Patient Name : Mr.
UMESH KAUSHIK Collected : 16/Jul/2025 12:37PM
Age/Gender : 37 Y 0 M 0 D /M Received : 16/Jul/2025 04:10PM
UHID/MR No : DMEE.0000013819 Reported : 16/Jul/2025 05:42PM
Visit ID : DMEEOPV27505 Status : Final Report
Ref Doctor : DR SHWETA KEDIA Client Name : PUP HM DIAGNOSTICS
IP/OP NO : Center location : Paschmin Vihar,West Delhi
DEPARTMENT OF BIOCHEMISTRY
Test Name Result Unit Bio. Ref. Interval Method
RHEUMATOID FACTOR , SERUM <10.0 IU/mL <14 Immunoturbidimetry
Comment:
Rheumatoid factor (RF) consists of autoantibodies of immunoglobulin isotypes IgM, IgA, IgG, and IgE. Most patients with
rheumatoid arthritis and Sjogren’s syndrome have elevated levels of RF. RF may also be elevated in scleroderma,
dermatomyositis, Waldenstrom’s disease, sarcoidosis, and systemic lupus erythematosus. There are also instances of elevated RF
without apparent disease or definable clinical disorders.
Test Name Result Unit Bio. Ref. Interval Method
CK CREATINE KINASE - (CPK) , 24.20 U/L 39-308 IFCC
SERUM
Comments:-
Creatinine kinase is an enzyme consisting of 3 major iso-enzymes, CK-BB(Brain), CK-MB(Heart) & CK –MM(Skeletal muscle).
It is used as a marker for injury of cardiac muscle with good specificity. It is used as a marker for injury of striated muscle
disorders.
Decreased muscle mass
Rheumatoid arthritis (two thirds of patients)
Cushing’s disease
Untreated hyperthyroidism
Metastatic tumor in liver
Multiple organ failure
Septicemia
Test Name Result Unit Bio. Ref. Interval Method
C-REACTIVE PROTEIN CRP 10.8 mg/L 0-5 Latex Particle
(QUANTITATIVE) , SERUM Immunoturbidimetric
Comment:
C-reactive protein (CRP) is one of the most sensitive acute-phase reactants for inflammation. Measuring changes in the
concentration of CRP provides useful diagnostic information about the level of acuity and severity of a disease. Unlike ESR, CRP
levels are not influenced by hematologic conditions such as anemia, polycythemia etc.
Page 1 of 3
SIN No:BI26854119
Patient Name : Mr.UMESH KAUSHIK Collected : 16/Jul/2025 12:37PM
Age/Gender : 37 Y 0 M 0 D /M Received : 16/Jul/2025 04:10PM
UHID/MR No : DMEE.0000013819 Reported : 16/Jul/2025 05:42PM
Visit ID : DMEEOPV27505 Status : Final Report
Ref Doctor : DR SHWETA KEDIA Client Name : PUP HM DIAGNOSTICS
IP/OP NO : Center location : Paschmin Vihar,West Delhi
DEPARTMENT OF BIOCHEMISTRY
Increased levels are consistent with an acute inflammatory process. After onset of an acute phase response, the serum CRP
concentration rises rapidly (within 6-12 hours and peaks at 24-48 hours) and extensively.Concentrations above 100 mg/L are
associated with severe stimuli such as major trauma and severe infection (sepsis).
Page 2 of 3
SIN No:BI26854119
Patient Name : Mr.UMESH KAUSHIK Collected : 16/Jul/2025 12:37PM
Age/Gender : 37 Y 0 M 0 D /M Received : 16/Jul/2025 04:16PM
UHID/MR No : DMEE.0000013819 Reported : 16/Jul/2025 07:45PM
Visit ID : DMEEOPV27505 Status : Final Report
Ref Doctor : DR SHWETA KEDIA Client Name : PUP HM DIAGNOSTICS
IP/OP NO : Center location : Paschmin Vihar,West Delhi
DEPARTMENT OF SEROLOGY
Test Name Result Unit Bio. Ref. Interval Method
ANTI CCP (CYCLIC CITRULLINATED 80.3 U/mL 0-17 ECLIA
PEPTIDE) , SERUM
Comment:
Comment (Table): Anti CCP Interpretation
<17 U/ml Negative
>= 17 U/ml Positive
Antibodies to citrullinated proteins are markers of RA, especially for early diagnosis of the disease. The sensitivity of CCP-IgG for
RA varies from about 50–75%, whereas specificity for RA is relatively high, usually >90%. Hence it is useful in differentiating RA
from other connective tissue diseases that may present with arthritis and may be positive for RF, such as HCV-associated
cryoglobulinemia, undifferentiated polyarthritis, and Sjögren syndrome.
Not all individuals with RA will have detectable anti-CCP antibodies, and elevated anti-CCP antibodies may be seen in individuals
with no evidence of clinical disease.
*** End Of Report ***
Page 3 of 3
SIN No:SE02775473
Patient Name : Mr.UMESH KAUSHIK Collected : 16/Jul/2025 12:37PM
Age/Gender : 37 Y 0 M 0 D /M Received : 16/Jul/2025 04:16PM
UHID/MR No : DMEE.0000013819 Reported : 16/Jul/2025 07:45PM
Visit ID : DMEEOPV27505 Status : Final Report
Ref Doctor : DR SHWETA KEDIA Client Name : PUP HM DIAGNOSTICS
IP/OP NO : Center location : Paschmin Vihar,West Delhi
TERMS AND CONDITIONS GOVERNING THIS REPORT
1. Reported results are for information and interpretation of the referring doctor or such other medical professionals, who understand
reporting units, reference ranges and limitation of technologies. Laboratories not be responsible for any interpretation whatsoever
2. This is computer generated medical diagnostics report that has been validated by an Authorized Medical Practitioner/Doctor. The
report does not need physical signature.
3. Partial reproduction of this report is not valid and should not be resorted to draw any conclusion.
4. In the case you are not the intended recipient of this report. Please immediately return the same to the concerned issuing desk. Any
disclosure, copy or distribution of any contents of this report, is unlawful and is strictly prohibited.
5. Results delays may occur due to unforeseen circumstances such as non-availability of kits, equipment breakdown, natural calamities,
IT downtime, logistic delays or any other unavoidable event. For certain tests based on analyte stability, criticality of results and in the
interest of patient for having appropriate medical diagnosis, the same test may be outsourced to other accredited laboratory.
6. It is presumed that the tests performed are, on the specimen / sample being to the patient named or identified and the verifications of
particulars have been confirmed by the patient or his / her representative at the point of generation of said specimen
7. The reported results are restricted to the given specimen only. Results may vary from lab to lab and from time to time for the same
parameter for the same patient (within subject biological variation).
8. The patient details along with their results in certain cases like notifiable diseases and as per local regulatory requirements will be
communicated to the assigned regulatory bodies
9. The patient samples can be used as part of internal quality control, test verification, data analysis purposes within the testing scope of
the laboratory.
10. This report is not valid for medico legal purposes. It is performed to facilitate medical diagnosis only
SIN No:SE02775473
