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Saturday, March 17, 2018

Advances in Hematology

Advances in Hematology

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Starting with the concept of blood circulation, which was introduced in 1628, numerous advances have been made in the field of hematology that have significantly improved the lives of patients with hematologic disorders and blazed a trail for advances in other fields. In the last 50 years alone, substantial strides have been made in the research, treatment, and prevention of blood diseases. Listed here are just a few, but those not mentioned are no less important. As past experience has shown us, even some of the most basic research taking place today has the potential to lead to promising life-saving treatments in the future.
A selection of major advances follows. To learn more about some of the top breakthroughs made in the field, please read "50 Years in Hematology: Research That Revolutionized Patient Care." To request copies of the brochure, contact the Webmaster.

Major Advances in Leukemia

  • Cure of Childhood Acute Lymphoblastic Leukemia (ALL)
    ALL was fatal for every child who was diagnosed in the 1960s, but today, after new combinations of drugs were developed and aggressive treatment of the brain and spinal fluid were incorporated, approximately 80 percent of children with the disease are cured. Learn more
  • Targeted Therapy ("smart" drugs) for Chronic Myelogenous Leukemia (CML)
    In the 1950s the only treatment for CML was radiation of the spleen, granting patients about 30 months of survival. The identification of the mutation in the BCR-ABL  caused by a specific chromosomal translocation (when a piece of one chromosome breaks off and attaches to another) led to the development of imatinib, a gene-targeting drug that is the paradigm of a new generation of "smart" drugs. Imatinib is the first drug that has been designed to be so specific that it targets and corrects only the molecular defect that leads to CML (unlike chemotherapy, which targets all rapidly dividing cells, both diseased and normal), sparing patients most of the toxic side-effects that usually come with chemotherapy. Treated with this non-toxic oral drug, more than 75 percent of patients diagnosed with CML now achieve a durable complete cytogenetic remission. This development introduced a new way to think about treating cancer patients. With the disease in long-term remission (inactive, but not necessarily cured) many CML patients can now expect a normal life span. Learn more.
  • Targeted Therapy for Acute Promyelocytic Leukemia (APL)
    APL was once described as the most malignant (rapidly worsening) form of acute leukemia. Leukemia cells contain molecules that disrupt normal function of the hemostatic system (which controls the flow of blood) and, as a result of initial treatments that triggered the release of these molecules, many APL patients bled to death before the chemotherapy they were given had a chance to work. A simple and effective therapy for this process was established in the 1980s that allowed chemotherapy drugs to kill the leukemia cells without initiating the deadly reaction. In combination with chemotherapy, targeted treatment has significantly improved survival in patients with APL and raised remission rates to about 85 percent. Today, the treatment of APL has become a model for treating cancer with targeted therapy.
  • Two major advances were required to develop an effective treatment for APL: the understanding of how and what causes the blood to clot (hemostasis) and the development of targeted therapy (as described for CML above).
  • Improved Survival in Acute Myeloid Leukemia (AML)
    More than 13,000 new cases of AML will be diagnosed in the United States this year. Without treatment, AML can progress quickly and become fatal in just a few months. However, over the past 30 years, new targeted therapies and aggressive chemotherapy have dramatically increased the rate of patients who stay in remission for years or are cured. Today, the initial remission rate is approximately 80 percent.

Major Advances in Lymphoma and Lymphoid Malignancies

  • Cure of Hodgkin Lymphoma
    Today, many patients survive Hodgkin lymphoma. Advancements in radiation therapy and chemotherapy have helped transform this once fatal disorder into a routinely cured disease. More than 80 percent of patients are cured after primary treatment, and the success of treating Hodgkin lymphoma has created hope for curing other forms of cancer. Learn more.
  • Immunotherapy for Non-Hodgkin Lymphoma
    The incidence of non-Hodgkin lymphoma has been increasing since the 1970s, making it the fifth most common cancer in the United States. Recent years have seen the development of promising immunotherapy treatments (which stimulate the body's immune system to fight disease) for patients, increasing survival rates. Studies have shown that five-year survival without recurrence of the lymphoma signals a high likelihood of cure. During the 1960s only 31 percent of patients reached that benchmark. Today, that number has more than doubled to 64 percent.
  • Improved Therapy and Survival in Multiple Myeloma
    There will be more than 19,000 new cases of multiple myeloma this year, and approximately 34 percent of patients survive five years after diagnosis. Unfortunately, there is not yet a cure; however, thanks to advancements in stem cell transplantation and treatment therapies, patients are living longer, healthier lives than they were 30 years ago.

Major Advances in Bleeding and Clotting

  • Development of Effective Treatments for Blood Clots
    Diseases such as heart attacks and strokes arise from clots that form in our blood vessels. These disorders are some of the most common causes of death in developed countries. However, developments in antithrombotic therapy (which prevents or treats clots) have had a huge impact on health. New antithrombotic treatments have lowered the risk of blood clots in leg veins by more than 70 percent, and deaths from heart attacks have been reduced by around 50 percent. Learn more.
  • Development of Clotting Factor Concentrates for Hemophilia Therapy
    For much of the 1960s, the only treatment for hemophilia was to give the patient large volumes of frozen plasma in order to stop bleeding episodes. Generally, children would have to spend three days in the hospital with this type of treatment, and many were reluctant to tell their parents about their injuries, further delaying treatment and gradually leading to chronic joint disease with crippling deformities. Today, clotting factor concentrates are portable and easily stored. Best of all, clotting factor concentrates can be used to treat bleeding episodes without a visit to the hospital. Learn more.
  • Improved Transfusion Therapy Through Screening for Infectious Agents
    In the 1980s patients with hemophilia lived in fear of contracting viruses such as HIV and hepatitis B through the regular blood transfusions they needed to manage the disease. Now, thanks to new recombinant DNA-derived technologies, safe and effective factor concentrates are available, allowing those with hemophilia to treat the bleeding disorder without the constant fear of viral infection. In addition, the development of highly sensitive techniques to screen for viruses has yielded exceptionally safe blood products so that those receiving transfusions can do so with unprecedented confidence. The hematology community continues to improve outcomes and manage risks related to transfusion. Learn more

Major Advances in Genetic Diseases

  • Effective Prenatal Diagnosis of Abnormal Hemoglobins
    Sickle cell disease and thalassemia are among the most common genetic diseases in the United States. Before 1983, there was no national neonatal screening program to detect either disorder. Today, newborns with these diseases greatly benefit from early detection. Those diagnosed with sickle cell disease have a greater rate of survival than children diagnosed later in life.
  • Development of Diagnostic Techniques to Prevent Stroke in Sickle Cell Disease
    Despite progress in understanding the causes of sickle cell disease, the health of patients with this disease was largely ignored until the 1970s. During the 1980s and 1990s, several studies worked to improve the quality of life for these patients. In 1998, transcranial screening allowed doctors to identify sickle cell patients at risk for stroke and treat them with blood transfusions to prevent stroke.

Major Advances in Stem Cell Research

  • Development of Successful Hematopoietic Stem Cell Transplantation
    Today, hematopoietic stem cell transplantation (HSCT) is an important approach for treating blood and bone marrow disorders, as well as certain types of cancer. The earliest work with HSCT began in the 1950s. By the 1960s this treatment was successfully used in patients with end-stage leukemia. Subsequent research in this area has led to improved transplantation techniques and improved survival rates for a number of diseases. Learn more.

Major Advances in Anemia

  • Cloning of Erythropoietin and Development of Recombinant Epo Clinical Use
    More than 50 years ago, patients suffering from anemia due to chemotherapy, chronic kidney disease, AIDS, or other disorders were dependent on frequent blood transfusions in order to replenish their red blood cells. In between transfusions, when their red blood cell counts dropped, they would suffer from weakness, fatigue, and shortness of breath. In the 1950s and 1960s scientists conclusively showed that a hormone in the body, erythropoietin, was responsible for regulating red cell production. Twenty years later, researchers developed a nearly identical, synthetic version of that hormone, known as epoetin alfa (Epo), that could be mass-produced and administered by injection under the skin. Today, millions of patients worldwide have benefited from Epo, one of the most widely used drugs created through recombinant DNA technology. Epo has allowed them to live active lives without the inconvenience and risk of repeated transfusions. Learn more.
  • Immunotherapy for Aplastic Anemia
    Aplastic anemia is a rare and serious condition that can be traced back to 1888. In the past, severe aplastic anemia was fatal to nearly half of all patients regardless of treatment, but with the development of immunosuppressive therapy combined with other treatments, survival rates have substantially improved, and more than 60 percent of patients experience successful responses to immunotherapy.

Blood Banking (Department of transfusion Medicine)

Blood bank

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A blood bank is a center where blood gathered as a result of blood donation is stored and preserved for later use in blood transfusion. The term "blood bank" typically refers to a division of a hospital where the storage of blood product occurs and where proper testing is performed (to reduce the risk of transfusion related adverse events). However, it sometimes refers to a collection center, and indeed some hospitals also perform collection.


Storage and management[edit]

Routine blood storage is 42 days or 6 weeks for stored packed red blood cells (also called "StRBC" or "pRBC"), by far the most commonly transfused blood product, and involves refrigeration but usually not freezing. There has been increasing controversy about whether a given product unit's age is a factor in transfusion efficacy, specifically on whether "older" blood directly or indirectly increases risks of complications.[15][16] Studies have not been consistent on answering this question,[17] with some showing that older blood is indeed less effective but with others showing no such difference; nevertheless, as storage time remains the only available way to estimate quality status or loss, a first-in-first-out inventory management approach is standard presently.[18] It is also important to consider that there is large variability in storage results for different donors, which combined with limited available quality testing, poses challenges to clinicians and regulators seeking reliable indicators of quality for blood products and storage systems.[19]
Transfusions of platelets are comparatively far less numerous, but they present unique storage/management issues. Platelets may only be stored for 7 days,[20] due largely to their greater potential for contamination, which is in turn due largely to a higher storage temperature.

RBC storage lesion[edit]

Insufficient transfusion efficacy can result from red blood cell (RBC) blood product units damaged by so-called storage lesion—a set of biochemical and biomechanical changes which occur during storage. With red cells, this can decrease viability and ability for tissue oxygenation.[21] Although some of the biochemical changes are reversible after the blood is transfused,[22] the biomechanical changes are less so,[23] and rejuvenation products are not yet able to adequately reverse this phenomenon.[24]
Current regulatory measures are in place to minimize RBC storage lesion—including a maximum shelf life (currently 42 days), a maximum auto-hemolysis threshold (currently 1% in the US), and a minimum level of post-transfusion RBC survival in vivo (currently 75% after 24 hours).[25] However, all of these criteria are applied in a universal manner that does not account for differences among units of product;[19] for example, testing for the post-transfusion RBC survival in vivo is done on a sample of healthy volunteers, and then compliance is presumed for all RBC units based on universal (GMP) processing standards. RBC survival does not guarantee efficacy, but it is a necessary prerequisite for cell function, and hence serves as a regulatory proxy. Opinions vary as to the best way to determine transfusion efficacy in a patient in vivo.[26] In general, there are not yet any in vitro tests to assess quality deterioration or preservation for specific units of RBC blood product prior to their transfusion, though there is exploration of potentially relevant tests based on RBC membrane properties such as erythrocyte deformability[27] and erythrocyte fragility (mechanical).[28]

Platelet storage lesion[edit]

Platelet storage lesion is a very different phenomenon from RBC storage lesion, due largely to the different functions of the products and purposes of the respective transfusions, along with different processing issues and inventory management considerations.[31]

Alternative inventory and release practices[edit]

Although as noted the primary inventory-management approach is first in, first out (FIFO) to minimize product expiration, there are some deviations from this policy—both in current practice as well as under research. For example, exchange transfusion of RBC in neonates calls for use of blood product that is five days old or less, to "ensure" optimal cell function.[32] Also, some hospital blood banks will attempt to accommodate physicians' requests to provide low-aged RBC product for certain kinds of patients (e.g. cardiac surgery).[33]

Blood Banking and Donation

Blood banking refers to the process of collecting, separating, and storing blood. The first U.S. blood bank was established in 1936. Today, blood banks collect blood and separate it into its various components so they can be used most effectively according to the needs of the patient. Red blood cells carry oxygen, platelets help the blood clot, and plasma has specific proteins that allow proper regulation of coagulation and healing. Although research has yielded drugs that help people's bone marrow produce new blood cells more rapidly, the body's response time can still take weeks, thus donated blood remains an important and more immediate life-saving resource.
Blood is the vital connection to having a healthy body, and according to the American Red Cross, nearly 5 million people receive blood transfusions each year. Thanks to years of research, much progress has been made towards making transfusions safer and more effective.


Sunday, March 31, 2013

MEDICAL LABORATORY TECHNOLOGY INFORMATION: Medical laboratory Technology:-A medical laborator...




A medical laboratory or clinical laboratory is a laboratory where tests are usually done on clinical specimens in order to obtain information about the health of a patient as pertaining to the diagnosis, treatment, and prevention of disease.[1] Clinical laboratories are thus focused on applied science mainly on a production-like basis, as opposed to research laboratories that focus on basic science on an academic basis.

Departments

Laboratory medicine is generally divided into two sections, each of which being subdivided into multiple units. These two sections are

Types of laboratory


In many countries, there are two main types of labs that process the majority of medical specimens. Hospital laboratories are attached to a hospital, and perform tests on patients. Private (or community) laboratories receive samples from general practitioners, insurance companies, clinical research sites and other health clinics for analysis. For extremely specialised tests, samples may go to a research laboratory. A lot of samples are sent between different labs for uncommon tests. It is more cost effective if a particular laboratory specializes in a rare test, receiving specimens (and money) from other labs, while sending away tests it cannot do.
In many countries there are mainly three types of Medical Laboratories as per the types of investigations carried out. 1. Clinical Pathology: Haematology, Histopathology, Cytology, Routine Pathology2. Clinical Microbiology: Bacteriology, Mycobacteriology, Virology, Mycology, Parasitology, Immunology, Serology.3. Clinical Biochemistry: Biochemical analysis, Hormonal assays etc.Blood Banks:- Blood bank is a separate body. Its laboratory need Microbiological analysis for infectious diseases that may be found in blood. Pathology to observe Blood grouping, Haematology & cross matching reactions. It also involves PRO department for the communication & contact for blood donations etc.. Molecular diagnostic lab or cytogenetics and molecular biology lab is the latest addition to the three types of medical laboratories listed above in many countries.


Medical laboratory accreditation

Credibility of medical laboratories is paramount to the health and safety of the patients relying on the testing services provided by these labs. The international standard in use today for the accreditation of medical laboratories is ISO 15189 - Medical laboratories - Requirements for quality and competence.
Accreditation is done by the Joint Commission, College of American Pathologists, AAB (American Association of Bioanalysts), and other state and federal agencies. CLIA 88 or the Clinical Laboratory Improvement Amendments also dictate testing and personnel.
The accrediting body in Australia is NATA, all laboratories must be NATA accredited to receive payment from Medicare.
In France, where accrediting body is COFRAC (COFRAC), in 2010, modification of legislation established ISO 15189 accreditation as an obligation for all clinical laboratories.[2]
In the United Arab Emirates, the Dubai Accreditation Department is the accreditation body that is internationally recognised[3] by the International Laboratory Accreditation Cooperation (ILAC) for many scopes including Medical Laboratories, Testing and Calibration Laboratories and Inspection Bodies.
In Hong Kong, the accrediting body is Hong Kong Accreditation Service (). On 16 February 2004, HKAS launched the medical testing accreditation programme.
In Canada, laboratory accreditation is not mandatory, but is becoming more and more popular. Accreditation Canada bis the national reference.