{"title":"免疫功能低下患者的脓毒症:韩国的现状","authors":"Kwangha Lee","doi":"10.4266/KJCCM.2015.30.4.239","DOIUrl":null,"url":null,"abstract":"Severely immunocompromised patients have increased risk of infection by common pathogens, as well as opportunistic infections by less virulent microorganisms of little concern to immunocompetent hosts. This highly developing risk of infection predisposes such individuals to increased risk of sepsis and septic shock.[1,2] The most common cause of severe, prolonged, immune compromise is systemic chemotherapy as a treatment for some forms of hematologic malignancies (e.g., induction chemotherapy for acute leukemia and lymphoreticular malignancies), delayed bone marrow recovery following allogenic hematopoietic stem cell transplantation, and solid organ transplantation. Less intensive chemotherapeutic regimens can cause a low incidence of neutropenia and short duration of bone marrow suppression, such as those regimens used for many solid organ malignancies. Also, the steroids used to treat various rheumatologic diseases and human immunodeficiency virus (HIV) infection contribute to immunosuppressive states. In addition, chronic medical illnesses, such as diabetes mellitus, chronic obstructive pulmonary disease, chronic kidney disease, liver cirrhosis, and heart failure, are often associated with immune abnormalities that increase the susceptibility of affected patients to specific life-threatening infections.[3] The frequency of community and hospitalized patients with immunocompromised host defenses has increased dramatically over recent decades such that it is common for intensive care unit (ICU) care physicians to routinely encounter immunocompromised hosts. Despite significant advances in the prevention, diagnosis, and treatment of infection in immunocompromised hosts, infection remains a major cause of morbidity, increased hospital stay, and increased total costs.[4] As a result, the mortality of these patients can be higher because of higher incidence of infection severity. However, the superimposition of compromised host defenses and acute catastrophic illness complicates the detection and management of infection in such patients. Moreover, while there is a rapidly increasing evidence base in critical care medicine, there are no documented management guidelines for sepsis in immunocompromised patients.[5] In Korea, there is no reported data about current status for sepsis in immunocompromised patients. In this issue of the Journal, Oh et al[6] reported the influence of immunosuppressants on in-hospital mortality from sepsis. The authors retrospectively collected data on patients with sepsis from data of Health Insurance Review & Assessment (HIRA) Service over a period of five years (from 2009 to 2013). In their study,","PeriodicalId":255255,"journal":{"name":"The Korean Journal of Critical Care Medicine","volume":"30 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2015-11-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sepsis in Immunocompromised Patients: Current Status in Korea\",\"authors\":\"Kwangha Lee\",\"doi\":\"10.4266/KJCCM.2015.30.4.239\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Severely immunocompromised patients have increased risk of infection by common pathogens, as well as opportunistic infections by less virulent microorganisms of little concern to immunocompetent hosts. This highly developing risk of infection predisposes such individuals to increased risk of sepsis and septic shock.[1,2] The most common cause of severe, prolonged, immune compromise is systemic chemotherapy as a treatment for some forms of hematologic malignancies (e.g., induction chemotherapy for acute leukemia and lymphoreticular malignancies), delayed bone marrow recovery following allogenic hematopoietic stem cell transplantation, and solid organ transplantation. Less intensive chemotherapeutic regimens can cause a low incidence of neutropenia and short duration of bone marrow suppression, such as those regimens used for many solid organ malignancies. Also, the steroids used to treat various rheumatologic diseases and human immunodeficiency virus (HIV) infection contribute to immunosuppressive states. In addition, chronic medical illnesses, such as diabetes mellitus, chronic obstructive pulmonary disease, chronic kidney disease, liver cirrhosis, and heart failure, are often associated with immune abnormalities that increase the susceptibility of affected patients to specific life-threatening infections.[3] The frequency of community and hospitalized patients with immunocompromised host defenses has increased dramatically over recent decades such that it is common for intensive care unit (ICU) care physicians to routinely encounter immunocompromised hosts. Despite significant advances in the prevention, diagnosis, and treatment of infection in immunocompromised hosts, infection remains a major cause of morbidity, increased hospital stay, and increased total costs.[4] As a result, the mortality of these patients can be higher because of higher incidence of infection severity. However, the superimposition of compromised host defenses and acute catastrophic illness complicates the detection and management of infection in such patients. Moreover, while there is a rapidly increasing evidence base in critical care medicine, there are no documented management guidelines for sepsis in immunocompromised patients.[5] In Korea, there is no reported data about current status for sepsis in immunocompromised patients. In this issue of the Journal, Oh et al[6] reported the influence of immunosuppressants on in-hospital mortality from sepsis. The authors retrospectively collected data on patients with sepsis from data of Health Insurance Review & Assessment (HIRA) Service over a period of five years (from 2009 to 2013). 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Sepsis in Immunocompromised Patients: Current Status in Korea
Severely immunocompromised patients have increased risk of infection by common pathogens, as well as opportunistic infections by less virulent microorganisms of little concern to immunocompetent hosts. This highly developing risk of infection predisposes such individuals to increased risk of sepsis and septic shock.[1,2] The most common cause of severe, prolonged, immune compromise is systemic chemotherapy as a treatment for some forms of hematologic malignancies (e.g., induction chemotherapy for acute leukemia and lymphoreticular malignancies), delayed bone marrow recovery following allogenic hematopoietic stem cell transplantation, and solid organ transplantation. Less intensive chemotherapeutic regimens can cause a low incidence of neutropenia and short duration of bone marrow suppression, such as those regimens used for many solid organ malignancies. Also, the steroids used to treat various rheumatologic diseases and human immunodeficiency virus (HIV) infection contribute to immunosuppressive states. In addition, chronic medical illnesses, such as diabetes mellitus, chronic obstructive pulmonary disease, chronic kidney disease, liver cirrhosis, and heart failure, are often associated with immune abnormalities that increase the susceptibility of affected patients to specific life-threatening infections.[3] The frequency of community and hospitalized patients with immunocompromised host defenses has increased dramatically over recent decades such that it is common for intensive care unit (ICU) care physicians to routinely encounter immunocompromised hosts. Despite significant advances in the prevention, diagnosis, and treatment of infection in immunocompromised hosts, infection remains a major cause of morbidity, increased hospital stay, and increased total costs.[4] As a result, the mortality of these patients can be higher because of higher incidence of infection severity. However, the superimposition of compromised host defenses and acute catastrophic illness complicates the detection and management of infection in such patients. Moreover, while there is a rapidly increasing evidence base in critical care medicine, there are no documented management guidelines for sepsis in immunocompromised patients.[5] In Korea, there is no reported data about current status for sepsis in immunocompromised patients. In this issue of the Journal, Oh et al[6] reported the influence of immunosuppressants on in-hospital mortality from sepsis. The authors retrospectively collected data on patients with sepsis from data of Health Insurance Review & Assessment (HIRA) Service over a period of five years (from 2009 to 2013). In their study,