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5.
Arch Pediatr ; 26(7): 407-410, 2019 Oct.
Article in English | MEDLINE | ID: mdl-31630900

ABSTRACT

The extravasation of a calcium solution into soft tissue constitutes a medical emergency, and a lack of adequate management can lead to significant functional and cosmetic sequelae. Here, we report on the management of and long-term outcome in two children who experienced calcium infusion leakage. We also describe the emergency procedures used in cases of extravasation and discuss the role of negative pressure wound therapy as an appropriate adjunct to conventional techniques for dealing with serious extravasation-related injuries.


Subject(s)
Calcium Chloride/adverse effects , Calcium Gluconate/adverse effects , Extravasation of Diagnostic and Therapeutic Materials/complications , Negative-Pressure Wound Therapy , Soft Tissue Injuries/etiology , Soft Tissue Injuries/therapy , Adolescent , Calcium Chloride/administration & dosage , Calcium Gluconate/administration & dosage , Extravasation of Diagnostic and Therapeutic Materials/diagnosis , Humans , Infant, Newborn , Infusions, Intravenous , Male
6.
Ginekol Pol ; 89(8): 407-413, 2018.
Article in English | MEDLINE | ID: mdl-30215458

ABSTRACT

OBJECTIVE: This study aimed to investigate and compare the pregnancy and live birth rates in IVF cycles of frozen-thawed embryo transfers and fresh embryo transfers in a group of women with a high risk of Ovarian hyperstimulation syndrome (OHSS). MATERIAL AND METHODS: The study group consisted of 254 women with a high level of response to controlled ovarian hyperstimulation. The patients who received fresh cycle embryo transfers with calcium infusions are referred to as the Fresh Ca+ group, and those without the calcium therapy are called the Fresh Ca- group; and we used correspondingly similar terminology for the Frozen group. RESULTS: We observed no statistically significant differences between the cycles of fresh and frozen-thawed embryo transfers in patients with a high risk of OHSS in terms of implantation, clinical pregnancy, and live birth rates. Furthermore, these implantation, clinical pregnancy and live birth rates were not different in the cycles with or without calcium treatment. There was no statistical difference in the OHSS rates between the fresh and frozen-thawed cycles; although, the OHSS rates were less in the two calcium infusion groups (Fresh Ca+ and Frozen-thawed Ca+) than in the without-calcium group. There was no OHSS development in the subjects of the Frozen-thawed Ca+ group. CONCLUSION: Our study results suggest that fresh and frozen-thawed embryo transfers have similar IVF results in patients with a high risk of OHSS. Calcium infusion is beneficial in preventing OHSS without altering pregnancy rates. Both IVF protocols with calcium infusion can safely be applied in high-responder patients without lowering success rates.


Subject(s)
Blastocyst , Calcium Gluconate/administration & dosage , Cryopreservation , Embryo Transfer , Fertility Agents, Female/administration & dosage , Fertility/drug effects , Infertility/therapy , Ovulation Induction , Sperm Injections, Intracytoplasmic , Adult , Calcium Gluconate/adverse effects , Embryo Culture Techniques , Embryo Transfer/adverse effects , Female , Fertility Agents, Female/adverse effects , Humans , Infertility/diagnosis , Infertility/physiopathology , Infusions, Intravenous , Live Birth , Ovarian Hyperstimulation Syndrome/etiology , Ovarian Hyperstimulation Syndrome/physiopathology , Ovarian Hyperstimulation Syndrome/prevention & control , Ovulation Induction/adverse effects , Pregnancy , Pregnancy Rate , Retrospective Studies , Risk Factors , Sperm Injections, Intracytoplasmic/adverse effects , Treatment Outcome , Young Adult
7.
Plast Reconstr Surg ; 142(3): 699-707, 2018 09.
Article in English | MEDLINE | ID: mdl-29927835

ABSTRACT

BACKGROUND: Calcium gluconate extravasation is a process that can cause serious lesions, such as necrosis and calcification of the soft tissues. The aim of the present study was to analyze the beneficial effects of four possible local antidotes for calcium gluconate extravasation: hyaluronidase, sodium thiosulfate, triamcinolone acetonide, and physiologic saline solution. METHODS: Seventy-four BALB/c mice were used in the study. The substances selected for use in this study were calcium gluconate (4.6 mEq/ml), hyaluronidase (1500 IU/ml), sodium thiosulfate (25%), triamcinolone acetonide (40 mg/ml 0.5 mg/kg), and saline solution 0.9%. Five minutes were allowed to lapse after the calcium gluconate infiltration, and then an antidote was infiltrated. After 3 weeks, a skin biopsy was performed and a radiographic and histologic study was carried out. RESULTS: Only in the group infiltrated with sodium thiosulfate did all skin lesions disappear after the 3-week period after infiltration. In the radiographic study, calcium deposits larger than 0.5 mm were observed in 40 percent of cases without an antidote, in 33 percent with triamcinolone acetonide, in 13 percent with a saline solution, and in none with thiosulfate and hyaluronidase. In the histologic study, calcium deposits were found in 53 percent of cases without antidote, 100 percent of cases with triamcinolone acetonide, 33 percent of cases with saline solution, and 13 percent of cases with sodium thiosulfate or hyaluronidase. CONCLUSION: Sodium thiosulfate and hyaluronidase prevent the development of calcium deposits after calcium gluconate extravasation.


Subject(s)
Antidotes/therapeutic use , Calcinosis/chemically induced , Calcinosis/prevention & control , Calcium Gluconate/adverse effects , Skin Diseases/chemically induced , Skin Diseases/prevention & control , Animals , Hyaluronoglucosaminidase/therapeutic use , Male , Mice , Mice, Inbred BALB C , Prospective Studies , Saline Solution/therapeutic use , Thiosulfates/therapeutic use , Treatment Outcome , Triamcinolone Acetonide/therapeutic use
8.
Cardiovasc Toxicol ; 18(3): 290-293, 2018 06.
Article in English | MEDLINE | ID: mdl-29383633

ABSTRACT

Using calcium salts in management of amlodipine overdose is challenging. A 25-year-old male with known history of adult polycystic kidney disease presented with hypotension, tachycardia, and intact neurological status after ingestion of 450 mg of amlodipine. Immediately, normal saline infusion and norepinephrine were initiated. Two grams of calcium gluconate was injected, followed by intravenous infusion of 1.16 mg/kg/h. The patient was put on insulin-glucose protocol to maintain euglycemia and hyperinsulinemia. Electrocardiography demonstrated junctional rhythm. Serum creatinine was 2.5 mg/dL with metabolic acidosis. By the end of 24 h post-admission, his consciousness, blood pressure, and urine output were normal. Almost 32 h post-admission, he became disoriented and his oxygen saturation decreased and therefore was mechanically ventilated. Second chest X-ray showed pulmonary edema. Serum calcium level increased to 26.1 mg/dL. Calcium was discontinued, and furosemide infusion and calcitonin were intravenously administrated. Urine output increased and hemodialysis improved pulmonary edema and serum calcium level with no change in consciousness. Three days after admission, the patient became anuric and developed multi-organ failure and died 5 days post-admission. To avoid the consequences of excessive infusion of calcium in renal failure patients, the minimum calcium dose with close monitoring is recommended.


Subject(s)
Amlodipine/poisoning , Calcium Channel Blockers/poisoning , Calcium Gluconate/adverse effects , Hypercalcemia/chemically induced , Hypotension/drug therapy , Iatrogenic Disease , Tachycardia/drug therapy , Adult , Amlodipine/administration & dosage , Calcium Channel Blockers/administration & dosage , Calcium Gluconate/administration & dosage , Electrocardiography , Fatal Outcome , Humans , Hypercalcemia/blood , Hypercalcemia/diagnosis , Hypercalcemia/physiopathology , Hypotension/chemically induced , Hypotension/diagnosis , Hypotension/physiopathology , Kidney/physiopathology , Kidney Failure, Chronic/complications , Kidney Failure, Chronic/physiopathology , Male , Multiple Organ Failure/chemically induced , Risk Factors , Suicide , Tachycardia/chemically induced , Tachycardia/diagnosis , Tachycardia/physiopathology
9.
Ann Plast Surg ; 79(5): 444-449, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28570460

ABSTRACT

INTRODUCTION: Calcium gluconate extravasation is a process, which, while not common, occurs more frequently in neonatal intensive care units. The aim of this study is to present a number of cases of calcium gluconate extravasation, which have occurred in our hospital, and to carry out a review of those clinical cases published in the literature to obtain relevant epidemiological data. METHODS: Data were gathered on the medical histories of 5 patients who presented lesions secondary to calcium gluconate extravasation in our center. A review of the literature was also performed to include clinical cases of calcium gluconate extravasation already published. RESULTS: Data were collected on 60 cases published in 37 articles. Most patients (55%) were neonates. The average age of these neonates was 8 days. The commonest location of injuries was the back of the hand and wrist (42%). The 2 most frequent symptoms were the appearance of erythema (65%) and swelling/edema (48%) followed by the appearance of skin necrosis (47%), indurated skin (33%), and yellow-white plaques or papules (33%). Most cases are cured within a period of 3 to 6 months. Fifty percent of patients required surgery, and in 13% of cases, skin grafts were performed. The most frequent histological finding was the presence of calcium deposits. Other histological findings described were the presence of necrosis, lymphohistiocytic infíltrate, and granulomas. Most histological findings were located in the dermis. Most x-rays showing calcium deposits had been performed at 3 to 4 weeks. CONCLUSIONS: Calcium gluconate extravasation is a process, which, although infrequent, is associated with serious skin and soft-tissue lesions, mainly affecting infants. Further studies are needed to determine possible specific procedures to be carried out in these cases.


Subject(s)
Calcium Gluconate/adverse effects , Extravasation of Diagnostic and Therapeutic Materials/etiology , Hypocalcemia/drug therapy , Skin/drug effects , Aged , Calcium Gluconate/administration & dosage , Extravasation of Diagnostic and Therapeutic Materials/physiopathology , Female , Follow-Up Studies , Humans , Hypocalcemia/diagnosis , Incidence , Infant , Infant, Newborn , Infusions, Intravenous , Male , Risk Assessment , Sampling Studies , Skin/pathology
10.
BMC Musculoskelet Disord ; 16: 114, 2015 May 13.
Article in English | MEDLINE | ID: mdl-25963758

ABSTRACT

BACKGROUND: A novel therapeutic management of osteoarthritis (OA) of the knee was assessed. The study aimed to evaluate the effect of monthly sodium bicarbonate with a single (SBCG1) or double dose (SBCG2) of calcium gluconate injections on OA of the knee; as well as the efficacy and safety of both SBCG interventions in the long term. METHODS: A double-blind parallel-group clinical trial with 74 knee OA patients was performed during 12 months, both SBCG interventions were followed-up for another 6mo after intervention. The outcome variables were the Western Ontario-McMaster University Osteoarthritis Index (WOMAC), the Lequesne's functional index and joint-space width changes from serial radiographs. RESULTS: After 12 months, group SBCG1 decreased -14.8 (95% CI:-14.2, -17.0) and group SBCG2 decreased -14.6 (-16.9, -12.4) in the global WOMAC score, the mean changes represent 80% and 82% lessened pain, respectively. In the Lequesne Functional Index scale, SBCG1 decreased -11.9 (-10.4, -14.2) and SBCG2 decreased -11.9 (-13.8, -10.0), representing 66 and 69% of improvement. Both mean scores were maintained after intervention discontinued. SBCG2 improved the knees' joint space width more than SBCG1 at 3 and 18 months. Both SBCG interventions were well tolerated after 12 months of treatment CONCLUSION: A solution of sodium bicarbonate and calcium gluconate is effective on reducing the symptoms associated with OA. Its beneficial effect is maintained for one year of continuous monthly administration and at least for 6 months after the administration is discontinued. When the dose of calcium gluconate is increased, it prevents further narrowing of joint-space. TRIAL REGISTRATION: Clinicaltrials.gov NCT00977444 September 11, 2009.


Subject(s)
Calcium Gluconate/administration & dosage , Osteoarthritis, Knee/drug therapy , Sodium Bicarbonate/administration & dosage , Adult , Calcium Gluconate/adverse effects , Disease Progression , Double-Blind Method , Drug Therapy, Combination , Female , Humans , Injections, Intra-Articular , Male , Middle Aged , Osteoarthritis, Knee/physiopathology , Pain/drug therapy , Pain/etiology , Sodium Bicarbonate/adverse effects
11.
Iran J Kidney Dis ; 9(1): 67-70, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25599740

ABSTRACT

Calciphylaxis is a complication of chronic kidney disease characterized by necrotic lesion in the skin. Histological examination reveals microcalcification of medium-sized blood vessels. We report on a 21-month-old girl with end-stage renal disease with severe calcium-phosphate imbalance. Calciphylaxis process started when she received calcium gluconate intravenously the day before the surgery to correct hypocalcemia and continued progressively despite peritoneal dialysis and forced stopping calcium-containing medication. Pamidronate, 0.5 mg/kg/d, was administered for 6 days and then once a week for 5 weeks. After 1 week, the skin lesion started to heal and circulation improved, and after 6 weeks, all skin lesions completely recovered. Pamidronate was effective to stop calciphylaxis in this case with advanced renal insufficiency and severe calcium-phosphate imbalance. Medical or surgical debridement are not suggested and lesions might recover without scar by pamidronate.


Subject(s)
Calciphylaxis/drug therapy , Calcium Gluconate/adverse effects , Diphosphonates/therapeutic use , Hypocalcemia/drug therapy , Kidney Failure, Chronic/complications , Biopsy , Calciphylaxis/diagnosis , Calciphylaxis/etiology , Debridement , Female , Humans , Hypocalcemia/diagnosis , Hypocalcemia/etiology , Kidney Failure, Chronic/diagnosis , Kidney Failure, Chronic/therapy , Pamidronate , Risk Factors , Time Factors , Treatment Outcome , Wound Healing/drug effects , Young Adult
12.
Food Funct ; 6(3): 816-23, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25588126

ABSTRACT

The nano-composites of whey protein hydrolysate (WPH) chelated with calcium were fabricated in aqueous solution at 30 °C for 20 min, with the ratio of hydrolysate to calcium 15 : 1 (w/w). UV scanning spectroscopy, fluorescent spectroscopy, Fourier transform infrared spectroscopy, dynamic light scattering and atomic force microscopy were applied to characterize the structure of the WPH-calcium chelate. The nano-composites showed the successful incorporation of calcium into the WPH, indicating the interaction between calcium and WPH. The chelation of calcium ions to WPH caused molecular folding and aggregation which led to the formation of a WPH-calcium chelate of nanoparticle size, and the principal sites of calcium-binding corresponded to the carboxyl groups and carbonyl groups of WPH. The WPH-calcium chelate demonstrated excellent stability and absorbability under both acidic and basic conditions, which was beneficial for calcium absorption in the gastrointestinal tract of the human body. Moreover, the calcium absorption of the WPH-calcium chelate on Caco-2 cells was significantly higher than those of calcium gluconate and CaCl2 in vitro, suggesting the possible increase in calcium bioavailability. The findings suggest that the WPH-calcium chelate has the potential in making dietary supplements for improving bone health of the human body.


Subject(s)
Bone Density Conservation Agents/chemistry , Calcium, Dietary/analysis , Dietary Supplements/analysis , Intestinal Absorption , Nanocomposites/chemistry , Protein Hydrolysates/chemistry , Whey Proteins/chemistry , Absorption, Physiological , Binding Sites , Bone Density Conservation Agents/administration & dosage , Bone Density Conservation Agents/adverse effects , Bone Density Conservation Agents/metabolism , Caco-2 Cells , Calcium Chelating Agents/adverse effects , Calcium Chelating Agents/chemistry , Calcium Chloride/adverse effects , Calcium Chloride/metabolism , Calcium Gluconate/adverse effects , Calcium Gluconate/metabolism , Calcium, Dietary/administration & dosage , Calcium, Dietary/adverse effects , Calcium, Dietary/metabolism , Cell Survival , Chemical Phenomena , Dietary Supplements/adverse effects , Endopeptidases/metabolism , Enterocytes/metabolism , Humans , Nanocomposites/adverse effects , Particle Size , Protein Folding , Protein Hydrolysates/adverse effects , Protein Hydrolysates/metabolism , Proteolysis , Solubility , Whey Proteins/adverse effects , Whey Proteins/metabolism
13.
Fa Yi Xue Za Zhi ; 30(4): 304-6, 2014 Aug.
Article in English | MEDLINE | ID: mdl-25434095

ABSTRACT

The combination use of dexamethasone and calcium gluconate can be applied to hypersensitivity. Severe hypokalemia is a usual complication of dexamethasone and calcium gluconate therapy, which occurs frequently with therapeutic use. Fatal cases, accidental and intentional, occur frequently in forensic practice. The current case report presented a 43-year-old man with diabetes mellitus with infection, to whom dexamethasone and calcium gluconate were administered in the private clinic. With the development of such clinical symptoms of severe hypokalemia as quadriplegia, he was confirmed to have severe hypokalemia through a biochemical test before dying of arrhythmia. And also it presented pathophysiologic mechanism underlying severe hypokalemia as well as suggestions for clinical practice regarding combination use of dexamethasone and calcium gluconate.


Subject(s)
Anti-Inflammatory Agents/adverse effects , Calcium Gluconate/adverse effects , Dexamethasone/adverse effects , Hypokalemia/chemically induced , Adult , Diabetes Mellitus , Fatal Outcome , Humans , Male
14.
Circ Cardiovasc Interv ; 7(6): 806-12, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25351198

ABSTRACT

BACKGROUND: We aimed to test, for the first time, the feasibility of intracoronary delivery of an innovative, injectable bioabsorbable scaffold (IK-5001), to prevent or reverse adverse left ventricular remodeling and dysfunction in patients after ST-segment-elevation myocardial infarction. METHODS AND RESULTS: Patients (n=27) with moderate-to-large ST-segment-elevation myocardial infarctions, after successful revascularization, were enrolled. Two milliliters of IK-5001, a solution of 1% sodium alginate plus 0.3% calcium gluconate, was administered by selective injection through the infarct-related coronary artery within 7 days after myocardial infarction. IK-5001 is assumed to permeate the infarcted tissue, cross-linking into a hydrogel and forming a bioabsorbable cardiac scaffold. Coronary angiography, 3 minutes after injection, confirmed that the injection did not impair coronary flow and myocardial perfusion. Furthermore, IK-5001 deployment was not associated with additional myocardial injury or re-elevation of cardiac biomarkers. Clinical assessments, echocardiographic studies, 12-lead electrocardiograms, 24-hour Holter monitoring, blood tests, and completion of Minnesota Living with Heart Failure Questionnaires were repeated during follow-up visits at 30, 90, and 180 days after treatment. During a 6-month follow-up, these tests confirmed favorable tolerability of the procedure, without device-related adverse events, serious arrhythmias, blood test abnormalities, or death. Serial echocardiographic studies showed preservation of left ventricular indices and left ventricular ejection fraction. CONCLUSIONS: This first-in-man pilot study shows that intracoronary deployment of an IK-5001 scaffold is feasible and well tolerated. Our results have promoted the initiation of a multicenter, randomized controlled trial to confirm the safety and efficacy of this new approach in high-risk patients after ST-segment-elevation myocardial infarction. CLINICAL TRIAL REGISTRATION URL: http://www.clinicaltrials.gov. Unique identifier: NCT01226563.


Subject(s)
Absorbable Implants , Alginates/administration & dosage , Calcium Gluconate/administration & dosage , Myocardial Infarction/therapy , Regenerative Medicine/methods , Tissue Engineering/methods , Tissue Scaffolds , Ventricular Dysfunction, Left/therapy , Ventricular Function, Left , Ventricular Remodeling , Absorbable Implants/adverse effects , Adult , Aged , Alginates/adverse effects , Belgium , Calcium Gluconate/adverse effects , Feasibility Studies , Female , Germany , Glucuronic Acid/administration & dosage , Glucuronic Acid/adverse effects , Heart Function Tests , Hexuronic Acids/administration & dosage , Hexuronic Acids/adverse effects , Humans , Hydrogels , Injections, Intra-Arterial , Male , Middle Aged , Myocardial Infarction/diagnosis , Myocardial Infarction/physiopathology , Pilot Projects , Predictive Value of Tests , Surveys and Questionnaires , Time Factors , Tissue Scaffolds/adverse effects , Treatment Outcome , Ventricular Dysfunction, Left/diagnosis , Ventricular Dysfunction, Left/physiopathology
16.
Acta pediatr. esp ; 72(3): e105-e110, mar. 2014. ilus
Article in Spanish | IBECS | ID: ibc-121822

ABSTRACT

Las lesiones cutáneas por extravasación se producen por la salida o introducción directa de fármacos o líquidos al tejido celular subcutáneo en el transcurso de un tratamiento intravenoso. Los fármacos que con mayor frecuencia producen daño por extravasación son las soluciones hiperosmolares, los agentes vasopresores y los quimioterápicos. El gluconato cálcico es un ácido débil que se comporta como una solución hipertónica. Los neonatos, los ancianos y los pacientes ingresados en unidades de cuidados intensivos son la población que presenta este tipo de complicación con mayor frecuencia y gravedad, debido a su mala perfusión y delgadez de la piel y a la incapacidad para localizar el dolor. Los casos descritos en la bibliografía de necrosis cutánea por gluconato cálcico en neonatos son excepcionales. No hay una única forma de tratamiento de este tipo de patología. Se han empleado pautas conservadoras o tratamientos agresivos, con escisión amplia de los tejidos y cierre mediante injerto. Presentamos los casos de 2 recién nacidos con necrosis cutánea secundaria a la extravasación de gluconato cálcico, sin infección asociada, que evolucionaron favorablemente con tratamiento conservador, consistente en el empleo de apósitos de colágeno de origen porcino. Según nuestra experiencia, ésta podría ser una alternativa terapéutica útil en pacientes con esta infrecuente patología (AU)


Cutaneous injury due to extravasation is produced by leakage or direct introduction of drugs or fluids into the subcutaneous tissue during intravenous therapy. Hyperosmolar solutions, vasopressor agents and chemotherapy are the most frequently agents related to extravasation injury. Calcium gluconate is a weak acid that acts as a hypertonic solution. Infants, elderly patients and intensive care unit patients are prone to this type of complication and more serious effects can be observed in this population because of poor skin perfusion, thinning of cutaneous tissue and the inability to locate the pain. In the literature cases described of skin necrosis by calcium gluconate in neonates are exceptional. There is not standard treatment established for this pathology. Both conservative or aggressive management like wide excision of tissue and grafting has been used to treatment of this complication. We report two cases of neonatal skin necrosis secondary due to extravasation of calcium gluconate in which conservative treatment with dressings porcine collagen was successful. In our experience, this could be a useful therapeutic alternative in patients with this rare disease (AU)


Subject(s)
Humans , Male , Female , Infant, Newborn , Calcium Gluconate/adverse effects , Extravasation of Diagnostic and Therapeutic Materials/complications , Necrosis/chemically induced , Bandages, Hydrocolloid , Collagen/therapeutic use , Dermatitis, Contact/diagnosis
17.
Endocrine ; 46(3): 549-53, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24272596

ABSTRACT

The aim of this study was to compare the side effects of the pentagastrin test and the calcium stimulation test in patients with increased basal calcitonin concentration, especially the gender-specific differences of side effects. A total of 256 patients (123 females and 133 males, mean age of 56 ± 27 years, range 21-83 years) had both pentagastrin and calcium stimulation tests. All patients filled in a questionnaire regarding the side effects within 30 min after completion of the stimulation tests. The differences of side effects between female and male patients as well as between the pentagastrin stimulation test and the calcium stimulation test were evaluated. Warmth feeling was the most frequent occurring side effect in all patients who had both pentagastrin and calcium stimulation tests, followed by nausea, altered gustatory sensation, and dizziness. The incidences of urgency to micturate (p < 0.05) and dizziness (p < 0.05) were significantly increased in the female patients as compared to male patients by calcium stimulation test. Significant higher incidences of urgency to micturate (p < 0.05) and warmth feeling (p < 0.05) were found by calcium stimulation test as compared with those by pentagastrin test in female patients. The incidences of nausea (p < 0.05) and abdominal cramping (p < 0.05) in male patients were significantly higher by pentagastrin stimulation test than by calcium stimulation test. There is a significant gender-specific difference in side effects induced by calcium stimulation test. Female patients have fewer side effects by pentagastrin test than by calcium stimulation test. Male patients may tolerate the calcium stimulation test better than the pentagastrin test.


Subject(s)
Calcitonin/blood , Calcium Gluconate/adverse effects , Carcinoma, Medullary/diagnosis , Pentagastrin/adverse effects , Thyroid Function Tests/adverse effects , Thyroid Neoplasms/diagnosis , Adult , Aged , Aged, 80 and over , Carcinoma, Medullary/blood , Female , Humans , Male , Middle Aged , Sex Factors , Surveys and Questionnaires , Thyroid Neoplasms/blood , Young Adult
19.
Journal of Forensic Medicine ; (6): 304-306, 2014.
Article in English | WPRIM (Western Pacific) | ID: wpr-983922

ABSTRACT

The combination use of dexamethasone and calcium gluconate can be applied to hypersensitivity. Severe hypokalemia is a usual complication of dexamethasone and calcium gluconate therapy, which occurs frequently with therapeutic use. Fatal cases, accidental and intentional, occur frequently in forensic practice. The current case report presented a 43-year-old man with diabetes mellitus with infection, to whom dexamethasone and calcium gluconate were administered in the private clinic. With the development of such clinical symptoms of severe hypokalemia as quadriplegia, he was confirmed to have severe hypokalemia through a biochemical test before dying of arrhythmia. And also it presented pathophysiologic mechanism underlying severe hypokalemia as well as suggestions for clinical practice regarding combination use of dexamethasone and calcium gluconate.


Subject(s)
Adult , Humans , Male , Anti-Inflammatory Agents/adverse effects , Calcium Gluconate/adverse effects , Dexamethasone/adverse effects , Diabetes Mellitus , Fatal Outcome , Hypokalemia/chemically induced
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