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COMPARATIVE STUDY OF ADVERSE DONOR EVENTS IN VOLUNTARY AND REPLACEMENT WHOLE BLOOD DONORS: NEED OF ROBUST DONOR HEMOVIGILANCE PROGRAM Dr Lubna Naseer,

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Presentation on theme: "COMPARATIVE STUDY OF ADVERSE DONOR EVENTS IN VOLUNTARY AND REPLACEMENT WHOLE BLOOD DONORS: NEED OF ROBUST DONOR HEMOVIGILANCE PROGRAM Dr Lubna Naseer,"— Presentation transcript:

1 COMPARATIVE STUDY OF ADVERSE DONOR EVENTS IN VOLUNTARY AND REPLACEMENT WHOLE BLOOD DONORS: NEED OF ROBUST DONOR HEMOVIGILANCE PROGRAM Dr Lubna Naseer, Dr Meena Sidhu PG 3rd year Govt. Medical college, Jammu

2 Background Adverse Event was recognized as symptoms or signs of donor discomfort of sufficient severity such that either the donor called for attention of the staff or they were noticed by the staff. Blood donation is safe, but small percentage of donors experience complications, mostly mild, that resolve promptly but are still unpleasant for donors, and blood services have an obligation to minimize them. Adverse donor reactions can result in injury and decrease the likelihood of donor return. 

3 Aims and Objectives The aim of this study was to compare the frequency and severity of AE’s in voluntary and replacement whole blood donors.

4 Material and Methods Retrospective study of donor reactions documented at Department of IHBT Government Medical College, Jammu over a period of 1 year from April 2017 to March 2018. Donors fulfilling national guidelines for blood donation were selected. Phlebotomy was performed by trained personnel's. Donors were observed during and following donation for 15 mints. Blood donors were asked to report for any delayed adverse events after they have left the premises.

5 American Red Cross Hemovigilance Program classifies complications into defined categories
Pre syncopal - pallor, sweating or light headedness without loss of consciousness. Syncopal complications are classified as; Minor- if there is a transient loss of consciousness lasting less than one minute, Major- prolonged loss of consciousness for more than a minute or complicated by loss of bowel/bladder control, seizures or convulsions Local adverse events -include small haematomas (<25.8 mm2) or large(>25.8 mm2), bruises, infiltration, allergic reaction and a tingling sensation.

6 Results Table II: Showing reaction rate in Male and Female donors.
Category No. Reaction Rate p value Total Donations 17527 641 3.65% Replacement Donations 10763 424 3.93% 0.012 Voluntary Donations 6764 217 3.2% Table 1: showing reaction rate in replacement and voluntary donors Category No. Reaction Rate P Value Total Male Donors 17011 606 3.6% 0.0001 Total Female Donors 516 35 6.8% Table II: Showing reaction rate in Male and Female donors.

7 results Table III: Showing reaction rate in 1st time and repeat donors
Category No. Reaction Rate p Value 1st Time Male Donors 4422 461 10.53% 0.0001 1st Time Female Donors 155 21 Repeat Male Donors 12589 145 1.22% Repeat Female Donors 361 14 Table III: Showing reaction rate in 1st time and repeat donors

8 Severity of Adverse Events

9 Types of Reaction

10 Symptoms of Vasovagal reaction

11 Donation site

12 Figure showing time of Reaction occurrence

13 Conclusion The reaction rate was 3.65% , mostly Vasovagal type of reactions were most common ,seen more in females, first-time donors, replacement donors which is comparable with other studies. So repeat, regular and voluntary donations should be encouraged This study has increased our knowledge of risk factors associated with blood donation and provided an insight into the importance of voluntary donation and need to increase the same and highlighting the need for specific guidelines for the management of prone donor groups

14 THANK YOU


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