Actual problems of infectious diseases and hiv infection



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Partial answer

  • Absence of answer

  • *All the above

  • What is organism answer of interferon therapy.

    1. Disappearance of markers of viral replication upon completion of course of therapy

    2. Normalization of activity of ALaT during the course of therapy

    3. Relapse in next 6 months

    4. Disappearance of icterus

    5. *All the above

  • Answer of interferon therapy are all, except.

    1. *Disappearance of markers of viral replication

    2. Normalization of ALaT activity

    3. Disappearance of icterus

    4. Normalization of patient general condition

    5. Normalization of a liver size

  • What investigation for confirming of viral hepatitis diagnosis.

    1. Total analysis of blood

    2. Determination of bilirubin level

    3. Determination of aminotransferases activity

    4. *Determination of HV markers by IFA

    5. All the above

  • What examination is helpful in confirming of viral hepatitis diagnosis.

    1. Complete analysis of blood

    2. Ultrasound of abdominal region

    3. Determination of activity of aminotransferase

    4. *Determination of antigen of viruses

    5. Duodenal probing

  • What is duration of incubation period for B hepatitis :

    1. 45 days

    2. *180 days

    3. 360 days

    4. 90 days

    5. 25 days

  • Parenteral way of transmission is present in spreding of hepatitis except:

    1. *A

    2. B

    3. C

    4. D

    5. TTV

  • Chronic course is possible for viral hepatitis except:

    1. *A

    2. B

    3. C

    4. D

    5. B+C

  • All the following medicines are interferons except:

    1. Intron

    2. Roferon

    3. Reaferon

    4. Leukinferon

    5. *Cycloferon

  • All the following medicines are hepatoprotective agents except:

    1. Carsil

    2. Silibor

    3. Legalon

    4. *Lomusol

    5. Arginine

  • What is mechanism of viral hepatitis A transmission:

    1. Contact

    2. Transmissive

    3. Vertical

    4. *Fecal-oral

    5. Air-drop

  • What is mechanism of hepatitis B transmission:

    1. *Contact

    2. Transmissive

    3. Alimentary

    4. Fecal-oral

    5. Air-drop

  • What is mechanism hepatitis C transmission:

    1. *Contact

    2. Transmissive

    3. Alimentary

    4. Fecal-oral

    5. Air-drop

  • What rash is present in case of haemorrhagic fevers with kidneys syndrome?

    1. Roseolar

    2. Maculo-papular

    3. Punctuate

    4. *Petechial

    5. Rash is not present

  • What rash is present in case of Congo hemorrhagic fever?

    1. Roseola

    2. Maculo-papular

    3. Punctulate

    4. *Petechial

    5. Rashes not is characteristic

  • What rashes is present in case of Crimea hemorrhagic fever?

    1. Roseolar

    2. Maculo-papular

    3. Punctulate

    4. *Petechial

    5. Rashes not is characteristic

  • How long the rash is present in case of haemorrhagic fever with kidneys syndrome?

    1. *During all feverish period

    2. Before the reconvalescense

    3. Before development of clinical features of kidneys insufficiency

    4. During whole disease

    5. Appears yet in a latent period and disappears in the period of early reconvalescense

  • A kidney syndrome at haemorrhagic fever with kidneys syndrome shows up usually:

    1. Only laboratory changes

    2. Only on BRIDLES

    3. *By pain in lumbar area, positive Pasternatsky symptom, development of oliguria

    4. By fever, polyuria, dyspepsia

    5. By paradoxical ischuria

  • What changes in biochemical blood test inherent for haemorrhagic fever with kidneys syndrome?

    1. Increase level of urea and bilirubin

    2. The level of urea and kreatinine falls

    3. The level of kreatinine grows and urea falls

    4. The level of urea grows and kreatinine falls

    5. *The level of urea and kreatinine grows

  • What changes in haemogram is typical for haemorrhagic fever with kidneys syndrome?

    1. Normochromic anaemia, leucocytosis with atypical mononucleosis, thrombocytopenia enhanceable ESR

    2. Erythrocytosis, lymphocytosis,ESR is enhanceable

    3. Normochromic anaemia, leucopenia with neutrophylosis, thrombocytopenia enhanceable ESR

    4. *Hypochromic anaemia, leucocytosis with neutrophylosis, thrombocytopenia enhanceable ESR

    5. Hyperchromic anaemia, leucocytosis with neutrophylosis, thrombocytopenia mionectic ESR

  • Polyuria in haemorrhagic fever with kidneys syndrome is a sign of:

    1. *Recovering

    2. . Chronic process

    3. Unfavorable flow of illness

    4. Development of complications

    5. Complete convalescence

  • In most patients with Congo hemorrhagic what type of fever is:

    1. Wunderlich’s type

    2. Botkin’s type

    3. Undulating

    4. Intermittent

    5. *Two-humped

  • What changes in haemogram inherent Congo hemorrhagic fever?

    1. Normochomic anaemia, leucocytosis mononuclear

    2. Erythrocytosis, lymphocytosis

    3. *Hypochromic anemia, erythrofilosis

    4. Hypochromic anemia, neutrofilosis

    5. Hyperchromic anemia, neutrofilosis

  • What is typical for the Lassa hemorrhagic fever:

    1. Effect of cardiovascular system

    2. Development of acute hepatic insufficiency

    3. Hundred-per-cent lethality

    4. *Defeat of breathing organs

    5. Development of paresis and paralysis

  • Confirm diagnosis of haemorrhagic fever with kidneys syndrome by a way of:

    1. Only virological methods

    2. Only bacteriological methods

    3. Bacteriological and serum methods

    4. Proper epidemiological information

    5. *Virologic and serum methods

  • Confirm the diagnosis of Lassa hemorrhagic fever by a way of:

    1. Only virological methods

    2. Only bacteriological methods

    3. Bacteriological and serum methods

    4. Proper epidemiological information

    5. *Virologic and serum methods

  • Confirm the diagnosis of Congo hemorrhagic fever by a way of:

    1. Only virological methods

    2. Only bacteriological methods

    3. Bacteriological and serum methods

    4. Proper epidemiological information

    5. *Virologic and serum methods

  • Confirm the diagnosis of Ebola fever by a way of:

    1. Growth of viruses on chicken embryons

    2. Only bacteriological methods

    3. Bacteriological and serum methods

    4. Proper epidemiological information

    5. *Selection of virus on the Vero culture

  • Confirm the diagnosis of Omsk fever by a way of:

    1. Growth of virus on chicken embryons

    2. Only bacteriological methods

    3. Bacteriological and serum methods

    4. Proper epidemiological information

    5. *Selection of virus on the Vero culture

  • Confirm the diagnosis of Marburg fever by a way of:

    1. Growth on chicken embryos

    2. Only bacteriological methods

    3. Bacteriological and serum methods

    4. Proper epidemiologys information

    5. *Selection of virus on the Vero culture

  • What etiothropic means use at treatment of haemorrhagic fever with kidneys syndrome:

    1. Benzylpenicillin

    2. Dopamine

    3. *Virolex

    4. Dexamethazone

    5. Etamsylatum

  • What etiothropic means use at treatment of patients with Lassa fever:

    1. Benzylpenicillin

    2. Dopamine

    3. *Ribavirin

    4. Dexamethazole

    5. Etamsylatum

  • What etiothropic means use at treatment of patients with Marburg fever:

    1. Benzypenicillin

    2. Dopamine

    3. *Ribavirin

    4. Dexamethazone

    5. Etamsylatum

  • What etiothropic means use at treatment of patients with Congo fever:

    1. Benzylpenicillin

    2. Dopamine

    3. *Ribavirin

    4. Dexamethazone

    5. Etamsylatum

  • What etiothropic means use at treatment of patients with Ebola fever:

    1. Benzylpenicillin

    2. Dopamine

    3. *Virolex

    4. Dexamethazone

    5. Etamsylatum

  • What etiothropic means use at treatment of patients with Crimea fever:

    1. Benzylpenicillin

    2. Dopamine

    3. *Ribavirin

    4. Dexamethazone

    5. Etamsylatum

  • Specific prevention of hemorrhagic fevers may perform by:

    1. Live vaccine

    2. Killed vaccine

    3. Specific immunoglobulin

    4. *Do not develop

    5. Polivalent vaccine

  • Who is the source of the causal agent in the Crimean-Congo haemorrhagic fever?

    1. Rodents, cattle, birds

    2. Tikes

    3. *Rodents, cattle, birds, sick people

    4. Sick man, reconvalescent, bacteriocarrier

    5. Rodents, cattle, birds, sick people, bacteriocarries

  • The source of infection of Omsk‘s hemorrhagic fever are muskrat, water rats and other rodents. Who are the carriers?

    1. Bee and flea

    2. *Pliers and flea

    3. Mosquitoes

    4. Fly

    5. Pliers and mosquitoes

  • Specific prevention of Crimean-Congo haemorrhagic fever are:

    1. *Vaccine and human immunoglobulin

    2. Serum

    3. Serum and human immunoglobulin

    4. Do not developed

    5. Antibacterial drugs

  • How to prevent malaria?

    1. Follow the rules of personal hygiene

    2. Do not drink raw water

    3. Vaccination

    4. *Chemoprophylaxis

    5. Heating of food

  • What group of infectious diseases malaria belong to?

    1. Intestinal

    2. Respiratory

    3. External covers

    4. Transmissive

    5. *Blood

  • What is the treatment of malaria attacks.

    1. Antibiotics

    2. Serum transfer

    3. Delagil

    4. Primaquine

    5. *Delagil + Primaquine

  • In a survey of donor blood microhametosis are found. Assign treatment.

    1. Delagil

    2. *Primaquine

    3. Antibiotics

    4. Fluoroquinolone

    5. Sulfanilamide

  • Malaria must be differentiated primarily with such diseases:

    1. Pyelonephritis

    2. Sepsis

    3. Viral hepatitis

    4. Leptospirosis

    5. *All of the above

  • The diagnosis of malaria can be confirmed by:

    1. Microscopy of urine

    2. Haemoculture

    3. Bacteriology of stool

    4. Serological reactions

    5. *Parazitoscopy of blood

  • Rules of hospitalization of patients with malaria:

    1. *In separate room

    2. In a respiratory infections department

    3. In the Meltser’s ward

    4. Patients are not hospitalized

    5. In a intestinal infections department

  • Why early relapse in malaria develops?

    1. The immune deficiency

    2. *Due to erythrocytic forms of shizonts

    3. Releasing of tissue shizonts to the blood stream

    4. Fresh contamination

    5. Availability of a blood gamonts

  • Why late relapses in malaria develops?

    1. Due to erythrocytic forms of shizonts

    2. *Releasing of tissue shizonts to the blood stream

    3. Fresh contamination

    4. Availability of a blood gamonts

    5. The immune deficiency

  • By what drug is possible to prevent early recurrence of malaria:

    1. *Delagil

    2. Immunoglobulin

    3. Antibiotics

    4. Primahin

    5. Glucocorticoids

  • By what drug is possible to prevent relapse of malaria:

    1. Delagil

    2. Immunoglobulin

    3. Antibiotics

    4. *Primahin

    5. Glucocorticoids

  • Radical treatment of malaria include:

    1. Primaquine within 2 weeks

    2. Glucocorticoids

    3. *Delagil + primahin

    4. Serum transfer

  • Indications for the appointment of hematoshizotrop antimalarial drugs:

    1. *Attack of malaria

    2. Preventing late relapse

    3. Prophylactic course after returning from areas difficult to malaria

    4. Antyretsidiv course for the rekonvalescents

    5. During a check-up

  • Indications for the appointment of histoshizotrop antimalarial drugs:

    1. Attack of malaria

    2. *Prevention of late relapse

    3. Complications of malaria

    4. Malaria chemoprophylaxis for a period of stay in endemic areas

    5. During a check-up

  • What do you need to give to the patients with malaria‘s coma?

    1. Glucocorticoids

    2. Antishok treatment

    3. *Intravenous delagil

    4. Blood transfusion

    5. Oxygen

  • Specific complications of malaria, except:

    1. Hemoglobinuria fever

    2. Spleen destruction

    3. Malaria‘s coma

    4. *Intestinal perforation

    5. Hemolytic anaemia

  • Reconvalences after malaria may descharged from a clinic no earlier than:

    1. After 2 weeks till complete clinical recovery

    2. After 2 weeks of a radical course of therapy

    3. *After a radical course of therapy with a negative results of parazitoscopy

    4. After 3 weeks with a negative blood culture results

    5. After 3 weeks, if the negative results of planting feces

  • Activities on contact with import cases of malaria:

    1. Parasitoscopy of blood

    2. The direction of the contact in the detention facility for 5 days

    3. Chemoprophylaxis

    4. Vaccination

    5. *Do not hold

  • What is malaria prevention for those who have returned from disadvantaged areas:

    1. Introduction of human immunoglobulin

    2. Interferon

    3. 6-days-prevention by streptomycin or tetracycline

    4. *Primaquine

    5. All the above

  • What measures must be taken in relation to people who had a contact with malaria case:

    1. Microscopy of periferal blood

    2. Isolation during 5 days

    3. Chimioprophylaxis

    4. Houses rounds

    5. *Does not conduct

  • Who would be a subject for inspection on malaria?

    1. Recovering of malaria persons

    2. Persons, returning from endemic regions of malaria

    3. Patients with fever more than 5 days

    4. Patients with spleenomegaly

    5. *All above enumerated

  • Methods for identification of sources of malaria:

    1. Stool culture test

    2. Haemoculture

    3. *Microscopic assessment of blood

    4. Byurne test

    5. All above enumerated

  • When should begin treatment of malaria patients?

    1. *Immediately after hospitalization

    2. After taking of material for research

    3. After of final diagnosis

    4. After laboratory and instrumental research

    5. All answers are correct

  • Delagil appoint in case of malaria in such doses:

    1. 0,5 g 3 times a day 3 days

    2. 0,5 g during a week

    3. *In the first day 1 g, then 0,5 g every 6 h

    4. 0,5 g a day during a month

    5. 0,5 g 2 times a day 3 days

  • There are etiotropic drugs of malaria, except:

    1. Delagilum

    2. Prymahin

    3. *Ceresyn

    4. Quinine

    5. Fansydar

  • The radical course of treatment of malaria includes:

    1. Five-day therapy of delagilum

    2. Prymahin during 2 weeks

    3. C. Delagilum + prymahin + fansydar

    4. *Delagilum + prymahin

    5. Delagilum + fansydar

  • What do you need for treatment of chlorochyn resistent forms of malaria?

    1. Bactrimum

    2. Dapson

    3. Fansydar

    4. Meflohin

    5. *All enumerated

  • The most effective antibiotics at the treatment of patients with leptospirosis are:

    1. *Penicillin

    2. Macrolids

    3. Cefalosporins

    4. Ftorhinolons

    5. Sulfanilamids

  • What daily doses of penicillin for leptospirosis treatment:

    1. 2-3 million units

    2. *3-12 million units

    3. 10-20 million units

    4. 20-40 million units

    5. Over 40 million units

  • All of these is an epidemic dangerous to leptospirosis except:

    1. Farm animals

    2. Wide rodents

    3. Domestic animals

    4. Foxes

    5. *Humans

  • How long lasts the incubation period of leptospirosis:

    1. 2 month

    2. 1-7 days

    3. *7-14 days

    4. 14-21 days

    5. 2-3 days

  • Which serotypes of leptospirosis caused the disease more frequent:

    1. L. interogans

    2. L. grippotyphosa

    3. L. canicola

    4. *L. icterohaemorrhagia

    5. L. Pomona

  • Agglutinines in leptospirosis arrive at a maximal titre:

    1. On the third day of illness

    2. *On the third week of illness and later

    3. On the fourth week of illness

    4. On the second month of illness

    5. On the second week of illness

  • Rules of hospitalization of patients with infectious mononucleosis:

    1. Patients are not hospitalized

    2. In a ward for the infections of respiratory tracts

    3. *In a separate ward

    4. In a ward for the infections of external covers

    5. In a ward for intestinal infections

  • What symptoms are not characteristic of infectious mononucleosis?

    1. Hepatomegaly

    2. *Oliguria

    3. Limfocytosis

    4. Tonsillitis

    5. Splenomegaly

  • How much atypical mononucleares present in infection mononucleosis?

    1. Less than 5 cells

    2. *10 and more cells

    3. 5 and more cells

    4. Less than10 cells

    5. 50 % cells

  • What is most possible complication occur in infectious mononucleosis?

    1. Oliguria

    2. Autoimmune process

    3. Meningitis

    4. *Spleen rupture

    5. Pneumonia

  • What additional inspections must be conducted to the patient with infectious mononucleosis?

    1. *IFA on HIV-infection, bacteriology inspection on diphtheria

    2. IFA on HIV-infection, bacteriology inspection on a scarlet fever

    3. Bacteriology inspection on diphtheria and typhoid fever

    4. Burne and Rihth-Heddlson reactions

    5. Paul-Bunnel reaction and punction of lymphatic node

  • What from the following symptoms are not characteristic of infectious mononucleosis?

    1. Fever

    2. *Defeat of kidneys

    3. Lymphadenopathy

    4. Tonsillitis

    5. Increasing of liver and spleen

  • For what disease characterize changes in a blood (presence of lymphomonocytes and atypical mononuclears?

    1. Flu

    2. *Infectious mononucleosis

    3. Measels

    4. AIDS

    5. Diphtheria

  • In a survey of donor blood found microhametosis. Assign treatment.

    1. Delagil

    2. *Primaquine

    3. Antibiotics

    4. Fluoroquinolone

    5. Sulfanilamide

  • Diagnosed a patient: chronic hepatitis in the stage of integration. What markers will be in patient in this stage disease?

    1. HBeAg

    2. Antibodies to HBeAg

    3. DNA OF HBV

    4. Viral DNA-polimerase

    5. *HBsAg, anti-НBе

  • As etiotropic therapy of sharp and chronic viral hepatitis B utillize:

    1. Corticosteroid

    2. Immunomodulate preparations

    3. Cytostatics

    4. Antibiotics

    5. *Antiviral preparations

  • Give recommendation for a patient in reconvalensent period of viral hepatitis during a clinical supervision after isolation.

    1. *Medical supervision during 6 months, periodic biochemical inspections.

    2. Control bacteriological examinations

    3. Full labor investigation

    4. To continue prophylactic inoculations

    5. Supervision is not needed

  • Etiotropic therapy of viral hepatitis is.

    1. Ribavirin

    2. Interferon

    3. Inductors of interferon

    4. Zefix

    5. *All the above

  • Choose the remedies for etiotropic therapy of viral hepatitis.

    1. *Ribavirin

    2. Vaccine

    3. Normal human immunoprotein

    4. Hepatoprotector

    5. Glucocorticoid

  • Choose the remedies for etiotropic therapy for viral hepatitis.

    1. Antibiotics

    2. *Interferon

    3. Probiotics

    4. Vaccine

    5. Normal human immunoprotein

  • The criteria for application of etiotropic therapy in viral hepatitis is.

    1. Protracted motion of HBV, HVD

    2. Any form of HV

    3. Biochemical activity

    4. Presence of virus replication

    5. *All the above

  • The criteria for application of etiotropic therapy for the patient with HCV.

    1. Clinical displays are insignificant

    2. Icterus is absent

    3. Moderate biochemical activity

    4. There is anti-HCV in blood

    5. *RNA of HCV +

  • Factors which are indications of successful interferon therapy in HV infections are all, except.

    1. Level of ALaT not more than 2-3 norm

    2. Low titre of HCV after the treatment

    3. Absence of cholestasis

    4. 2th and 4th genotypes of HCV

    5. *Expressed fibrosis

  • Indirect action of interferon therapy.

    1. Influenza-like syndrome

    2. Nausea

    3. Itching

    4. Para-hypnosis

    5. *All the above||

  • Indirect action of interferons.

    1. Flatulence

    2. Diarrhea

    3. Nausea

    4. Depression

    5. *All the above

  • Indirect action of interferon therapy are all except.

    1. Influenza-like syndrome

    2. Nausea

    3. Depression

    4. Intensification of autoimmune diseases

    5. *Progress of fibrosis

  • Basic principles of antiviral therapy for viral hepatitis.

    1. Individual selection of dose and rhythm of application of preparations

    2. Duration of introduction of preparations

    3. Control of amount of erytrocytes, leucocytes and thrombocytes, in blood

    4. Control of iron level in blood

    5. *All the above

  • Contra-indications for antiviral therapy of viral hepatitis.

    1. Decompensatory cirrhosis of liver

    2. Thrombocytopenia <50000 in 1 мм3

    3. Psychic disorders

    4. Leucocytopenia <1500 in 1 мм3

    5. *All the above

  • Contra-indications for antiviral therapy of viral hepatitis.

    1. Decompensatory cirrhosis of liver

    2. Autoimmune disease

    3. Alcoholism and other drug addictions

    4. Coinfection by HIV

    5. *All the above

  • Choose the indexes of efficiency of interferon therapy.

    1. *Disappearance| of markers of viral replication

    2. Improvement of the general state

    3. Normalization of the liver size

    4. Disappearance of icterus

    5. All the above

  • Choose the indexes of efficiency of interferon therapy.

    1. Improvement of the general state

    2. *Normalization of activity of ALaT

    3. Normalization of the liver size

    4. Disappearance of icterus

    5. All the above

  • Types of answer for interferon therapy are.

    1. Stable remission

    2. Unsteady

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