This document summarizes gastrointestinal protozoal infections. It discusses various protozoa including Entamoeba histolytica, Giardia lamblia, Cryptosporidium parvum, Balantidium coli, and Isospora belli. It covers the morphology, life cycles, clinical manifestations, diagnosis, and treatment of these protozoa. Risk factors for infection include developing countries, poor sanitation, homosexuality, and immunocompromised states like HIV/AIDS. Protozoal infections commonly cause diarrhea but can also lead to more severe complications in vulnerable groups. Diagnosis involves microscopic examination of stool samples, and treatment consists of antimicrobial agents like metronidazole and nitazox
Shigellosis = inflammation of intestines (especially the colon) with accompanying severe abdominal cramps, tenesmus and frequent, low-volume stools containing blood, mucus and fecal leukocytes.
The new virus has made the jump from pigs to humans and has demonstrated it can also pass from human to human. This is why it is demanding so much attention from health authorities. The virus passes from human to human like other types of flu, either through coughing, sneezing, or by touching infected surfaces, although little is known about how the virus acts on humans.
The genus Shigella exclusively infects human intestine.
Shigella dysenteriae is the causative agent of bacillary dysentery or shigellosis in humans.
It is a diarrheal illness which is characterized by frequent passage of blood stained mucopurulent stools.
The four important species of the genus Shigella are:
Shigella dysenteriae
Shigella flexneri
Shigella sonnei
Shigella boydii.
shigellosis presentation , communicable diseases lecture, community medicine master , university of Khartoum
contains basic information about the disease, its clinical features and treatment
Shigellosis = inflammation of intestines (especially the colon) with accompanying severe abdominal cramps, tenesmus and frequent, low-volume stools containing blood, mucus and fecal leukocytes.
The new virus has made the jump from pigs to humans and has demonstrated it can also pass from human to human. This is why it is demanding so much attention from health authorities. The virus passes from human to human like other types of flu, either through coughing, sneezing, or by touching infected surfaces, although little is known about how the virus acts on humans.
The genus Shigella exclusively infects human intestine.
Shigella dysenteriae is the causative agent of bacillary dysentery or shigellosis in humans.
It is a diarrheal illness which is characterized by frequent passage of blood stained mucopurulent stools.
The four important species of the genus Shigella are:
Shigella dysenteriae
Shigella flexneri
Shigella sonnei
Shigella boydii.
shigellosis presentation , communicable diseases lecture, community medicine master , university of Khartoum
contains basic information about the disease, its clinical features and treatment
Entre los parásitos más comunes, la AMIBA Y GIARDIA LAMBLIA ambas son adquiridas a través de los alimentos y el agua respectivamente la cual ha sido infestada con materia fecal por lo general humana.
Existen grandes diferencias entre una y la otra pero quizá las más importante para fines de comprensión es el sitio donde se ubican y los síntomas que ocasionan.
La ameba es un parasito que se deposita en el intestino grueso, y también puede emigrar hacia el hígado y la piel. En cambio la Giardia lamblia se deposita en el intestino delgado, preferentemente en el duodeno sitio donde se llevan a cabo muchos intercambios nutricionales sobre todo el manejo de las grasas.
CHRONIC DYSPEPSIA
Seminar Prepared by :-
Ali Abdulazeem
Shilan Adnan Abdulrahman
Alaa Shamil
Guldan Hameed
Internal Medicine
College of Medicine - University of Kirkuk
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- 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
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
Anti ulcer drugs and their Advance pharmacology ||
Anti-ulcer drugs are medications used to prevent and treat ulcers in the stomach and upper part of the small intestine (duodenal ulcers). These ulcers are often caused by an imbalance between stomach acid and the mucosal lining, which protects the stomach lining.
||Scope: Overview of various classes of anti-ulcer drugs, their mechanisms of action, indications, side effects, and clinical considerations.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
MANAGEMENT OF ATRIOVENTRICULAR CONDUCTION BLOCK.pdfJim Jacob Roy
Cardiac conduction defects can occur due to various causes.
Atrioventricular conduction blocks ( AV blocks ) are classified into 3 types.
This document describes the acute management of AV block.
2. Introduction:
• Protozoan
• Greek: protos- first, and zoon- animal
• Protozoology
• A protozoan can be defined as a motile
eucaryotic unicellular organism
• Entamoeba histolytica infects all age groups but
has its most profound effects in adults.
• Giardia lamblia and Cryptosporidium parvum
have their major impact in childrens
3. Protozoa
• Moisture is necessary protozoa because they
are susceptible to desiccation.
• Most protozoa are free living and inhabit
freshwater or marine environments.
• Many terrestrial protozoa can be found in
decaying organic matter, in soil, and even in
beach sand
• Some are parasitic in plants or animals.
4. Nutrition of protozoa
• Holozoic nutrition : bacteria are acquired by
phagocytosis and the subsequent formation of
phagocytic vacuoles.
• Saprozoic nutrition: soluble nutrients such as
amino acids and sugars cross the plasma
membrane by pinocytosis, diffusion, or carrier
mediated transport
• Significant role in the food web of nature
7. Cysts
• They protect against adverse changes in the
environment
• They are sites for nuclear reorganization and
cell division (reproductive cysts)
• They serve as a means of transfer between
hosts in parasitic species.
8. E histolytica G lambia
Isospora oocyst Cryptosporidium oocysts
CYSTS
B. coli cyst
10. Epidemiology
• Race – not associated
• Sex – no association ( except in amoebic liver
abscess M:F= 10:1 )
• 53.8% school children are infected
• 36.8% of pregnant women are infected
• In rural southern India: 23.1% was infected by
one variety and 74.3% are infected by more
than 1 group
12. In HIV
• Diarrhoea is the most common GI manifestation
• The diagnosis and management of diarrhoea in a PLHIV is a
major challenge.
• There are multiple reasons for the high occurrence of
diarrhoea:
• Immune dysfunction of the intestinal epithelial cells.
• Reduced IgA levels.
• Poor gastric acid secretion and nutritional deficiencies.
13. • Protozoa isolated from the stools of PLHIV
without any symptoms, although the isolation of
parasites was shown to be more common in
patients with diarrhoea.
• The most common pathogen identified in those
with diarrhoea was Isospora belli.
• In asymptomatic patients were more likely to
shed Giardia in their stools
14. • Enteric pathogens in stool:
– 57.4% of diarrhoeal patients
– 40% without diarrhoea (P >0.05)
• Protozoal pathogens 71.8%
• Most commonly isolated pathogens:
– Chronic diarrhoea: Isospora belli (25%)
– Controls: Giardia lamblia (16%)
• In patients with acute diarrhoea, there is no definite
prominent pathogen
17. Diagnosis of Intestinal Protozoa
•Suspect: acute or chronic GI symptoms
•Confirmed: detection of parasite in feces
•3 non-consecutive days (inconsistent excretion)
•copro-antigens or molecular probes
•Cryptosporidium
•acid-fast stain
•Giardia
•duoenal aspirates or biopsy
•presumptive treatment in chronic cases
•Entamoeba
•sigmoidoscopy (lesions, aspirates, biopsy)
•extra-intestinal disease
18. • Sometimes even after repeated stool testing, no
pathogen can be isolated.
• May not be related to technique, but due to fact that
the shedding of pathogens may be intermittent.
• The relationship between the pathogen and diarrhoea is
unclear.
• Many of the pathogens have been isolated from stools
of asymptomatic PLHIV.
19. • Stool cultures
• Endoscopic studies
• Biopsies and histo-pathological studies
• Electron microscopy and other special studies
20. Diagnosis of Extraintestinal Disease
• Symptoms associated with
specific organ
• History of dysentery
• Hepatic
• right upper quadrant pain
• enlarged liver
• Serology
• Imaging (CT, MRI, ultrasound)
• Abscess aspiration
• only select cases
• reddish brown liquid
• trophozoites at abscess wall
21. Non specific treatment
• Maintaining adequate hydration
• Adequate nutritional supplements and
specific vitamins and minerals replacement
are essential.
• Initiate ART : Initiation of ART is important in
controlling diarrhoea especially in conditions
where diarhhoea due to cryptosporiodia,
isospora and microspora.
22. Giardiasis
Salient features
• First observed by Leeuwenhoek
in 1681 and described by Vilem
dusan lambl in 1859
• Giardiasis intestinalis /
G lamblia / G duodenalis
• Worldwide distribution
• Cross infectivity between animals
and humans
• Largely devoid of cytoplasmic
organelles (including
mitochondria)
• First organism to emerge from
the prokaryotic to the eukaryotic
state.
25. Role of bile and bile salts
• Bile has been shown to promote growth of Giardia
both in vivo and in vitro
• The final stage of the life cycle, encystation, can also be
completed following exposure of trophozoites to high
concentrations of conjugated bile salts at neutral pH.
• Thus, bile and bile salts may have a dual role in the
parasite life cycle.
• On one hand promoting growth and multipli cation,
while at the same time ensuring that the parasite
completes its life cycle by encystation
31. Diagnosis
• The traditional diagnosis for giardiasis consists
of performing an ova and parasite (O+P) exam
of one to three stool specimens on non-
consecutive days (sensitivity: 85-90%)
• Several days of specimen collection are
needed to improve sensitivity
• Stool microscopy is relatively inexpensive, but
it does require a skilled technician and may be
a time consuming process
32. • These alternative diagnostic methods should
only be used when stool examination is
repeatedly negative and there is a high clinical
suspicion of infection
• Duodenal aspirate biopsy and collection of
duodenal fluid with the string test
33. Enterotest
• This test requires the patient to swallow a
gelatin capsule containing a string. The
proximal end of the string is taped to the
patient's cheek and the distal end in the
capsule moves to the duodenum after the
capsule dissolves in the stomach. Several (4-6)
hours later, the string is removed and
microscopically examined for trophozoites.
34. Treatment
• Metronidazole 400 mg TID for 5 days OR
2 g OD for 3 days
• Tinidazole 2 g stat dose
• Nitazoxanide 500 mg BD for 3 days
• Furazolidone 100 mg QID for 7-10 days
• In refractory cases
Metronidazole 750 mg TID for 21 days
35. Amoebiasis
• Amoebiasis : has been defined by WHO as the
condition of harbouring the protozoan parasite
E.histolytica with or without clinical
manifestations
• Entamoeba histolytica
• Entamoeba dispar
• Symptomatic infection occur in <10% of infected
individuals and 1% develops invasive or
extraintestinal amebiasis
36. • Feco-oral route
• Oro-anal route
• No animal reservoirs
• World-wide distribution with major problem
in China, south east and west Asia and Latin
America
• Affects about 15% of the Indian population.
37. Risk factors
• People who have traveled to tropical places
that have poor sanitary conditions
• Immigrants from tropical countries that have
poor sanitary conditions
• People who live in institutions that have poor
sanitary conditions
• Men who have sex with men
42. Intestinal amoebiasis
• Abdominal discomfort, loose motions or frank
diarrhoea
• Constitutional symptoms are not prominent
• Tenesmus occurs in half of the patients and is
always associated with rectosigmoid
involvement
• Tenderness may be localized anywhere in the
lower abdomen but is usually over the
caecum, transverse colon or sigmoid
43. • The disease may involve the terminal ileum
rarely.
• Rarely occasions involvement of the blood
vessels at the base of the ulcer may produce
brisk bleeding.
• Fulminant colitis clinical picture is virtually
indistinguishable from that of fulminant
ulcerative colitis
45. Amoeboma or amoebic granuloma
• Amoeboma is non-fibrotic and contains granulation tissue
with lymphocytes, plasma cells, eosinophils and giant cells.
There is remarkably little inflammation and most of the
swelling is due to oedema.
• Repeated invasion of the colon by E. histolytica,
complicated by pyogenic infection.
• Lesions are usually single and involve a short segment of
the colon.
• Occurs commonly in caecum (40%) and rectosigmoid
junction (20%).
46. Amoebic liver abscess
• Most common extraintestinal form
• 10 times more frequent in adults than in children
• Frequent in males than in females
• Common in the poorest sectors
• 20% of patients have a past history of dysentery
• Parasite can be detected in faeces in less than
50% of cases
• Onset of symptoms is usually abrupt
47.
48.
49.
50. 1. Peritoneal amoebiasis
2. Pericardial amoebiasis
• most serious complication
• necessary to perform open drainage
3. Pleuropulmonary amoebiasis
• 15% of patients with liver abscess.
4. Cerebral amoebiasis
• Metronidazole- immediate use will improve the prognosis
51. 5. Genitourinary amoebiasis
• Renal amoebiasis usually respond well to
aspiration and medical therapy
• Genital lesions are usually caused by fistulas from
a liver abscess or rectocolitis & they are painful,
punched-out ulcers with profuse discharge.
Medical treatment is usually sufficient
6. Cutaneous amoebiasis
• Perforation of an abscess or surgical
52. Diagnosis
• Stool or rectal smears for cyst and trophozoite
(within 30 min)
• Rectosigmoidoscopy and colonoscopy of mild or
moderate cases usually reveals the presence of small
ulcers (3–5 mm in diameter)
• Serology can be useful in the diagnosis of amoebiasis,
particularly in non-endemic areas. Antibody response
is present in 85–95% of patients with invasive disease.
53.
54. Tissue amebicides
Metronidazole
• 500mg TID IV for 7-10 days
(for extraintestinal)
• 400mg TID orally for 7-10
days
Tinidazole: 2 g/day for 3 days
Ornidazole : 1.5 g/ day for 3
days
Secnidazole : 2g single dose
Luminal infection
• Paromomycin 30mg/kg qid
PO in 3 divided doses
• Diloxanide furate: 500mg
TID for 10 days
• Iodoquinol 500mg PO BD
for 10 days
57. Cryptosporidium
Tyzzer in 1907, was the first to describe Cryptosporidium
(c.muris) in the gastric mucosa of laboratory mice.
Currently 13 species are present
2 species infecting humans
•C. parvum: cattle and other mammals
•C. hominis: only humans
Self-limiting diarrhea in immunocompetent persons
Profuse, watery diarrhea associated with AIDS (life
threatening)
58.
59. The Milwaukee Outbreak
NEJM 331:161 (1994)
•Massive cryptosporidiosis outbreak following
spring thaw
• >400,000 people may have been affected
• based on clinical symptoms (acute watery diarrhea)
• ~100-fold higher prevalence of Cryptosporidium oocysts
in stools than normal
•Treated water had high levels of turbidity
60. • Substantial outbreaks of water-borne
diarrhoea in the immunocompetent, and for
diarrhoea in travellers and in children.
• Cryptosporidiosis is an important contributor
to childhood diarrhoea, with a prevalence
among children with diarrhoea of 1–3% in the
industrialized world and 4–17% in developing
countries.
61. • Recognized to represent a threat to HIV-
infected individuals, with a lifetime risk of
infection of around 10%
• AIDS-related cryptosporidiosis, the dominant
site of infection was the distal small intestine
and right side of the colon.
62.
63. Diagnosis and treatment
• Conventional stool examination for ova and
parasites does not detect Cryptosporidium (4-6
µm round in shape).
• Nitazoxanide : 500 mg twice daily for 3 days
and for 2 weeks in PLHIV
• Biliary tract obstruction may
require papillotomy or
T-tube placement.
64. Balantidium coli
• Reported in tropical and subtropical regions,
particularly Central and South America, Iran,
Papua New Guinea and the Philippines.
• Prevalence is usually <1%
• Higher rates are reported in hyperendemic
areas and some residential institutions.
• Swine - important animal reservoir
• Closely resembles amoebic colitis
65.
66. B. coli
Invade
Distal ileal and colonic mucosa
penetrate
hyaluronidase
Mucosa and submucosa, and muscle layers
inflammation products of parasite
inflammatory cells
Inflammation
67. Iron hematoxylin stain Bailenger’s stain
Mayer’s hematoxylin Phase contrast microscopy
Iodine stain
Wet mount preparation
68. Diagnosis
• Large motile trophozoites can be detected
using hand lens
• Serology : specific antibody can be detected
Management
• Tetracycline 500 mg four times daily for 10
days
69. Isospora belli
• Faecal-oral spread
• Associated with mild to a subtotal villous
atrophy
• Inflammatory cells and eosinophils are seen in
the lamina propria.
• Watery diarrhoea, cramping abdominal pain
and nausea.
• Associated with wasting and dehydration
70. • Stool examination using
wet preparations and
modified Ziehl–Neelsen
acid-fast stained smears
• Co-trimoxazole QID for 10
days and then 1 DS tablet
three times daily for three
weeks
71. Cyclospora
• Cyclospora cayetanensis
• Single host to complete its entire life cycle
• History of foreign travel and those infected with
HIV.
• 4–7% has been reported in foreign residents in
Nepal( as seasonal outbreak)
• In 1996, a major outbreak of cyclosporiasis was
investigated in the USA, which was found to be
due to the ingestion of Guatemalan raspberries
72. • Responsible for persistent diarrhoea in both
immunocompetent and immunocompromised
individuals.
• Abdominal gas , bloating and weight loss are
also commonly associated features.
• Guillain–Barré syndrome.
• Cyst concentration techniques
• TMP-SMX 160–800 mg twice dailyfor 7 days
73. Microspora
• Found since the outbreak of the HIV
• Enterocytozoon bieneusi
• No mitochondria
• Sclerosing cholangitis like syndrome
indistinguishable from cryptococcus induced
• Diagnosis : gold standard is the electron
microscopy of intestinal epithelial cells
• Detection of spores using chromotope in stool
74. Treatment :
• No effective therapy
• Albendazole 7.5mg/kg/dose (max 400mg) bid 2-4
weeks
• Nitazoxanide :
• For Children aged 1-3 years: 100 mg bid 3 days
• For Children aged 4-11 years: 200 mg bid 3 days
75. Dientamoeba fragilis
• Most cases are asymptomatic. D. fragilis is a
small (6–12 mm) cosmopolitan parasite.
• Only trophozoites are known
• Presence of two nuclei in the majority of them.
• Detection : Trichrome stain
Culture
PCR
76. Examination: Assess for perforated Viscous
Investigation: CBC, MP, Widal Test, Stool Examination for routine & for leucocytes
Advice, if culture is available
Abdominal pain?
Fever?
Check: Hypotension, Pain Abdomen, Nausea, Vomiting
Treat for salmonella typhi, shigella, sepsis
Give Ceftrixone ig IV 2 g X 5-7 days
Provide hydration and evaluate for surgery
Provide oral
Rehydration and
observe
Stool Evaluation: Positive for ova
or parasites?
Tenesmus or Bloody stools Bloating / Flatulence?
Treat for
Giardiasis
Treat for
Amoebiasis
Treat Empirically for
Cyclosporiasis and
Giardiasis
Treat for Shigella sp,
Yersinia sp and
Salmonella sp.
NoYes
NoYes
Yes NoYes
Yes No
No
Give Specific Treatment
77. Problems with Diagnosis
and Management
• Failure to detect pathogens
• Relationship between enteric pathogens and
chronic diarrhoea is uncertain
• Pathogens may not have effective /
convenient treatment
• Laboratory facilities and expertise are needed
• Quality of life and functional status have
received little attention
78. • In PLHIV, Very often the episodes of diarrhoea are recurrent
and severely compromise the quality of life.
• Frequent absence from work and need to access medical
care.
• This has not been well studied.
• Although the initial evaluation is quite simple, if no
pathogen is isolated, then further testing may be required
and this is expensive.
• Lab facilities and expertise of this nature is not available in
most institutions.
• Finally, the cost needs to be considered.
• These include cost to the health care, to the patient- both
direct and indirect (due to loss of wages).
79. Approach in a resource poor settings
Management Approach
• Treat empirically with cotrimoxazole or quinolones first for
a period of 5-7 days
• If no improvement, treat with metronidazole for 7
days
• Cotrimoxazole DS 2 bid for three weeks and ciprofloxacin
750 mg bid for 1 week as empirical regimen is quite
effective
• May be combined with metronidazole or albendazole
• Investigate for the pathogen separately
82. Prevention
1. Sanitation : safe disposal of human excreta
coupled with washing hands after defecation
and before eating
2. Water supply: protecting the water supplies
from fecal contamination cysts are not killed by
chlorination
3. Uncooked vegetables can be disinfected with
acetic acid or full sterngth vinegar
4. Education periodical examination and treatment
of food handlers
83. Safe to drink:
• Bottled water
• Tap water that has been boiled for at least 1
minute
• Carbonated (bubbly) water from sealed cans
or bottles
• Carbonated (bubbly) drinks (like soda) from
sealed cans or bottles
84. Filters that are designed to remove the parasite
should have one of the following labels:
• Reverse osmosis,
• Absolute pore size of 1 micron or smaller,
• Tested and certified by NSF Standard 53 for
cyst removal, or
• Tested and certified by NSF Standard 53 for
cyst reduction
85. References
• API medicine update 2013
• Harrison's Principles of Internal Medicine – 18th edition
• Davidson's Principles and Practice of Medicine 21st edition
• Manson's Tropical Diseases 22nd ed. - G. Cook, et. al., (Saunders,
2009)
• Parasitology in relation to clinical medicine by K D Chatterjee
• Park’ textbook of preventive and social medicine, 21st edition
• Parasitology Research journal, October 2005, Volume 97, Issue 4,
pp 270-273
86. References:
• Gastrointestinal Manifestations in PLHIV, NACO guidelines-
September 2013
• www.dpd.cdc.gov
• Enteric pathogens in southern Indian HIV-infected patients
with & without diarrhoea, Mukhopadhya A. Indian Journal
of Medical Research 1999; 109: 85-90.
• Attili SV, Gulati AK, Singh VP, Varma DV, Rai M, Sundar S.
Diarrhea, CD4 counts and enteric infections in a hospital -
based cohort of HIV-infected patients around Varanasi,
India. BMC Infect Dis. 2006 Mar 1;6:39.
Editor's Notes
Although many of the pathogens can be detected by simple stool examination, the diagnosis and management of diarrhoea in a PLHIV is a major challenge.
Sometimes even after repeated stool testing, no pathogen can be isolated.
May not be related to technique, but due to fact that the shedding of pathogens may be intermittent.
The relationship between the pathogen and diarrhoea is unclear.
Many of the pathogens have been isolated from stools of asymptomatic PLHIV.
This is probably because the bowel may be colonized fairly early in the life of the PLHIV by the pathogen, and it produces diarrhoea when the immunity wanes.
Although many of the pathogens can be detected by simple stool examination, the diagnosis and management of diarrhoea in a PLHIV is a major challenge.
Sometimes even after repeated stool testing, no pathogen can be isolated.
May not be related to technique, but due to fact that the shedding of pathogens may be intermittent.
The relationship between the pathogen and diarrhoea is unclear.
Many of the pathogens have been isolated from stools of asymptomatic PLHIV.
This is probably because the bowel may be colonized fairly early in the life of the PLHIV by the pathogen, and it produces diarrhoea when the immunity wanes.
In his own stools!! Giardia lacks mitochondria and mitochondrial enzymes, and respires in the presence of oxygen by a flavin, iron-sulphur protein-mediated electron transport system.
Giardia is known to produce a variety of proteinases that could find cleavage sites in proteins of the microvillous membrane. Giardia also has a mannose-binding surface lectin, which could interact with mannose residues on relatively immature enterocytes and again contribute to epithelial damage. Other dietary plant lectins are known to be able to produce substantial abnormalities of villous architecture.
patient is extremely febrile and toxic, and shows signs of hypovolaemia and electrolyte imbalance.
ulcers are initially superfi cial with hyperaemic borders and a necrotic base covered with a yellowish exudate. There is normal mucosa between sites of invasion.
Amoebae are scanty and diffi cult to demonstrate. Fibrous tissue is formed later.
10% of patients have diarrhoea or dysentery at the time of diagnosis
1.In some instances the perforation may be smaller and the abdominal signs are more localized.
2. because of the development of loculations and thickened pericardium.
3 mounts: saline solution, saline +iodine, saline plus methylene blue
The Entamoeba histolytica II kit – DIFF between dispar and histolytica
Nitazoxanide 500mg tid 3 days and chloroquine as adjuanct to metronidazole for 21 days
First human case reported in 1976
initially believed to be rare and exotic
now known to be common human pathogen
oocysts identified in ice made during this period
specific testing must be requested. Detection is enhanced by evaluation of stools (obtained on multiple days) by several techniques, including modified acid-fast and direct immunofluorescent stains and enzyme immunoassays
1)the asymptomatic carrier state (2) acute and acute fulminant colitis (3) chronic infection.
relapse in 50%,usually within 12 weeks
2. First detected
Associated with such as diarrhoea and abdominal pain
Studies from India have evaluated the efficacy of co-trimoxazole and ciprofloxacin and found them to be quite effective.