|Year : 2016 | Volume
| Issue : 2 | Page : 143-146
Profile of pneumocystis infection in a tertiary care institute in North India
Ravinder Kaur1, Pragyan Swagatika Panda1, Richa Dewan2
1 Department of Microbiology, Maulana Azad Medical College and Associated Hospitals, New Delhi, India
2 Department of Medicine, Maulana Azad Medical College and Associated Hospitals, New Delhi, India
|Date of Web Publication||13-Oct-2016|
Department of Microbiology, Maulana Azad Medical College and Associated Hospitals, Bahadur Shah Zafar Marg, New Delhi - 110 002
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Context: Pneumocystis jirovecii pneumonia (PcP) is still remains a common opportunistic disease in human immunodeficiency virus (HIV) infected individuals. Study on PcP in developing countries are scarce. Aims: To study the occurrence of P. jirovecii infection in clinically suspected individuals in a tertiary care institute. Settings and Design: Retrospective study conducted in a tertiary care hospital. Materials and Methods: Two years data regarding respiratory sample analysis, HIV status, and cluster of differentiation 4 (CD4) cell count of clinically suspected pneumocystis infection patients with known/unknown HIV status were analyzed. Results: Data of 45 eligible patients were analyzed. The majority of the patients were male (between 21 and 50 years of age). Total 26 (57.7%) patients were HIV reactive, of which 14 had CD4 count of <200 cells/mm3. 20 patients (9 HIV reactive and 11 unknown HIV status) were confirmed with pneumocystosis by direct fluorescent antibody (DFA) staining. Four of 14 HIV reactive individuals who had CD4 count of <200 cells/mm3 and 5 of 12 HIV reactive individuals who had CD4 count of >200 cells/mm3 were positive for pneumocystosis. Conclusions: Pneumocystis pneumonia is still prevalent in North India and is mainly affecting patients in economically productive and sexually active age group. To diagnose pneumocystosis, DFA is an easily available method in resource-limited settings. Appreciating the actual HIV or immunodeficiency status and the CD4 profile of an individual with symptoms of pneumocystis infection will help the clinicians in early diagnosis and initiation appropriate therapy in individuals living with the disease.
Keywords: Cluster of differentiation 4 count, human immunodeficiency virus status, North India, pneumocystosis
|How to cite this article:|
Kaur R, Panda PS, Dewan R. Profile of pneumocystis infection in a tertiary care institute in North India. Indian J Sex Transm Dis 2016;37:143-6
|How to cite this URL:|
Kaur R, Panda PS, Dewan R. Profile of pneumocystis infection in a tertiary care institute in North India. Indian J Sex Transm Dis [serial online] 2016 [cited 2017 Apr 27];37:143-6. Available from: http://www.ijstd.org/text.asp?2016/37/2/143/185501
| Introduction|| |
Pneumocystis jirovecii pneumonia (PcP) is an opportunistic infection (OI) causing life-threatening pneumonia in immunocompromised patients and it still remains a common opportunistic disease in human immunodeficiency virus (HIV) infected individuals. As compared to developed countries, the epidemiology and clinical spectrum of PcP have not been clearly defined and well documented in developing countries. Hence, studies on the profile of pneumocystis infection in individuals with clinical suspicion of HIV in developing countries are needed to be carried out. This retrospective study was carried out in a tertiary care institution to study the occurrence of P. jirovecii infection in clinically suspected individuals and to study its association with HIV status and cluster of differentiation 4 (CD4) cell count of those patients.
| Materials and Methods|| |
Our laboratory records were reviewed to collect 2 years data (January 2012 to December 2013) of respiratory sample analysis of clinically suspected pneumocystis infection patients with known/unknown HIV status and CD4 counts. During the study data inclusion period, both expectorated and induced sputum samples from clinically suspected pneumocystis infection were processed in our laboratory. Uniform sample processing and staining procedure were followed in all patients. The smears were prepared and fixed with acetone as per the manufacturer's instruction and were subjected to direct fluorescent antibody (DFA) stain using a commercially available kit (MERIFLUOR ® Pneumocystis - Meridian Bioscience, Inc., Italy). The stained slides were screened using a fluorescent microscope with a ×10 followed by ×40 dry objective for the presence of trophozoites and cysts with typical apple green fluorescence. To assess reproducibility, two slides were made for each specimen and were examined separately. We collected the data regarding the HIV status and CD4 cell counts of the study group. The CD4 count was done only for HIV reactive individual in our institution.
| Results|| |
Data of 45 eligible patients were analyzed in our study. The patients included in the study ranged from 2 to 60 years of age with male:female ratio of 31/14 (2.2:1). The mean age of the study cohort was 35.1 years. Most of the male patients (34/45; 75%) belonged to age groups of 21–50 years and the majority of the female patients (6/45; 13.3%) belonged to 21–30 years age group [Table 1]. Of all the patients, 26 (57.7%) were HIV reactive [7 out of 13 (53.8%)patients in 2012 and 19
|Table 1: Patient demography of human immunodeficiency virus reactive and human immunodeficiency virus status unknown patients|
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out of 32 (59.3%) patients in 2013], whereas, 19 (42.2%) were of unknown HIV status. Among the HIV reactive individuals 69.2% (18/26) and among the unknown HIV status individuals 68.4% (13/19) were males. The result of CD4 count done for the HIV reactive individuals is shown in [Table 2]. Fourteen out of 26 (53.8%) had CD4 count of <200 cells/mm 3 whereas, 12 (46.2%) patients had CD4 count of >200 cells/mm 3.
|Table 2: Cluster of differentiation 4 count (cells/mm3) of human immunodeficiency virus reactive individuals|
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The result of DFA staining of the patients is shown in [Table 3]. 20 patients (8 in 2012 and 12 in 2013) were confirmed with pneumocystosis by DFA (15 male and 5 female) irrespective to their HIV status. Most of the males belonged to 21–40 years of age group, whereas most females were of the age group of 11–60 years. Among the pneumocystis positive individuals 9 were HIV reactive (4 in 2012 and 5 in 2013), whereas 11 were of unknown HIV status. Among the 14 HIV reactive individuals who had CD4 count of <200 cells/mm 3 4 were positive and 10 were negative for pneumocystosis with DFA staining. Among the 12 HIV reactive individuals who had CD4 count of >200 cells/mm 3 5 were positive and 7 were negative for pneumocystosis with DFA staining.
|Table 3: CD4 count and direct fluorescent antibody staining profile of human immunodeficiency virus reactive and individuals with unknown human immunodeficiency virus status|
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| Discussion|| |
Opportunistic Infections are an important cause of morbidity and mortality among HIV-infected individuals. The use of highly active anti-retroviral therapy (HAART) and pneumocystis prophylaxis have dramatically reduced the number of cases of PcP. Moreover, pneumocystosis continues to occur among persons who are unaware of their HIV infection, and also in patients who fail to seek medical care, or adhere to or respond to anti-retro viral therapy (ART) or pneumocystis prophylaxis.
World Health Organization (WHO) recommends starting of empiric therapy for PcP on the basis of its clinical case definition by a number of local guidelines which have been incorporated into the management protocols in resource-limited settings. This approach may be acceptable in the correct clinical and epidemiological context, but inaccurate diagnosis carries a number of important implications in resource-poor countries. Moreover, large and increasing numbers of patients with HIV-associated respiratory diseases has necessitated the use of rapid and accurate diagnostic tests for the identification of P. jirovecii. The DFA stain is a sensitive and convenient method for detection of P. jirovecii. It has the advantage of being simpler requiring less time and fewer reagents than indirect fluorescent-antibody, Gomori methenamine silver, and modified toluidine blue O stains., Hence, we used DFA staining in our study.
Among the 45 patients with a clinical suspicion of pneumocystinosis included in our study, 19 (42.2%) had unknown HIV status. This highlights the importance of unknown HIV status in patients with clinically suspected pneumocystis infection in our country. The mean age of HIV reactive state in our study was 35.1 years, which is similar to that reported in previous studies.,, In contrast to male (21–50 years) female patients in our study were of slightly younger age group (21–30 years). This finding is similar to that reported previously.,,,, This could be due to the general trend of having younger female partners in India. Another important observation in our study is that HIV infection still prevalent in patients in economically productive age group.
In our study, 20 out of 45 patients (44.4%) were positive for pneumocystinosis by DFA. Among the HIV reactive individuals, 34.6% (9 out of 26) of patients were positive for pneumocystinosis by DFA. In their study, Choe et al. reported 55.3% HIV reactive patients to be positive for PcP by DFA. Earlier studies in the USA showed PcP as the most frequent cause of pulmonary infections (85%) and was also the first cause of hospital admission in HIV patients. However, The reported incidence of PcP is between 32% and 45% in the current literature.,,,
Among the individuals diagnosed to have pneumocystinosis by DFA, 15/20 (75%) were male and 5/20 (25%) were female in our study. Most males belonged to 21–40 years of sexually active age group and the females belonged to age group of 11–60 years. In a study in South Africa, out of 41 patients, 77.7% (23 out of 27 females were positive for P. jirovecii, whereas, 50% (7 out of 14) males were positive for P. jirovecii. The females mostly belonged to 20–39 years of age who were older than in our study, whereas 5/7 (71.4%) males were of 20–39 years of age, which was similar to our study.
The CD4 counts <200 cells/mm 3 is an important risk factor for OIs in HIV infection and CD4 count is considered the best short-term predictor of OIs. Currently, The National Institutes of Health, the Centers for Disease Control and Prevention and the HIV Medicine Association of the Infectious Diseases Society of America guidelines mentions that prophylaxis against PcP may be discontinued safely in HIV-infected individuals when CD4 counts are maintained >200 cells/mm 3 for over 3 months on antiretroviral therapy. Jensen et al. and Masur et al. in their respective studies have reported that around 95% of their patients with of PcP had a CD4 count of <250 cells/mm 3. However, in our study, 44.4% (4 out of 9) among the DFA positive individuals had a CD4 count <200 cells/mm 3 which indicates a poor correlation between CD4 count and DFA positivity in the diagnosis of pneumocystosis. The discrepancy between CD4 count and the DFA positive cases of pneumocystosis [Table 3] in our study could be due to the time difference between CD4 count increase and clearance of pneumocystis antigen from the body. We cannot comment the about the later because we did not have the data about the duration of HAART or pneumocystis prophylaxis received by the patients.
Nearly 58% (11 out of 19) individuals with unknown HIV status were DFA positive for pneumocystosis in our study. The CD4 count was not known in them because, as per National AIDS Control Organization (NACO) guidelines CD4 count being an expensive test is to be done only in HIV reactive individuals as a guide to therapy. Hence, HIV status unknown patients might had HIV infections or any other immunodeficiency state that predisposed them to PcP infection. Our finding emphasizes the need for increasing resources in a developing country like ours to diagnose HIV, other immune deficiency states in patients with pneumocystis infection.
The major limitation of our study is that our study is a retrospective one. Hence, data regarding the duration of HAART and/or pneumocystis prophylaxis was not available to us. Another limitation in our study was that we did not have any data about the immune status and CD4 count of patients with unknown HIV status. Their actual HIV status and the CD4 count would help in knowing the actual PcP infection burden in the society and for an effective HAART therapy to be implemented to help in lessening the disease burden in the community.
| Conclusion|| |
Pneumocystis pneumonia is still prevalent in North India and is mainly affecting patients in economically productive and sexually active age group. To diagnose pneumocystosis, DFA remains an easily available method in resource-limited settings where the polymerase chain reaction assay cannot be developed and standardized to be followed routinely. As a rapid screening method, DFA can be used to detect P. jirovecii in respiratory specimens. Appreciating the actual HIV or immunodeficiency status and the CD4 profile of an individual with symptoms of pneumocystis infection will help the clinicians in early diagnosis and initiation appropriate therapy in individuals living with the disease.
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Conflicts of interest
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[Table 1], [Table 2], [Table 3]