Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 20 de 101
Filtrar
1.
J Med Case Rep ; 18(1): 183, 2024 Mar 28.
Artículo en Inglés | MEDLINE | ID: mdl-38539274

RESUMEN

INTRODUCTION: Brain abscesses are rare but potentially fatal condition and can be associated with cyanotic congenital heart disease of which 5-18.7% of these patients that develop cerebral abscess commonly have tetralogy of Fallot (TOF). CASE PRESENTATION: We report a case of 3-year-old Muganda male that presented with convulsions, cyanosis and difficulty in breathing. The patient had a combination intervention of medical treatment and surgical drainage of the abscess. Post-operative Computerized tomography scan images and pre-operative brain Computerized tomography scans were compared. The multiple rings enhancing lesions were reduced in number and sizes. The largest measured ring was 44 × 22.5×16mm compared to the previous; 42 × 41×36mm. The mass effect had reduced from 16 mm to 7.5 mm. The periventricular hypodensities persisted. Findings showed radiological improvement with residual abscesses, subacute subdural hematoma and pneumocranium. The patient was treated with intravenous ceftriaxone 1 g OD for six weeks and he showed marked improvement and was discharged home after 3 months. CONCLUSION: A comprehensive strategy involving medications, surgical drainage, and early neurosurgical consultation is vital in treating brain abscesses in uncorrected TOF. Early identification of the pathogen, appropriate antibiotic therapy, and vigilant follow-up through clinical assessments and imaging are crucial, potentially spanning a 4-8-week treatment.


Asunto(s)
Absceso Encefálico , Cardiopatías Congénitas , Tetralogía de Fallot , Preescolar , Humanos , Masculino , Antibacterianos/uso terapéutico , Absceso Encefálico/complicaciones , Absceso Encefálico/diagnóstico por imagen , Ceftriaxona/uso terapéutico , Cianosis/tratamiento farmacológico , Cardiopatías Congénitas/complicaciones , Tetralogía de Fallot/complicaciones , Tetralogía de Fallot/diagnóstico por imagen , Tetralogía de Fallot/cirugía
3.
BMC Infect Dis ; 22(1): 538, 2022 Jun 13.
Artículo en Inglés | MEDLINE | ID: mdl-35692038

RESUMEN

BACKGROUND: Bronchiolitis, the most common cause of hospitalization in infancy has not yet a definitive treatment. This study was conducted to assess the effect of Zinc and vitamin D on treatment of infants with bronchiolitis. METHODS: In this double blind, randomized clinical trial, 94 infants aged 2 to 23 months, admitted in Mousavi Hospital in Zanjan, Iran, with the diagnosis of acute bronchiolitis were randomly assigned into 3 groups. The control group was only treated with hypertonic saline. The two case groups received either 100 unit/kg/day of Vitamin D or 20 mg/day of zinc in addition to hypertonic saline. Wheezing, duration of hospital stay, cough, cyanosis, respiratory distress and the respiratory rate in the first, third and seventh day of hospitalization were evaluated. RESULTS: There was no significant difference between groups in terms of age, sex, weight, passive smoking, wheezing, oxygen saturation, cyanosis and type of delivery. On the third day of hospitalization, the respiratory rate/min in the control group, the groups receiving vitamin D and zinc were 45.2 ± 10.7, 37.8 ± 3.9 and 41.1 ± 9.1 respectively and the result of repeated measure analysis didn't show any significant difference between the 3 groups (P = 0.562). Duration of hospitalization in the group receiving Vitamin D or zinc and in controls were 4.2 ± 2.6, 4.4 ± 2.2 and 5.1 ± 2.4 days respectively and this difference was not significant. Zinc receiving patients did not differ from the control group regarding to respiratory rate, cyanosis and wheezing. CONCLUSION: Vitamin D or zinc administration was not effective in reducing respiratory rate in children with bronchiolitis. Trial registration This project was approved by the Institutional Ethics Committee (IR, ZUMS.REC.1396.50), and registered on IRCT (IRCT20131217015835N7).


Asunto(s)
Bronquiolitis , Nebulizadores y Vaporizadores , Bronquiolitis/tratamiento farmacológico , Broncodilatadores/uso terapéutico , Niño , Cianosis/tratamiento farmacológico , Suplementos Dietéticos , Método Doble Ciego , Humanos , Lactante , Ruidos Respiratorios , Solución Salina Hipertónica/uso terapéutico , Índice de Severidad de la Enfermedad , Resultado del Tratamiento , Vitamina D/uso terapéutico , Zinc/uso terapéutico
4.
J Med Case Rep ; 16(1): 244, 2022 Jun 21.
Artículo en Inglés | MEDLINE | ID: mdl-35725643

RESUMEN

BACKGROUND: Methemoglobinemia is an excess of oxidized hemoglobin in the blood, affecting oxygen transportation. It is characterized by central cyanosis that does not respond to oxygen therapy. Prognosis is excellent when treated adequately and rapidly. We present a case report of a 38-year-old Caucasian man suffering from methemoglobinemia due to the use of poppers. CASE PRESENTATION: A 38-year-old Caucasian man known as a smoker and addicted to cocaine was admitted to the emergency department with dyspnea, agitation, and central cyanosis that started approximately 3 hours before admission. The persistent hypoxia despite high-flow oxygen therapy and a history of poppers use helped to reveal a condition known as methemoglobinemia. CONCLUSIONS: Our case highlighted a typical clinical presentation of methemoglobinemia. This possible life-threatening condition can occur after ingestion or inhalation of poppers, commonly sold in sex shops for recreational purposes. This can be easily confirmed by the methemoglobin level of the blood gases, provided the emergency physician considers this diagnosis. Rapid treatment with intravenous methylene blue is effective and leads to a favorable prognosis.


Asunto(s)
Cocaína/toxicidad , Metahemoglobinemia , Adulto , Cianosis/inducido químicamente , Cianosis/tratamiento farmacológico , Humanos , Hipoxia , Masculino , Metahemoglobinemia/inducido químicamente , Metahemoglobinemia/diagnóstico , Metahemoglobinemia/tratamiento farmacológico , Azul de Metileno/uso terapéutico , Oxígeno , Fumar
5.
Clin Toxicol (Phila) ; 60(8): 970-973, 2022 08.
Artículo en Inglés | MEDLINE | ID: mdl-35438593

RESUMEN

INTRODUCTION: While 4-chloro-1-nitrobenzene has oxidising properties and can lead to methaemoglobinaemia and haemolysis, such reports are rare. We herein describe two cases of 4-chloro-1-nitrobenzene poisoning after skin exposure and detail relevant clinical characteristics and treatment outcomes. CASE PRESENTATION: A 45-year-old man and his 32-year-old male co-worker presented at our department shortly after skin exposure to 4-chloro-1-nitrobenzene. They developed similar symptoms, including dizziness, dyspnoea, excessive fatigue, and coma. Patients' chest inspection yielded normal findings. Despite maximal oxygen supplementation, neither patient exhibited improvements in the following clinical parameters: diffuse cyanosis, chocolate-coloured blood, and decreased pulse oximetry. For patients 1 and 2, methaemoglobin levels at admission were 78.6% and 63.6%, and 4-chloro-1-nitrobenzene concentrations were 4.12 µg/mL and 2.89 µg/mL, respectively. Their symptoms and methaemoglobin levels improved after we cautiously administered methylene blue; we subsequently detected oxidative haemolysis (confirmed by peripheral blood smears) that later resolved without further aggravation. No further episodes of anaemia were documented via telephone follow-up for eight months after hospital discharge for either patient. DISCUSSION: Typical features of methaemoglobinaemia included diffuse cyanosis, dark chocolate-coloured blood, elevated partial pressure of oxygen, and decreased pulse oximetry saturation. Haemolysis likely occurred secondary to the toxic effects of 4-chloro-1-nitrobenzene.


Asunto(s)
Metahemoglobinemia , Adulto , Cianosis/tratamiento farmacológico , Hemólisis , Humanos , Masculino , Metahemoglobina , Metahemoglobinemia/tratamiento farmacológico , Azul de Metileno/uso terapéutico , Persona de Mediana Edad , Nitrobencenos , Oxígeno , Absorción Cutánea
6.
Transfus Apher Sci ; 61(2): 103299, 2022 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-34740513

RESUMEN

INTRODUCTION: Acquired methemoglobinemia may cause cyanosis and tissue ischemia unresponsive to oxygen supplementation. METHODS: We performed a literature search to identify cases of acquired methemoglobinemia published between 1980 and 2020. Clinical, diagnostic, and treatment details were extracted from eligible cases. RESULTS: A total of 76 reports involving 87 cases were analyzed. The median age at presentation was 32.5 with male to female ratio of 1.6. Cyanosis and SpO2 <90 % were reported in 82 % and 60 % of cases, respectively. Dapsone or cocaine-based anesthetics were causative in 52 % of cases; most anesthetic-related cases occurred in the peri-procedural setting. Methylene blue (MB) and red cell transfusion were given in 71 % and 10 % of cases, respectively. Compared to MB untreated patients, MB treated patients were more likely to be cyanotic (91.9 % vs 54.2 %), had higher proportions (%) and levels (g/dL) of methemoglobin (MetHb) - 33.2 % vs 15.3 % and 3.1 g/dL vs 1.2 g/dL, respectively. We found that among cyanotic cases, the median MetHb level was 3.0 g/dL (0.4-12.3 g/dL) with 74 % of values ≥ 1.5 g/dL. An SaO2:SpO2 ratio of >1 was not universally present, but always coincided with an [SaO2-SpO2] delta value greater than zero. CONCLUSIONS: Cyanosis and hypoxemia were not universal findings of acquired methemoglobinemia in our series. In addition, not all patients had cyanosis at MetHb ≥ 1.5 g/dL or an SaO2:SpO2 ratio of >1. All those with an SaO2:SpO2 >1 did, however, have a delta value greater than zero - a finding not previously reported which we feel holds diagnostic value.


Asunto(s)
Metahemoglobinemia , Cianosis/complicaciones , Cianosis/tratamiento farmacológico , Femenino , Humanos , Hipoxia , Masculino , Metahemoglobinemia/etiología , Metahemoglobinemia/terapia , Azul de Metileno , Oxígeno
9.
Expert Rev Clin Pharmacol ; 13(11): 1263-1270, 2020 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-32969724

RESUMEN

BACKGROUND: Cyanotic breath-holding spells (CBHS) are self-limited conditions among younger children. Frequent spells cause parents' fear and anxiety. Seizures, brain damage and sudden death have been rarely reported with BHS. Some reported spells' frequency reduction with iron or piracetam. We evaluated the effectiveness of valproic acid (VPA) to treat CBHS and predictors of improvement. METHODS: Participants were 90 children with CBHS (≥4/week) (age: 1.6±0.4yrs). They were treated with VPA (5 mg/kg/d). Follow-ups occurred after 3-≥6 months. Autonomic nervous system functions were evaluated. RESULTS: The majority (74.4%) had daily spells and 19% had ≥2 spells/d. Crying or anger provoked spells. Postural hypotension was found in 46.7%. They had normal electroencephalography and QT, QTc interval or QTd or QTcd and heart rate. Compared to controls, postural fall in systolic (>20mmHg) and diastolic (>10mmHg) blood pressures and mean arterial pressure (>10mmHg) were observed in 46.7%, 74.4% and 72.2% and miosis observed with 0.125% pilocarpine in 28.9% (P=0.001). Spells' frequency reduction (P=0.001) occurred within 3 months with VPA. The independent prdictors for spell' frequency reduction were reduction of anger and crying [OR=4.52(95%CI=2.35-6.04), P =0.01]. CONCLUSION: VPA therapy reduces CBHS' frequency. Mood improvement is a suggestive effective mechanism. CLINICAL TRIAL REGISTRATION: www.clinicaltrials.gov identifier is NCT04482764.


Asunto(s)
Anticonvulsivantes/uso terapéutico , Contencion de la Respiración/efectos de los fármacos , Cianosis/tratamiento farmacológico , Ácido Valproico/uso terapéutico , Afecto/efectos de los fármacos , Preescolar , Cianosis/etiología , Electroencefalografía , Femenino , Compuestos Ferrosos/uso terapéutico , Estudios de Seguimiento , Humanos , Lactante , Masculino , Proyectos Piloto , Piracetam/uso terapéutico , Estudios Prospectivos
10.
Am J Health Syst Pharm ; 76(22): 1835-1837, 2019 Oct 30.
Artículo en Inglés | MEDLINE | ID: mdl-31665765

RESUMEN

PURPOSE: Carfentanil is a synthetic opioid with an estimated potency that is 10,000 times more than that of morphine and 100 times more than that of fentanyl. Although there is a paucity of evidence, when considering the potency of carfentanil, it is reasonable to speculate that larger doses of naloxone may be required to resuscitate patients after carfentanil ingestion. This case report discusses the use of high-dose naloxone in 2 patients with suspected carfentanil overdose presenting to a small community hospital. SUMMARY: Two patients with suspected carfentanil overdose presented to a 30-bed emergency department at a community hospital in New Hampshire. Cyanosis and respiratory distress were noted in both instances, and airway intervention was ultimately deemed necessary. Patient 1 required a total of 12 mg of naloxone to be successfully resuscitated, while patient 2 required a total of 10 mg for resuscitation. Both patients were successfully resuscitated with high doses of naloxone. The use of high-dose naloxone prevented the need for intubation in these patients. CONCLUSION: While more robust studies should be considered, emergency personnel should be comfortable using higher-than-standard doses of naloxone in appropriate cases.


Asunto(s)
Analgésicos Opioides/envenenamiento , Sobredosis de Droga/tratamiento farmacológico , Fentanilo/análogos & derivados , Naloxona/administración & dosificación , Naloxona/uso terapéutico , Antagonistas de Narcóticos/administración & dosificación , Antagonistas de Narcóticos/uso terapéutico , Trastornos Relacionados con Opioides/tratamiento farmacológico , Adulto , Reanimación Cardiopulmonar/métodos , Cianosis/inducido químicamente , Cianosis/tratamiento farmacológico , Femenino , Fentanilo/envenenamiento , Hospitales Comunitarios , Humanos , Masculino , Esquizofrenia/complicaciones , Trastornos Relacionados con Sustancias/complicaciones
11.
Arch. argent. pediatr ; 116(4): 612-615, ago. 2018. ilus, tab, graf
Artículo en Español | LILACS, BINACIS | ID: biblio-950053

RESUMEN

La metahemoglobinemia es una patología caracterizada por la presencia de altas concentraciones de metahemoglobina en sangre. Esta es una forma oxidada de la hemoglobina, muy afín al oxígeno, que es incapaz de cederlo a los tejidos. Es una entidad poco frecuente, con baja sospecha diagnóstica. Aunque puede ser congénita en recién nacidos con cianosis, es más frecuente la adquirida por fármacos y tóxicos. En la Argentina, no se conoce la incidencia real de esta patología. El objetivo es comunicar un caso de metahemoglobinemia en una paciente pediátrica que ingresó al Hospital Magdalena V. de Martínez con cianosis en la cara y las extremidades, en mal estado general, con el antecedente de ingesta de varios comprimidos de dapsona, y se constató concentración sérica de metahemoglobina del 35%. El tratamiento consistió en la administración endovenosa de azul de metileno. Su evolución fue favorable.


Methemoglobinemia is a condition characterized by a high blood concentration of methemoglobin. Methemoglobinemia is a disorder that occurs when hemoglobin in the blood is oxidized to form methemoglobin, rendering it unable to transport oxygen. Although it can be congenital in cyanotic newborn, it is more often an adverse medication effect. The aim is to report a pediatric methemoglobinemia case, assisted in Magdalena V. de Martínez Hospital, with cyanosis in face and limb, in poor condition, that consumed dapsone accidentally. Her methemoglobin concentration was 35%. Intravenous methylene blue was administered with favorable outcome.


Asunto(s)
Humanos , Femenino , Niño , Cianosis/inducido químicamente , Metahemoglobinemia/inducido químicamente , Cianosis/tratamiento farmacológico , Dapsona/envenenamiento , Inhibidores Enzimáticos/administración & dosificación , Metahemoglobinemia/tratamiento farmacológico , Azul de Metileno/administración & dosificación
12.
Arch Argent Pediatr ; 116(4): e612-e615, 2018 08 01.
Artículo en Español | MEDLINE | ID: mdl-30016042

RESUMEN

Methemoglobinemia is a condition characterized by a high blood concentration of methemoglobin. Methemoglobinemia is a disorder that occurs when hemoglobin in the blood is oxidized to form methemoglobin, rendering it unable to transport oxygen. Although it can be congenital in cyanotic newborn, it is more often an adverse medication effect. The aim is to report a pediatric methemoglobinemia case, assisted in Magdalena V. de Martínez Hospital, with cyanosis in face and limb, in poor condition, that consumed dapsone accidentally. Her methemoglobin concentration was 35%. Intravenous methylene blue was administered with favorable outcome.


La metahemoglobinemia es una patología caracterizada por la presencia de altas concentraciones de metahemoglobina en sangre. Esta es una forma oxidada de la hemoglobina, muy afín al oxígeno, que es incapaz de cederlo a los tejidos. Es una entidad poco frecuente, con baja sospecha diagnóstica. Aunque puede ser congénita en recién nacidos con cianosis, es más frecuente la adquirida por fármacos y tóxicos. En la Argentina, no se conoce la incidencia real de esta patología. El objetivo es comunicar un caso de metahemoglobinemia en una paciente pediátrica que ingresó al Hospital Magdalena V. de Martínez con cianosis en la cara y las extremidades, en mal estado general, con el antecedente de ingesta de varios comprimidos de dapsona, y se constató concentración sérica de metahemoglobina del 35%. El tratamiento consistió en la administración endovenosa de azul de metileno. Su evolución fue favorable.


Asunto(s)
Cianosis/inducido químicamente , Dapsona/envenenamiento , Metahemoglobinemia/inducido químicamente , Niño , Cianosis/tratamiento farmacológico , Inhibidores Enzimáticos/administración & dosificación , Femenino , Humanos , Metahemoglobinemia/tratamiento farmacológico , Azul de Metileno/administración & dosificación
16.
Medicine (Baltimore) ; 96(24): e7105, 2017 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-28614229

RESUMEN

RATIONALE: Few studies had reported syndromes that include patent ductus arteriosus (PDA) with Eisenmenger syndrome and congenital deafness clustered in male siblings without facial, skeletal, or mental abnormalities. PATIENT CONCERNS: Two brothers, who were deaf and had PDA with Eisenmenger complex, were first seen at our Cardiology clinic at the ages of 25 and 41, respectively. They presented with progressive dyspnea on exertion. Upon physical examination, both brothers had clubbing and/or cyanotic toes, normal fingers, and without facial, skeletal, ophthalmological, or mental abnormalities. DIAGNOSES AND INTERVENTIONS: Echocardiography and multidetector computed tomography revealed large PDAs in both brothers. Cardiac catheterization showed bidirectional shunting via the PDA. OUTCOMES AND LESSONS: Familial clustering of Eisenmenger PDA and congenital deafness is rare. Further studies are warranted to define possible genetic links.


Asunto(s)
Cianosis/complicaciones , Sordera/complicaciones , Conducto Arterioso Permeable/complicaciones , Complejo de Eisenmenger/complicaciones , Adulto , Cianosis/diagnóstico , Cianosis/tratamiento farmacológico , Sordera/diagnóstico , Sordera/tratamiento farmacológico , Diagnóstico Diferencial , Conducto Arterioso Permeable/diagnóstico , Conducto Arterioso Permeable/tratamiento farmacológico , Complejo de Eisenmenger/diagnóstico , Complejo de Eisenmenger/tratamiento farmacológico , Humanos , Hermanos
18.
Croat Med J ; 58(6): 424-430, 2017 Dec 31.
Artículo en Inglés | MEDLINE | ID: mdl-29308834

RESUMEN

This is the first report describing a severe form of cold agglutinin-induced acrocyanosis with cutaneous necrosis after Mycoplasma infection in a 9-year-old patient without any other severe symptoms and laboratory alterations. We also present the results of two non-invasive methods used to determine the viability of tissues, degree of tissue perfusion impairment, and the responsiveness of the microvasculature. Laser Doppler flowmetry and laser speckle contrast imaging, both suitable to measure tissue blood perfusion non-invasively, have been used in the diagnosis and follow-up of various peripheral vascular diseases. In our patient, we demonstrated remarkably reduced microcirculation before the treatment and a significant perfusion increase in the acral regions after pentoxifylline therapy. The investigational techniques were useful tools to assess and quantify the severity of peripheral perfusion disturbances and to monitor the efficacy of the treatment in our patient.


Asunto(s)
Cianosis/etiología , Hemaglutininas/efectos adversos , Mycoplasma pneumoniae/aislamiento & purificación , Neumonía por Mycoplasma/complicaciones , Administración Oral , Antibacterianos/uso terapéutico , Anticuerpos Antibacterianos/sangre , Niño , Claritromicina/uso terapéutico , Crioglobulinas/efectos adversos , Cianosis/tratamiento farmacológico , Quimioterapia Combinada , Ecocardiografía , Femenino , Humanos , Infusiones Intravenosas , Flujometría por Láser-Doppler , Pentoxifilina/uso terapéutico , Neumonía por Mycoplasma/tratamiento farmacológico , Neumonía por Mycoplasma/inmunología , Vasodilatadores/uso terapéutico
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA
...