Pub Date : 2026-02-01Epub Date: 2025-12-01DOI: 10.1055/a-2703-7643
Kathrin Knochel, Marie-Christin Fritzsche, Tanja Henking, Sebastian Schleidgen, Anna-Henrikje Seidlein, Orsolya Friedrich
Medical indications are based on a synthesis of medical expertise, professional ethical standards, and legal requirements. This paper examines the extent to which value judgments influence these determinations and how they can be ethically approached.The interdisciplinary conceptual and normative analysis incorporates theoretical approaches from medical science, case studies, empirical findings, and legal considerations to identify and critically discuss the various levels of value judgments involved in the indication process.Value judgments influence determining medical indications, particularly with regard to the choice of one of the goals of medicine and how probabilities, uncertainties, personal attitudes, and social norms, are handled. Some judgments do not fall within the physician's scope of responsibility, at least not in the context of medical indication, e.g., economic or allocation considerations. For clarity, it is essential to differentiate physicians' assessments and patients' preferences, to explicate professional values, and to integrate assessments and individual values within decision-making processes.Value judgments made in determining a medical indication are unavoidable and must be carefully considered. Values should be made transparent in order to justify medical interventions that are judged to be indicated or not by physicians on a case-by-case basis and to strengthen patients' self-determination. A social debate is needed on how to appropriately address considerations (such as economic) which should not be mixed up with medical indications.
{"title":"[Value judgments in the determination of a medical indication - An interdisciplinary analysis].","authors":"Kathrin Knochel, Marie-Christin Fritzsche, Tanja Henking, Sebastian Schleidgen, Anna-Henrikje Seidlein, Orsolya Friedrich","doi":"10.1055/a-2703-7643","DOIUrl":"10.1055/a-2703-7643","url":null,"abstract":"<p><p>Medical indications are based on a synthesis of medical expertise, professional ethical standards, and legal requirements. This paper examines the extent to which value judgments influence these determinations and how they can be ethically approached.The interdisciplinary conceptual and normative analysis incorporates theoretical approaches from medical science, case studies, empirical findings, and legal considerations to identify and critically discuss the various levels of value judgments involved in the indication process.Value judgments influence determining medical indications, particularly with regard to the choice of one of the goals of medicine and how probabilities, uncertainties, personal attitudes, and social norms, are handled. Some judgments do not fall within the physician's scope of responsibility, at least not in the context of medical indication, e.g., economic or allocation considerations. For clarity, it is essential to differentiate physicians' assessments and patients' preferences, to explicate professional values, and to integrate assessments and individual values within decision-making processes.Value judgments made in determining a medical indication are unavoidable and must be carefully considered. Values should be made transparent in order to justify medical interventions that are judged to be indicated or not by physicians on a case-by-case basis and to strengthen patients' self-determination. A social debate is needed on how to appropriately address considerations (such as economic) which should not be mixed up with medical indications.</p>","PeriodicalId":93975,"journal":{"name":"Deutsche medizinische Wochenschrift (1946)","volume":" ","pages":"e9-e15"},"PeriodicalIF":0.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145656575","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2026-02-09DOI: 10.1055/a-2647-5908
Klara-Luisa Budau, Robert Thimme, Lukas Sturm
Acute-on-chronic liver failure (ACLF) is a life-threatening syndrome in patients with decompensated cirrhosis and is characterized by acute failure of one or more organ systems. Despite advances in clinical management, ACLF continues to be associated with high short-term mortality.This article provides an up-to-date, guideline-based overview of the classification, diagnosis, and therapeutic approaches to ACLF, drawing on the latest literature and consensus definitions.ACLF is defined by acute decompensation of cirrhosis accompanied by failure of the liver and/or other organs including the kidneys, cardiovascular system, lungs, central nervous system, and coagulation. The EASL-CLIF Consortium criteria distinguish three grades of ACLF based on the number and type of organ failures; increasing grade correlates with sharply rising short- and medium-term mortality. Pathophysiologically, ACLF is characterized by an overwhelming systemic inflammatory response typically triggered by bacterial infections, severe alcoholic hepatitis, or gastrointestinal bleeding. Prognostication is guided by CLIF-C OF, CLIF-C ACLF, and CLIF-C AD scores, which can also help to identify patients at high risk for further decompensation. Management focuses on rapid identification and reversal of precipitating factors, organ support, and early evaluation for liver transplantation, as it remains the sole curative option in non-reversible ACLF. Preemptive TIPS placement is reserved for selected cases, with individualized risk assessment being critical due to the increased complication rate in severe multiorgan failure.ACLF remains the most severe complication of cirrhosis, marked by high short-term mortality. Early, guideline-based interventions and multidisciplinary management can improve outcomes. Accurate risk stratification and timely consideration of liver transplantation are essential to enhance patient survival.
{"title":"[Acute-on-chronic liver failure].","authors":"Klara-Luisa Budau, Robert Thimme, Lukas Sturm","doi":"10.1055/a-2647-5908","DOIUrl":"https://doi.org/10.1055/a-2647-5908","url":null,"abstract":"<p><p>Acute-on-chronic liver failure (ACLF) is a life-threatening syndrome in patients with decompensated cirrhosis and is characterized by acute failure of one or more organ systems. Despite advances in clinical management, ACLF continues to be associated with high short-term mortality.This article provides an up-to-date, guideline-based overview of the classification, diagnosis, and therapeutic approaches to ACLF, drawing on the latest literature and consensus definitions.ACLF is defined by acute decompensation of cirrhosis accompanied by failure of the liver and/or other organs including the kidneys, cardiovascular system, lungs, central nervous system, and coagulation. The EASL-CLIF Consortium criteria distinguish three grades of ACLF based on the number and type of organ failures; increasing grade correlates with sharply rising short- and medium-term mortality. Pathophysiologically, ACLF is characterized by an overwhelming systemic inflammatory response typically triggered by bacterial infections, severe alcoholic hepatitis, or gastrointestinal bleeding. Prognostication is guided by CLIF-C OF, CLIF-C ACLF, and CLIF-C AD scores, which can also help to identify patients at high risk for further decompensation. Management focuses on rapid identification and reversal of precipitating factors, organ support, and early evaluation for liver transplantation, as it remains the sole curative option in non-reversible ACLF. Preemptive TIPS placement is reserved for selected cases, with individualized risk assessment being critical due to the increased complication rate in severe multiorgan failure.ACLF remains the most severe complication of cirrhosis, marked by high short-term mortality. Early, guideline-based interventions and multidisciplinary management can improve outcomes. Accurate risk stratification and timely consideration of liver transplantation are essential to enhance patient survival.</p>","PeriodicalId":93975,"journal":{"name":"Deutsche medizinische Wochenschrift (1946)","volume":"151 4","pages":"171-178"},"PeriodicalIF":0.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146151404","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2026-02-09DOI: 10.1055/a-2754-4758
Jakob Leonhardi, Charlotte Ackmann, Anne Beeskow
{"title":"[81-year-old patient with unclear shortness of breath].","authors":"Jakob Leonhardi, Charlotte Ackmann, Anne Beeskow","doi":"10.1055/a-2754-4758","DOIUrl":"https://doi.org/10.1055/a-2754-4758","url":null,"abstract":"","PeriodicalId":93975,"journal":{"name":"Deutsche medizinische Wochenschrift (1946)","volume":"151 4","pages":"147-148"},"PeriodicalIF":0.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146151455","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2026-02-09DOI: 10.1055/a-2647-5748
Christian Labenz
Hepatic encephalopathy (HE) is a common and serious complication of liver cirrhosis, associated with significant morbidity and mortality. Pathophysiologically, it results from a complex interplay of hyperammonemia, systemic inflammation, neuroinflammatory processes, and microbial dysbiosis. Clinically, HE ranges from subtle cognitive impairments (minimal HE) to coma (grade 4 HE). Diagnosis requires thorough clinical assessment and the use of specialized testing methods, particularly to detect subclinical alterations. In everyday practice, ammonia levels have limited diagnostic value but may be useful for differential diagnosis. The acute treatment of overt hepatic encephalopathy (OHE) is primarily based on the administration of lactulose, optionally supplemented with intravenous L-ornithine-L-aspartate. For secondary prophylaxis lactulose is the treatment of choice and in patients with recurrent episodes, the combination of rifaximin and lactulose is well established. Nutritional recommendations are a key component of therapy, especially to prevent sarcopenia. In cases of refractory HE or recurrent relapses despite guideline-based treatment, liver transplantation should always be considered. In general, early detection and individualized management of HE is essential to preserve and improve quality of life, prognosis, and functional independence of the affected patients.
肝性脑病(HE)是肝硬化的一种常见且严重的并发症,发病率和死亡率都很高。病理生理上,它是高氨血症、全身炎症、神经炎症过程和微生物生态失调等复杂相互作用的结果。临床上,HE的范围从轻微的认知障碍(轻度HE)到昏迷(4级HE)。诊断需要彻底的临床评估和使用专门的检测方法,特别是检测亚临床改变。在日常实践中,氨水平的诊断价值有限,但可能有助于鉴别诊断。公开性肝性脑病(OHE)的急性治疗主要基于乳果糖的施用,选择性地辅以静脉注射l -鸟氨酸- l -天冬氨酸。对于二级预防,乳果糖是治疗的选择,对于反复发作的患者,利福昔明和乳果糖的联合治疗是很好的。营养建议是治疗的关键组成部分,特别是预防肌肉减少症。对于难治性HE或经指导治疗后复发的病例,应始终考虑肝移植。总的来说,早期发现和个体化治疗对于维持和改善患者的生活质量、预后和功能独立性至关重要。
{"title":"[Hepatic encephalopathy in liver cirrhosis].","authors":"Christian Labenz","doi":"10.1055/a-2647-5748","DOIUrl":"https://doi.org/10.1055/a-2647-5748","url":null,"abstract":"<p><p>Hepatic encephalopathy (HE) is a common and serious complication of liver cirrhosis, associated with significant morbidity and mortality. Pathophysiologically, it results from a complex interplay of hyperammonemia, systemic inflammation, neuroinflammatory processes, and microbial dysbiosis. Clinically, HE ranges from subtle cognitive impairments (minimal HE) to coma (grade 4 HE). Diagnosis requires thorough clinical assessment and the use of specialized testing methods, particularly to detect subclinical alterations. In everyday practice, ammonia levels have limited diagnostic value but may be useful for differential diagnosis. The acute treatment of overt hepatic encephalopathy (OHE) is primarily based on the administration of lactulose, optionally supplemented with intravenous L-ornithine-L-aspartate. For secondary prophylaxis lactulose is the treatment of choice and in patients with recurrent episodes, the combination of rifaximin and lactulose is well established. Nutritional recommendations are a key component of therapy, especially to prevent sarcopenia. In cases of refractory HE or recurrent relapses despite guideline-based treatment, liver transplantation should always be considered. In general, early detection and individualized management of HE is essential to preserve and improve quality of life, prognosis, and functional independence of the affected patients.</p>","PeriodicalId":93975,"journal":{"name":"Deutsche medizinische Wochenschrift (1946)","volume":"151 4","pages":"149-155"},"PeriodicalIF":0.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146151573","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2026-02-09DOI: 10.1055/a-2647-5812
Valerie Ohlendorf, Laura Buttler, Benjamin Maasoumy
Liver cirrhosis is considered as a multisystemic disease that affects also the immune system. The spectrum of immunological alterations that can be found in patients with liver cirrhosis is summarized as cirrhosis-associated immune dysfunction (CAID). The mechanisms that are involved in the development of CAID are complex. Next to immune-mediated mechanisms causing the development of liver cirrhosis, one of the key mechanisms in the development of CAID is portal hypertension, leading to an impaired gut-liver-axis with an increased bacterial translocation to the blood stream. CAID can be assigned in the two key components systemic inflammation and immune deficiency. The intensity of components is variable and dynamic and depends on the stage of liver cirrhosis as well as the presence of incidental events (e.g. bacterial infections). In return, CAID increases the risk of infections and worsens the prognosis of the patient. The reduction of portal hypertension, inter alia by the insertion of a transjugular intrahepatic portosystemic shunt seems to be an important approach in the modulation of CAID. Further therapeutic approaches include the reduction of bacterial components to the blood and the modulation of impaired immune cell functions. Nevertheless, the only targeting approach of liver cirrhosis and CAID is still liver transplantation.
{"title":"[Cirrhosis-associated immune dysfunction (CAID)].","authors":"Valerie Ohlendorf, Laura Buttler, Benjamin Maasoumy","doi":"10.1055/a-2647-5812","DOIUrl":"https://doi.org/10.1055/a-2647-5812","url":null,"abstract":"<p><p>Liver cirrhosis is considered as a multisystemic disease that affects also the immune system. The spectrum of immunological alterations that can be found in patients with liver cirrhosis is summarized as cirrhosis-associated immune dysfunction (CAID). The mechanisms that are involved in the development of CAID are complex. Next to immune-mediated mechanisms causing the development of liver cirrhosis, one of the key mechanisms in the development of CAID is portal hypertension, leading to an impaired gut-liver-axis with an increased bacterial translocation to the blood stream. CAID can be assigned in the two key components systemic inflammation and immune deficiency. The intensity of components is variable and dynamic and depends on the stage of liver cirrhosis as well as the presence of incidental events (e.g. bacterial infections). In return, CAID increases the risk of infections and worsens the prognosis of the patient. The reduction of portal hypertension, inter alia by the insertion of a transjugular intrahepatic portosystemic shunt seems to be an important approach in the modulation of CAID. Further therapeutic approaches include the reduction of bacterial components to the blood and the modulation of impaired immune cell functions. Nevertheless, the only targeting approach of liver cirrhosis and CAID is still liver transplantation.</p>","PeriodicalId":93975,"journal":{"name":"Deutsche medizinische Wochenschrift (1946)","volume":"151 4","pages":"156-162"},"PeriodicalIF":0.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146151491","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2026-02-09DOI: 10.1055/a-2647-5845
Alexander Zipprich, Cristina Ripoll
Ascites, spontaneous bacterial peritonitis (SBP), and hepatorenal syndrome-acute kidney injury (HRS-AKI) are frequent and clinically significant complications in patients with cirrhosis, each conferring a substantial increase in mortality risk. Their pathogenesis is fundamentally driven by the development of splanchnic and systemic vasodilation secondary to portal hypertension, compounded by intestinal bacterial translocation. The diagnosis of ascites and SBP should be established without delay, employing a combination of laboratory testing and imaging modalities. In contrast, the diagnosis of HRS-AKI relies on the presence of cirrhosis with ascites together with the exclusion of alternative, more common causes of kidney injury. Management strategies vary by complication: ascites is typically addressed with diuretic therapy and placement of a transjugular intrahepatic portosystemic shunt (TIPS); SBP requires prompt initiation of antibiotic therapy combined with albumin administration; and HRS-AKI is treated with vasoconstrictor agents in conjunction with albumin.
{"title":"[Ascites, spontaneous bacterial peritonitis and hepatorenal syndrome - Complications of circulatory failure in cirrhosis].","authors":"Alexander Zipprich, Cristina Ripoll","doi":"10.1055/a-2647-5845","DOIUrl":"https://doi.org/10.1055/a-2647-5845","url":null,"abstract":"<p><p>Ascites, spontaneous bacterial peritonitis (SBP), and hepatorenal syndrome-acute kidney injury (HRS-AKI) are frequent and clinically significant complications in patients with cirrhosis, each conferring a substantial increase in mortality risk. Their pathogenesis is fundamentally driven by the development of splanchnic and systemic vasodilation secondary to portal hypertension, compounded by intestinal bacterial translocation. The diagnosis of ascites and SBP should be established without delay, employing a combination of laboratory testing and imaging modalities. In contrast, the diagnosis of HRS-AKI relies on the presence of cirrhosis with ascites together with the exclusion of alternative, more common causes of kidney injury. Management strategies vary by complication: ascites is typically addressed with diuretic therapy and placement of a transjugular intrahepatic portosystemic shunt (TIPS); SBP requires prompt initiation of antibiotic therapy combined with albumin administration; and HRS-AKI is treated with vasoconstrictor agents in conjunction with albumin.</p>","PeriodicalId":93975,"journal":{"name":"Deutsche medizinische Wochenschrift (1946)","volume":"151 4","pages":"163-170"},"PeriodicalIF":0.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146151478","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2026-02-09DOI: 10.1055/a-2725-3723
Nicolai Savaskan, Alexandra Roth, Mesut Yavuz
In 2025, Germany faces a dual transformation: the institutionalization of a federal Ministry for Digital Affairs and a controversial relaxation of data protection regulations, i.e. register for mentally ill people. These developments coincide with increasing political polarization, which not only shapes public discourse but also exerts measurable effects on health behavior, trust in institutions, and access to care. Despite operating one of the world's most expensive health systems, structural inequalities in Germany persist, with life expectancy differing by up to eight years across socioeconomic groups. Public health authorities (Öffentlicher Gesundheitsdienst, ÖGD) could act as a corrective force, yet they remain underfunded, digitally underdeveloped, and vulnerable to political influence. This article argues that polarization has emerged as a social determinant of health, comparable in significance to income or education. We highlight the urgent need for institutional trustworthiness. We present the OSCADO-AI ethical code, an open-source, inter-operational, and privacy-conscious digital standard designed to enhance the resilience of public health institutions. By enabling transparent data use, secure communication, real-time surveillance, and collaborative platforms, OSCADO-AI strengthens both evidence-based decision-making and public trust. Case examples from Frankfurt illustrate how digital sovereignty and open infrastructures can protect democratic institutions against partisan interference while fostering citizen-centered health governance. Ultimately, the future of the German public health system depends on its capacity to combine medical independence, digital innovation, and civic accountability to reduce inequality and safeguard democracy.
{"title":"[Standards and conditions for the success of digitalization for Public health authorities].","authors":"Nicolai Savaskan, Alexandra Roth, Mesut Yavuz","doi":"10.1055/a-2725-3723","DOIUrl":"https://doi.org/10.1055/a-2725-3723","url":null,"abstract":"<p><p>In 2025, Germany faces a dual transformation: the institutionalization of a federal Ministry for Digital Affairs and a controversial relaxation of data protection regulations, i.e. register for mentally ill people. These developments coincide with increasing political polarization, which not only shapes public discourse but also exerts measurable effects on health behavior, trust in institutions, and access to care. Despite operating one of the world's most expensive health systems, structural inequalities in Germany persist, with life expectancy differing by up to eight years across socioeconomic groups. Public health authorities (Öffentlicher Gesundheitsdienst, ÖGD) could act as a corrective force, yet they remain underfunded, digitally underdeveloped, and vulnerable to political influence. This article argues that polarization has emerged as a social determinant of health, comparable in significance to income or education. We highlight the urgent need for institutional trustworthiness. We present the OSCADO-AI ethical code, an open-source, inter-operational, and privacy-conscious digital standard designed to enhance the resilience of public health institutions. By enabling transparent data use, secure communication, real-time surveillance, and collaborative platforms, OSCADO-AI strengthens both evidence-based decision-making and public trust. Case examples from Frankfurt illustrate how digital sovereignty and open infrastructures can protect democratic institutions against partisan interference while fostering citizen-centered health governance. Ultimately, the future of the German public health system depends on its capacity to combine medical independence, digital innovation, and civic accountability to reduce inequality and safeguard democracy.</p>","PeriodicalId":93975,"journal":{"name":"Deutsche medizinische Wochenschrift (1946)","volume":"151 4","pages":"180-184"},"PeriodicalIF":0.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146151517","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ingo Eitel, Insa Emrich, Stephan von Haehling, Birgit Schleß, Roland Schmitt, Frank Strutz, Sven Wassmann, Markus van der Giet
Chronic hyperkalemia is an electrolyte imbalance that occurs mainly in patients with progressive kidney failure. It usually develops over a long period of time and symptoms are often mild. As chronic hyperkalemia is associated with increased morbidity and mortality, it should be treated. Treatment begins with a review of the medications that may be responsible for the hyperkalemia and careful therapy and correction of the metabolism. Dietary assessment now focuses on potassium intake from non-vegetable sources. Reducing the dose and/or discontinuing renin-angiotensin-aldosterone inhibitors should be discouraged, as these drugs improve the prognosis in patients with heart failure and proteinuric kidney disease. In addition to other conservative measures, specific potassium-binding substances should be used.
{"title":"[Paradigm shift in the treatment of chronic hyperkalaemia to optimise cardiorenal patient prognosis].","authors":"Ingo Eitel, Insa Emrich, Stephan von Haehling, Birgit Schleß, Roland Schmitt, Frank Strutz, Sven Wassmann, Markus van der Giet","doi":"10.1055/a-2755-3785","DOIUrl":"https://doi.org/10.1055/a-2755-3785","url":null,"abstract":"<p><p>Chronic hyperkalemia is an electrolyte imbalance that occurs mainly in patients with progressive kidney failure. It usually develops over a long period of time and symptoms are often mild. As chronic hyperkalemia is associated with increased morbidity and mortality, it should be treated. Treatment begins with a review of the medications that may be responsible for the hyperkalemia and careful therapy and correction of the metabolism. Dietary assessment now focuses on potassium intake from non-vegetable sources. Reducing the dose and/or discontinuing renin-angiotensin-aldosterone inhibitors should be discouraged, as these drugs improve the prognosis in patients with heart failure and proteinuric kidney disease. In addition to other conservative measures, specific potassium-binding substances should be used.</p>","PeriodicalId":93975,"journal":{"name":"Deutsche medizinische Wochenschrift (1946)","volume":" ","pages":""},"PeriodicalIF":0.7,"publicationDate":"2026-01-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146004881","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01Epub Date: 2026-01-20DOI: 10.1055/a-2656-0698
Anette Scholz, Sophie Peter, Achim Mortsiefer
When discharging geriatric patients from inpatient care, hospital and family doctors must consider numerous factors to ensure seamless and safe follow-up treatment. Geriatric patients are usually multimorbid, take many medications (polypharmacy), and have an increased risk of functional limitations or complications after discharge.
{"title":"[Aftercare -Discharge of geriatric patients from hospital - What do hospitals and family doctors need to bear in mind?]","authors":"Anette Scholz, Sophie Peter, Achim Mortsiefer","doi":"10.1055/a-2656-0698","DOIUrl":"https://doi.org/10.1055/a-2656-0698","url":null,"abstract":"<p><p>When discharging geriatric patients from inpatient care, hospital and family doctors must consider numerous factors to ensure seamless and safe follow-up treatment. Geriatric patients are usually multimorbid, take many medications (polypharmacy), and have an increased risk of functional limitations or complications after discharge.</p>","PeriodicalId":93975,"journal":{"name":"Deutsche medizinische Wochenschrift (1946)","volume":"151 3","pages":"103-110"},"PeriodicalIF":0.7,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146013210","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}