ISSN: 0973-7510
E-ISSN: 2581-690X
In this study, the rapid detection of Clostridium difficile and its toxins (A/B) in admitting patients in hospitals were offered the possibility of prevention of the bacterium spread into other patients. This bacterium is the most common cause of hospital-acquired diarrhea in patients treated with antibiotics, chemotherapeutic agents and other drugs that alter the normal equilibrium of the intestinal flora. The Stool samples were cultured on specific agar media with anaerobically growth equipment. The C. difficile toxins A and B were detected in fecal samples by using enzyme-linked immunosorbent assay (EIA). In this study, there was a higher incidence of C. Difficile infection among the hospitalized patients in different hospital wards, especially in the renal ward, hepatic ward and oncology ward. The using of EIA technique for pathogen detection is very useful and significant method for the rapid detection of the C. difficile strains.
Clostridium difficile, Toxins A/B, Renal patients, Hepatic patients, Oncology patients
The Clostridium difficile is a gram-positive, spore-forming bacterium, usually spread by the fecal-oral route. It is non-invasive and produces toxins A/B that is causing disease. This disease is ranging either from asymptomatic carriage to mild diarrhea, colitis or pseudo-membranous colitis1, but C. difficile emerged as a major enteric pathogen with worldwide distribution2.
In the United States, C. difficile was nosocomial pathogen. In 2011 were identified 453,000 cases with C. difficile infection, in addition there were 29,000 death cases associated with C. difficile infection 3. The Nosocomial risks of C. difficile infection was more than the cost of treatments and hospitalizations (4). Increasing the annual expenditures were approximately $1.5 billion in the United States5.
The incidence of C. difficile infections among hospitalized patients were varied widely from different times and in different locations, but has generally been increasing to almost 15 cases per 1000 hospital discharges6 and approximately 20 cases per 100,000 persons/year in the community7.
The enzyme immunoassay (EIA) is more common diagnostic test today. It can be used to detect glutamated-hydrogenase (so-called common antigen) and/or major Toxins A/B. It is inexpensive, rapid and easy to perform. A drawback of EIA toxin tests is a lack of sensitivity, but conversely EIA tests, have better specificity, as they cannot distinguish toxigenic from nontoxigenic C. difficile. Glutamate dehydrogenase is a good screening test, but the positive specimens must be subjected to another test, that used to detect the toxin A and/or B or the toxin genes8.
Patients: This study carried out at Menoufia University hospital admitted patients in the period between December 2016 and March 2017. The 81 cases include 41 males (50.61%) and 40 females (49.4%). All patients were divided into three groups; group 1 was 25 patients from renal ward, group 2 included 33 patients from hepatic ward and the other cases in group 3 included 23 patients from oncology ward. All patients under the this study were classified into another two groups, diabetic group (N=46 cases) and non-diabetic group (N=35 cases). The inclusion criteria of adult men or women were 16-85 years old of patients with equal duration of admission to hospital wards (more than two days). The collected stool samples were diarrhea (N = 59), enema (N = 2) and semi formed stool samples (N = 19).
The age, sex, duration of hospital admission and drug usage (antibiotics and chemotherapy) is obtained from the patient’s clinical data. The case history of diabetes, liver diseases, kidney impairment and cancer are confirmed by the histopathology data. Every patient fulfilling the inclusion criteria was allocated to the intervention group. The written consent was obtained from all patients prior to enrollment in the study and ethical committee of Faculty of Medicine Hospital Menoufia University approved the protocol, which was in accordance with the ethical guidelines of the 1975 Declaration of Helsinki.
Stool samples: The stool samples available are collected after the patient’s admission in sterilized plastic containers and transported to the microbiology lab for the screening of the presence of C. difficile bacterium and A/B toxins.
Methods
Culture technique: Stool samples collected one by one and cultured anaerobically on selective media agar base (M836) with culture supplement (FD010).
Gram stain: All slides of bacteria examined under the oil immersion lens.
EIA detection of toxin A/B: The RIDASCREEN® Clostridium difficile toxin A/B is an enzyme immunoassay for determining toxin A and toxin B, specifically and simultaneously in the stool samples of patients using monoclonal antibodies. The reliable results were taken after only 2 hours and the effect of therapeutic measures were taken promptly.
Statistical analysis: The data were collected, tabulated and analyzed by SPSS (statistical package for social science) version 17.0 on IBM compatible computer (SPSS Inc., Chicago, IL, USA). The highly significant P value if it was less than 0.001, significant if it was less than 0.05 and not significant if it was more than 0.05.
The stool specimens were collected from selected hospitalized 81 patients under this study, were classified into three groups by gender of males in renal cases males were 4% and females were 96.0% of hepatic cases males were 69.7% and females were 30.3%, in oncology cases males were 73.9% and females were 26.1%. The patient’s duration before stool sample collection in hospital possible ranged from 5 to 10 days as follows; about 10 days to patients of the renal group, 5 days for the hepatic group and 8 days for oncology patients (table 1).
Table (1):
Different patient’s duration of the stay in hospital for all groups.
Duration |
Renal group (1) (N = 25) |
Hepatic group (2) (N = 33) |
Oncology group (3) (N = 23) |
Test of significance |
P value |
|---|---|---|---|---|---|
Days in hospital M ± SD |
10.48±6.61 |
5.67±2.83 |
8.13±10.05 |
U 2.08** 0.12* 0.11* |
< 0.051 > 0.052 > 0.053 |
U (Mann Whitney U test), * (t- test), ** (Mann Whitney U test), M ± SD (mean + standard deviation) & N (number of patients).1= comparison between renal cases and oncology cases.2= comparison between hepatic cases and oncology cases.3= comparison between renal cases and hepatic cases.
The consistency of stool samples in renal cases is 36.0% of semi-formed and 64% with diarrhea. In hepatic group patients stool consistency is 30.3% with semi-formed, 63.6% with diarrhea and 6.1% with an enema, but oncology patients the stool consistency are diarrhea 100% (table 2).
Table (2):
Stool consistency in different patient groups.
| Stool consistency | Renal group (1) (N = 25) |
Hepatic group (2) (N = 33) |
Oncology group (3) (N = 23) |
Test of significance | P value | |||
|---|---|---|---|---|---|---|---|---|
| N | % | N | % | N | % | X2 | ||
| Semi formed Diarrhea Enema |
9 16 0 |
36.0 64.0 0.0 |
10 21 2 |
30.3 63.6 6.1 |
0 23 0 |
0.0 100 0.0 |
10.19# 10.64 10.05 |
<0.051 <0.052 <0.053 |
# = Fisher’s Exact test.X2 (Chi Square test), % (percentage) & N (number of patients).1 = comparison between renal cases and oncology cases.2 = comparison between hepatic cases and oncology cases.3 = comparison between renal cases and hepatic cases
In this study among 81 studied cases 1 case its stool sample showed no growth of Clostridium difficile Agar media (1.2%), 80 cases their stool sample showed growth of gram-positive bacilli (98.8%). The bacterial growth was 100% in hepatic and oncology group, but was 96% in renal group patients (table 3). The bacterial toxin A/B production are highly elevated in hepatic and oncology groups, 69 cases showed the positive result for EIA for toxin A/B (85.2%) and 12 cases showed negative results for the same test (14.8%). The positive bacilli grow in hepatic and oncology groups are showing highly significant growth in comparison of different groups with each other, but the toxin production is 56% positive and 44% negative toxin production in renal patients under this study (table 3).
Table (3):
Growth on Clostridium difficile agar medium and toxin A/B production.
| Growth on agar media | Renal group (1) (N = 25) |
Hepatic group (2) (N = 33) |
Oncology group (3) (N = 23) |
Test of significance | P value | |||
|---|---|---|---|---|---|---|---|---|
| No growth Gram positive bacilli. |
N | % | N | % | N | % | X2 | > 0.051 > 0.051 > 0.053 |
| 1 24 |
4.0 96.0 |
0 33 |
0.0 100 |
0 23 |
0.0 100 |
0.94# 1.34 |
||
| Toxin A/B production | N | % | N | % | N | % | X2 | P value |
| Positive Negative |
14 11 |
56.0 44.0 |
32 1 |
97.0 3.0 |
23 0 |
100 0.0 |
13.13 0.71# 14.6 |
< 0.0011 > 0.052 < 0.0013 |
# = Fisher’s Exact test.
X2 (Chi Square test), % (percentage) & N (number of patients).
1= comparison between renal cases and oncology cases.
2 = comparison between hepatic cases and oncology cases.
3 = comparison between renal cases and hepatic cases.
The C. difficile growth is in diabetic patients in the different group was 97.8 % and 100% in non-diabetic patients. The possibilities of toxin A/B production are highly elevated in comparing with diabetic patients (table 4).
Table (4):
Growth on Clostridium difficile agar medium and toxin A/B in diabetic and non-diabetic groups.
| Growth on agar media | Diabetic (N = 46) |
Non diabetic (N = 35) |
Fisher’s Exacts | P value | ||
|---|---|---|---|---|---|---|
| N | % | N | % | |||
| No growth Gram positive bacilli |
1 45 |
2.2 97.8 |
0 35 |
0.0 100 |
FE 0.77 |
> 0.051 |
| Toxin A/B production | N | % | N | % | ||
| Positive Negative |
36 10 |
78.3 21.7 |
33 2 |
94.3 5.7 |
4.05* | < 0.051 |
FE = Fisher’s Exact test. X2 (Chi Square test), % (percentage) & N (number of patients).
1= comparison between diabetic cases and non diabetic cases
Table 5 appears gram-positive growth with highly significant increasing (94.1%) in chronic kidney disease without dialysis, but renal failure with dialysis group the growth are 100%. The toxin A/B production positivity is about 50% renal failure in dialysis cases and 58.8% of chronic kidney disease patients. The last table number 6 showed the different antibiotic and chemotherapy using in all patients of different three groups under this study with impaired pathogen growth.
Table (5):
Growth on Agar medium and toxin A/B production in chronic kidney disease patients with no dialysis and renal failure patients on dialysis.
| Growth on agar media | Renal Cases | Test of significance | P value | |||
|---|---|---|---|---|---|---|
| Chronic kidney disease No dialysis N=17 |
Renal failure on dialysis N = 8 |
|||||
| N | % | N | % | FE | ||
| No growth Gram positive bacilli |
1 16 |
5.9 94.1 |
0 8 |
0 100 |
0.49 | > 0.051 |
| Toxin A/B production | N | % | N | % | FE | > 0.051 |
| Positive Negative |
10 7 |
58.8 41.2 |
4 4 |
50 50 |
0.17 | |
FE = Fisher’s Exact test.
Table (6):
Drugs used in patients of study groups with bacteria growth.
| Drugs/ Growth | Renal group (1) (N = 25) |
Hepatic group (2) (N = 33) |
Oncology group (3) (N = 23) |
Test of significance | P value | |||
|---|---|---|---|---|---|---|---|---|
| N | % | N | % | N | % | x2 | ||
| No drugs Antibiotics Chemotherapy Both |
1 24 0 0 |
4.0 96.0 0.0 0.0 |
2 31 0 0 |
6.1 93.9 0 0 |
0 0 15 8 |
0.0 0.0 65.2 34.8 |
48.0 56.0 0.12* |
<0.0011 <0.0012 0.7203 |
| Antibiotics | N=24 | % | N=31 | % | N=8 | % | x2 | >0.051 >0.052 >0.053 |
| Single Combined |
13 11 |
54.2 45.8 |
16 15 |
51.6 48.4 |
6 2 |
75.0 25.0 |
1.08* 1.41* 0.04* |
|
| A type of antibiotic used | N=24 | % | N=31 | % | N=8 | % | x2 | >0.051 >0.052 >0.053 |
| Cephotax Unasyn Cephotax + unasyn Cephotax +cipro Unasyn +cipro Other combination |
12 1 5 1 2 3 |
50.0 4.2 20.8 4.2 8.3 12.5 |
16 0 8 1 1 5 |
51.6 0 25.8 3.2 3.2 16.1 |
4 2 1 0 0 1 |
50.0 25.0 12.5 0.0 0.0 12.5 |
4.0 8.81 2.24 |
|
* = Fisher’s Exact test.X2 (Chi Square test), % (percentage) & N (number of patients).1 = comparison between renal cases and oncology cases.2 = comparison between hepatic cases and oncology cases.3= comparison between renal cases and hepatic cases
The older age was independently associated with the development of severe complicated C. difficile infection in the hospitalized patients9. The most important primary risk factors include age more than 65 years, age less than 1 year with co-morbidity or underlying conditions10. The age over 70 years is an independent risk factor of severe C. difficile associated disease and adverse outcome, including death11, age were positively associated with the incidence of C. difficile infection and its relationship to disease severity remains controversial12. This previous suggestion was agreed with our observation where was significantly a difference between hepatic and oncology cases as regards age, on the other hand, there was no significant difference between renal and oncology group (P value < 0.05). It was argued that older patients may not be able to mount an effective immune response to the C. difficile infection 13 thus, leading to severe disease and poor outcome in the elderly. The male gender was associated with severe disease14, as in our foundation the hepatic and oncology groups, male gender were 69.7% and 73.9 % respectively, in contrast, the renal group that has 96% females.
The highest incidence rate of C. difficile infection and acquired within the long-term care facility, were indicating a substantial degree of transmission15, these infections can lead to major complications for the patient’s health (16), these agreements with this study duration and hospital stay for patients in hepatic unit was 5.67 and for oncology ward is 8.13 and for renal ward was 10.48 days (table 1). The clinical importance of C. difficile toxigenicity founded in liquid stool samples of hospitalized patients and the possibility of asymptomatic carrying in 2% of patients with formed stool17, the quantitative colony counts were sufficiently high to detect the bacterium irrespective of stool consistency and the semi-formed stool should be sought for the pathogen in symptomatic patients with frequent stools18. These are discussed, the majority of our collected stool samples were diarrhea; the minority of specimens are semi-formed and few with an enema (table 2).
The main of diagnosis is the detection of C. difficile toxins in a diarrheal sample, but a few laboratories made cultures of the organism. This combination of tests should include culture (with toxin testing of the isolate), demonstration of toxin directly from the feces and the detection of C. difficile antigen19 and this was in agreement with this study as we first used the culture technique then the demonstration of toxin using EIA technique. The EIA has a sensitivity ranging from 60 to 70% and specificity of 98%, but symptomatic patients with negative tests should be tested by another more sensitive method20. The stool culture is the most sensitive test and is essential for epidemiological studies1.
The patients with diarrhea were detected positive for C. difficile toxins A/B in stool specimens by EIA screen test in cases 74 % with diarrhea, 23.5% with semi-formed stool and 2.5% from enema21, these were supported our observed significant difference data of toxin A/B were 56.0% with renal, 97.0% with hepatic and 100% with oncology patients (table 3). Acute renal dysfunction can be used to define severe C. difficile infection22 and the dialysis patients have impaired host defense mechanisms and frequently require antibiotics for various infective complications23, this appear the high growth bacterium in our renal patients (96.0%) in addition to low toxin A/B production (56.0%).
In our results were100 0% growth of C. difficile Agar medium and 97.0% were positive for the production of toxin A/B using the EIA test in agreement with previous studies24. In addition to the formerly suggestions, the C. difficile infection is common amongst liver transplantation (22%) patients, cirrhotic liver disease25, 26 and cirrhosis-related complications26, 27, although diarrhea on hospital admission has been reported for 13% cirrhotic patients with C. difficile infection26. Recent evidence suggests that liver disease patients have increased morbidity, mortality and health care costs28.
The cancer patients have a higher risk for C. difficile infection as compared to non-cancer patients29, this confirms the 100% growth and toxin production of oncology group of our work. In the other recent foundation, there were no cancer-specific factors were identified to be related to C. difficile carriage. However, a younger age and a longer hospital stay may represent the characteristics of more aggressive and immunosuppressive oncologic disease 30.
In this study we found that 8 cases from 25 cases were admitted to renal unit were renal failure in dialysis and 2 cases from these 8 cases were showed positive growth on Clostridium difficile and we found that, 50% of renal failure on dialysis cases including two cases of the previous showed positive test for toxin A\B and 50% of cases show negative test for toxin A\B and this was in agreement with a study which indicated that, the dialysis process might be at high risk for the development of C. difficile associated disease, especially if the symptoms develop in dialysis patients31, this risk of pathogen infection increased hospital-associated morbidity and mortality was greater in dialysis than of chronic kidney disease patients not undergoing dialysis32.
Our significant difference between diabetic and non-diabetic cases as regards the production of toxin A/B (P-value <0.05) and this was in agreement with a study which demonstrated that, diabetes is an important risk factor for recurrence of C. difficile associated disease33. In addition, the diabetes-related hospitalization increases the risk of recurrent bacterium infection34.
The patients who take antibiotics are most at risk for developing C. difficile infections because the beneficial bacteria that are normally present in the human gut and protect against infection can be suppressed for several weeks to months, during this time the patients can get sick from C. difficile picked up from contaminated surfaces or spread person to person35. The C. difficile infection in cancer patients receiving chemotherapy is 2.3 to 8.2% of these patients develop severe intestinal colitis36.
Risk factors for bacterium infection in immune suppressed cancer patients appear to be their frequent hospitalizations and receipt of chemotherapeutic agents and antimicrobials that make them more susceptible to this disease37 and this was in agreement with our study as all oncology patients were received chemotherapy and show positive production of C. difficile toxin A/B. Some chemotherapeutic drugs such as; methotrexate and 5-fluorouracil are most commonly reported to be associated with pathogen infection risk may be from the drug’s ability to cause intense intestinal mucositis 37. Several other chemotherapeutic agents, including cyclophosphamide, doxorubicin, cisplatin, paclitaxel, and vinorelbine, have been associated with C. difficile infection38. This was confirmed the obtaining significant difference between renal and oncology cases as regards taken drugs (P-value <0.001), there was a highly significant difference between hepatic and oncology cases as regards taken drugs (P-value is <0.001). The taken drugs include antibiotics, chemotherapy or both.
This study must be introduced into the infection control units of many hospital in Egypt, specially in Faculty of Medicine Hospital, Menoufia University. It is concluded that, C. difficile bacterium is widely spread among hospitalized patients in hospital wards, renal ward (56%), hepatic ward (97%) and oncology ward (100%). The immunosorbent assay for the detection of toxin A/B is a significant technique for the rapid detection of pathogenic C. difficile strain in patient’s stool specimen.
ACKNOWLEDGMENTS
We introduce the acknowledgment to all members of the Faculty of Medicine Hospital, Menoufia University and patients who were agreed to undergo this study.
CONFLICT OF INTEREST
The authors declare that there is no conflict of interest.
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