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1.
Enferm. nefrol ; 26(2): 178-184, Abr-Jun 2023. tab, graf
Artigo em Espanhol | IBECS | ID: ibc-222847

RESUMO

Descripción del caso: Paciente con enfermedad renal crónica terminal en tratamiento de hemodiálisis desde hace 1 año. Acude a sesión de hemodiálisis refiriendo lesiones cutáneas muy dolorosas con aspecto necrótico de 2 semanas de evolu-ción en extremidades inferiores distales sugestivas de calcifi-laxis. Dados los antecedentes clínicos de fibrilación auricular paroxística, anticoagulada con acenocumarol y los factores de riesgo que presenta, se inician medidas inmediatas dado el mal pronóstico de dicha enfermedad. Descripción/evaluación del plan de cuidados: Se suspende tratamiento con acenocumarol iniciando anticoagulación con heparina de bajo peso molecular, también se suspenden los suplementos de vitamina D. Se inicia administración de bifos-fonatos como inhibidores del calcio, de tiosulfato de sodio como vasodilatador y quelante del fósforo. Se instaura pauta de analgesia siendo uno de los objetivos más importantes del plan de cuidados, el control del dolor, con la administración de opiáceos, antiinflamatorios no esteroideos o mórficos. Aunque fue de difícil manejo, el papel de enfermería ha sido fundamental para procurar el máximo confort. También fue muy importante la vigilancia y el cuidado de las lesiones para prevenir infecciones y controlar la enfermedad observándose una adversa y rápida evolución a pesar de las terapias coad-yuvantes, puesto que cuando se diagnosticó ya presentaba lesiones necróticas. Conclusiones: La calcifilaxis es una complicación poco fre-cuente pero grave que suele observarse en pacientes con enfermedad renal crónica, sobre todo en hemodiálisis. Eltratamiento es multidisciplinar y es importante identificar precozmente a estos pacientes. Desgraciadamente, como en nuestro caso, los resultados no son siempre favorables.(AU)


Case description: Patient with end-stage renal disease undergoing hemodialysis treatment for 1 year. The patient presents to the hemodialysis session with extremely painful necrotic-looking skin lesions on the distal lower extremities, suggestive of calciphylaxis, which have been present for 2 weeks. Given the patient’s medical history of paroxysmal atrial fibrillation and anticoagulation with acenocoumarol, along with the risk factors present, immediate measures are initiated due to the poor prognosis of this condition. Description/evaluation of the care plan: Acenocoumarol treatment is discontinued, and anticoagulation with low molecular weight heparin is initiated. Vitamin D supplements are also discontinued. Bisphosphonates are started as calcium inhibitors, sodium thiosulfate is administered as a vasodilator, and phosphate binder. An analgesic regimen is established, with pain control being one of the most important goals of he care plan. This includes the administration of opioids, nonsteroidal anti-inflammatory drugs, or morphine. Although challenging, the nursing role has been crucial in providing maximum comfort. Close monitoring and wound care are also important to prevent infections and control the disease, although an adverse and rapid progression was observed despite the adjunctive therapies, as necrotic lesions were already present at the time of diagnosis. Conclusions: Calciphylaxis is a rare but serious complication often observed in patients with chronic kidney disease, especially in those undergoing hemodialysis. Treatment is multidisciplinary, and early identification of these patients is important. Unfortunately, as in our case, the outcomes are not always favorable.(AU)


Assuntos
Humanos , Feminino , Idoso , Diálise Renal , Insuficiência Renal Crônica/complicações , Insuficiência Renal Crônica/tratamento farmacológico , Insuficiência Renal Crônica/mortalidade , Calciofilaxia , Cuidados de Enfermagem , Planejamento de Assistência ao Paciente , Nefrologia , Nefropatias , Pacientes Internados , Exame Físico
2.
Acta méd. colomb ; 47(2): 35-38, Apr.-June 2022. tab, graf
Artigo em Inglês | LILACS-Express | LILACS | ID: biblio-1419922

RESUMO

Abstract The advanced stages of chronic kidney disease are associated with mineral and bone metabolism disorders, which increase the risk of serious complications such as uremic calciphylaxis. Below we present the case of a 65-year-old male patient with multiple comorbidities, including stage 5 chronic kidney disease with long-term hemodialysis treatment, who presented refractory secondary hyperparathyroidism complicated by penile necrosis secondary to uremic calciphylaxis. We believe this case may be useful in sensitizing the medical community on the seriousness of uremic calciphylaxis, emphasizing the importance of prevention and early diagnosis before complications such as necrosis occur. (Acta Med Colomb 2022; 47. DOI:https://doi.org/10.36104/amc.2022.2224).


Resumen Los estadios avanzados de la enfermedad renal crónica se asocian a alteraciones en el metabolismo mineral óseo, lo cual aumenta el riesgo de complicaciones graves como la calcifilaxis urémica. A continuación se presenta el caso de un paciente masculino de 65 años, con múltiples comorbilidades, entre ellas enfermedad renal crónica estadio 5 en terapia de hemodiálisis durante largo tiempo, quien presentó hiperparatiroidismo secundario de difícil manejo y se complicó con necrosis peneana secundaria a calcifilaxis urémica. Se considera que este caso puede ser útil para sensibilizar a la comunidad médica sobre la gravedad de la calcifilaxis urémica por lo cual es muy importante la prevención y realización de un diagnóstico temprano antes de que se produzcan complicaciones como la necrosis. (Acta Med Colomb 2022; 47. DOI:https://doi.org/10.36104/amc.2022.2224).

3.
Dermatol. argent ; 27(4): 170-172, oct. - dic. 2021. il, graf
Artigo em Espanhol | LILACS, BINACIS | ID: biblio-1390655

RESUMO

La calcifilaxis o arteriolopatía urémica calcificante es una enfermedad rara que conlleva elevada morbilidad y una mortalidad de 40-80%. Se produce por la calcificación de los vasos de pequeño calibre y afecta sobre todo a los pacientes con insuficiencia renal crónica. Suele iniciarse con cambios en la coloración de la piel. Luego se produce ulceración, dolor y necrosis cutánea. Se presenta el caso de un varón de 70 años con insuficiencia renal crónica que desarrolló lesiones cutáneas dolorosas en los miembros inferiores.


Calciphylaxis or calcifying uremic arteriolopathy is a rare disease that carries high morbidity and mortality between 40% and 80%. It is produced by calcification of small caliber vessels and mainly affects patients with chronic renal failure. It usually begins with a change in skin color and then ulceration, pain and skin necrosis occur. We present a 70-year-old man with chronic renal failure who developed painful skin lesions on his lower limbs.


Assuntos
Humanos , Masculino , Idoso , Calciofilaxia/diagnóstico , Necrose , Extremidade Inferior , Insuficiência Renal
4.
Rev. argent. reumatolg. (En línea) ; 32(3): 15-18, set. 2021. ilus
Artigo em Espanhol | LILACS, BINACIS | ID: biblio-1365496

RESUMO

La calcifilaxis se caracteriza por una intensa deposición de calcio en pequeños vasos sanguíneos, piel y otros órganos, descripta principalmente en pacientes con insuficiencia renal crónica, trasplante renal o disfunción paratiroidea. Hasta la fecha, solo hay siete casos descriptos en la literatura de calcifilaxis que imita arteritis de células gigantes (ACG). En esta revisión presentamos el octavo caso documentado patológicamente.


Calciphylaxis is characterized by intense deposition of calcium in small blood vessels, skin, and other organs, described mainly in patients with chronic renal insufficiency, renal transplant of parathyroid dysfunction. To date, there are only seven cases described in literature of calciphylaxis mimicking giant cell arteritis (GCA). In this review, we present the eighth case pathologically documented.


Assuntos
Humanos , Masculino , Pessoa de Meia-Idade , Artérias Temporais/patologia , Arterite de Células Gigantes/diagnóstico , Calciofilaxia/diagnóstico , Calciofilaxia/patologia , Diagnóstico Diferencial
5.
Actas dermo-sifiliogr. (Ed. impr.) ; 112(8): 757-762, sept. 2021. tab
Artigo em Espanhol | IBECS | ID: ibc-213459

RESUMO

En los últimos años se han producido importantes avances en el conocimiento de la calcifilaxis, al haberse identificado nuevos factores de riesgo para su desarrollo, y hallazgos histológicos que podrían ser de ayuda al diagnóstico. Nuestro propósito al realizar este estudio ha sido revisar retrospectivamente los casos de calcifilaxis atendidos en nuestro hospital en los últimos 13 años, con especial atención a los aspectos más novedosos de esta patología. Se incluyó un total de 16 pacientes, 62,5% mujeres, con edad media de 67,9 años. Entre los factores asociados destacaron, aparte de la enfermedad renal avanzada (75%), los tratamientos relacionados con el metabolismo fosfocálcico (75%) y la anticoagulación (62,5%), en su mayoría con fármacos antagonistas de la vitamina K. En el estudio histológico se hallaron alteraciones en las fibras elásticas solo en un 25% de las biopsias. Once de los pacientes han fallecido, siendo la sepsis la primera causa de muerte (AU)


Recent years have seen important advances in our understanding of calciphylaxis, especially regarding newly identified risk factors and histologic findings that may aid diagnosis. This retrospective study of cases of calciphylaxis treated in our hospital in the last 13 years focuses on newly revealed aspects of this disease. We describe 16 patients (62.5% women; mean age, 67.9 years). In addition to advanced kidney disease (in 75% of our patients), other factors associated with the presence of calciphylaxis were a history of treatments related to phosphorus and calcium metabolism (75%) and anticoagulation (62.5%), usually with vitamin-K antagonists. Histology showed alterations in elastic fibers in only 25% of the biopsy specimens. Eleven of the patients died: sepsis was most often the cause (AU)


Assuntos
Humanos , Masculino , Feminino , Pessoa de Meia-Idade , Idoso , Idoso de 80 Anos ou mais , Atenção Terciária à Saúde , Calciofilaxia/diagnóstico , Calciofilaxia/patologia , Fatores de Risco
6.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-33939992

RESUMO

Recent years have seen important advances in our understanding of calciphylaxis, especially regarding newly identified risk factors and histologic findings that may aid diagnosis. This retrospective study of cases of calciphylaxis treated in our hospital in the last 13 years focuses on newly revealed aspects of this disease. We describe 16 patients (62.5% women; mean age, 67.9 years). In addition to advanced kidney disease (in 75% of our patients), other factors associated with the presence of calciphylaxis were a history of treatments related to phosphorus and calcium metabolism (75%) and anticoagulation (62.5%), usually with vitamin-K antagonists. Histology showed alterations in elastic fibers in only 25% of the biopsy specimens. Eleven of the patients died: sepsis was most often the cause.

8.
Actas Dermosifiliogr (Engl Ed) ; 112(2): 103-117, 2021 Feb.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-33075291
9.
Rev. argent. dermatol ; 101(1): 61-70, mar. 2020. graf
Artigo em Espanhol | LILACS | ID: biblio-1125807

RESUMO

Resumen La calcifilaxis es una enfermedad poco frecuente, aunque presenta una elevada tasa de mortalidad debido sobre todo a complicaciones como sepsis o gangrena. Generalmente se asocia a insuficiencia renal severa. Se define como la calcificación de la capa media de vasos de pequeño y mediano tamaño de la dermis y tejido celular subcutáneo. Clínicamente se manifiesta como un síndrome de livedoracemosa que progresa a púrpura retiforme y necrosis cutánea. La primera línea de tratamiento es el tiosulfato sódico.


Abstract Calciphylaxis is a rare disease, although it has a high mortality rate due mainly to complications such as sepsis or gangrene. It is usually associated with severe renal failure. It is defined as the calcification of the middle layer of small and medium-sized vessels of the dermis and subcutaneous cellular tissue. Clinically it manifests as a livedoracemosa syndrome that progresses to retinal purpura and cutaneous necrosis. The first line of treatment is sodium thiosulfate.


Assuntos
Humanos , Masculino , Pessoa de Meia-Idade , Calciofilaxia/diagnóstico , Calciofilaxia/terapia , Sepse/prevenção & controle , Calciofilaxia/mortalidade , Diagnóstico Diferencial , Necrose/complicações
10.
Rev. argent. dermatol ; 100(4): 71-80, dic. 2019. graf
Artigo em Espanhol | LILACS-Express | LILACS | ID: biblio-1092397

RESUMO

Resumen La calcifilaxis es un síndrome caracterizado por la calcificación de la pared media de las arteriolas de pequeño y mediano calibre de dermis y tejido celular subcutáneo, que se caracteriza clínicamente por úlceras necróticas, intensamente dolorosas, que afectan sobre todo miembros inferiores. Existen factores de riesgo para su desarrollo, como insuficiencia renal crónica, hiperparatiroidismo, sexo femenino, raza caucásica, diabetes, uso de anticoagulantes, entre otros. Si bien no existe un protocolo estandarizado para su tratamiento, se ha propuesto el uso del tiosulfato sódico como primera elección. Se presenta el caso de una paciente de sexo femenino de 75 años de edad con diagnóstico de calcifilaxis.


Abstract Calciphylaxis is a syndrome characterized by calciphication of the media of small and medium vessels of dermis and subcutaneous celular tissue, clinically characterized by extremely painful, necrotic ulcers, that affects especially lower limbs. There are risk factors for its development, such as renal failure, hyperparathyroidism, female gender, caucasian race, diabetes, use of anticoagulants, among others. Although there is not a standarized protocol for the treatment, it has been proposed the use of sodium thiosulfate as first line. We report a case of a woman of 75 years old with calciphylaxis.

11.
Rev. colomb. nefrol. (En línea) ; 6(1): 69-73, ene.-jun. 2019. tab, graf
Artigo em Espanhol | LILACS, COLNAL | ID: biblio-1093028

RESUMO

Resumen La calcifilaxis es una de las complicaciones menos comunes de la enfermedad renal crónica avanzada, sobretodo en terapia de sustitución renal, se desconoce la fisiopatología exacta de aparición, pero se cree, que es por una alteración en el metabolismo óseo-mineral. Se describe un caso clínico, de un paciente con enfermedad renal crónica, que presentó como complicación grave calcifilaxis, llegando a dicho diagnóstico gracias a las imágenes características de dicha patología tomadas del banco del servicio de imagenología del hospital. En conclusión, la calcifilaxis, a pesar de ser una patología difícil de encontrar en la actualidad, debido al mejor control del metabolismo óseo-mineral, se debe considerar en aquellos pacientes con progresión rápida de la enfermedad renal y con presencia de lesiones calcificadas supurativas en extremidades.


Abstract Calciphylaxis is one of the less common complications of Chronic Advanced Kidney Disease, especially in renal replacement therapy, the exact pathophysiology of its appearance is unknown, but it is believed that it is due to an alteration in bone-mineral metabolism. We describe a clinical case of a patient with chronic kidney disease, who presented as a serious complication calciphylaxis, reaching this diagnosis thanks to the characteristic images of this pathology taken from the bank of the Hospital's imaging service. In conclusion, calciphylaxis, despite being a pathology difficult to find nowadays due to better control of bone-mineral metabolism, should be considered especially in those patients with rapid progression of renal disease and presence of suppurative calcified lesions in extremities.


Assuntos
Humanos , Masculino , Feminino , Calciofilaxia , Terapia de Substituição Renal , Distúrbio Mineral e Ósseo na Doença Renal Crônica , Equador , Insuficiência Renal Crônica
12.
Colomb. med ; 49(4): 288-291, Oct.-Dec. 2018. graf
Artigo em Inglês | LILACS | ID: biblio-984310

RESUMO

Abstract Introduction: Calciphylaxis is an infrequent disease that almost exclusively affects patients with chronic kidney disease, although cases have been observed in patients without renal function impairment. The diagnosis is mainly made by clinical manifestations and subsequently confirmed by radiological and histological study. The optimal treatment is not known, although there is a consensus that a multifactorial approach is required. Clinical Case: A 68-year-old woman on hemodialysis for 2 years, who presented a painful nodular lesion in the left thigh, a skin biopsy was performed resulting in a diagnosis of calciphylaxis. Treatment and Outcome: Treatment was started with intravenous sodium thiosulfate. Pamidronate is added intravenously, three months later, due to an unfavorable evolution. After 6 months of treatment, improvement in nodular lesions and healing of the ulcerated lesion was observed to be generally well tolerated treatment. Conclusion: The combined treatment of sodium thiosulfate, pamidronate and calcitomimetics has been effectiveand safe for the treatment of calciphylaxis, inducing complete remission.


Resumen: Introducción: La calcifilaxis es una enfermedad infrecuente que afecta casi exclusivamente a pacientes con insuficiencia renal, aunque se han observado casos en pacientes sin deterioro de la función renal. El diagnóstico es clínico confirmándose con estudio radiológico e histológico. No se conoce con exactitud el tratamiento óptimo, aunque hay consenso en que se requiere un abordaje multifactorial. Caso Clínico: Mujer de 68 años en hemodiálisis desde hace 2 años, que presenta una lesión nodular dolorosa en muslo izquierdo, resultando un diagnostico compatible con calcifilaxis, tras biopsia cutánea. Tratamiento y resultado: Inicia tratamiento con tiosulfato de sodio vía venosa. Tres meses más tarde y ante la evolución desfavorable, se añade al tratamiento pamidronato vía intravenosa. Tras 6 meses de tratamiento se observa mejoría de las lesiones nodulares y cicatrización de la lesión ulcerada, habiéndose experimentado buena tolerancia. Conclusión: El tratamiento combinado de tiosulfato de sodio, pamidronato y calcimiméticos ha resultado efectivo y seguro para el tratamiento de la calcifilaxis, induciendo su remisión completa.


Assuntos
Idoso , Feminino , Humanos , Tiossulfatos/administração & dosagem , Calciofilaxia/tratamento farmacológico , Pamidronato/administração & dosagem , Falência Renal Crônica/complicações , Calciofilaxia/etiologia , Calciofilaxia/patologia , Quelantes/administração & dosagem , Diálise Renal/métodos , Resultado do Tratamento , Quimioterapia Combinada , Administração Intravenosa , Falência Renal Crônica/terapia
13.
Nefrologia (Engl Ed) ; 38(6): 579-586, 2018.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-30415999

RESUMO

Calciphylaxis, also known as calcific uraemic arteriolopathy, is a rare syndrome that typically causes skin necrosis and usually affects dialysis patients. Its pathogenesis is multifactorial and is the consequence of many factors causing ectopic calcifications in patients with chronic kidney disease, such as calcium-phosphate metabolism disorders, hyper- or hypo-parathyroidism, diabetes, obesity, systemic inflammation and the use of vitamin K antagonists, among others. From a clinical point of view, calciphylaxis may progress from painful purpura to extensive areas of skin necrosis that can potentially lead to superinfection and the death of the patient due to sepsis. Treatment is primarily based on managing the wounds, eliminating all the possible precipitating factors of ectopic calcification and administering agents which are capable of inhibiting the process of calcification.


Assuntos
Calciofilaxia/etiologia , Insuficiência Renal Crônica/complicações , Calciofilaxia/diagnóstico , Calciofilaxia/terapia , Humanos , Diálise Renal , Insuficiência Renal Crônica/terapia , Fatores de Risco
14.
Medicina (B.Aires) ; 77(4): 331-333, ago. 2017. ilus
Artigo em Espanhol | LILACS | ID: biblio-894489

RESUMO

La calcifilaxis es una vasculopatía caracterizada por isquemia y necrosis cutánea dolorosa debida a calcificación, fibroplastia de la íntima y trombosis de las arteriolas paniculares. Compromete más frecuentemente a pacientes con insuficiencia renal crónica terminal y tiene muy elevada mortalidad. La biopsia de las lesiones cutáneas se utiliza como método diagnóstico. No se han registrado hallazgos específicos de laboratorio. Las lesiones cutáneas generalmente comienzan en las extremidades a modo de moteado violáceo doloroso similar al livedo reticularis. La evolución natural es hacia úlceras y escaras. La primera línea de tratamiento consiste en el cuidado de las lesiones cutáneas y antibioticoterapia. El tiosulfato sódico se utiliza como tratamiento debido a su actividad como antioxidante y quelante. Se presentan dos casos clínicos.


Calciphylaxis is vasculopathy characterized by ischemia and painful skin necrosis due to calcification and intimal fibroplasia of thrombosis of the panicular arterioles. It most frequently compromises patients with terminal chronic renal failure and has a high mortality rate. Biopsy of skin lesions is used as a diagnostic method. No specific laboratory findings have been recorded. Skin lesions usually begin in the extremities like a painful purplish mottling similar to "livedo reticularis". The natural evolution is to ulcers and bedsores. The first line of treatment involves the care of skin lesions and antibiotic therapy. Sodium thiosulfate is used as treatment due to its antioxidant activity and as a chelating. Two clinical cases are here reported.


Assuntos
Humanos , Feminino , Adulto , Pessoa de Meia-Idade , Calciofilaxia/diagnóstico , Falência Renal Crônica/complicações , Calciofilaxia/etiologia , Calciofilaxia/terapia , Terapia Combinada , Desbridamento
15.
Nefrologia ; 37(5): 501-507, 2017.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-28390776

RESUMO

INTRODUCTION: Calcific uraemic arteriolopathy (CUA), also called calciphylaxis, is a rare but potentially fatal vascular disorder that almost exclusively affects patients with chronic renal failure. The objective of this study was to analyse various risk factors for developing CUA and its subsequent clinical course according to the treatment received. MATERIALS AND METHODS: A retrospective study that included patients diagnosed with CUA from December 1999 to December 2015. Various risk factors, clinical course and treatment options were analysed. RESULTS: A total of 28 patients (53.6% females) with a mean age of 67.2±11.8 (38-88) years were included. At the time of diagnosis, 53.6% were on haemodialysis, 25% were kidney transplant patients and 21.4% had normal renal function. The use of steroids (100%, P=.001) was the main risk factor in renal transplant patients. Skin lesions resolved in 60.7% (especially in those receiving multitargeted therapy). Patient survival at 12 months was 29% in transplant patients, 57% in haemodialysis patients and 100% in normal renal function patients (log-rank 6.88, P=.032). Chronic renal failure (P=.03) and hypoalbuminaemia (P=.02) were the main risk factor for CUA mortality. CONCLUSIONS: Although the incidence of CUA remains low, CUA mortality is very high, Special attention to its occurrence in kidney transplant patients and «non-renal¼ CUA forms is required. Oral anticoagulants and steroids appear to be the main risk factors, CUA is a challenge; a registry of patients and determining standard therapy are required.


Assuntos
Calciofilaxia/etiologia , Corticosteroides/efeitos adversos , Adulto , Idoso , Idoso de 80 Anos ou mais , Amputação Cirúrgica , Calciofilaxia/mortalidade , Calciofilaxia/terapia , Terapia por Quelação , Cinacalcete/uso terapêutico , Terapia Combinada , Difosfonatos/uso terapêutico , Feminino , Humanos , Hipoalbuminemia/complicações , Estimativa de Kaplan-Meier , Falência Renal Crônica/complicações , Falência Renal Crônica/cirurgia , Falência Renal Crônica/terapia , Transplante de Rim , Masculino , Pessoa de Meia-Idade , Pentoxifilina/uso terapêutico , Complicações Pós-Operatórias/etnologia , Complicações Pós-Operatórias/etiologia , Diálise Renal , Estudos Retrospectivos , Fatores de Risco , Resultado do Tratamento
16.
Nefrologia ; 37(1): 20-28, 2017.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-27697413

RESUMO

Phytate, or myo-inositol 1,2,3,4,5,6-hexakis dihydrogen phosphate (InsP6), is a naturally occurring phosphorus compound that is present in many foods, mainly legumes, whole grains and nuts. Patients with chronic kidney disease (CKD) have cardiovascular disease mortality up to 30times higher than the general population. Vascular calcifications (VCs) directly contribute to overall morbidity and mortality, especially in CKD. In part, this high mortality is due to elevated levels of phosphorus in the blood. Therefore, control of dietary phosphorus is essential. Dietary phosphorus can be classified according to its structure in organic phosphorus (plant and animal) and inorganic (preservatives and additives). Plant-phosphorus (legumes and nuts), mainly associated with InsP6, is less absorbable by the human gastrointestinal tract as the bioavailability of phosphorous from plant-derived foods is very low. Recent data indicate that restriction of foods containing plant phosphates may compromise the adequate supply of nutrients that have a beneficial effect in preventing cardiovascular events, such as InsP6 or fibre found in legumes and nuts. Experimental studies in animals and observational studies in humans suggest that InsP6 can prevent lithiasis and VCs and protect from osteoporosis. In conclusion, we need prospective studies to elucidate the potential benefits and risks of phytate (InsP6) through the diet and as an intravenous drug in patients on haemodialysis.


Assuntos
Calcinose/prevenção & controle , Doenças Cardiovasculares/prevenção & controle , Hiperfosfatemia/complicações , Fosfatos/metabolismo , Fósforo na Dieta/farmacocinética , Ácido Fítico/metabolismo , Insuficiência Renal Crônica/metabolismo , Urolitíase/prevenção & controle , Animais , Antioxidantes/metabolismo , Arteriosclerose/prevenção & controle , Disponibilidade Biológica , Calcinose/etiologia , Doenças Cardiovasculares/etiologia , Doenças Cardiovasculares/mortalidade , Distúrbio Mineral e Ósseo na Doença Renal Crônica/etiologia , Distúrbio Mineral e Ósseo na Doença Renal Crônica/prevenção & controle , Cinacalcete/uso terapêutico , Estudos Transversais , Fabaceae , Humanos , Hiperfosfatemia/mortalidade , Masculino , Estrutura Molecular , Nozes , Estudos Observacionais como Assunto , Osteoporose/tratamento farmacológico , Osteoporose/etiologia , Fósforo na Dieta/administração & dosagem , Fósforo na Dieta/efeitos adversos , Ácido Fítico/farmacologia , Ácido Fítico/uso terapêutico , Estudos Prospectivos , Ratos , Insuficiência Renal Crônica/complicações , Insuficiência Renal Crônica/dietoterapia , Urolitíase/etiologia
17.
Med. leg. Costa Rica ; 33(2): 123-132, sep.-dic. 2016. ilus
Artigo em Espanhol | LILACS | ID: lil-795913

RESUMO

Resumen:La calcifilaxis es una alteración vascular considerada como un síndrome multifactorial, que afecta la túnica media de las arterias más pequeñas causando isquemia del pene y esto a su vez una gangrena de rápida evolución.Su etiopatogenia aun no es muy clara y la bibliografía acerca de esta condición es escasa, a pesar de que su incidencia ha ido en aumento en los últimos años. La calcifilaxis del pene es una condición casi exclusiva para pacientes con insuficiencia renal crónica que reciben diálisis y frecuentemente es subdiagnosticada por los profesionales de la salud. Sus manifestaciones clínicas son altamente agresivas y de rápida evolución, además asocia una alta morbi-mortalidad por lo que debe diagnosticarse con la mayor brevedad posible. El manejo de los pacientes con calcifilaxis es multidisciplinario, en el intervienen tanto el urólogo como el nefrólogo y su tratamiento debe personalizarse según las condiciones de cada paciente, iniciando como primera medida con un manejoconservador y posteriormente quirúrgico si no se logra la respuesta deseada.


Abstract:Calciphylaxis is a vascular disorder, considered a multifactorial syndrome that affects the media of small caliber vessels, causing penile ischemia and in turn, rapidly evolving gangrene. Despite the raising incidence rates in recent years, literary information is limited, and its pathogenesis remains unclear. This condition is almost entirely attributed to chronic kidney disease patients receiving dialysis treatment, and is often clinically underdiagnosed by health care professionals. Clinically, calciphylaxis is considered to be rapidly evolving and highly aggressive, associated with high morbility and mortality rates, making prompt diagnosis imperative.


Assuntos
Humanos , Doenças do Pênis/complicações , Pênis/patologia , Calciofilaxia/complicações , Insuficiência Renal Crônica/complicações , Calcificação Vascular/diagnóstico , Costa Rica , Necrose
18.
Nefrologia ; 36(6): 597-608, 2016.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-27595517

RESUMO

Cardiovascular (CV) calcification is a highly prevalent condition at all stages of chronic kidney disease (CKD) and is directly associated with increased CV and global morbidity and mortality. In the first part of this review, we have shown that CV calcifications represent an important part of the CKD-MBD complex and are a superior predictor of clinical outcomes in our patients. However, it is also necessary to demonstrate that CV calcification is a modifiable risk factor including the possibility of decreasing (or at least not aggravating) its progression with iatrogenic manoeuvres. Although, strictly speaking, only circumstantial evidence is available, it is known that certain drugs may modify the progression of CV calcifications, even though a direct causal link with improved survival has not been demonstrated. For example, non-calcium-based phosphate binders demonstrated the ability to attenuate the progression of CV calcification compared with the liberal use of calcium-based phosphate binders in several randomised clinical trials. Moreover, although only in experimental conditions, selective activators of the vitamin D receptor seem to have a wider therapeutic margin against CV calcification. Finally, calcimimetics seem to attenuate the progression of CV calcification in dialysis patients. While new therapeutic strategies are being developed (i.e. vitamin K, SNF472, etc.), we suggest that the evaluation of CV calcifications could be a diagnostic tool used by nephrologists to personalise their therapeutic decisions.


Assuntos
Insuficiência Renal Crônica/complicações , Calcificação Vascular/diagnóstico , Calcificação Vascular/tratamento farmacológico , Calcimiméticos/uso terapêutico , Doença Crônica , Distúrbio Mineral e Ósseo na Doença Renal Crônica , Progressão da Doença , Humanos , Diálise Renal
19.
Rev. nefrol. diál. traspl ; 36(2): 99-102, mar. 2016. ilus
Artigo em Espanhol | LILACS | ID: biblio-1006119

RESUMO

Se presenta un caso clínico de una paciente de 23 años con enfermedad renal crónica estadio IIIa (ERC EIIIa), secundaria a glomerulopatía focal y segmentaria, que evoluciona con lesiones ulceradas de fondo necrótico dolorosas con biopsia compatible con calcifilaxis. Se suspende tratamiento inmunosupresor, bloqueante cálcicos y calcitriol e inicia tratamiento antibiótico, con buena evolución. La calcifilaxis es una enfermedad que afecta principalmente a pacientes con enfermedad renal terminal. Debido a su alta mortalidad, se deben aumentar los esfuerzos en la prevención de los factores de riesgo modificables y en el reconocimiento temprano. Reportamos el caso de una paciente con un Clearance de Creatinina de 53.8 ml/min. por CKD-EPI y factores predisponentes no convencionales para el desarrollo de la enfermedad demostrando que la calcifilaxis no es una entidad exclusiva de pacientes con enfermedad renal estadio V en terapia de sustitución


Calciphylaxis is a disease that affects mainly end-stage renal disease patients. Due to its high mortality, every effort should be taken to prevent modifiable risk factors and to make an early diagnosis. We report the case of a 23 year old patient with chronic renal disease stage IIIa (CKD IIIa) secondary to focal segmental glomerulopathy and 53.8 ml/min glomerular filtration rate calculated with the CKD-EPI formula, with non-conventional predisposing risk factors for disease development. Immunosuppressive treatment, calcium blockers, and calcitriol were stopped and antibiotic treatment was applied with good evolution. This case shows that calciphylaxis in not an exclusive entity seen in patients with stage V CKD on renal replacement therapy.


Assuntos
Calciofilaxia , Glomerulosclerose Segmentar e Focal , Insuficiência Renal Crônica
20.
Rev. nefrol. diál. traspl ; 36(1): 12-20, ene. 2016. ilus
Artigo em Espanhol | LILACS | ID: biblio-1005985

RESUMO

INTRODUCCIÓN: La calcifilaxis (CFX) es un síndrome caracterizado por depósito de calcio en la capa íntima y media de los vasos, proliferación, fibrosis y trombosis luminal, isquemia y necrosis tisular. Su reporte inicial y descripciones posteriores estuvieron asociados a la insuficiencia renal crónica terminal (IRCT). Hay poca información sobre el efecto que la recuperación de la función renal secundaria al trasplante renal produce en la incidencia de esta patología. MATERIAL Y MÉTODOS: Estudio retrospectivo unicéntrico. Se realizó un análisis retrospectivo de la cohorte de los 448 pacientes trasplantados de riñón y riñón y páncreas entre el 1 de enero de 2001 y el 1 de enero de 2014 en nuestro Servicio. RESULTADOS: Tres pacientes presentaron CFX confirmada por biopsia. En los 3 pacientes la CFX se asoció a hipercalcemia (calcemia promedio 11.5 mg/dl), en 2 de ellos al momento del diagnóstico. La Paratohormona intacta (PTHi) al momento del diagnóstico fue 2pg/ml, 62,3pg/ml y 3561pg/ml respectivamente. Dos pacientes eran diabéticos. Se halló hipoalbuminemia en los 3 pacientes. Sólo un paciente presentó obesidad, hiperfosfatemia y anticoagulación como factores de riesgo agregados. En todos los casos la biopsia proporcionó el diagnóstico de certeza para CFX. La mediana de la creatininemia en el momento del diagnóstico de CFX fue de 1,5 mg/dl (1,2mg/dl; 1,2mg/dl y 2mg/dl respectivamente) y el promedio de tiempo entre el trasplante y el desarrollo de CFX fue de 32 meses. En todos los casos se realizó un estricto control del fósforo, la hipercalcemia, las lesiones dérmicas y se administró tiosulfato de sodio IV durante 7 meses promedio. Se observó hipercalcemia al año post trasplante en el 19,59 % de los 448 pacientes estudiados, la evolución fue favorable dos pacientes, con control de la calcemia y mejoría de las manifestaciones cutáneas, y conservación de la función renal. CONCLUSIONES: La prevalencia de CFX luego de un TxR sobre un total de 448 pacientes trasplantados de riñón y de riñón y páncreas para el periodo 2001/2014 fue del 0,66%, inferior a los reportes de incidencia de CFX en diálisis. Los factores asociados a CFX en nuestros pacientes fueron la hipercalcemia al año post trasplante y al momento del evento, la hipoalbuminemia, la diabetes y los desórdenes de la glándula paratiroidea. La persistencia de la hipercalcemia al año post-trasplante renal debe ser un elemento de alta sospecha clínica de esta complicación


INTRODUCTION: Calciphylaxis (CFX) is a syndrome characterized by deposition of calcium in the intima and media of vessels, intimal proliferation, fibrosis, luminal thrombosis, tissue ischemia and necrosis. Its initial report and subsequent descriptions were associated with chronic renal failure. There is little information regarding the possible effect of the recovery of renal function secondary to kidney transplantation in the incidence of this disease. METHODS: Center retrospective study. We analyze in this report the three cases of patients who developed CFX after a renal transplant within a cohort of 448 kidney and kidney-pancreas transplant patients from January 1th 2001 to January 1th 2014 in our Hospital. RESULTS: Three patients were found to have CFX. All of them had hypercalcemia (serum calcium average 11.5 mg/dl) at first year post transplant and 2 patients at diagnosis of CFX. PTHi in the three CFX patients was 2 pg/ml, 62,3pg/ml and 3561pg/ml respectively. Hypoalbuminemia was found in all patients. Two patients were diabetic. Only one patient was obese and under anticoagulation treatment. In all cases a biopsy provided the diagnosis of certainty for calciphylaxis. Median serum creatinine at diagnosis was 1.5 mg/dl (1.2 mg/dl 1.2 mg/dl and 2 mg/dl, respectively) and the average time between transplantation and calciphylaxis diagnosis was 32 months. In all cases, strict control of phosphorus and hypercalcemia and sodium IV thiosulfate treatment was performed. The evolution was successful in two patients, controlling blood calcium and improving cutaneous manifestations with preservation of renal function. CONCLUSIONS: CFX prevalence in a cohort of 448 kidney and kidney-pancreas transplant patients from 2001 to 2014 was 0.66%, less than reported in dialysis patients. Factors associated with CFX in our patients were hypercalcemia in the first year after renal transplant and at the time of the event, hypoalbuminemia, diabetes and disorders of the parathyroid gland. The persistence of hypercalcemia in the first year after renal transplant should be an element of high clinical suspicion of this complication in the kidney transplant recipients


Assuntos
Humanos , Calciofilaxia , Transplante de Rim , Transplante de Pâncreas , Hipercalcemia
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