Bacterial Infections

Opportunistic Infections

Opportunistic infections are those caused by organisms that do not ordinarily harm healthy people but occur in people with impaired defenses (immuno-compromised hosts). Broadly, immuno-compromised hosts are categorized into three categories:

  1. Primary immunodeficiency syndromes, mostly congenital.
  2. Secondary immunodeficiency syndromes e.g. AIDS, haematological malignancies, splenectomy etc.
  3. Therapeutic immunosuppression.
Salient featuresThe type of immunosuppression may give clue to the likely pathogens to produce opportunistic infections e.g.

  • Neutropenia predisposes an individual to bacteriaemia particularly with gram-negative organisms, Staphylococcus and Candida albicans.
  • Immunosuppression due to corticosteroids predisposes to infections with M. tuberculosis & fungi e.g. Candida, Cryptococcus.
  • HIV/AIDS predisposes to infections with mycobacteria, fungi, cytomegalo virus, Pneumocystis carinii, protozoal infections like toxoplasma and many more organisms.
  • The duration of immunosuppression and speed of progression of immunosuppression also determines the likely pathogen. In splenectomized patients, capsulated bacteria are the likely pathogens.
  • The diagnosis of specific infection is made by appropriate investigation, choice depending upon the clinical suspicion and the type of immunosuppression.

Treatment

Nonpharmacological

General hygienic measures for prevention of infection, barrier nursing for neutropenic patient.

Pharmacological (Specific treatment of opportunistic pathogens)

Candidiasis

Vulvovaginal candidiasis
Tab. Fluconazole 150 mg single dose.
Oral thrush
Clotrimazole oral troches five times a day till infection clears.
Oesophageal
Tab. Fluconazole 200 mg on first day followed by 100 mg daily for 7-14
days.
Or
Nystatin Susp. 100,000 units/ml, 10-20 ml 6 hourly for 15 days.
If it fails, Tab. Itraconazole 100-200 mg once daily for 15 days.
Recurrent oropharyngeal candidiasis in HIV positive patients – treat for each individual episode.
In resistant cases Amphotericin lozenges are used for 7-10 days followed by Nystatin or Fluconazole for as long as the host resistance remains low (in AIDS patients).
Disseminated infection
Inj. Amphotericin B IV 0.5-0.7 mg/kg/day for 2 weeks after the patient becomes afebrile.
Pneumocystis Pneumonia
Tab. Trimethoprim + Sulfamethoxazole (TMP-SMZ) 15-20 mg TMP + 75-100 mg SMZ/kg/day in 3-4 divided doses for 14 days in non-HIV patients and 21 days in HIV positive patients.
Or
Tab. TMP 15 mg/kg/day orally + Tab. Dapsone 100 mg/day for mild cases of PCP.
Or
Inj. Pentamidine 4 mg/kg/day slow IV infusion as a single dose.
In HIV positive patients with severe PCP i.e. Arterial pO2 of 70 mmHg or less, Alveolar arterial pO2 difference of 35 mmHg or more.
Steroids are recommended as adjunct therapy:
Tab. Prednisolone 40 mg 2 times a day for 1-5 days; 40 mg once daily on days 6-10 and 20 mg once daily on days 11-20.
Cryptococcosis (In patients with AIDS)
Inj. Amphotericin B 0.7 mg/kg/day for a minimum 2 weeks or till condition is stable, followed by Tab. Fluconazole 400 mg/day till infection is controlled, followed by Tab. Fluconazole 200 mg day indefinitely.
Cryptococcosis (In patients without AIDS)
Inj. Amphotericin B, doses as above till cultures from all positive sites become negative, with a maximum of 10 weeks.

References

  1. Infection in the Immuno-compromised Host. In: Oxford Textbook of Medicine, Weatherall DJ, Ledingham JGG, Warrell DA (eds), 1996, Oxford University Press, pp 1027-35.
  2. Diagnosis and Treatment of Fungal infections. In: Harrison’s Principles of Internal Medicine, Braunwald E., Fauci AS, Kasper DL et al (eds), 15th Edition, 2001, McGraw Hill Company Inc., pp 1168-70.
  3. Pneumocystis carini Infection. In: Harrison’s Principles of Internal Medicine, Braunwald E., Fauci AS, Kasper DL et al (eds), 15th Edition, 2001, McGraw Hill Company Inc., pp 1168-70.

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Tetanus

An acute neurological disorder resulting from contamination of a wound (may be a trivial one) by an obligate anaerobic organism, C lostridium tetani.

Salient features

  • Generalized tetanus, the most common form usually starts with trismus or lockjaw followed by rigidity, violent, painful, generalized muscle spasms and seizures provoked by slightest stimulation.
    Generalized muscle spasms may compromise respiration. Fever and tachycardia may be present. Mentation is not impaired.
  • Prognosis and management depends on grade.

Grade I or Mild – muscle rigidity with few or no spasms.
Grade II or Moderate – trismus, dysphagia, rigidity, and shortlasting spasms.
Grade III or Severe – frequent explosive spasms, autonomic dysfunction particularly sympathetic over-activity may be present.
Grade IV or very severe – features of grade III plus violent autonomic disturbances involving the CVS – severe hypo or hypertension.

  • Other presentations include local, cephalic (cranial nerves) or neonatal tetanus (within 2 weeks of life).
  • Complications include respiratory failure, respiratory infections, barometric trauma due to prolonged ventilator support, persistent hypotension, labile hypertension, cardiac arrhythmia, sepsis and sudden death.

Treatment

Nonpharmacological

Admit in a quiet room/ICU with minimum stimulation, cardiopulmonary monitoring, protection of airways/respiratory support (intubation / tracheostomy) with or without ventilation, cleaning/exploration/ debridement of wound. Maintain hydration and enteral/parenteral nutrition with high calorie and high protein diet.

Pharmacological

Grade I tetanus

  1. As above.
  2. Tab. Diazepam 5-20 mg 3 times a day in mild tetanus; slow IV infusion in moderate to severe tetanus. Not to exceed a dose of 80-100 mg in 24 hours.
    If spasms not controlled.
    Inj. Phenobarbitone 200 mg IM every 8-12 hours.
    Or
    Inj. Chlorpromazine 50 mg IM in adults 4 times a day.
    The ideal sedative and muscle relaxant schedule for each patient should be individualized. An objective guide to decrease in rigidity is relaxation of abdominal muscles.

Grade II

  1. As above.
  2. Tracheostomy.

Grade III and IV

  1. As above.
  2. Ventilator support.
  3. Inj. Pancuronium 2-4 mg IV.
    Or
    Inj. Gallamine 20-40 mg IV.
  4. In case of hypotension
    Inj. Dopamine/Dobutamine 10-40 mcg/kg/min infusion titrated to maintain systolic BP of 100 mm Hg.
    If bradyarrhythmias Inj. Atropine 0.6-1.2 mg IV.
    If hypertension (for details see section on hypertension)

In addition give following to all the patients
Inj. Crystalline penicillin 2 mega units 6 hourly IV for 10 days.
Or
Inj. Metronidazole 500 mg 8 hourly or 1 g 12 hourly.
(Other antibiotics may be required according to need of infected wound).
Inj. Human tetanus immunoglobulin (TIG) 3000-5000 units IV or IM.
Or
Inj. Equine antiserum, 10,000 units by slow IV Injection after sensitivity test (If human TIG is not available).
Antiserum should be given before local manipulation of the wound.
(CAUTION: Tetanus immunoglobulin does not produce natural immunity and a full course of immunization with tetanus toxoid should be administered once the patient has recovered).

References

  1. Tetanus. In: Harrison’s Principles of Internal Medicine. Braunwald E., Fauci AS, Kasper DL et al (eds), 15th Edition, 2001, McGraw Hill Company Inc., pp. 918-20.
  2. Tetanus. In:Oxford Textbook of Medicine, Weatherall DJ, Ledingham JGG, Warrell DA (eds), 1996, Oxford University Press, pp 624-30.

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Typhoid (Enteric Fever)

It is caused by Salmonella typhi and paratyphi.

Salient features

  • Continuous fever (temperature upto 40oC), may be associated with headache, malaise, abdominal discomfort, constipation or diarrhoea (pea-soup stool).
  • Complications usually occur in the 3rd week and may include lower GI bleed, intestinal perforation, disseminated intravascular coagulation and jaundice.
  • Examination may reveal a toxic look with relative bradycardia and mild soft splenomegaly. Diagnosis is suggested by rising titres of ‘O’ antibodies (Widal Test) and confirmed by isolation of organism in blood, bone-marrow, urine or stool.

Treatment

Nonpharmacological

Cold sponging, rest and normal diet.

Pharmacological

  1. Tab. Paracetamol 500-1000 mg 6 to 8 hourly to reduce headache and fever (for details see section on fever).
  2. Tab. Ciprofloxacin 10 mg/kg in 2 divided doses, upto a maximum of 750 mg twice a day for 10-14 days (for 1 week after the fever subsides).
    Or
    Inj. Ciprofloxacin 200 mg IV twice a day (initial treatment in severely ill hospitalized patient).

    If no response after 5 days,
    Inj. Ceftriaxone 50-60 mg/kg per day IV or IM in 2 divided doses or as a single dose for 7-10 days (preferred in pregnant women patients, children or patients resistant to quinolones).
    Or
    Inj. Cefixime 20 mg/kg per day in 2 divided doses for 14 days.
    If there is no response after 5 days, alternative diagnosis should be considered.

    Report to the physician immediately if abdominal symptoms worsen or occurrence of bleeding per rectum or alteration in sensorium and shock (severe typhoid with high risk of fatality).

  3. Severe typhoid with shock or patients with enteric encephalopathy should be hospitalized and treated as above plus Inj. Dexamethasone 3 mg/kg IV first dose followed by 1 mg/kg IV every 6 hourly for 8 doses.
    Chronic Carrier State (patients who continue to excrete bacilli in stool for more than 1 year).
    Tab. Ciprofloxacin 750 mg twice a day for 28 days.

Patient education

  • Small frequent feeds should continue. Give plenty of oral fluids and compensate for increased fluid loss from the body due to high grade fever.
  • Fever usually lasts 5-7 days even after starting effective treatment in most cases. Frequent change of therapy should therefore be avoided.
  • The treatment should be completed till the patient has been afebrile for at least 7 days as incomplete treatment increases the risk of relapse and emergence of resistance.
  • Three types of vaccines are available to prevent this disease. (see section on immunization for details).

References

Salmonellosis. In: Harrison’s Principles of Internal Medicine. Braunwald E, Fauci AS, Kasper DL et al (eds), 15th Edition, 2001, McGraw Hill Company Inc., pp 970-975.

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