Salmonella Infections
Salmonella Infections
Salmonella Infections
Salmonella Infections
Complications
Extra-intestinal
infectious complications
recognition
of these can prevent a delay in diagnosis
can
occur
and
Intestinal
The two most serious complications of enteric fever are intestinal
haemorrhage and perforation, which usually occur when the
sloughs overlying the Peyers patches separate during the late
second or early third week of the illness.
Haemorrhage
Clinical signs of haemorrhage are :
- a sharp fall in body temperature and blood pressure,
- and sudden tachycardia.
- The blood passed per rectum is usually bright red but may
be altered if intestinal stasis is present. Sometimes there
may not be any passage of blood when frank ileus is
present.
Management of haemorrhage is conservative, with sedation and
transfusion unless there is evidence of perforation, when surgery
is indicated.
Perforation
Clinical sign :
- Unlike other causes of intestinal perforation, typhoid
perforation occurs in a patient who already had a vaguely
tender distended abdomen with scanty bowel sounds.
Therefore, recognition of perforation can be diffi cult.
- Usually, pain and tenderness worsen, the pulse rises and
the temperature falls suddenly.
Nervous system
A toxic confusional state, characterized by disorientation, delirium
and restlessness, is characteristic of late-stage typhoid but
occasionally these and other neurpsychiatric features may
dominate the clinical picture from an early stage. Facial twitching
or convulsion(s) may be the presenting feature; sometimes,
paranoid psychosis or catatonia may develop during
convalescence.
Meningism is not uncommon but bacterial meningitis caused by
S. Typhi is a rare, but recognized, complication. Encephalomyelitis
may develop and the underlying pathology may be that of
demyelinating leukoencephalopathy.Rarely, transverse myelitis,
polyneuropathy or cranial mononeuropathy may develop.
Haematological and renal
Subclinical disseminated intravascular coagulation occurs
commonly in typhoid fever; this rarely manifests as haemolytic
uraemic syndrome. Haemolysis may also be associated with
glucose 6-phosphate dehydrogenase (G6PD) defi ciency. Immune
complex glomerulitis has been reported and IgM immunoglobulin,
C3 and S. Typhi antigen can be demonstrated in the glomerular
capillary wall. Nephrotic syndrome may complicate chronic S.
Typhi bacteraemia associated with urinary schistosomiasis.
Musculoskeletal and other systems
Skeletal muscle characteristically shows Zenkers degeneration (a
hyaline degeneration of muscle fi bres), particularly affecting the
Diagnosis
The definitive diagnosis of enteric fever requires the isolation of S.
Typhi or S. Paratyphi from blood, bone marrow, other sterile sites,
rose spots, stool, or intestinal secretions.. Isolation from stool or
urine provides strong presumptive evidence only in the presence
of a characteristic clinical picture.
Blood and bone marrow culture
The defi nitive diagnosis of typhoid is by the isolation of the
organism from a sterile site. Isolation of the organism from the
stool is useful information but may be a false positive due to
longterm carriage. Thus, in patients with suspected typhoid, blood
or bone marrow cultures should be performed. Modern automated
systems rapidly detect the presence of the organism, but
conventional non-automated methods also have a high diagnostic
yield
Faecal and urine cultures
With modern techniques, faecal cultures are often positive even
during the first week, though the percentage positivity rises
steadily thereafter. Urine cultures are positive less often.
Serology
The traditional Widal test measures antibodies against flagellar
(H) and somatic (O) antigens of the causative organism. In acute
infection, O antibody appears first, rising progressively, later
falling and often disappearing within a few months. H antibody
appears a little later but persists for longer. Rising or high O
antibody titre generally indicates acute infection, whereas raised
H antibody helps to identify the type of enteric fever.
However, the Widal test has many limitations :