Savita Kumari

Savita Kumari

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Savita Kumari

Department of General Medicine, MM Institute of Medical Sciences and Research, Ambala, India

Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2007 in Leukemia & Lymphoma
Verified
Journal Article
Closed access
PMPankaj Malhotra
Pankaj Malhotra
SVSubhash Varma
Subhash Varma
NVNeelam Varma
Neelam Varma
SKSavita Kumari
Savita Kumari
RDReena Das
Reena Das
SRSrinivasan Radhika
Srinivasan Radhika
Cure rates for adult acute lymphoblastic leukemia (ALL) in developing countries are significantly lower because of problems unique to these countries. We assessed some of the problems in adult ALL patients (>12 years of age) in a tertiary care hospital of northwest India with modified BFM regimen. The diagnosis of ALL was made according to FAB criteria. The protocol consisted of Phase I & II induction, consolidation, reinduction and maintenance phases. CNS prophylaxis was administered with 24 Gy radiation and intrathecal methotrexate. One hundred and eighteen patients (72.9% males), aged 12 – 68 years (median 23 years) were treated from January 1997 till December 2003. Follow-up of patients was done till December 2005. Complete remission (CR) was achieved in 85.6% patients after induction therapy and 40% patient relapsed. Most patients (23.7%) relapsed during the maintenance phase or after completion of chemotherapy. At least 15% of patients (15/101) after successful induction abandoned the treatment because of financial constraints, prolonged travel time to treatment facility and switching over to alternative medicines. Fatal infectious complications occurred in 19.5% of patients. The 3-year and 5-year event free survival rates were 29.8% and 21.6% respectively. In conclusion, modified BFM regimen resulted in high induction rates but relatively poor 5-year event free survival. Infections related death and post induction abandonment of treatment were the main reasons for poor overall results.

1 March 2019 in Journal of Family Medicine and Primary Care
Verified
Journal Article
Open access
PDF file
DSDheeraj Sharma
Dheeraj Sharma
VSVikas Suri
Vikas Suri
APAshok K. Pannu
Ashok K. Pannu
SASavita V. Attri
Savita V. Attri
NVNeelam Varma
Neelam Varma
SKSavita Kumari
Savita Kumari
Background: Geriatric anemia is a global health problem because of its high prevalence and associated significant morbidity and mortality. Aim: The objectives of this study were to estimate the pattern of anemia in the elderly patients and the underlying etiology of anemia. Research Design and Methods: This was a hospital-based prospective observational study, conducted in patients aged 60 years and above at PGIMER, Chandigarh, a tertiary care center of North India. Anemia is defined as hemoglobin level less than 13 g/dl in men and 12 g/dl in women. Results: Among the 105 older patients with anemia, the mean value of hemoglobin was 8.8 ± 2.3 g/dl. The etiological distribution of anemia was iron deficiency in 26 patients (24.8%), chronic disease in 24 patients (22.9%), hematological disorders in 21 (20%), chronic kidney disease in 13 (12.4%), multifactorial in 8 (7.6%), vitamin B12 deficiency in 2 (1.9%), folate deficiency in 1 (0.9%), and hypothyroidism in 1 patient (0.9%). No etiology could be found in 9 patients (8.6%). 57.6% of the iron-deficient patients had upper gastrointestinal lesions and 30.7% had a nutritional cause. Common chronic diseases causing anemia were malignancy (36.6%) and liver disease (29.1%). The myelodysplastic syndrome was the commonest hematological disorder. 53.35% of the patients had normocytic anemia, 40% had microcytic anemia, and 6.6% had macrocytic anemia. Conclusions: In most of the cases, anemia in the elderly had a treatable cause. Thus, a thorough investigation including gastrointestinal endoscopy is warranted. Unexplained progressive or unresponsive anemia requires bone marrow examination.

1 October 2020 in Asian Journal of Psychiatry
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Journal Article
Closed access
AMAseem Mehra
Aseem Mehra
VSVikas Suri
Vikas Suri
SKSavita Kumari
Savita Kumari
AAAjit Avasthi
Ajit Avasthi
SGSandeep Grover
Sandeep Grover

25 October 2012 in Indian Journal of Hematology and Blood Transfusion
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Journal Article
Closed access
PDF file
PCPuneet Chhabra
Puneet Chhabra
ALArjun Datt Law
Arjun Datt Law
USUpender Sharma
Upender Sharma
VSVikas Suri
Vikas Suri
MSMan Updesh Singh Sachdeva
Man Updesh Singh Sachdeva
PMPankaj Malhotra
Pankaj Malhotra

1 November 2013 in Leukemia & Lymphoma
Verified
Journal Article
Closed access
PDF file
DLDeepesh P. Lad
Deepesh P. Lad
PMPankaj Malhotra
Pankaj Malhotra
AKAlka Khadwal
Alka Khadwal
GPGaurav Prakash
Gaurav Prakash
VSVikas Suri
Vikas Suri
SVSubhash Varma
Subhash Varma
Treatment for hairy cell leukemia (HCL) has evolved over the years from splenectomy to interferon to purine analogs to monoclonal antibody based therapy [1]. Until three decades ago, splenectomy wa...

1 May 2003
Verified
Journal Article
Closed access
PMP Malhotra
P Malhotra
SKSavita Kumari
Savita Kumari
SSS Singh
S Singh
SVS Varma
S Varma