• 제목/요약/키워드: acute renal injury

검색결과 146건 처리시간 0.021초

급성 신손상을 가진 소아의 지속적 신대체 요법 (Overview of Pediatric Continuous Renal Replacement Therapy in Acute Kidney Injury)

  • 박세진;신재일
    • Childhood Kidney Diseases
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    • 제15권2호
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    • pp.107-115
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    • 2011
  • 소아에서 급성 신손상의 흔한 원인들로는 신허혈, 신독성 약물들, 그리고 패혈증 등이 있으며, 신대체요법 시작시의 저혈압, 신대체 요법 동안 승압제의 사용, 그리고 신대체 요법 시작시의 수액 과부하 정도가 환자의 생존(소아 중환자실 퇴원)에 영향을 미치는 요인들로 알려져 있다. 지속적 신대체 요법의 빠른 시작은 급성 신손상을 가진 환자들에게서 사망률과 예후에 나쁜 영향을 미치는 수액 과부하를 감소시키는 것으로 보고되었다. 이에 저자들은 소아 환자에게서 지속적 신대체 요법의 실제 처방과 급성 신손상, 수액 과부하, 그리고 지속적 신대체 요법간의 연관성 및 치료결과를 살펴보고자 한다. 결론적으로, 급성 신손상을 가진 소아의 치료에 있어서 과도한 수액 과부하가 발생하기 전에 빠른 지속적 신대체 요법의 시작이 필요하다고 제시하는 바이다.

Aurantio-obtusin exerts an anti-inflammatory effect on acute kidney injury by inhibiting NF-κB pathway

  • Haiyan Xiang;Yun Zhang;Yan Wu;Yaling Xu;Yuanhao Hong
    • The Korean Journal of Physiology and Pharmacology
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    • 제28권1호
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    • pp.11-19
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    • 2024
  • Acute kidney injury (AKI) is one of the major complications of sepsis. Aurantio-obtusin (AO) is an anthraquinone compound with antioxidant and anti-inflammatory activities. This study was developed to concentrate on the role and mechanism of AO in sepsis-induced AKI. Lipopolysaccharide (LPS)-stimulated human renal proximal tubular epithelial cells (HK-2) and BALB/c mice receiving cecal ligation and puncture (CLP) surgery were used to establish in vitro cell model and in vivo mouse model. HK-2 cell viability was measured using MTT assays. Histological alterations of mouse renal tissues were analyzed via hematoxylin and eosin staining. Renal function of mice was assessed by measuring the levels of serum creatinine (SCr) and blood urea nitrogen (BUN). The concentrations of pro-inflammatory cytokines in HK-2 cells and serum samples of mice were detected using corresponding ELISA kits. Protein levels of factors associated with nuclear factor kappa-B (NF-κB) pathway were measured in HK-2 cells and renal tissues by Western blotting. AO exerted no cytotoxic effect on HK-2 cells and AO dose-dependently rescued LPS-induced decrease in HK-2 cell viability. The concentrations of pro-inflammatory cytokines were increased in response to LPS or CLP treatment, and the alterations were reversed by AO treatment. For in vivo experiments, AO markedly ameliorated renal injury and reduced high levels of SCr and BUN in mice underwent CLP operation. In addition, AO administration inhibited the activation of NF-κB signaling pathway in vitro and in vivo. In conclusion, AO alleviates septic AKI by suppressing inflammatory responses through inhibiting the NF-κB pathway.

SCL22A12 유전자의 R90H 돌연변이를 동반한 신성 저요산혈증과 반복적인 운동유발성 급성 신부전 1예 (A Case of Recurrent Exercise-Induced Acute Renal Failure and Renal Hypouricemia with R90H Mutation in a SCL22A12 Gene)

  • 김애진;박수용;정지용;장제현;이현희;정우경;노한
    • Journal of Yeungnam Medical Science
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    • 제29권2호
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    • pp.150-152
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    • 2012
  • Acute renal failure with severe loin pain and patch renal ischemia after anaerobic exercise (ALPE) is a rare cause of exercise-induced acute kidney injury. Some ALPE patients also have renal hypouricemia. Mutations in the SCL22A12 gene are among the major factors of hypouricemia. Education for the prevention of relapse and genetic counseling should be recommended to ALPE patients with renal hypouricemia. This paper reports a 25-year-old man who showed recurrent exercise-induced ARF and renal hypouricemia with R90H mutation in his SCL22A12 gene.

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소아에서 방광 요관역류가 동반된 급성 신우신염 및 신장 농양으로 인한 급성 신부전 1례 (Acute Kidney Injury Accompanied by Acute Pyelonephritis and Renal Abscess in a Child with Vesicoureteral Reflux)

  • 박철;김민상;김미경;임형은;유기환;홍영숙;이주원
    • Childhood Kidney Diseases
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    • 제16권1호
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    • pp.63-67
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    • 2012
  • 소아에서 급성 신우신염은 상대적으로 흔한 세균 감염 질환이다. 이전에 건강했던 소아에서 요로계의 폐쇄, 저혈압에 의한 신장 허혈, 신장 독성물질에의 노출 등이 없이는 급성 신우신염의 결과로 급성 신부전이 생기기는 매우 드물다. 저자들은 이전에 건강했던 소아에서 방광요관 역류가 동반된 급성 신우신염과 신장 농양에 따른 급성 신부전이 발생한 예를 보고하는 바이다. 환자는 적절한 수액 치료와 항생제 치료를 통해 호전되었다. 증례를 통해 저자들은 급성 신우신염이 급성 신부전의 감별진단에포함되어야 하며, 신장기능의 완전한 회복을 위해서는 적절한 항생제 치료가 수반되어야 함을 제시하는 바이다.

급성 허혈성 신손상 후 여러 성장인자 발현의 변화 (Alteration of Growth Factor Expression after Acute Ischemic Renal Injury)

  • 고양심;이수연;김원;조수철;황평한;김정수;이대열
    • Clinical and Experimental Pediatrics
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    • 제46권7호
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    • pp.687-694
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    • 2003
  • 목 적 : 급성 허혈성 신손상 후 손상된 세뇨관 상피세포의 재생은 순환하거나 국소적으로 생성된 성장인자나 cytokine, 생리적 인자 및 주위 환경들의 조절에 의해 매개되는 것으로 알려져 있다. 따라서 급성 허혈성 신손상 후 신기능 회복에 따른 혈중 IGF-I의 변화와 전체 신장조직과 각 부위에 따른 IGF-I, -II, VEGF, $TGF-{\beta}1$, CTGF의 mRNA 발현의 변화를 알아보는데 연구의 목적이 있다. 방 법 : 체중이 250-300 g의 백서를 대상으로 급성 허혈성 신손상을 시켜 유발된 급성 신부전 모델을 이용하여 급성 신부전의 진행과정에 따라 혈청 IGF-I치와 여러 성장인자 발현의 변화를 측정하였다. 급성 신부전 진행은 혈청 크레아티닌을 측정하여 평가하였고 혈청 IGF-I 농도는 iodinated IGF-I과 polyclonal anti-IGF-I 항체를 이용한 방사면역 측정법을 이용하여 측정하였다. 신장에서 성장인자의 발현은 RT-PCR을 이용하였고 신장조직에서의 RNA 추출은 통상적인 방법에 준하였다. 신장에서의 IGF-I과 CTGF의 분포는 anti-IGF-I 항체와 anti-CTGF 항체를 이용한 면역조직화학법을 이용하였다. 결 과 : 1) 양측 신동맥을 결찰한 후 1일째부터 체중 감소와 혈청 크레아티닌치의 증가가 관찰되었는데 이러한 변화는 3일째에 가장 현저하였다. 혈청 IGF-I은 신손상 후 1일 째 현저하게 감소하였고 신손상 3일째에 더 증가되었다가 5일째부터는 신손상 전으로 회복되었다. 2) 신기능 회복에 따른 성장인자의 변화는 거의 유사하였다. IGF-I, IGF-II, $TGF-{\beta}1$ 및 VEGF의 mRNA 발현은 허혈성 신손상 후 1일째에 현저하게 감소하였고 신손상 3일째에는 신손상 전에 비해 증가하였으며 7일째에는 거의 신손상 전의 수준으로 회복되었다. 3) IGF-I과 IGF-II는 정상 신장에서는 주로 수질부 특히 바 깥쪽 수질부에서 발현되었고 허혈성 신손상 1일째에 현저하게 감소하였다가 3일째에는 정상 수준으로 회복되었다. $TGF-{\beta}1$은 정상에서 신수질부에서 주로 발현되었고 1일째는 현저하게 감소하였다가 회복되는 소견을 보였다. CTGF와 VEGF는 정상 신장의 수질부와 피질부 모두에서 발현되었으며 신손상 1일째에 현저하게 감소되었다가 3일째부터 정상 수준으로 회복되는 소견을 보였다. 4) 정상 백서의 신장에서 IGF-I은 주로 피질부위의 신세뇨관에 분포하였고 사구체에서는 발견되지 않았는데 급성 허혈성 신손상 후 1일째 신장의 피질부위에서는 IGF-I가 현저히 감소되었다. CTGF는 정상 백서의 신장에서는 주로 혈관에 분포하는 소견을 보였는데 신손상 3일째에는 세뇨관에서 현저한 증가가 관찰되었다. 결 론: 이번의 연구로 저자들은 IGF-I, IGF-II, $TGF-{\beta}1$, CTGF, VEGF 등과 같은 성장인자가 급성 허혈성 신손상 후 신기능과 세뇨관세포의 회복과정에 발현의 변화가 초래된다는 사실을 알 수 있었다. 따라서 신기능 회복을 촉진시키기 위해 여러 성장인자를 급성신부전 치료제로 사용할 수 있을 것으로 생각되고 이에 대한 연구가 더 필요할 것으로 생각된다.

폐 이식 후 신부전 발생 환자에서 유지 면역억제제로서 basiliximab의 사용 평가 (Medication Utilization Analysis of Basiliximab as a Maintenance Immunosuppressant in Renal Failure Patients Undergoing Lung Transplantation)

  • 서예진;금민정;이경아;김재송;손은선;유윤미
    • 한국임상약학회지
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    • 제30권3호
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    • pp.149-160
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    • 2020
  • Background: Basiliximab is used as an alternative to tacrolimus in patients with decreased renal function. However, studies on basiliximab as a maintenance immunosuppressant, particularly in patients with lung transplantation, are limited. Therefore, here, we investigated the efficacy and safety of basiliximab in patients with lung transplantation. Methods: Adult patients with acute kidney injury (AKI) who received lung transplantation at a single general hospital between July 1, 2014 and June 30, 2018, were selected and classified in tacrolimus and basiliximab groups. Both groups received a triple-drug regimen (tacrolimus, mycophenolate mofetil, and steroids). However, tacrolimus was discontinued in the basiliximab group when AKI occurred, and two or more repeat basiliximab doses were administered within 3 months after transplantation. The electronic medical records were analyzed retrospectively. Results: Of the 85 patients who met the selection criteria, 61 and 24 were assigned to the tacrolimus and basiliximab groups, respectively. Significant improvement in renal function was observed in the basiliximab group (p <0.001). However, there were no differences in acute and chronic rejection rates in both the groups. No difference was observed in the incidence rate of complications between the groups, except for chronic kidney disease, which showed higher incidence in the basiliximab group (25.0% vs. 4.9%; p =0.013). Conclusions: We suggest the use of basiliximab as an immunosuppressant alternative to tacrolimus in patients with acute renal failure after lung transplantation. Basiliximab demonstrated effectiveness as an immunosuppressant and improved renal function. Therefore, basiliximab can be used in patients with decreased renal function.

New Insights for Febrile Urinary Tract Infection (Acute Pyelonephritis) in Children

  • Lee, Kyung-Yil
    • Childhood Kidney Diseases
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    • 제20권2호
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    • pp.37-44
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    • 2016
  • Although asymptomatic bacteriuria, cystitis, and acute pyelonephritis (APN) have been categorized as urinary tract infections (UTIs), the immunopathogenesis of each disease is different. APN shows an age predilection; the majority of children (over 70-80%) with APN are under 1-2 years of age, with a male predominance. After 1-2 years of age, female predominance has been reported. This finding suggests that the immature immune state of infancy may be associated with the pathogenesis of APN. Escherichia coli is the most common etiologic agent; other uropathogens associated with UTIs originate from the host and comprise normal flora that are continuously altered by environmental factors. Therefore, uropathogens may have characteristics different from those of extraneous bacterial pathogens. Although antibiotic-resistant uropathogens, including extended-spectrum beta-lactamase-producing strains, are increasing in Korea and worldwide, treatment failure is rare in immune-competent children. The immunopathogenesis of APN remains unknown. Intact bacteria may not be the causative substances in renal cell injury; rather, smaller substances produced during bacterial replication may be responsible for renal cell injury and scarring. Moreover, substances from host cells such as proinflammatory cytokines may be involved in renal cell injury. A dimercaptosuccinic acid scan is used to detect the site of bacterial replication in the renal parenchyma, and may be influenced by the size of the focus and the stage of APN. Traditional aggressive studies used to identify vesicoureteral reflux after the first episode of APN have been modified because of rare cases of chronic kidney disease in patients with recurrent UTI.

Spontaneous Tumor Lysis Syndrome Presenting Acute Kidney Injury with Extreme Hyperuricemia and Urinary Stone: A Rare Case of Spontaneous Tumor Lysis Syndrome

  • Kim, Seong Heon;Yang, Eu Jeen;Lim, Young Tak;Kim, Su Young
    • Childhood Kidney Diseases
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    • 제21권1호
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    • pp.31-34
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    • 2017
  • Tumor lysis syndrome is a serious complication of malignancy, resulting from the massive and rapid release of cellular components into the blood. Generally, it occurs after initiation of chemotherapy. The onset of spontaneous tumor lysis syndrome (STLS) before anti-cancer treatment is rare and occurs mostly in Burkitt lymphoma and non-Hodgkin's lymphoma. There are only a few case reports in children. Here, we report a case of STLS secondary to T-cell acute lymphoblastic leukemia (ALL), which presented with urinary stone and subsequent acute kidney injury with severe hyperuricemia. Occult malignancy should be considered in case of unexplained acute kidney injury with extreme hyperuricemia.

Acute tubular necrosis as a part of vancomycin induced drug rash with eosinophilia and syste­mic symptoms syndrome with coincident post­infectious glomerulonephritis

  • Kim, Kyung Min;Sung, Kyoung;Yang, Hea Koung;Kim, Seong Heon;Kim, Hye Young;Ban, Gil Ho;Park, Su Eun;Lee, Hyoung Doo;Kim, Su Young
    • Clinical and Experimental Pediatrics
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    • 제59권3호
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    • pp.145-148
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    • 2016
  • Drug rash with eosinophilia and systemic symptoms (DRESS) syndrome is a rare and potentially fatal condition characterized by skin rash, fever, eosinophilia, and multiorgan involvement. Various drugs may be associated with this syndrome including carbamazepine, allopurinol, and sulfasalazine. Renal involvement in DRESS syndrome most commonly presents as acute kidney injury due to interstitial nephritis. An 11-year-old boy was referred to the Children's Hospital of Pusan National University because of persistent fever, rash, abdominal distension, generalized edema, lymphadenopathy, and eosinophilia. He previously received vancomycin and ceftriaxone for 10 days at another hospital. He developed acute kidney injury with nephrotic range proteinuria and hypocomplementemia. A subsequent renal biopsy indicated the presence of acute tubular necrosis (ATN) and late exudative phase of postinfectious glomerulonephritis (PIGN). Systemic symptoms and renal function improved with corticosteroid therapy after the discontinuation of vancomycin. Here, we describe a biopsy-proven case of severe ATN that manifested as a part of vancomycin-induced DRESS syndrome with coincident PIGN. It is important for clinicians to be aware of this syndrome due to its severity and potentially fatal nature.

급성(急性) 신부전(腎不全)이 동반(同伴)된 근양사(筋壤死)에 있어서의 $^{99m}Tc$-MDP 골주사(骨走査) ($^{99m}Tc$-MDP Bone Scan in the Cases of Muscle Necrosis Associated with Acute Renal Failure)

  • 문희범;한진석;김삼용;조보연;이정상;고창순;조경삼
    • 대한핵의학회지
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    • 제14권2호
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    • pp.61-66
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    • 1980
  • We studied four patients with muscle necrosis associated with acute renal failure to evaluate the diagnostic value of the bone scan in this disease. The illness followed carbon monoxide poisoning in two patients, acute physical exertion in one and contaminated intramuscular injection in the other. Whole-body rectilinear bone scans using technetium 99m-methyldiphosphonate were done. In all patients, increased muscle labelling at the regions of suspected muscle injury was showed, and in one, it was after normalization of serum muscle enzyme levels. In one patient, the bone scan was rechecked 8 months later and showed no residual abnormality. Above all, the site and precise extent of muscle injury could be detected and the degree of muscle labelling seemed to correlate with the severy of muscle injury. These findings suggest that isotope scanning may be useful in the diagnosis of patients with acute muscle necrosis.

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