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Prolactin (PRL)
Investigation Result Units Biological Reference Interval

Prolactin (PRL) 18.87 ng/mL 6 - 29.9

• Sample Type: Serum. • Method : ECLIA. • Comments : PRL is a polypeptide produced by the lactotrophs of the pituitary gland. Since prolactin is secreted in a pulsatile manner and is also influenced by a variety of physiologic stimuli, it is recommended to test 3 specimens at 20-30 minute intervals after pooling. Major circulating form of Prolactin is a nonglycosylated monomer, but several forms of Prolactin linked with immunoglobulin occur which can give falsely high Prolactin results. Macroprolactin assay is recommended if prolactin levels are elevated, but signs and symptoms of hyperprolactinemia are absent or pituitary imaging studies are normal • Clinical Use : 1.Diagnosis & management of pituitary adenomas. 2.Differential diagnosis of male & female hypogonadism increased levels. 3.Physiologic:-Sleep, stress, postprandially, pain, coitus, pregnancy, nipple stimulation or nursing. 4.Systemic disorders:-Chest wall or thoracic spinal cord lesions, Primary/Secondary hypothyroidism, Adrenal insufficiency, Chronic renal failure, Cirrhosis 5.Medications:-Psychiatric medications like Phenothiazine, Haloperidol, Risperidone, Domperidone, Fluoexetine, Amitriptylene, MAO inhibitors etc., Antihypertensives: Alphamethyldopa, Reserpine, Verapamil Opiates: Heroin, Methadone, Morphine, Apomorphine Estrogens Oral contraceptives Cimetidine / Ranitidine 6.Prolactin secreting pituitary tumors:-Prolactinoma, Acromegaly 7.Miscellaneous:-Polycystic ovarian disease, Epileptic seizures, 8.Ectopic secretion of prolactin by non-pituitary tumors, pressure / transaction of pituitary stalk, macroprolactinemia 9.Idiopathic Decreased levels:-Pituitary deficiency (Pituitary necrosis / infarction), Bromocriptine administration, Pseudohypoparathyroidism

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FSH - Follicle Stimulating Hormone
Investigation Result Units Biological Reference Interval

FSH - Follicle Stimulating Hormone 9.61 mIU/mL Follicular Phase 3.03 - 8.08
Mid-Cycle Peak 2.56 - 16.69
Luteal Phase 1.38 - 5.47
Post-menopausal 26.72 - 133.41

• Sample Type: Serum. • Method : ECLIA. Clinical Use : 1) Diagnosis of gonadal, hypothalamic function disorders, Diagnosis & Management of infertility in both genders. Increased levels : 1) Primary hypogonadism(anorchia, testicular failure, menopause), Gonadotropin secreting pituitary tumors, Precocious puberty (secondary to CNS lesion or idiopathic), Complete testicular feminization syndrome, Luteal phase of menstrual cycle. Decreased levels : 1) Hypothalamic GnRH deficiency, Pituitary FSH deficiency, Ectopic steroid hormone production. Disclaimer : 1) The above result relate only to the specimens received and tested in laboratory and should be always correlate with clinical findings and other laboratory markers. 2) Improper specimen collection, handling, storage and transportation may result in false negative/Positive results.

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LH-Luteinizing Hormone
Investigation Result Units Biological Reference Interval

LH-Luteinizing Hormone 17.11 mIU/mL Follicular Phase : 1.8 - 11.78
Mid Cycle Phase : 7.59 - 89.08
Luteal Phase : 0.56 - 14
Postmenopausal Phase : 5.16 - 61.99
Males : 0.57 - 12.07

• Sample Type: Serum. • Method : ECLIA. Clinical Use : 1) Diagnosis of gonadal function disorders, Diagnosis of pituitary disorders. Increased levels : 1) Primary hypogonadism, Gonadotropin secreting pituitary tumors. Decreased levels : 2) Hypothalamic GnRH deficiency, Pituitary LH deficiency, GnRH analog treatment, Ectopic steroid hormone production. Disclaimer : 1) The above result relate only to the specimens received and tested in laboratory and should be always correlate with clinical findings and other laboratory markers. 2) Improper specimen collection, handling, storage and transportation may result in false negative/Positive results.

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Thyroid Function Test (TFT)
Investigation Result Units Biological Reference Interval

T3 (Triiodothyronine) 1.36 ng/mL 0.8 - 2.0
• Sample Type : Serum.
• Method : ECLIA.
T4 (Thyroxine) 6.91 ug/dl 5.1 - 14.1
• Sample Type : Serum.
• Method : ECLIA.
ULTRA Thyroid Stimulating Hormone (TSH) 1.18 uIU/mL 0.27 - 4.2
Frist trimester: 0.3- 4.5
Second trimester : 0.5 -4.6
Third trimester : 0.8 -5.2
• Sample Type : Serum.
• Method : ECLIA.

1) TSH levels are subject to circadian variation, reaching peak levels between 2 - 4.a.m. and at a minimum between 6-10 pm. The variation is of the order of 50% . hence time of the day has influence on the measured serum TSH concentrations. 2) Recommended test for T3 and T4 is unbound fraction or free levels as it is metabolically active. 3) Physiological rise in Total T3 / T4 levels is seen in pregnancy and in patients on steroid therapy. Clinical Use : • Primary Hypothyroidism • Hyperthyroidism • Hypothalamic – Pituitary hypothyroidism • Inappropriate TSH secretion • Nonthyroidal illness • Autoimmune thyroid disease • Pregnancy associated thyroid disorders. • References : - Henry’s Clinical Diagnosis and Management, 23rd edition. -Tietz Fundamentals of Clinical Chemistry and Molecular Diagnosis, 7th edition. •Disclaimer: 1) The above result relate only to the specimens received and tested in laboratory and should be always correlate with clinical findings and other laboratory markers. 2) Improper specimen collection, handling,storage and transportation may result in false negative/Positive results.

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