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1.
Chinese Journal of Nephrology ; (12): 393-397, 2023.
Article in Chinese | WPRIM | ID: wpr-994991

ABSTRACT

Calciphylaxis is a vascular disease caused by a combination of multiple factors, and the calcified ischemic lesion results in the severe skin damage accompanied by unbearable pain. Calciphylaxis tends to occur in patients with end-stage renal disease, and the treatment of this disease faces enormous challenges. Current treatment recommendations are mainly based on clinical experience and observational research reports, and there is still a lack of clinical practice standards or consensus for managing calciphylaxis. Therefore, this paper will review the effective treatment methods and off-label use of calciphylaxis based on literature reports, providing reference for the clinical treatment of the disease.

2.
Acta méd. colomb ; 47(2): 35-38, Apr.-June 2022. tab, graf
Article in English | LILACS-Express | LILACS | ID: biblio-1419922

ABSTRACT

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.
Chinese Journal of Nephrology ; (12): 313-319, 2022.
Article in Chinese | WPRIM | ID: wpr-933862

ABSTRACT

Objective:To observe the efficacy and safety of roxadustat in the treatment of renal anemia in calciphylaxis dialysis patients who had poor response to recombinant human erythropoietin (rHuEPO).Methods:This study was a prospective cohort study. The dialysis patients who were diagnosed with calciphylaxis and had previous regular use of rHuEPO≥3 months with hemoglobin (Hb) levels<110 g/L in the Department of Nephrology of Zhong Da Hospital affiliated to Southeast University from January 1, 2019 to March 28, 2021 were recruited. The effect of oral roxadustat in calciphylaxis dialysis patients with renal anemia was analyzed by self-comparison method.Results:There were totally 18 calciphylaxis dialysis patients with renal anemia enrolled in the study and the age was (49.7±16.2) years old, including 11 males and 7 females, and 14 cases on hemodialysis and 4 cases on peritoneal dialysis. The high-sensitivity C-reactive protein level was 27.3(15.6, 48.5) mg/L(reference value 0-3 mg/L) at baseline. The baseline Hb level was (85.4±11.6) g/L, and after 3 months of oral roxadustat, the Hb level was (105.8±15.2) g/L ( t=-9.282, P<0.001). The Hb compliance rate was 44.4%(8/18). Ferritin decreased significantly at 3 months compared with the baseline level [208.0(59.0, 306.3) μg/L vs 229.0(127.3, 385.2) μg/L, Z=-3.637, P<0.001]. The total iron binding capacity level increased significantly compared with the baseline level [127.0(65.0, 211.5) μmol/L vs 105.5(43.8, 153.7) μmol/L, Z=-2.156, P=0.031]. Transferrin saturation level at 3 months was lower than that at baseline, but there was no significant difference [20.2%(14.2%, 27.7%) vs 20.5%(18.7%, 34.9%), Z=-1.546, P=0.122]. No adverse reactions occurred during the observation period. Conclusion:The application of roxadustat can effectively correct Hb level and improve iron metabolism with high safety in calciphylaxis dialysis patients with renal anemia under inflammatory status.

4.
Dermatol. argent ; 27(4): 170-172, oct. - dic. 2021. il, graf
Article in Spanish | LILACS, BINACIS | ID: biblio-1390655

ABSTRACT

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.


Subject(s)
Humans , Male , Aged , Calciphylaxis/diagnosis , Necrosis , Lower Extremity , Renal Insufficiency
5.
Rev. argent. reumatolg. (En línea) ; 32(3): 15-18, set. 2021. ilus
Article in Spanish | LILACS, BINACIS | ID: biblio-1365496

ABSTRACT

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.


Subject(s)
Humans , Male , Middle Aged , Temporal Arteries/pathology , Giant Cell Arteritis/diagnosis , Calciphylaxis/diagnosis , Calciphylaxis/pathology , Diagnosis, Differential
6.
J. bras. nefrol ; 43(2): 274-278, Apr.-June 2021. tab, graf
Article in English, Portuguese | LILACS | ID: biblio-1286939

ABSTRACT

ABSTRACT Introduction: The clinical impact of vascular calcification is well established in the context of cardiovascular morbidity and mortality, but other clinical syndromes, such as calciphylaxis, although less frequent, have a significant impact on chronic kidney disease. Methods: Case report of a 27-year-old woman, who had complained of bilateral pain in her toes for 3 days, with the presence of small necrotic areas in the referred sites. She had a history of type 1 diabetes (25 years ago), with chronic kidney disease, on peritoneal dialysis, in addition to rheumatoid arthritis. She was admitted to the hospital, which preceded the current condition, due to exacerbation of rheumatoid arthritis, evolving with intracardiac thrombus due to venous catheter complications, when she started using warfarin. Ischemia progressed to her feet, causing the need for bilateral amputations. Her chirodactyls were also affected. Thrombophilia, vasculitis, endocarditis or other embolic sources were investigated and discarded. Her pathology report evidenced skin necrosis and superficial soft parts with recent arterial thrombosis, and Monckeberg's medial calcification. We started treatment with bisphosphonate and sodium thiosulfate, conversion to hemodialysis and replacement of warfarin with unfractionated heparin. Despite all the therapy, the patient died after four months of evolution. Discussion: Calciphylaxis is a rare microvasculature calcification syndrome that results in severe ischemic injuries. It has pathogenesis related to the mineral and bone disorder of chronic kidney disease combined with the imbalance between promoters and inhibitors of vascular calcification, with particular importance to vitamin K antagonism. Conclusion: The preventive strategy is fundamental, since the therapy is complex with poorly validated effectiveness.


RESUMO Introdução: O impacto clínico da calcificação vascular está bem estabelecido no âmbito de morbimortalidade cardiovascular, mas outras síndromes clínicas, como a calcifilaxia, apesar de menos frequente, têm significante impacto na doença renal crônica. Métodos: Relato de caso de mulher, 27 anos, com queixa de dor em pododáctilos bilateralmente havia 3 dias, com presença de pequenas áreas necróticas nos locais referidos. Antecedente pessoal de diabetes tipo 1 (há 25 anos), com doença renal crônica, em diálise peritoneal, além de artrite reumatoide. Teve internação hospitalar, que antecedeu o quadro atual, devido à exacerbação da artrite reumatoide, evoluindo com trombo intracardíaco por complicação de cateter venoso, quando iniciou uso de varfarina. A isquemia progrediu para pés com necessidade de amputações bilaterais. Quirodáctilos também foram acometidos. Trombofilias, vasculites, endocardite ou outras fontes emboligênicas foram pesquisadas e descartadas. Anatomopatológico evidenciou: necrose de pele e partes moles superficiais com trombose arterial recente e calcificação medial de Monckeberg. Tratamento foi instituído com bisfosfonato e tiossulfato de sódio, conversão para hemodiálise e substituição de varfarina por heparina não fracionada. Apesar de toda a terapia, a paciente foi a óbito após quatro meses de evolução. Discussão: A calcifilaxia é uma rara síndrome de calcificação da microvasculatura que resulta em graves lesões isquêmicas. Tem patogênese relacionada ao distúrbio mineral e ósseo da doença renal crônica combinado com o desbalanço entre promotores e inibidores de calcificação vascular, com particular importância ao antagonismo da vitamina K. Conclusão: A estratégia preventiva é fundamental, uma vez que a terapia é complexa e de eficácia pouco validada.


Subject(s)
Humans , Female , Adult , Calciphylaxis/complications , Kidney Failure, Chronic , Heparin , Dialysis , Extremities , Necrosis
7.
Rev. argent. dermatol ; 101(1): 61-70, mar. 2020. graf
Article in Spanish | LILACS | ID: biblio-1125807

ABSTRACT

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.


Subject(s)
Humans , Male , Middle Aged , Calciphylaxis/diagnosis , Calciphylaxis/therapy , Sepsis/prevention & control , Calciphylaxis/mortality , Diagnosis, Differential , Necrosis/complications
8.
Philippine Journal of Urology ; : 19-22, 2020.
Article in English | WPRIM | ID: wpr-962129

ABSTRACT

@#Penile calciphylaxis is a rare penile condition associated with end-stage renal disease and is found in 1-4% of hemodialysis patients. The condition has an overall mortality of 64%. Literature has yet to provide a gold standard for the management of this condition. The first case is a 58-year-old diabetic and hypertensive on hemodialysis who presented with ulcerating lesions on the penis. The patient underwent partial penectomy. The patient contracted pneumonia during recovery and expired 3 months after the procedure. The second case is a 56-year-old diabetic with end stage renal disease on dialysis who presented with dry gangrene of the penis. He underwent partial penectomy and was sent home after recovery.

9.
Rev. argent. dermatol ; 100(4): 71-80, dic. 2019. graf
Article in Spanish | LILACS-Express | LILACS | ID: biblio-1092397

ABSTRACT

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.

10.
Rev. colomb. nefrol. (En línea) ; 6(1): 69-73, ene.-jun. 2019. tab, graf
Article in Spanish | LILACS, COLNAL | ID: biblio-1093028

ABSTRACT

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.


Subject(s)
Humans , Male , Female , Calciphylaxis , Renal Replacement Therapy , Chronic Kidney Disease-Mineral and Bone Disorder , Ecuador , Renal Insufficiency, Chronic
11.
Colomb. med ; 49(4): 288-291, Oct.-Dec. 2018. graf
Article in English | LILACS | ID: biblio-984310

ABSTRACT

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.


Subject(s)
Aged , Female , Humans , Thiosulfates/administration & dosage , Calciphylaxis/drug therapy , Pamidronate/administration & dosage , Kidney Failure, Chronic/complications , Calciphylaxis/etiology , Calciphylaxis/pathology , Chelating Agents/administration & dosage , Renal Dialysis/methods , Treatment Outcome , Drug Therapy, Combination , Administration, Intravenous , Kidney Failure, Chronic/therapy
12.
An. bras. dermatol ; 93(3): 397-404, May-June 2018. tab, graf
Article in English | LILACS | ID: biblio-949898

ABSTRACT

Abstract: Purpura is defined as a visible hemorrhage in the skin or mucosa, which is not evanescent upon pressure. Proper classification allows a better patient approach due to its multiple diagnoses. Purpuras can be categorized by size, morphology, and other characteristics. The course varies according to the etiology, as do the diagnostic approach and treatment. This review discusses pigmented purpuras and some cutaneous vascular occlusion syndromes.


Subject(s)
Humans , Pigmentation Disorders/diagnosis , Purpura/diagnosis , Skin Diseases, Vascular/diagnosis , Purpura/etiology , Purpura/pathology , Skin/blood supply , Syndrome , Calciphylaxis/pathology , Antiphospholipid Syndrome/complications , Antiphospholipid Syndrome/pathology , Skin Diseases, Vascular/pathology , Diagnosis, Differential , Purpura Fulminans/pathology
13.
Rev. Soc. Bras. Clín. Méd ; 16(1): 41-44, 20180000. ilus
Article in Portuguese | LILACS | ID: biblio-884993

ABSTRACT

A calcifilaxia é uma vasculopatia obliterativa caracterizada por necrose isquêmica cutânea, com instalação aguda e progressiva, secundária à calcificação de vasos sanguíneos de pequeno ou médio calibre. Habitualmente, é uma complicação observada nos pacientes com hiperparatireoidismo secundário à insuficiência renal crônica. Sua patogênese ainda é desconhecida e, provavelmente, multifatorial. Este estudo descreve o caso de um paciente com calcifilaxia idiopática submetido ao tratamento clínico, desbridamento cirúrgico e curativos, com resolução completa após 6 meses. Apesar de ser uma afecção rara e grave na população em geral, o diagnóstico e o tratamento precoce da calcifilaxia permitem a evolução clínica favorável e a melhoria da qualidade de vida do paciente.(AU)


The calciphylaxis is an obliterative vasculopathy characterized by cutaneous ischemic necrosis, with acute and progressive installation, secondary to calcification of small or medium-sized blood vessels. Usually, is a complication observed in patients with hyperparathyroidism secondary to chronic renal failure. Its pathogenesis is still unknown and probably multifactorial. This study describes a case of a patient with idiopathic calciphylaxis, which was submitted to clinical treatment, surgical debridement and dressings, with complete resolution after 6 months. Although being a rare and serious disease in the general population, the early diagnosis and treatment of calciphylaxis allow favorable clinical evolution and improvement of patient's quality of life.(AU)


Subject(s)
Humans , Male , Middle Aged , Calciphylaxis/drug therapy , Debridement , Leg Ulcer , Vasculitis
14.
Palliative Care Research ; : 63-68, 2018.
Article in Japanese | WPRIM | ID: wpr-688859

ABSTRACT

Purpose: To describe a patient receiving maintenance hemodialysis complicated with calcific uremic arteriolopathy (calciphylaxis) in whom ulcer pain control was successfully achieved by buprenorphine. Case: A 75-year-old man was admitted due to intractable, extreme pain, which was accompanied by skin ulcers of the lower extremities. By a series of examinations including skin biopsy, the lesion was diagnosed to be calcific uremic arteriolopathy. The pain was not controllable with non-steroidal anti-inflammatory drugs and even by the nerve block. Buprenorphine, a partial agonist for the opioid receptor, markedly alleviated the mixed pain which was attenuated from Numerical Rating Scale (NRS) 10/10 to 0-2/10. Conclusion: Buprenorphine was very effective for the refractory pain control in a patient with skin ulcer due to calcific uremic arteriolopathy.

15.
Rev. cienc. cuidad ; 15(1): 110-122, 2018.
Article in Spanish | LILACS, BDENF, COLNAL | ID: biblio-906371

ABSTRACT

Objetivo: Revisar la literatura científica publicada en las principales bases de datos, entre los años 1962 y 2016, cuyo objetivo fue abordar el tema de la calcifilaxia y sus principales características. Metodología: Se llevó a cabo una revisión de la literatura en las principales bases de datos de las Ciencias de la Salud y las Ciencias Sociales (medline-pubmed, cinhal, web of science, lilacs, sociological abstracts, cuiden, embase, psycoinfo e isi web of knowledge). Se emplearon descriptores en español, inglés y portugués: Calcifilaxis, diálisis, hiperparatiroidismo, necrosis, gangrena, calcificación vascular, cuidados de enfermería y diagnósticos de enfermería. Se hizo una revisión sistemática de los artículos seleccionados utilizando un protocolo para extraer los datos. Resultado: Se encontraron 45 artículos que cumplían con los criterios de búsqueda establecidos, 35 reportaron los resultados de ensayos clínicos o estudios cualitativos, 4 correspondían a revisiones sistemáticas y 6 se catalogaron como estudios retrospectivos. Los autores señalaron las principales características de la enfermedad, de los pacientes y los tratamientos más usados, pero poco del cuidado que debe brindar el profesional enfermero. Conclusión: En los estudios analizados se identificaron principalmente aspectos sobre el curso de la enfermedad y el tratamiento; se reportó la efectividad de algunos tratamientos utilizadas en la atención de dichos pacientes, pero ninguna de ellas definitiva, lo que permite proponer algunas acciones desde la disciplina enfermera.


Objective: To analyze the scientifi c literature published in the main databases between 1962 and 2016, whose objective was to address the issue of calciphylaxis and its main characteristics? Methodology: A literature review was carried out in the main databases of the Health Sciences and Social Sciences (medline-pubmed, cinhal, web of science, lilacs, sociological abstracts, cuiden, embase, psycoinfo and isi web of knowledge). An analytical review of the selected articles was made using a protocol to extract the data. Results: 45 articles were found that fulfi lled the established search criteria, 35 reported the results of clinical trials or qualitative studies, 4 corresponded to systematic reviews and 6 were classifi ed as retrospective studies. The authors pointed out the main characteristics of the disease, the patients and the most used treatments, but little of the care that should be provided by the nurse practitioner. Conclusion: In the analyzed studies, aspects regarding the course of the disease and treatment were identifi ed; it was reported the effectiveness of some treatments used in the care of these patients, but none of them defi nitive, which allows to propose some actions from the nurse discipline.


Objetivo: Revisar a literatura científica publicada nas principais bases de dados, entre os anos 1962 e 2016, cujo objetivo era abordar o tema da calcifilaxia e suas principais características. Metodologia: Uma revisão da literatura foi realizada nas principais bases de dados das Ciências da Saúde e das Ciências Sociais (Medline-Pubmed, Cinhal, Web of Science, Lilacs, Sociological abstracts, Cuiden, Embase, Psycoinfo e Isi Web of Knowledge). Foram usados descritores em espanhol, inglês e português: calcifilaxia, diálise, hiperparatiroidismo, necrose, gangrena, calcificação vascular, cuidados de enfermagem e diagnósticos de enfermagem. Foi feita uma revisão sistemática dos artigos selecionados utilizando um protocolo para extrair os dados. Resultados: Encontraram-se 45 artigos que cumpriam com os critérios de busca estabelecidos, 35 reportaram os resultados de ensaios clínicos ou estudos qualitativos, quatro (4) correspondiam a revisões sistemáticas e seis (6) se catalogaram como estudos retrospectivos. Os autores apontaram as principais características da doença, dos pacientes e os tratamentos mais usados, mas pouco do cuidado que debe oferecer o professional da enfermagem. Conclusão: Nos estudos analisados se identificaram principalmente aspectos sobre o curso da doença e o tratamento; se reportou a efetividade de alguns tratamentos utilizados no atendimento desses pacientes, mas nenhum deles definitivo, o que permite propor algumas ações desde a profissão da enfermagem.


Subject(s)
Calciphylaxis
16.
Medicina (B.Aires) ; 77(4): 331-333, ago. 2017. ilus
Article in Spanish | LILACS | ID: biblio-894489

ABSTRACT

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.


Subject(s)
Humans , Female , Adult , Middle Aged , Calciphylaxis/diagnosis , Kidney Failure, Chronic/complications , Calciphylaxis/etiology , Calciphylaxis/therapy , Combined Modality Therapy , Debridement
17.
Med. leg. Costa Rica ; 33(2): 123-132, sep.-dic. 2016. ilus
Article in Spanish | LILACS | ID: lil-795913

ABSTRACT

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.


Subject(s)
Humans , Penile Diseases/complications , Penis/pathology , Calciphylaxis/complications , Renal Insufficiency, Chronic/complications , Vascular Calcification/diagnosis , Costa Rica , Necrosis
18.
Rev. nefrol. diál. traspl ; 36(2): 99-102, mar. 2016. ilus
Article in Spanish | LILACS | ID: biblio-1006119

ABSTRACT

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.


Subject(s)
Calciphylaxis , Glomerulosclerosis, Focal Segmental , Renal Insufficiency, Chronic
19.
Rev. nefrol. diál. traspl ; 36(1): 12-20, ene. 2016. ilus
Article in Spanish | LILACS | ID: biblio-1005985

ABSTRACT

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


Subject(s)
Humans , Calciphylaxis , Kidney Transplantation , Pancreas Transplantation , Hypercalcemia
20.
Kidney Research and Clinical Practice ; : 55-58, 2016.
Article in English | WPRIM | ID: wpr-110775

ABSTRACT

Warfarin skin necrosis (WSN) is an infrequent complication of warfarin treatment and is characterized by painful ulcerative skin lesions that appear a few days after the start of warfarin treatment. Calciphylaxis also appears as painful skin lesions caused by tissue injury resulting from localized ischemia caused by calcification of small- to medium-sized vessels in patients with end-stage renal disease. We report on a patient who presented with painful skin ulcers on the lower extremities after the administration of warfarin after a valve operation. Calciphylaxis was considered first because of the host factors; eventually, the skin lesions were diagnosed as WSN by biopsy. The skin lesions improved after warfarin discontinuation and short-term steroid therapy. Most patients with end-stage renal disease have some form of cardiovascular disease and some require temporary or continual warfarin treatment. It is important to differentiate between WSN and calciphylaxis in patients with painful skin lesions.


Subject(s)
Humans , Biopsy , Calciphylaxis , Cardiovascular Diseases , Hyperparathyroidism, Secondary , Ischemia , Kidney Failure, Chronic , Lower Extremity , Necrosis , Peritoneal Dialysis , Skin Ulcer , Skin , Ulcer , Warfarin
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