Trypanosomiasis is a vector-borne parasitic disease caused by Trypanosoma parasites. There are two main forms: African trypanosomiasis (sleeping sickness) transmitted by tsetse flies, and American trypanosomiasis (Chagas disease) transmitted by triatomine bugs. African trypanosomiasis is found in Central and East Africa and causes a slow progression of symptoms, while American trypanosomiasis is found in Latin America and causes an initial acute phase followed by a chronic phase in some patients. Both forms require treatment with drugs to eliminate the parasites from the body.
Trypanosomiasis, also known as sleeping sickness, is caused by protozoan parasites that are transmitted to humans via the bites of infected tsetse flies or reduviid bugs. There are two forms: African trypanosomiasis, which is found in central and eastern Africa, and Chagas disease, found in Latin America. Both forms initially cause fever, joint pain, and swelling and if left untreated can spread to the central nervous system, causing behavioral changes, confusion, and eventually death. Diagnosis involves examining blood or cerebrospinal fluid samples microscopically for parasites. Treatment depends on the stage of the disease and involves pentamidine, suramin, melarsoprol,
Trypanosomiasis, also known as sleeping sickness, is caused by infection with Trypanosoma brucei parasites transmitted through bites from tsetse flies. There are two main forms: West African trypanosomiasis caused by T. b. gambiense transmitted by Glossina palpalis flies, and East African trypanosomiasis caused by T. b. rhodesiense transmitted by Glossina morsitans flies. The disease progresses in stages from an initial skin lesion and fever to later invasion of the central nervous system causing neurological symptoms. Diagnosis involves microscopic examination of blood, lymph node aspirates, or cerebrospinal fluid for the motile parasites
Malaria is caused by a parasite transmitted via mosquito bites. It causes cyclical fevers and other flu-like symptoms. The parasite travels to the liver and bloodstream, infecting and destroying red blood cells. Early diagnosis and treatment are important to prevent severe illness and death. Control relies on preventing mosquito bites, chemoprophylaxis for travelers, larviciding, and rapid treatment of cases.
African trypanosomiasis is caused by the protozoan Trypanosoma brucei, which is transmitted to humans via the bite of infected tsetse flies. There are two subspecies that cause distinct forms of the disease: T. b. gambiense causes chronic West African sleeping sickness while T. b. rhodesiense causes acute East African sleeping sickness. The parasite infects the blood and lymphatic system initially, then the central nervous system, causing neurological symptoms like disrupted sleep patterns that give the disease its name. Diagnosis involves microscopic identification of the parasite in samples like blood, lymph nodes or cerebrospinal fluid. Treatment depends on the stage and subtype, but may include drugs
Variola virus causes the acute, contagious disease smallpox. It was effectively eradicated through global vaccination efforts led by the WHO between 1966-1979. Smallpox is characterized by an initial fever and flu-like symptoms followed by a distinctive pustular rash. It spreads through respiratory droplets or direct contact with infected individuals or contaminated objects. Vaccination provided effective immunity and was a major factor in eliminating smallpox worldwide by 1980, making it the only human infectious disease to be fully eradicated.
Trypanosomiasis, also known as sleeping sickness, is caused by protozoan parasites that are transmitted to humans via the bites of infected tsetse flies or reduviid bugs. There are two forms: African trypanosomiasis, which is found in central and eastern Africa, and Chagas disease, found in Latin America. Both forms initially cause fever, joint pain, and swelling and if left untreated can spread to the central nervous system, causing behavioral changes, confusion, and eventually death. Diagnosis involves examining blood or cerebrospinal fluid samples microscopically for parasites. Treatment depends on the stage of the disease and involves pentamidine, suramin, melarsoprol,
Trypanosomiasis, also known as sleeping sickness, is caused by infection with Trypanosoma brucei parasites transmitted through bites from tsetse flies. There are two main forms: West African trypanosomiasis caused by T. b. gambiense transmitted by Glossina palpalis flies, and East African trypanosomiasis caused by T. b. rhodesiense transmitted by Glossina morsitans flies. The disease progresses in stages from an initial skin lesion and fever to later invasion of the central nervous system causing neurological symptoms. Diagnosis involves microscopic examination of blood, lymph node aspirates, or cerebrospinal fluid for the motile parasites
Malaria is caused by a parasite transmitted via mosquito bites. It causes cyclical fevers and other flu-like symptoms. The parasite travels to the liver and bloodstream, infecting and destroying red blood cells. Early diagnosis and treatment are important to prevent severe illness and death. Control relies on preventing mosquito bites, chemoprophylaxis for travelers, larviciding, and rapid treatment of cases.
African trypanosomiasis is caused by the protozoan Trypanosoma brucei, which is transmitted to humans via the bite of infected tsetse flies. There are two subspecies that cause distinct forms of the disease: T. b. gambiense causes chronic West African sleeping sickness while T. b. rhodesiense causes acute East African sleeping sickness. The parasite infects the blood and lymphatic system initially, then the central nervous system, causing neurological symptoms like disrupted sleep patterns that give the disease its name. Diagnosis involves microscopic identification of the parasite in samples like blood, lymph nodes or cerebrospinal fluid. Treatment depends on the stage and subtype, but may include drugs
Variola virus causes the acute, contagious disease smallpox. It was effectively eradicated through global vaccination efforts led by the WHO between 1966-1979. Smallpox is characterized by an initial fever and flu-like symptoms followed by a distinctive pustular rash. It spreads through respiratory droplets or direct contact with infected individuals or contaminated objects. Vaccination provided effective immunity and was a major factor in eliminating smallpox worldwide by 1980, making it the only human infectious disease to be fully eradicated.
This document discusses the Reduviid bug and its association with Chagas disease. It describes the classification, morphology, feeding habits, and life cycle of the Reduviid bug, which transmits the parasite Trypanosoma cruzi that causes Chagas disease. Chagas disease results in acute and chronic inflammatory changes and affects the heart, intestines and other tissues. It is most prevalent in rural areas of Mexico, South America and Central America, and transmission occurs through the bite of infected Reduviid bugs or consumption of contaminated food. Prevention focuses on education, insecticide use, housing modifications and screening of blood supplies.
Malaria is a mosquito-borne infectious disease caused by Plasmodium parasites. P. falciparum is the most dangerous species and a major cause of mortality in developing countries. It is transmitted via the bites of infected female Anopheles mosquitoes. Symptoms include fever, chills, and flu-like illness. Diagnosis involves examining blood films under a microscope for parasites. Treatment depends on the species and severity, but uncomplicated cases are typically treated with artemisinin-based combination therapies over 3 days. Nursing care, chemoprophylaxis, and controlling the mosquito vector are also important aspects of malaria control and management.
Malaria remains a major global health problem, with an estimated 219 million cases and 435,000 deaths in 2017. The disease is caused by Plasmodium parasites and transmitted via the bites of infected Anopheles mosquitoes. The WHO African Region carries the largest burden, with 92% of cases and 93% of deaths. Young children, pregnant women, and non-immune travelers are most at risk. Diagnosis is via blood smear examination, with treatment using artemisinin combination therapies. Prevention relies on mosquito control measures and the use of insecticide-treated bed nets. Efforts aim to eventually eliminate and eradicate the disease globally.
This document discusses two genera of parasites, Leishmania and Trypanosoma, that cause diseases in humans. It describes the four major Leishmania pathogens, their life cycles involving sandflies, clinical manifestations including visceral leishmaniasis and cutaneous leishmaniasis, and methods of laboratory diagnosis. It also discusses the three major Trypanosoma pathogens, their life cycles involving reduviid bugs or tsetse flies, diseases caused including Chagas disease and sleeping sickness, clinical features, and diagnosis. The document provides detailed information on the pathogenesis, epidemiology, symptoms and laboratory identification of infections caused by these important parasites.
Leishmaniasis is a parasitic disease transmitted through sandfly bites that causes three main forms: cutaneous (skin lesions), visceral (liver, spleen, bone marrow), and mucocutaneous (mouth, nose). It is endemic in 88 countries, infecting 12 million people annually. In the Middle East, L. major causes cutaneous disease while L. tropica causes cutaneous and sometimes visceral disease. Diagnosis requires biopsy identification of the parasite. Treatment depends on the form, with antimony recommended for cutaneous and mucocutaneous disease and liposomal amphotericin B for visceral disease.
powerpoint for mapeh 8 (health 8) quarter 3.pptxELLAMAYDECENA2
- Pathogens are organisms that cause disease and include viruses, bacteria, fungi, protozoa, and parasites.
- Bacteria and fungi are important in ecosystems but some species can cause illness in humans. Viruses and parasites rely on living hosts.
- Common diseases result from pathogens like influenza and SARS-CoV-2 viruses, malaria protozoa, and roundworm infections. Those with weak immune systems face higher risks. Prevention focuses on hygiene, sanitation, and treatment of infections.
Leishmania is a genus of protozoan parasites that cause leishmaniasis, a vector-borne disease transmitted by sandflies. It is endemic in many parts of Africa, Asia and South America. There are several species that cause different clinical manifestations depending on the part of the body affected. Visceral leishmaniasis affects internal organs while cutaneous and mucocutaneous leishmaniasis affect the skin and mucous membranes. The parasite has two forms - amastigotes found inside host cells and promastigotes found in the sandfly vector. There is no vaccine and treatment involves drugs like pentavalent antimonials or amphotericin B. Control relies on reducing vector populations
The name is derived from Greek word,
Trypano means (borer)
Soma means (body)
They are unicellular flagellate protozoa.
Have corkscrew like motion.
Oftenly transmitted by a vector.
Malaria is a major public health problem that affects many countries and causes nearly 1 million deaths annually. It is caused by a protozoan parasite (Plasmodium) transmitted via the bites of infected Anopheles mosquitoes. There are four human malaria parasite species, with P. falciparum being the most deadly. Malaria transmission is influenced by factors like temperature, human and mosquito behavior, drug resistance, and control measures. The WHO classifies malaria epidemiology into several types based on transmission patterns and intensity in different geographic areas.
This document summarizes several important blood protozoa: Trypanosoma brucei causes African sleeping sickness and is transmitted by tsetse flies; Trypanosoma cruzi causes Chagas disease and is transmitted by triatomine bugs; Leishmania species cause leishmaniasis which exists in visceral, cutaneous, and mucocutaneous forms; and Plasmodium species cause malaria with different species having distinct life cycles and host cell preferences. It provides details on the morphology, life cycles, transmission routes, geographical distribution and clinical stages of these protozoan parasites.
Neglected-tropical-diseasesindia and world.pptxAdhyaDubey1
This document discusses neglected tropical diseases (NTDs), a group of infectious diseases that plague millions worldwide in tropical areas with weak infrastructure. It outlines several specific NTDs, including their causative agents, transmission cycles, geographical distribution, symptoms, impacts on health and socioeconomics, current prevalence figures, and treatment approaches. The WHO's integrated strategy to control NTDs through preventive chemotherapy, vector control, veterinary public health, water and sanitation, and innovative disease management is also summarized.
Neglected-tropical-diseasesindia and world.pptxAdhyaDubey1
This document discusses neglected tropical diseases (NTDs), a group of infectious diseases that plague millions worldwide in tropical areas with weak infrastructure. It outlines several specific NTDs, including their causative agents, transmission cycles, geographical distribution, symptoms, impacts on health and socioeconomics, current prevalence figures, and treatment approaches. The WHO's integrated strategy to control NTDs through preventive chemotherapy, vector control, veterinary public health, water and sanitation, and innovative disease management is also summarized.
Flagellated and amoebozoid parasitic protozoansMerlyn Denesia
Parasitic protozoans can be flagellated, amoeboid, sporozoans, or ciliated. This document focuses on several disease-causing flagellated protozoans including Trypanosoma, Leishmania, and Chilomastix. Trypanosoma brucei causes African sleeping sickness while Trypanosoma cruzi causes Chagas disease. Leishmania species cause leishmaniasis. These parasites have complex life cycles involving insect vectors and mammalian hosts. They can cause acute and chronic infections impacting multiple organ systems. Diagnosis involves microscopic examination, serology, PCR and treatment consists of drugs like melarsoprol, nifurtimox
The document discusses leprosy and plague. It provides information on the causative agents, symptoms, transmission, diagnosis and treatment of both diseases. For leprosy, it describes Mycobacterium leprae and the different classifications of the disease. It also discusses the WHO recommended multidrug therapy. For plague, it outlines the bacterium Yersinia pestis and the different forms it can take including bubonic, septicemic and pneumonic plague. Diagnosis and treatment options for plague are also presented.
This document summarizes information about four pathogens - Leishmania donovani, Leishmania tropica, Trypanosoma cruzi, and Trypanosoma gambiense/rhodesiense. It describes their life cycles, which involve transmission between hosts via sandfly or tsetse fly vectors. It also discusses the diseases they cause, including visceral leishmaniasis, cutaneous leishmaniasis, Chagas disease, and sleeping sickness. Signs and symptoms are provided for each disease's acute and chronic stages. Methods for laboratory diagnosis focus on identifying the pathogens in blood, tissue, or spinal fluid samples via microscopy or serology.
The document discusses several protists from the class Zoomastigota, including Trypanosoma brucei, Leishmania species, and Trichomonas vaginalis. It describes their morphology, life cycles, hosts, transmission methods, locations in the host body, and the diseases they cause. The diseases covered are African trypanosomiasis, leishmaniasis, Chagas disease, and trichomoniasis. Diagnosis and prevention methods for these diseases are also summarized.
Leishmaniasis is caused by protozoan parasites of the genus Leishmania transmitted by sandfly bites. It presents clinically as cutaneous, mucocutaneous, or visceral leishmaniasis depending on the infecting species. Cutaneous leishmaniasis causes skin lesions while mucocutaneous involvement can also affect mucosal tissues. Visceral leishmaniasis affects internal organs like the liver and spleen and can be fatal if not treated. Diagnosis involves identifying the parasites in tissues or cultures and treatment depends on the clinical form and involves antimonial drugs or amphotericin B.
Leishmaniasis is caused by protozoan parasites of the genus Leishmania transmitted by sandfly bites. It presents clinically as cutaneous, mucocutaneous, or visceral leishmaniasis depending on the infecting species. Cutaneous leishmaniasis causes skin lesions while mucocutaneous involvement can also affect mucosal tissues. Visceral leishmaniasis affects internal organs like the liver and spleen and can be fatal if not treated. Diagnosis involves identifying the parasites in tissues or cultures and treatment depends on the clinical form and involves antimonial drugs or amphotericin B. Prevention focuses on reducing sandfly bites and reservoirs.
Leishmaniasis is caused by protozoan parasites of the genus Leishmania transmitted by sandfly bites. It presents clinically as cutaneous, mucocutaneous, or visceral leishmaniasis depending on the infecting species. Cutaneous leishmaniasis causes skin lesions while mucocutaneous involvement can also affect mucosal tissues. Visceral leishmaniasis affects internal organs like the liver and spleen and can be fatal if not treated. Diagnosis involves identifying the parasites in tissues or cultures and treatment depends on the clinical form and involves antimonial drugs or amphotericin B.
Patiwnt notes, history taking systematic screwing if patients to arrive at impression. Examination guide on assessment of patient normal anatomy and physiology by review of the body systems, central nervous system, Gastrointestinal , Cardiopulmonary , Genitourinary and Muskuloskeleal system review and examination
The anatomy of the cerebrum. External features of the CEREBRUM, sulci and gyri , folds and groves on the cerebral cortex. The cerebral hemispheres and their division s.
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This document discusses the Reduviid bug and its association with Chagas disease. It describes the classification, morphology, feeding habits, and life cycle of the Reduviid bug, which transmits the parasite Trypanosoma cruzi that causes Chagas disease. Chagas disease results in acute and chronic inflammatory changes and affects the heart, intestines and other tissues. It is most prevalent in rural areas of Mexico, South America and Central America, and transmission occurs through the bite of infected Reduviid bugs or consumption of contaminated food. Prevention focuses on education, insecticide use, housing modifications and screening of blood supplies.
Malaria is a mosquito-borne infectious disease caused by Plasmodium parasites. P. falciparum is the most dangerous species and a major cause of mortality in developing countries. It is transmitted via the bites of infected female Anopheles mosquitoes. Symptoms include fever, chills, and flu-like illness. Diagnosis involves examining blood films under a microscope for parasites. Treatment depends on the species and severity, but uncomplicated cases are typically treated with artemisinin-based combination therapies over 3 days. Nursing care, chemoprophylaxis, and controlling the mosquito vector are also important aspects of malaria control and management.
Malaria remains a major global health problem, with an estimated 219 million cases and 435,000 deaths in 2017. The disease is caused by Plasmodium parasites and transmitted via the bites of infected Anopheles mosquitoes. The WHO African Region carries the largest burden, with 92% of cases and 93% of deaths. Young children, pregnant women, and non-immune travelers are most at risk. Diagnosis is via blood smear examination, with treatment using artemisinin combination therapies. Prevention relies on mosquito control measures and the use of insecticide-treated bed nets. Efforts aim to eventually eliminate and eradicate the disease globally.
This document discusses two genera of parasites, Leishmania and Trypanosoma, that cause diseases in humans. It describes the four major Leishmania pathogens, their life cycles involving sandflies, clinical manifestations including visceral leishmaniasis and cutaneous leishmaniasis, and methods of laboratory diagnosis. It also discusses the three major Trypanosoma pathogens, their life cycles involving reduviid bugs or tsetse flies, diseases caused including Chagas disease and sleeping sickness, clinical features, and diagnosis. The document provides detailed information on the pathogenesis, epidemiology, symptoms and laboratory identification of infections caused by these important parasites.
Leishmaniasis is a parasitic disease transmitted through sandfly bites that causes three main forms: cutaneous (skin lesions), visceral (liver, spleen, bone marrow), and mucocutaneous (mouth, nose). It is endemic in 88 countries, infecting 12 million people annually. In the Middle East, L. major causes cutaneous disease while L. tropica causes cutaneous and sometimes visceral disease. Diagnosis requires biopsy identification of the parasite. Treatment depends on the form, with antimony recommended for cutaneous and mucocutaneous disease and liposomal amphotericin B for visceral disease.
powerpoint for mapeh 8 (health 8) quarter 3.pptxELLAMAYDECENA2
- Pathogens are organisms that cause disease and include viruses, bacteria, fungi, protozoa, and parasites.
- Bacteria and fungi are important in ecosystems but some species can cause illness in humans. Viruses and parasites rely on living hosts.
- Common diseases result from pathogens like influenza and SARS-CoV-2 viruses, malaria protozoa, and roundworm infections. Those with weak immune systems face higher risks. Prevention focuses on hygiene, sanitation, and treatment of infections.
Leishmania is a genus of protozoan parasites that cause leishmaniasis, a vector-borne disease transmitted by sandflies. It is endemic in many parts of Africa, Asia and South America. There are several species that cause different clinical manifestations depending on the part of the body affected. Visceral leishmaniasis affects internal organs while cutaneous and mucocutaneous leishmaniasis affect the skin and mucous membranes. The parasite has two forms - amastigotes found inside host cells and promastigotes found in the sandfly vector. There is no vaccine and treatment involves drugs like pentavalent antimonials or amphotericin B. Control relies on reducing vector populations
The name is derived from Greek word,
Trypano means (borer)
Soma means (body)
They are unicellular flagellate protozoa.
Have corkscrew like motion.
Oftenly transmitted by a vector.
Malaria is a major public health problem that affects many countries and causes nearly 1 million deaths annually. It is caused by a protozoan parasite (Plasmodium) transmitted via the bites of infected Anopheles mosquitoes. There are four human malaria parasite species, with P. falciparum being the most deadly. Malaria transmission is influenced by factors like temperature, human and mosquito behavior, drug resistance, and control measures. The WHO classifies malaria epidemiology into several types based on transmission patterns and intensity in different geographic areas.
This document summarizes several important blood protozoa: Trypanosoma brucei causes African sleeping sickness and is transmitted by tsetse flies; Trypanosoma cruzi causes Chagas disease and is transmitted by triatomine bugs; Leishmania species cause leishmaniasis which exists in visceral, cutaneous, and mucocutaneous forms; and Plasmodium species cause malaria with different species having distinct life cycles and host cell preferences. It provides details on the morphology, life cycles, transmission routes, geographical distribution and clinical stages of these protozoan parasites.
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This document discusses neglected tropical diseases (NTDs), a group of infectious diseases that plague millions worldwide in tropical areas with weak infrastructure. It outlines several specific NTDs, including their causative agents, transmission cycles, geographical distribution, symptoms, impacts on health and socioeconomics, current prevalence figures, and treatment approaches. The WHO's integrated strategy to control NTDs through preventive chemotherapy, vector control, veterinary public health, water and sanitation, and innovative disease management is also summarized.
Neglected-tropical-diseasesindia and world.pptxAdhyaDubey1
This document discusses neglected tropical diseases (NTDs), a group of infectious diseases that plague millions worldwide in tropical areas with weak infrastructure. It outlines several specific NTDs, including their causative agents, transmission cycles, geographical distribution, symptoms, impacts on health and socioeconomics, current prevalence figures, and treatment approaches. The WHO's integrated strategy to control NTDs through preventive chemotherapy, vector control, veterinary public health, water and sanitation, and innovative disease management is also summarized.
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Parasitic protozoans can be flagellated, amoeboid, sporozoans, or ciliated. This document focuses on several disease-causing flagellated protozoans including Trypanosoma, Leishmania, and Chilomastix. Trypanosoma brucei causes African sleeping sickness while Trypanosoma cruzi causes Chagas disease. Leishmania species cause leishmaniasis. These parasites have complex life cycles involving insect vectors and mammalian hosts. They can cause acute and chronic infections impacting multiple organ systems. Diagnosis involves microscopic examination, serology, PCR and treatment consists of drugs like melarsoprol, nifurtimox
The document discusses leprosy and plague. It provides information on the causative agents, symptoms, transmission, diagnosis and treatment of both diseases. For leprosy, it describes Mycobacterium leprae and the different classifications of the disease. It also discusses the WHO recommended multidrug therapy. For plague, it outlines the bacterium Yersinia pestis and the different forms it can take including bubonic, septicemic and pneumonic plague. Diagnosis and treatment options for plague are also presented.
This document summarizes information about four pathogens - Leishmania donovani, Leishmania tropica, Trypanosoma cruzi, and Trypanosoma gambiense/rhodesiense. It describes their life cycles, which involve transmission between hosts via sandfly or tsetse fly vectors. It also discusses the diseases they cause, including visceral leishmaniasis, cutaneous leishmaniasis, Chagas disease, and sleeping sickness. Signs and symptoms are provided for each disease's acute and chronic stages. Methods for laboratory diagnosis focus on identifying the pathogens in blood, tissue, or spinal fluid samples via microscopy or serology.
The document discusses several protists from the class Zoomastigota, including Trypanosoma brucei, Leishmania species, and Trichomonas vaginalis. It describes their morphology, life cycles, hosts, transmission methods, locations in the host body, and the diseases they cause. The diseases covered are African trypanosomiasis, leishmaniasis, Chagas disease, and trichomoniasis. Diagnosis and prevention methods for these diseases are also summarized.
Leishmaniasis is caused by protozoan parasites of the genus Leishmania transmitted by sandfly bites. It presents clinically as cutaneous, mucocutaneous, or visceral leishmaniasis depending on the infecting species. Cutaneous leishmaniasis causes skin lesions while mucocutaneous involvement can also affect mucosal tissues. Visceral leishmaniasis affects internal organs like the liver and spleen and can be fatal if not treated. Diagnosis involves identifying the parasites in tissues or cultures and treatment depends on the clinical form and involves antimonial drugs or amphotericin B.
Leishmaniasis is caused by protozoan parasites of the genus Leishmania transmitted by sandfly bites. It presents clinically as cutaneous, mucocutaneous, or visceral leishmaniasis depending on the infecting species. Cutaneous leishmaniasis causes skin lesions while mucocutaneous involvement can also affect mucosal tissues. Visceral leishmaniasis affects internal organs like the liver and spleen and can be fatal if not treated. Diagnosis involves identifying the parasites in tissues or cultures and treatment depends on the clinical form and involves antimonial drugs or amphotericin B. Prevention focuses on reducing sandfly bites and reservoirs.
Leishmaniasis is caused by protozoan parasites of the genus Leishmania transmitted by sandfly bites. It presents clinically as cutaneous, mucocutaneous, or visceral leishmaniasis depending on the infecting species. Cutaneous leishmaniasis causes skin lesions while mucocutaneous involvement can also affect mucosal tissues. Visceral leishmaniasis affects internal organs like the liver and spleen and can be fatal if not treated. Diagnosis involves identifying the parasites in tissues or cultures and treatment depends on the clinical form and involves antimonial drugs or amphotericin B.
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Patiwnt notes, history taking systematic screwing if patients to arrive at impression. Examination guide on assessment of patient normal anatomy and physiology by review of the body systems, central nervous system, Gastrointestinal , Cardiopulmonary , Genitourinary and Muskuloskeleal system review and examination
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Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
- Video recording of this lecture in Arabic language: https://youtu.be/SINlygW1Mpc
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
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Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
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Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
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• Building trust with communities online and offline
• Equipping health professionals to address questions, concerns and health misinformation
• Assessing risk and mitigating harm from adverse health narratives in communities, health workforce and health system
2. TWO FORMS OF TRYPANOSOMIASIS
• Trypanosomiasis is a vector borne parasitic disease
• Two types:
a) African Trypanosomiasis (sleeping sickness)
b) American Trypanosomiasis (chagas disease)
4. INTRODUCTION
• Caused by infection with protozoan parasite , Trypanosoma brucei
• Transmitted to humans by vector, Tsetse fly (glossina species)
• The vector, Tsetse fly is found only in the African regions
• T.brucei gambiense – West African sleeping sickness
• T.brucei rhodesiense – East African sleeping sickness
5. EPIDEMIOLOGY
• Sleeping sickness occurs only in 36 sub-Saharan African countries
• T.brucei gambiense accounts for > 98% of cases of sleeping sickness
• Annual number of cases – 7000 to 10000
• In 1998 – 40000 cases
• In 2009 – 9478 cases
• In 2013 – 7216 cases
6. EPIDEMICS IN THE PAST
• One between 1896 and 1906 – Uganda & Congo basin
• One in 1920 – number of African countries
• Recent epidemic in 1970 and lasted till late 1990s
• 1920 epidemic was controlled by mobile teams which screened millions of
people
• <5000 cases reported in mid-sixties
• After this success, surveillance measures were relaxed which led to
reappearing of the disease
8. MODES OF TRANSMISSION
• The most common method of transmission is by the bite of the tsetse
fly
• Mother to child transmission
• Mechanical transmission
• Accidental infection from laboratories
9. CLINICAL FEATURES
• Two stages:
a) Haemolymphatic stage: multiplies in peripheral
circulation, subcutaneous tissues and lymph
b) Neurological/Meningoencephalic stage: enters CNS by
crossing blood brain barrier
Without treatment the disease is fatal…
10. CLINICAL FEATURES
Characteristic T.b.gambiense T.b.rhodesiense
Disease progression Slow Rapid
Stage I Symptoms Fever, headache, malaise Fever, swollen
lymphnodes, itching
Time of CNS invasion 1 to 2 years 4 to 5 weeks
Stage II Symptoms Daytime sleepiness with
Night time sleep
disturbance, paralysis,
coma
Mental deterioration
Time to death 2 to 4 years Within months
11. DIAGNOSIS
• Screening:
Serological tests are used(available only for T.gambiense)
Serological tests are not reliable
• Microscopic Examination:
Lymph & blood – Stage I infection
CSF – Stage II infection & for staging
Parasites are not easily visible in T.gambiense infections and so
concentration techniques may be used
• Clinical Examination:
For Posterior cervical lymphadenopathy
Not a Preferred method for diagnosis
12. TREATMENT FOR STAGE I
• Pentamidine:
- discovered in 1941
- used against T.b.gambiense
- generally well tolerated
• Suramin:
- discovered in 1921
- used against T.b.rhodesiense
- causes Urinary tract problems and allergic reactions
13. TREATMENT FOR STAGE II
• Melarsoprolol:
- discovered in 1949(derived from arsenic)
- used against both the species
- causes reactive encephalopathy which can be fatal
• Eflornithine:
- discovered in 1990
- effective against T.b.gambiense only
- treatment regimen is strict but less toxic than melarsoprolol
• Combination of nifurtimox & eflornithine is used since 2009, effective
against T.b.gambiense only.
15. VECTOR(TSETSE FLY)
• Morphology:
Glossinae are bloodsucking flies
Resembles the common housefly in appearance
Yellow or Dark-brown in colour
Measures about half an inch
Pair of wings are present which when folded, overlap each other
Rigid and non-retractile proboscis for sucking blood is seen
Found only in Africa
16. TSETSE FLY
• Life history:
The female does not lay eggs, but gives birth to a living larva, one
at a time, 10 day intervals
The larva crawls to a suitable place and buries at an inch or so
from the surface
Pupation starts in a few hours and lasts for a month
At the end of pupation, adult fly emerges
It lives for 100 days
17. TSETSE FLY
• Species and Habits:
More than 30 species are found but only 4 are dangerous to man
G.palpalis
G.tachinoides
G.morsitans
G.pallidepes
• Both the male and female flies bites
Riverine species
Savannah species
Attacks man
Attacks game
18. CONTROL OF AFRICAN SLEEPING SICKNESS
• Control involves 2 strategies:
1) Control of the reservoir
2) Control of the vector
• Control of the reservoir:
Humans are the major vectors for T.b.gambiense and so control is
mainly by population screening and treatment of the disease in those
who are having the disease
Various animal hosts acts as reservoir for T.b.rhodesiense
infections, hence control of reservoir is very difficult with rhodesiense.
19. CONTROL OF THE VECTOR(TSETSE FLIES)
• 1) Insecticides: DDT(25%) and Dieldrin(20%) are used. The insecticide
is applied from aircraft when large areas are to be covered
• 2) Clearing of vegetation: where tsetse flies live and breed. It gives
very slow results
• 3) Game destruction: Large tracts of Africa has been cleared of the
tsetse flies by this method in the past but now given up
• 4) Genetic control: Through “sterile male technique”
• 5) Fly traps: Used widely nowadays. Blue coloured traps coated with
insecticides are used.
20. PREVENTION OF AFRICAN TRYPANOSOMIASIS
• Long-sleeved shirts and Medium-weight pants with neutral colours
can be used
• Vehicles should be thoroughly inspected before entering an area of
residents
• Avoiding bushes
• Permethrin impregnated clothing and repellents can be used.
22. INTRODUCTION
• Chagas disease is a potentially life-threatening disease, caused by the
protozoan parasite, T.cruzi
• Found mainly in 21 endemic Latin American countries
• Usually transmitted by contact with faeces of Triatomine bugs, which
acts as a vector for this disease
• Chagas disease was once entirely present in Latin America but now it
has spread to other continents
23. EPIDEMIOLOGY
• About 7 to 8 million of cases of chagas has been reported worldwide
• Most of the cases are from Latin America alone which is an endemic
area for American trypanosomiasis
• In the past decades cases have been reported from other countries
too
• It is mainly due to population from Latin America to rest of the world.
25. MODES OF TRANSMISSION
• T.cruzi infection is mainly spread by the contact with faeces of
Triatomine bugs
• Infection can also occur from:
mother-to-baby (congenital),
contaminated blood products (transfusions),
an organ transplanted from an infected donor,
laboratory accident, or
contaminated food or drink (rare)
26. CLINICAL FEATURES
• Chagas disease has an acute and chronic phase
• Acute phase:
It occurs immediately after the parasite entry into the body and
may last for 2 months
Infection may be mild or asymptomatic
Parasites are usually found in the blood during this phase
The symptoms includes fever, headache, enlarged lymph glands,
pallor, muscle pain , difficulty in breathing, etc…
In 50% of patients bitten by the bug, the characteristic purplish
swelling of eyelid is seen on one eye.
27. CLINICAL FEATURES
• Chronic phase:
After the acute phase most patients go into the “chronic
indeterminate” phase, where parasites are not found on blood
Patients are unaware and may remain asymptomatic for life
About 30% may develop cardiac complications and upto 10%
may develop G.I. complications and neurological problems
In later years, patient may die from progressive cardiac failure
due to destruction of heart wall by the parasite.
28. ROMANA’S SIGN
• T.cruzi is present in the faeces of
Triatomine bug
• The bug defaecates while biting a
man
• When the faeces is rubbed by the
host, the parasite may enter into
the host through breaks in the skin
or through eye or through mucous
membrane
• Swelling occurs in such sites of
inoculation
• Swelling of the eyelid on one eye is
known as Romana’s sign.
29. DIAGNOSIS
• Acute phase:
Blood smears are used for diagnosis of acute phase
Both thick and thin smears can be made and stained for
microscopic visualization of the parasite
• Chronic phase:
Clinical findings along with clinical history is used for diagnosis of
chronic phase
Two or more serological tests are also necessary to support the
diagnosis.
30. TREATMENT
• Acute phase:
Benznidazole and nifurtimox are 100% effective against the
parasite during the acute phase
Drugs lose their efficacy as the disease progresses
• Chronic phase:
Cardiac drugs may be given as per the symptoms of the patient
Benznidazole and nifurtimox are effective in immunosuppressed
patients and in children
32. MORPHOLOGY
• Cone nosed bugs, assassin bugs, kissing bugs, barber bugs
• Reduviid bugs are relatively larger (20 mm to 28 mm)
• Body can be divided into Head , Thorax and Abdomen
• Head – Cone shaped, 3 segmented rostrum, pair of eyes & antennae
• Thorax – 3 pairs of legs & 2 pairs of wings (forewings,hindwings)
• Abdomen – large in females & slender in males
- Pointed at tip in females & rounded at tip in males
- not fully covered by wings, flattened at uncovered areas
33. LIFECYCLE
• Life duration ranges between 4 and 24 months
• Incomplete metamorphosis
• Egg develops into 1st instar(nymph)
• Successively passes through 2nd,3rd,4th and 5th instar to develop into
adults
• Adults are morphologically similar to the nymphal stages except that
they are bigger in size
• Each bug undergoes one or two lifecycles per year
34.
35. BEHAVIOUR
• During daytime, the bugs rests in dark crevices, behind pictures, palm
thatched roof, among furnitures, boxes, clothes and in beds
• At night, the bugs bites and sucks blood
• Average feeding time is 15 to 25 minutes
36. PREVENTION AND CONTROL
• Improvement of houses to reduce or eliminate the hiding places is
the best method
• Spraying of the walls and roofs of the houses with insecticides
- not suitable for porous walls(mud walls)
- synthetic pyrethroids are the insecticides of choice
• Insecticidal paints can be used for mud or porous walls
- contains 8.3% malathion emulsifiable concentrate mixed with
polyvinyl acetate
- forms a thin film on the wall
37.
38. REFERENCES
• http://www.who.int/mediacentre/factsheets/fs259/en/ [internet] ;
accessed on 10/03/15
• http://www.cdc.gov/parasites/chagas/gen_info/index.html [internet];
accessed on 10/03/15
• http://www.cdc.gov/parasites/sleepingsickness/ [internet]; accessed
on 10/03/15
• Maxcy, K. F., Rosenau, M. J., Last, J. M., & Wallace, R. B.
(1998). Maxcy-Rosenau-Last public health & preventive medicine