated with maternal death, and the odds of maternal mortality increase by 1.08 per percentage increase of TBSAB (P < 0.001). Fetal survival depends on maternal survival (P ≤ 0.001). Maternal survival declines incrementally when TBSAB exceeds 55%, and inhalation injury further exacerbates maternal-perinatal risk. CONCLUSIONS: Emergent assessment of the pregnant burn victimincludes determination of gestational age, extent of TBSAB, presence of inhalation injury, and continuous fetal monitoring. If gestational age is 24 weeks or longer and TBSAB exceeds 55%, urgent cesarean delivery appears desirable for the mother and baby. RELEVANCE: A specific analysis of maternal-perinatal outcome based on TBSAB and gestational age is relevant to obstetric and emergency providers who provide care to pregnant burn patients.


Subject(s)
Burns/therapy , Health Personnel/standards , Practice Guidelines as Topic , Pregnancy Complications/therapy , Burns/diagnosis , Female , Fetal Monitoring , Fetal Mortality , Gestational Age , Humans , Maternal Health Services , Maternal Mortality , Perinatology , Pregnancy , Pregnancy Complications/diagnosis
3.
Clin Toxicol (Phila) ; 43(4): 243-53, 2005.
Article in English | MEDLINE | ID: mdl-16035200

ABSTRACT

Methyl parathion (MP) was used illegally to spray homes for insect control over approximately an 8-yr period. In an attempt to determine if there were any adverse health effects from this, health-screening evaluations were performed on 353 individuals living in homes that were illegally sprayed. The average subject spent 15.5 h a day in the home. Subjects from homes with high levels of MP (exposure group) were compared to controls that lived in homes with minimal or no MP. Subjects were aware of the levels of MP found in their homes and recall bias was likely. There were no significant differences in the symptoms reported or by the physician assessment of subacute or chronic toxicity between those in the exposure group and controls. No significant differences were found in growth and developmental evaluations. Three subjects were identified who most likely suffered acute toxicity from the initial exposure and were not appropriately diagnosed and treated. Cholinesterase determinations also did not differ between those in the exposure group and controls. When subjects from the exposure group were stratified by the level of MP in their home, those from homes with the highest levels appeared to have an increased likelihood of subacute toxicity and reported an increased number of neuropsychiatric symptoms (OR 2 for both evaluations).


Subject(s)
Insecticides/toxicity , Methyl Parathion/toxicity , Adolescent , Adult , Autonomic Nervous System Diseases/chemically induced , Autonomic Nervous System Diseases/epidemiology , Child , Child, Preschool , Cholinesterases/blood , Environmental Exposure , Female , Health , Humans , Infant , Insect Control , Insecticides/analysis , Insecticides/blood , Male , Methyl Parathion/analysis , Methyl Parathion/blood , Middle Aged , Parasympathetic Nervous System/drug effects , Risk Assessment
4.
J Intensive Care Med ; 20(1): 34-42, 2005.
Article in English | MEDLINE | ID: mdl-15665258

ABSTRACT

The authors performed a multicenter prospective observational study to evaluate the feasibility and safety of intravenous antihypertensive protocol for acute hypertension in patients with intracerebral hemorrhage (ICH). Twenty-seven patients with ICH and acute hypertension (mean age 61.37 +/- 14.27; 10 were men) were treated to maintain the systolic blood pressure (BP) below 160 mm Hg and diastolic BP below 90 mm Hg within 24 hours of symptom onset. Neurological deterioration (defined as a decrease in initial Glasgow Coma Scale score > or = 2) was observed in 2 (7.4%) of 27 patients during treatment. Among patients who underwent follow-up computed tomography, hematoma expansion (more than 33% increase in hematoma size at 24 hours) was observed in 2 (9.1%) of 22 patients. Patients treated within 6 hours of symptom onset were more likely to be functionally independent (modified Rankin scale < or = 2) at 1 month compared with patients who were treated between 6 and 24 hours (8 of 18 versus 0 of 9,P = .03). Aggressive pharmacological treatment of acute hypertension in patients with ICH can be initiated early with a low rate of neurological deterioration and hematoma expansion.


Subject(s)
Antihypertensive Agents/therapeutic use , Cerebral Hemorrhage/drug therapy , Hypertension/drug therapy , Acute Disease , Algorithms , Analysis of Variance , Cerebral Hemorrhage/complications , Cerebral Hemorrhage/diagnostic imaging , Cerebrovascular Circulation/drug effects , Feasibility Studies , Female , Humans , Hypertension/etiology , Male , Middle Aged , Prospective Studies , Tomography, X-Ray Computed
5.
Am J Emerg Med ; 20(6): 524-7, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12369026

ABSTRACT

This study was undertaken to determine the usually used approach to fetal monitoring in the emergency department (ED) of the less severely injured obstetric patient who has sustained blunt trauma. A written survey was sent to clinical directors of teaching programs in emergency medicine (EM) with inquiries on the usual way of monitoring, what studies were performed, and the usual disposition of the less-injured obstetric patient. From the 112 teaching programs surveyed in early 1996, there were 87 responses (78%). Seventy-eight percent of programs generally have fetal monitoring performed for 2 to 4 hours in obstetric trauma patients when the trauma is more than minor extremity injury. In 68%, fetal monitoring was not performed in the ED from the time of the initial assessment of fetal heart tones until the mother went to an obstetric area even though the average estimated time to radiographically clear a cervical spine was 36 minutes. In 92% of programs residents are taught cardiotocographic changes indicative of fetal distress but only 15% have such monitoring equipment in their department. However, 51% do have sonographic equipment in their department. Given a patient with a viable fetus who has no abdominal pain, 46% routinely use fetal monitoring if the mechanism is a simple fall whereas 92% use monitoring only if the mechanism is a rollover motor vehicle collision or a strike to the abdomen. It is generally recognized that fetal distress may occur subtly without overt clinical signs and that obstetric area monitoring for a period of several hours should take place. However, most teaching programs do not institute continuous fetal monitoring during the first 30 to 60 minutes that the mother is undergoing her work-up even though residents are taught such monitoring.


Subject(s)
Emergency Medical Services , Extremities/blood supply , Extremities/injuries , Pregnancy Complications , Wounds, Nonpenetrating , Abdominal Pain/etiology , Cardiotocography , Decision Making , Extremities/diagnostic imaging , Female , Fetal Monitoring , Heart Rate, Fetal/physiology , Humans , Maternal Welfare , Pregnancy , Pregnancy Complications/diagnostic imaging , Radiography , Trauma Severity Indices , Wounds, Nonpenetrating/complications , Wounds, Nonpenetrating/diagnostic imaging
6.
J Emerg Med ; 23(2): 191-7, 2002 Aug.
Article in English | MEDLINE | ID: mdl-12359290

ABSTRACT

Cardiac memory is an uncommonly recognized entity in which T wave inversions on electrocardiogram (EKG) appear consistent with ischemia. Persistent deep T wave inversions are seen after return of normal depolarization in leads where the T waves were normal before pacing. These changes are generally recognized to occur in association with artificial pacemakers but may occur with other entities with intrinsic ventricular ectopic focus of depolarization, such as intermittent left bundle branch block. Although consideration of ischemia should be given priority, awareness of the benign nature of cardiac memory may allow some patients to avoid unnecessary work-up and admission. Sometimes the diagnosis cannot be confirmed definitively in the Emergency Department (ED) because many patients who have pacemakers also have coronary artery disease and only after a negative work-up for ischemia can one retrospectively presume cardiac memory as the likely etiology.


Subject(s)
Cardiac Pacing, Artificial , Electrocardiography , Heart Conduction System/physiopathology , Adult , Aged , Atrial Flutter/therapy , Coronary Disease/diagnosis , Female , Humans , Male , Sick Sinus Syndrome/therapy
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