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Pre-Eclampsia Predictor (sFLT-1 Test

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Pre-Eclampsia Predictor (sFLT-1 Test

Short Name: sFLT-1:PIGF Ratio Test

Also known as: sFlt-1/PlGF Ratio Test, Pre-eclampsia Screening Test, Soluble fms-Like Tyrosine Kinase-1 to Placental Growth Factor Ratio, Preeclampsia Predictor Panel

Pre-Eclampsia Predictor (sFLT-1 Test test available at DNA Labs India for ₹4,500. Uses ECLIA (Electrochemiluminescence Immunoassay) on Serum samples. Results in Same-day reporting available when the sample is received on Tuesday, Thursday, or Saturday by 9 am.. Free home collection in 300+ cities across India.

Panel TestFemalePregnant Women (20+ Weeks Gestation)🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the sFLT-1:PIGF ratio panel test is to assist in the early prediction and risk stratification of pre-eclampsia in pregnant women from 20 weeks gestation onwards. By measuring the ratio of sFLT-1 to PlGF in maternal serum, the test helps clinicians identify women at high risk of developing pre-eclampsia or those with suspected pre-eclampsia. A low ratio provides reassurance and may reduce unnecessary hospital admissions, while a high ratio signals the need for closer surveillance, additional investigations, and possible intervention. This test is designed to complement, not replace, standard clinical assessment.

Test Code
1389
ICD Code
O14.9
Price
₹4,500
Sample Type
Serum
Result Time
Same-day reporting available when the sample is received on Tuesday, Thursday, or Saturday by 9 am.
Fasting Required
No
Method
ECLIA (Electrochemiluminescence Immunoassay)
Step 1

Sample Collection

No special preparation, fasting, or dietary restrictions are required before this test. Inform your healthcare provider about any current medications or pre-existing medical conditions. Continue all prescribed medications unless advised otherwise by your doctor.

Method: Venipuncture

Step 2

Laboratory Analysis

A trained phlebotomist will collect approximately 2 mL of blood from a vein in your arm (venipuncture) using standard aseptic technique. The procedure typically takes only a few minutes and may involve minimal discomfort at the puncture site.

Step 3

Report Delivery

After blood collection, slight bruising or soreness at the puncture site may occur, which typically resolves within a day. Apply gentle pressure with cotton if needed. You can resume normal activities immediately after sample collection.

Timeline: Same-day reporting available when the sample is received on Tuesday, Thursday, or Saturday by 9 am.

Patient Instructions

1
Before the Test:No special preparation or fasting is required. Bring your doctor's prescription and ensure you are at or beyond 20 weeks of gestation. Inform the sample collection team about any current medications.
2
During the Test:A blood sample of approximately 2 mL will be drawn from a vein in your arm using a standard venipuncture procedure. The entire process typically takes 5-10 minutes. No imaging or invasive procedure is involved.
3
After the Test:After the blood draw, you may resume normal activities immediately. Apply pressure to the puncture site if needed. Report any prolonged bleeding or unusual symptoms to your healthcare provider. Results will be communicated via online portal, email, or WhatsApp.

About This Test

Who Should Get This Test

The purpose of the sFLT-1:PIGF ratio panel test is to assist in the early prediction and risk stratification of pre-eclampsia in pregnant women from 20 weeks gestation onwards. By measuring the ratio of sFLT-1 to PlGF in maternal serum, the test helps clinicians identify women at high risk of developing pre-eclampsia or those with suspected pre-eclampsia. A low ratio provides reassurance and may reduce unnecessary hospital admissions, while a high ratio signals the need for closer surveillance, additional investigations, and possible intervention. This test is designed to complement, not replace, standard clinical assessment.

How to Prepare

  • No fasting is required before sample collection
  • Stay hydrated and drink adequate water before the test
  • Wear loose-fitting clothing that allows easy access to the arm
  • Inform the phlebotomist if you have a history of fainting during blood draws
  • Bring your doctor's prescription or referral form
  • Sample should be collected on Tuesday, Thursday, or Saturday by 9 am for same-day reporting

Doctor's Notes

Reviewed by — MBBS, MD (Biochemistry) · Reg. No. 21504

"The sFLT-1/PlGF ratio is a valuable adjunctive tool in the assessment of suspected pre-eclampsia. When used alongside standard clinical evaluation including blood pressure monitoring and urine protein assessment, it can significantly improve diagnostic confidence. A ratio below 38 at or after 20 weeks gestation has a high negative predictive value, helping to rule out pre-eclampsia within the subsequent week. This can reduce unnecessary hospital admissions and interventions. However, a high ratio warrants close clinical monitoring and timely intervention. This test should always be interpreted in the context of the complete clinical picture by a qualified obstetrician."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeSerum
Sample Volume2 mL (1 mL minimum)
ContainerSST (Serum Separator Tube)
Collection MethodVenipuncture

Sample Stability

Room Temperature: Up to 2 hours
Refrigerated (2-8°C): Up to 8 hours
Frozen (-20°C): Up to 1 month
Sample Rejection Criteria:
  • Haemolysed samples
  • Lipaemic samples
  • Samples received beyond stability period
  • Insufficient sample volume (less than 1 mL)
  • Improperly labelled or unlabelled samples
  • Samples collected in incorrect tube type

Understanding Your Results

The sFLT-1/PlGF ratio is interpreted in the context of the gestational age, clinical presentation, and other diagnostic findings. The following risk categories are based on established clinical evidence and guidelines:
📊

A ratio below 38 indicates a low probability of developing pre-eclampsia within the next week (negative predictive value approximately 99%). This result supports the clinical decision to avoid unnecessary hospitalisation. Continued routine antenatal monitoring is advised.

Range: sFLT-1/PlGF Ratio < 38

📊

An intermediate ratio warrants cautious clinical evaluation. While not definitively high risk, closer monitoring of blood pressure, urine protein, and symptoms is recommended. Repeat testing may be considered within 2-3 weeks.

Range: sFLT-1/PlGF Ratio 38-85

📊

A ratio above 85 is associated with a significantly increased risk of pre-eclampsia. Immediate clinical assessment, closer monitoring, and potential hospitalisation may be required. The treating obstetrician will determine the appropriate management plan, which may include antihypertensive therapy, corticosteroids for fetal lung maturity, or planned early delivery depending on gestational age and severity.

Range: sFLT-1/PlGF Ratio > 85

⚠️ When to Consult a Doctor:

Consult your obstetrician or gynaecologist immediately if you experience any of the following symptoms during pregnancy: persistent high blood pressure readings, sudden swelling of the hands and face, severe headaches that do not resolve with usual measures, visual disturbances such as blurred vision or seeing spots, pain in the upper right abdomen, sudden weight gain, or a significant decrease in fetal movements. Early consultation is critical for timely diagnosis and management of pre-eclampsia.

Limitations

  • This test is intended as a risk assessment tool and does not independently diagnose pre-eclampsia
  • Must be used in conjunction with clinical judgement, blood pressure measurement, and other investigations
  • The test is validated for use from 20 weeks gestation until delivery; results before 20 weeks may not be reliable
  • Cut-off values may vary slightly between assays and laboratories
  • False positives and false negatives can occur; clinical context must always be considered
  • Not a replacement for regular antenatal check-ups and monitoring

Risks & Considerations

  • Minimal: slight bruising or discomfort at the venipuncture site
  • Rare: mild dizziness or lightheadedness during blood draw
  • Very rare: infection at the puncture site (standard aseptic precautions are followed)

Interfering Factors

  • Severe maternal renal impairment may affect protein levels
  • Multiple gestation (twins or higher-order pregnancies) may alter baseline biomarker levels
  • Conditions affecting placental function such as intrauterine growth restriction (IUGR)
  • Pre-existing chronic hypertension or autoimmune conditions
  • Haemolysed or lipaemic samples may affect assay accuracy
  • Extremely early gestational age (before 20 weeks) may yield unreliable results

Compare With Similar Tests

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ComparisonPre-Eclampsia Predictor (sFLT-1

Frequently Asked Questions

What is the sFLT-1:PIGF ratio panel test?
The sFLT-1:PIGF ratio panel test is a blood-based screening test that measures two placenta-derived proteins — soluble fms-like tyrosine kinase-1 (sFLT-1) and placental growth factor (PlGF) — in the mother's blood. The ratio of these two proteins helps predict the risk of developing pre-eclampsia, a serious pregnancy complication characterised by high blood pressure and organ damage.
Who should take the pre-eclampsia predictor test?
This test is recommended for pregnant women from 20 weeks gestation onwards, particularly those with clinical suspicion of pre-eclampsia (e.g., elevated blood pressure, headaches, visual disturbances, proteinuria), a history of pre-eclampsia in a previous pregnancy, or known risk factors such as chronic hypertension, diabetes, obesity, or multiple gestation. Your obstetrician will advise whether this test is appropriate for you.
At what stage of pregnancy should this test be done?
The sFLT-1:PIGF ratio panel test can be performed from 20 weeks of gestation until delivery. It is typically ordered when clinical suspicion of pre-eclampsia arises during antenatal visits. The test is not validated for use before 20 weeks gestation.
How is the test performed and does it require fasting?
The test involves a simple blood draw (venipuncture) from a vein in your arm, collecting approximately 2 mL of blood into a serum separator tube (SST). No fasting or special preparation is required. The procedure is quick, safe, and involves minimal discomfort.
What does a low sFLT-1/PlGF ratio mean?
A low ratio (less than 38) indicates a low probability of developing pre-eclampsia within the subsequent week, with a negative predictive value of approximately 99%. This result provides reassurance and supports the clinical decision to continue routine antenatal monitoring without unnecessary hospitalisation.
What does a high sFLT-1/PlGF ratio mean?
A high ratio (greater than 85) indicates a significantly elevated risk of pre-eclampsia. This result warrants immediate clinical assessment, closer monitoring by your obstetrician, and potentially hospitalisation. Your doctor will determine the appropriate management plan based on the complete clinical picture, including gestational age and severity of symptoms.
Can this test alone diagnose pre-eclampsia?
No. The sFLT-1/PlGF ratio is a risk assessment tool designed to complement clinical judgement and other diagnostic investigations. It does not independently diagnose pre-eclampsia. A definitive diagnosis requires a combination of blood pressure readings, urine protein assessment, laboratory investigations, and clinical evaluation by a qualified healthcare provider.
Is the sFLT-1:PIGF ratio test safe for the mother and baby?
Yes. The test requires only a standard blood draw from the mother's arm and involves no direct risk to the baby. The procedure carries the same minimal risks as any routine venipuncture, such as slight bruising or temporary discomfort at the puncture site.
What is the cost of the pre-eclampsia predictor test at DNA Labs India?
The cost of the pre-eclampsia predictor (sFLT-1:PIGF ratio) panel test at DNA Labs India is Rs 4500. This price includes home sample collection at no additional charge. The cost is consistent across all cities in India where the service is available.
When will I receive my test results?
Same-day reporting is available when the blood sample is received on Tuesday, Thursday, or Saturday by 9 am. Results are delivered through the online portal, email, or WhatsApp for your convenience. Please check with the sample collection team for specific scheduling in your area.
How accurate is the sFLT-1:PIGF ratio test for predicting pre-eclampsia?
Clinical studies, including the landmark PROGNOSIS study, have demonstrated that the sFLT-1/PlGF ratio has a high negative predictive value (approximately 99%) for ruling out pre-eclampsia within one week when the ratio is below 38. It is considered one of the most reliable blood-based tools for pre-eclampsia risk assessment. However, no test is 100% accurate, and results must always be interpreted alongside clinical findings.
Is home sample collection available for this test?
Yes. DNA Labs India offers free home sample collection for the pre-eclampsia predictor test across numerous cities in India, including Mumbai, Delhi, Bangalore, Hyderabad, Chennai, Kolkata, Pune, Ahmedabad, and many more. You can book your sample collection online and a trained phlebotomist will visit your home at the scheduled time.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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