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Page 1 of 136BIDDING DOCUMENT procurement OF COMPONENT PACKAGE: 1.2 INTERNATIONAL COMPETITIVE BIDDING (ICB) SUPPLY AND INSTALLATION OF INTRAAORTIC BALLOON PUMP (IAP) FOR TERTIARY CARE HOSPITALS AT

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How to fill out intra-aortic balloon pump effects

01

Ensure proper patient identification and consent before starting the procedure.

02

Position the patient in a supine position on the bed with head slightly elevated.

03

Prepare the balloon pump system by connecting the catheter to the balloon pump console.

04

Insert the catheter into the femoral artery using the Seldinger technique under sterile conditions.

05

Inflate the balloon with helium gas to provide circulatory support during diastole.

06

Monitor the patient closely for any signs of complications or adverse effects.

07

Document the procedure and the patient's response to the intra-aortic balloon pump effects.

Who needs intra-aortic balloon pump effects?

01

Patients suffering from cardiogenic shock

02

Patients undergoing high-risk cardiac procedures

03

Patients with acute myocardial infarction complicated by heart failure

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What is intra-aortic balloon pump effects?

Intra-aortic balloon pump effects refer to the impact of using a device to assist the heart in pumping blood.

Who is required to file intra-aortic balloon pump effects?

Healthcare providers and medical facilities that use intra-aortic balloon pumps are required to file reports on the effects of these devices.

How to fill out intra-aortic balloon pump effects?

Fill out the reports on intra-aortic balloon pump effects by documenting the patient's response to the device, any complications, and overall outcomes.

What is the purpose of intra-aortic balloon pump effects?

The purpose of reporting on intra-aortic balloon pump effects is to monitor the safety and effectiveness of these devices in clinical practice.

What information must be reported on intra-aortic balloon pump effects?

Information that must be reported on intra-aortic balloon pump effects includes patient outcomes, device-related complications, and any adverse events.

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