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Background:
Clostridium difficile (CD) is implicated in 20 to 30% of patients with
antibiotic-associated diarrhoea, in 50 to 70% of those with
antibiotic-associated colitis and in more than 90% of those with
antibiotic-associated pseudomembranous colitis1-4. The incidence of CD
associated diarrhoea ranges from 1 in 100 to 1 in 1,000 hospital discharges
depending on the antibiotic prescribing habits of the hospital5-7.
The consequences of CD can be severe. At one academic medical center over a
three-year period, 21 of 710 cases (3%) of CD colitis required intensive care
unit admission or died as a result of their infection8. These deaths were
associated with co-morbid conditions such as malignancy, chronic obstructive
pulmonary disease or renal failure and therapies such as immunosuppressive
drugs, anti-peristaltic medications or the prior administration of clindamycin9.
At another university hospital the morbidity of the infection was higher and 24
of 157 patients (15.3%) with CD colitis died from their infection10. The new
variant of CD - which is capable of secreting much higher amounts of toxin A & B
and is more resistance to standard antibiotic therapy - results in greater
incidence in hospitalized patients11, a greater need for urgent colectomy for
toxic colitis and a significantly higher mortality rate12. The economic
consequences of CD infection can also be severe, with one report finding a mean
cost of $10,970 (US$) per patient for the treatment of the infection and its
complications13.
Due to the high incidence of CD infection on a 24-bedded ward in a busy district
general hospital in Merseyside - UK, all microbiologically confirmed infections
over a period of one month were identified and studied for predictors of
mortality and morbidity.
Aims:
The primary objective of our study was to determine the baseline characteristics
of in-patients with hospital acquired Clostridium difficile and to ascertain
their eventual outcomes, and thus evaluate the effectiveness of disease severity
in predicting mortality, morbidity at discharge and discharge destination.
Secondary aims included an analysis of the
epidemiology of the infected population and if
antibiotic-related infection varied in prognosis to sporadic
(antibiotic-unrelated) infection.
Methods:
All patients with diarrhoea admitted to a 24-bedded (cohort) ward in at Whiston
Hospital, Merseyside – UK over a four week period (May 2008) were prospectively
identified and their case-notes were retrospectively reviewed. The study was
approved by the Clinical Governance Department of the hospital.
Case definitions and
measures
Clostridium difficile (CD) infection: A patient admitted to the cohort wart
during the period of the study with symptoms and microbiological confirmation of
Clostridium difficile infection.
Antibiotic-related infection: A case of confirmed Clostridium difficile
infection with documented receipt of oral or parenteral antibiotic therapy as an
in-patient or in the community within 6 weeks prior to the onset of symptoms.
Measures of morbidity: Karnofsky14 and Zubrod (also called ECOG [Eastern
Cooperative Oncology Group]) 15 scoring systems were employed in determining the
morbidity of the infected population at diagnosis and at the eventual outcome. A
Karnofsky score of </= 40 (40 being the requirement of special care and
assistance [disabled], and 0 being death) and a Zubrod score of >/=3 (3 being
limited self care with confinement to a bed/chair for >50% of waking hours, and
5 being death) signified increased morbidity.
Measure of disease severity: Severity of infection was determined using the
Clostridium difficile Severity Assessment Scoring System of the UK’s Department
of Health (2008). A score of >/=3 was identified as ‘severe disease’ and a score
of <3 as ‘non-severe disease’.
Outcome measures: Outcome measures were death (resulting directly from the
infection), morbidity scores at discharge and discharge destination.
All results were expressed as mean or percentages. Fisher’s T test was employed
to explore statistical significance.
Results:
16 patients with confirmed CD infection were identified during the period of the
study. The mean age of the infected population was 80 years (age range: 59-89
years, median: 82 years).
Pre-admission morbidity state:
The average pre-admission Karnofsky and Zubrod scores of the studied population
were 50 and 2.57 respectively, suggestive of some disability even before the
onset of the infection. The average number of pre-existing co-morbidities was 5.
Eventual outcomes:
The average eventual morbidity scores of the population was Karnofsky 33.75 and
Zubrod 3.32 with 68.8% (11 cases) having a score of </= 40 and >/=3
respectively, denoting a significant decline in their morbidity status. 31.25%
(5 cases) died in hospital as a result of their infection. However, 54.5% (6
cases) of the 11 survivors were fully dependent and eventually required
institutional care at discharge.
Disease severity as a predictor of eventual outcome:
The mean disease severity score of the identified population was 3.72. 9
patients (56.3%) had an infection severity score of >/=3 (signifying ‘severe
disease’) while the remaining 7 had non-severe disease. Increased morbidity and
mortality was noted in the population with severe disease. 7 (77.8%) of the 9
patients with severe disease had an eventual Karnofsky score of </=40 and an
eventual Zubrod score of >/=3 (increased morbidity) while increased morbidity
was noted in 4 (57.1%) of the 7 patients with non-severe disease [p=0.37].
Similarly, 44.4% (4 cases) of patients with severe disease died and another
44.4% (4 cases) required institutional care on discharge compared to 14.3% and
28.6% respectively in patients with non-severe disease [p values of 0.3 and 0.45
respectively]. This is demonstrated in Table 1.
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Table
1: Disease
severity as a predictor of outcome in CD infection
|
|
Severity
score >/=3
N=9 |
Severity
score <3
N=7 |
Total
N=16 |
P value |
|
Eventual K score </= 40 |
7 (77.8%) |
4 (57.1%) |
11 (68.8%) |
0.3654 |
|
Eventual Z score >/= 3 |
7 (77.8%) |
4 (57.1%) |
11 (68.8%) |
0.3654 |
|
Institutional care on discharge
|
4 (44.4%) |
2 (28.6%) |
6 (37.5%) |
0.4510 |
|
Death |
4 (44.4%) |
1 (14.3%) |
5 (31.3%) |
0.3077 |
|
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Prognostic difference between antibiotic-related and antibiotic-unrelated
infection: 13 patients (81%) were confirmed to have antibiotic-related
infection. Significantly increased morbidity and mortality was noted in the
population with antibiotic un-related infection. 8 (61.5%) of the 13 patients
with antibiotic-related disease had an eventual Karnofsky score of </=40 and an
eventual Zubrod score of >/=3 in comparison to all 3 patients (100%) with
antibiotic-unrelated infection [p=0.29]. And while 15.4% of patients with
antibiotic-related disease died, the mortality rate in those with
antibiotic-unrelated infection was 100% [p=0.036]. Table 2 provides details of
these findings.
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Table
2: Outcome
difference between antibiotic-related and antibiotic-unrelated disease
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Antibiotic-related infection
(N=13) |
Antibiotic-unrelated infection
(N=3) |
Total
N=16 |
P value |
|
Eventual K score </= 40 |
8 (61.5%) |
3(100%) |
11 (68.8%) |
0.2946 |
|
Eventual Z score >/= 3 |
8 (61.5%) |
3(100%) |
11 (68.8%) |
0.2946 |
|
Death |
2 (15.4%) |
3(100%) |
5 (31.3%) |
0.0179 |
|
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Discussion:
Our study confirms that CD is a disease that affects a predominantly elderly and
frail population with multiple co-morbidities and poor performance status, and
carries a large mortality and morbidity burden. This is in keeping with the
findings of previous studies which have highlighted that pre-existing morbidity
is a significant risk factor to acquiring the infection and that the overall
prognosis of this patient group is generally poor16, 17.
Disease severity scores seem to have a reasonably realistic predictory value of
eventual outcome of the infection. In our study, those patients identified as
having a severe disease course did have a higher rate of mortality than those
with non-severe disease, and those who survived the infection were left with
elevated morbidity and a poorer performance status, with most requiring
institutional care on discharge.
Antibiotic use was the single most important contributing factor to developing
the infection. Over three-quarters of our inpatients with confirmed CD infection
were noted to have had oral or parenteral antibiotics in the preceding 6 weeks
and this corroborates with the findings in existent medical literature6.
However, a notable finding of our study is that prognosis and mortality rates
are significantly worse in those with antibiotic-unrelated CD infection. This
should be taken into consideration in the formulation of appropriate treatment
strategies in order to combat the high levels of mortality and morbidity ensuing
from antibiotic-unrelated Clostridium difficile infection.
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