CASE PRESENTATION ON BLOOD
TRANSFUSION REACTION
Student Name : SRIDHAR P
Date:17.02.2025
Preceptor Name: Dr. G. K. SADAGOBAN
Ward : OBSTRECTICS AND GYNAECOLOGY
Introduction
A blood transfusion reaction is a harmful immune system response to donor blood.
Reactions can occur right away or much later, and can be mild or severe.
EPIDEMIOLOGY:
In India there is a transfusion reaction frequency of 0.27%. Allergic reactions were
the most common, accounting for 0.19% of cases, followed by febrile non-hemolytic
transfusion reactions (FNHTR) at 0.036%. The studies also noted that females
experienced a higher incidence of transfusion reactions compared to males.
Transfusion reactions accounted for 0.5% of transfusions. Febrile non-hemolytic
transfusion reactions were the most common reactions (51.4%) followed by allergic
reactions (40%), fluid overload (5.7%) and anaphylactic reactions (2.9%). Majority of
these reactions were seen with PRBC transfusions (74.3%) followed by platelet
transfusions (25.7%)
5/10/2024 Arulmigu Kalasalingam College of Pharmacy - DPP 2
Subjective
Evidence
Patient ID: 16574 Age : 26 years
Sex : Female
Date of Admission:27.12.2024
Date of Discharge: 2.1.2025
Weight: 53kg
Weight gain during pregnancy:
12 kg
Height: 153 cm
BMI:23
Blood group: B+ve
Lmp:29.3.24
Edd: 05.01.25
G2A1
EFW:2.7-2.9
5/10/2024 Arulmigu Kalasalingam College of Pharmacy - DPP 3
CHEIF COMPLAINTS:
C/O fever
C/O itching
C/O pruritus
C/O restlessness
PAST MEDICAL HISTORY:
H/O Anaemia
H/O G1 abortion 4 ½ weeks
PAST MEDICATION HISTORY:
2 Packs of PCT august 2024
Allergies
yes – dust ,pollen
Occupation
cotton mill
Family History
Anemia for Mother
Objective Evidence
ON EXAMINATION
FHR:152/min
EFW:2.7-2.9
5/10/2024 Arulmigu Kalasalingam College of Pharmacy - DPP 4
GENERAL EXAMINATION:
BP: 100/70 mmHg
PR : 98 bpm
RR : 30 bpm
Temp : 100.2°F
SYSTEMIC EXAMINATION:
CVS: S1S2 (+)
RS : Bilateral Air Entry (+)
CNS: NFND
P/A : Soft.
5
6
Signs/
symptoms
0-5min 15min 30min 45min 1hr
Temp 98.4° 98.4° 98.4° 98.4° 100.2°
pulse 88/m 88/m 89/m 87/m 86/m
BP 120/70 120/70 110/70 110/70 100/60
SKIN
RASHES/UTICA
RIA
NO NO NO NO YES
LABORATORY INVESTIGATION
7
PARAMETERS OBSERVED VALUE NORMAL RANGE
Hemoglobin 9.9 g/dL↓ 13-17 g/dL
Total RBC count 3.2 millions/mm³↓ 3.8-4.8 millions/mm³
WBC count 11500 cells/mm³↑ 4000-10000 cells/mm³
Platelet count 5.06 lakh/µL ↑ 2.0-4.5 lakh/µL
Other investigation
1.Mast cell tryptase test
17.5 ng/ml Normal range<11.4ng/ml
2.Serum IgA and IgE test:
IgE- 140IU/ml Normal range <100IU/ml
IgA-380mg/DL Normal range 70-400mg/dl
8
9
3.Repeat blood grouping and repeat crossmatch
Test Anti-A Anti-B
Anti-D (Rh
Factor)
Interpretation
Forward
Grouping (RBC
Test)
No Agglutination
(-)
Agglutination (+) Agglutination (+) B Rh-Positive (B )
⁺
(Recipient’s serum + Donor
RBCs)
No agglutination (-) Compatible (safe for
transfusion)
Assessment
5/10/2024 Arulmigu Kalasalingam College of Pharmacy - DPP 10
1.Patient has an history of allergies to dust and pollen in his life which in
turn increases the risk of IgE mediated histamine reaction and thus
potential risk for blood transfusion reaction.
2.Based on the history collected from the patient and the IgE antibody
investigation the patient is assessed to have allergic reaction [grade1]
and not ABO compatibility or haemolysis.
11
SEVERITY( Ring and messmer Scale)
The patient is assessed to a Grade 1 allergic
symptoms
Therapeutic Goals
SHORT TERM GOALS
• To reduce fever.
• To reduce the itching and prurits
• To reduce the levels of serum IgE level from 140IU/ml to 100IU/ml
• LONG TERM GOALS
• To prevent the recurrence of the reaction as the patient is aneamic.
• To treat anaemia by improving hb level to 12mg/dl
• To monitor the reduce the risks too the fetus .
5/10/2024 Arulmigu Kalasalingam College of Pharmacy - DPP 12
Plan
5/10/2024 Arulmigu Kalasalingam College of Pharmacy - DPP 13
DRUG NAME BRAND NAME DOSE ROA FREQUENCY 27/
12
28
/1
2
29/
12
30
/1
2
31
/1
2
1/
12
5
Inj.cetrizine Quzyttir 10 mg IV OD    ✓
T. prednisolone Omnacortil 40 mg Oral OD    ✓
Inj.paracetamol Parapher 500 mg IV Q6H    
T.Ranitidine Rantac 50 mg Oral Q6H    
T.Ferrous sulphate Ferosol 200mg Oral BD      ✓
T.Folic acid Folvite 400 mg Oral OD    ✓ ✓ ✓
Drug-drug interaction
No drug-drug interactions were found.
14
Dose calculation
Prednisolone normal dose for adults- 0.5-2 mg/kg/day
Prednisolone pregnancy safe Dose - <80mg/day
Patient weight= 53kg
Per kg Dose = 1mg kg
Dose = 53mg
Given dose = 40 mg
It is well between the therapeutic range
15
Pharmacist Intervention
HEAMOVIGILANCE MONITORING AND REPORTING:
16
17
CAUSALITY ASSESSMENT
In this case the assessment made is that
the reaction is excluded with conclusive
evidence.
Therapeutic outcome
• Patient’s admission complaints were rectified.
18
PARAMETERS DAY OF ADMISSION DAY OF DISCHARGE
Temperature 101º F ↑ 98.6º F
Symptoms of
uticaria
(rashes,itching,
pruritus)
GRADE 1 symptoms Normal
Hb level 9.9 g/dL↓ 3.8-4.8 millions/mm³
Discharge medication
19
DRUG NAME DOSE FREQUENCY
Tab. Ferrous sulphate 250 mg OD * 4 days
Tab.folic acid 400 mg OD* 4days
REVIEW AFTER 3 days
Patient counselling
Counselling was provided to patient.
• Advised as “Your reaction may have been due to a mild immune response. We’ve
given medications like antihistamines (for allergic reactions) or antipyretics (for
fever) to help manage it.”
• Avoid allergic triggering foods such as diary product ,Brinjal and nuts and wear
mask to avoid dust and allergen which could trigger another allergic condition.
• Monitor and report any allergic reactions such as rash,itching or any other
unpleasant sensations.
• As it is a grade 1 allergic reactions there is none to relatively very less effect on the
featus.
• Anaemia is treated with ferrous sulphate as long term because you have a allergic
reaction to blood transfusion.
20
Clinical Pearls
21
1.I learnt about Haemovigilance in India
National Institute of Biologicals https://nib.gov.inHaemovigilance
Programme of India (HvPI)
2.I also learned about Ring and messmer scale which is used for severity
of Allergic reactions.
Refference
1.https://jmsh.ac.in/articles/a-study-of-transfusion-related-adverse-
events-at-a-tertiary-care-center-in-central-india-a-retrospective-
evaluation?
2.Pai S. Surveillance of Transfusion Related Adverse Reactions in a
Tertiary Care Centre in Bangalore: A 4-Year Hemovigilance Initiative.
Indian J Hematol Blood Transfus. 2020;36(4):733-739.
doi:10.1007/s12288-020-01312-w
3.https://www.researchgate.net/figure/Ring-and-Messmer-grading-
scale-for-allergic-reactions-25_tbl1_371121943
4.https://www.mayoclinic.org/drugs-supplements/prednisolone-oral-
route/description/drg-20075189
5.https://nib.gov.in/haemovigilance.aspx 22

Blood transfusion reactioncase presentation in soap.pptx

  • 1.
    CASE PRESENTATION ONBLOOD TRANSFUSION REACTION Student Name : SRIDHAR P Date:17.02.2025 Preceptor Name: Dr. G. K. SADAGOBAN Ward : OBSTRECTICS AND GYNAECOLOGY
  • 2.
    Introduction A blood transfusionreaction is a harmful immune system response to donor blood. Reactions can occur right away or much later, and can be mild or severe. EPIDEMIOLOGY: In India there is a transfusion reaction frequency of 0.27%. Allergic reactions were the most common, accounting for 0.19% of cases, followed by febrile non-hemolytic transfusion reactions (FNHTR) at 0.036%. The studies also noted that females experienced a higher incidence of transfusion reactions compared to males. Transfusion reactions accounted for 0.5% of transfusions. Febrile non-hemolytic transfusion reactions were the most common reactions (51.4%) followed by allergic reactions (40%), fluid overload (5.7%) and anaphylactic reactions (2.9%). Majority of these reactions were seen with PRBC transfusions (74.3%) followed by platelet transfusions (25.7%) 5/10/2024 Arulmigu Kalasalingam College of Pharmacy - DPP 2
  • 3.
    Subjective Evidence Patient ID: 16574Age : 26 years Sex : Female Date of Admission:27.12.2024 Date of Discharge: 2.1.2025 Weight: 53kg Weight gain during pregnancy: 12 kg Height: 153 cm BMI:23 Blood group: B+ve Lmp:29.3.24 Edd: 05.01.25 G2A1 EFW:2.7-2.9 5/10/2024 Arulmigu Kalasalingam College of Pharmacy - DPP 3 CHEIF COMPLAINTS: C/O fever C/O itching C/O pruritus C/O restlessness PAST MEDICAL HISTORY: H/O Anaemia H/O G1 abortion 4 ½ weeks PAST MEDICATION HISTORY: 2 Packs of PCT august 2024 Allergies yes – dust ,pollen Occupation cotton mill Family History Anemia for Mother
  • 4.
    Objective Evidence ON EXAMINATION FHR:152/min EFW:2.7-2.9 5/10/2024Arulmigu Kalasalingam College of Pharmacy - DPP 4 GENERAL EXAMINATION: BP: 100/70 mmHg PR : 98 bpm RR : 30 bpm Temp : 100.2°F SYSTEMIC EXAMINATION: CVS: S1S2 (+) RS : Bilateral Air Entry (+) CNS: NFND P/A : Soft.
  • 5.
  • 6.
    6 Signs/ symptoms 0-5min 15min 30min45min 1hr Temp 98.4° 98.4° 98.4° 98.4° 100.2° pulse 88/m 88/m 89/m 87/m 86/m BP 120/70 120/70 110/70 110/70 100/60 SKIN RASHES/UTICA RIA NO NO NO NO YES
  • 7.
    LABORATORY INVESTIGATION 7 PARAMETERS OBSERVEDVALUE NORMAL RANGE Hemoglobin 9.9 g/dL↓ 13-17 g/dL Total RBC count 3.2 millions/mm³↓ 3.8-4.8 millions/mm³ WBC count 11500 cells/mm³↑ 4000-10000 cells/mm³ Platelet count 5.06 lakh/µL ↑ 2.0-4.5 lakh/µL
  • 8.
    Other investigation 1.Mast celltryptase test 17.5 ng/ml Normal range<11.4ng/ml 2.Serum IgA and IgE test: IgE- 140IU/ml Normal range <100IU/ml IgA-380mg/DL Normal range 70-400mg/dl 8
  • 9.
    9 3.Repeat blood groupingand repeat crossmatch Test Anti-A Anti-B Anti-D (Rh Factor) Interpretation Forward Grouping (RBC Test) No Agglutination (-) Agglutination (+) Agglutination (+) B Rh-Positive (B ) ⁺ (Recipient’s serum + Donor RBCs) No agglutination (-) Compatible (safe for transfusion)
  • 10.
    Assessment 5/10/2024 Arulmigu KalasalingamCollege of Pharmacy - DPP 10 1.Patient has an history of allergies to dust and pollen in his life which in turn increases the risk of IgE mediated histamine reaction and thus potential risk for blood transfusion reaction. 2.Based on the history collected from the patient and the IgE antibody investigation the patient is assessed to have allergic reaction [grade1] and not ABO compatibility or haemolysis.
  • 11.
    11 SEVERITY( Ring andmessmer Scale) The patient is assessed to a Grade 1 allergic symptoms
  • 12.
    Therapeutic Goals SHORT TERMGOALS • To reduce fever. • To reduce the itching and prurits • To reduce the levels of serum IgE level from 140IU/ml to 100IU/ml • LONG TERM GOALS • To prevent the recurrence of the reaction as the patient is aneamic. • To treat anaemia by improving hb level to 12mg/dl • To monitor the reduce the risks too the fetus . 5/10/2024 Arulmigu Kalasalingam College of Pharmacy - DPP 12
  • 13.
    Plan 5/10/2024 Arulmigu KalasalingamCollege of Pharmacy - DPP 13 DRUG NAME BRAND NAME DOSE ROA FREQUENCY 27/ 12 28 /1 2 29/ 12 30 /1 2 31 /1 2 1/ 12 5 Inj.cetrizine Quzyttir 10 mg IV OD    ✓ T. prednisolone Omnacortil 40 mg Oral OD    ✓ Inj.paracetamol Parapher 500 mg IV Q6H     T.Ranitidine Rantac 50 mg Oral Q6H     T.Ferrous sulphate Ferosol 200mg Oral BD      ✓ T.Folic acid Folvite 400 mg Oral OD    ✓ ✓ ✓
  • 14.
    Drug-drug interaction No drug-druginteractions were found. 14
  • 15.
    Dose calculation Prednisolone normaldose for adults- 0.5-2 mg/kg/day Prednisolone pregnancy safe Dose - <80mg/day Patient weight= 53kg Per kg Dose = 1mg kg Dose = 53mg Given dose = 40 mg It is well between the therapeutic range 15
  • 16.
  • 17.
    17 CAUSALITY ASSESSMENT In thiscase the assessment made is that the reaction is excluded with conclusive evidence.
  • 18.
    Therapeutic outcome • Patient’sadmission complaints were rectified. 18 PARAMETERS DAY OF ADMISSION DAY OF DISCHARGE Temperature 101º F ↑ 98.6º F Symptoms of uticaria (rashes,itching, pruritus) GRADE 1 symptoms Normal Hb level 9.9 g/dL↓ 3.8-4.8 millions/mm³
  • 19.
    Discharge medication 19 DRUG NAMEDOSE FREQUENCY Tab. Ferrous sulphate 250 mg OD * 4 days Tab.folic acid 400 mg OD* 4days REVIEW AFTER 3 days
  • 20.
    Patient counselling Counselling wasprovided to patient. • Advised as “Your reaction may have been due to a mild immune response. We’ve given medications like antihistamines (for allergic reactions) or antipyretics (for fever) to help manage it.” • Avoid allergic triggering foods such as diary product ,Brinjal and nuts and wear mask to avoid dust and allergen which could trigger another allergic condition. • Monitor and report any allergic reactions such as rash,itching or any other unpleasant sensations. • As it is a grade 1 allergic reactions there is none to relatively very less effect on the featus. • Anaemia is treated with ferrous sulphate as long term because you have a allergic reaction to blood transfusion. 20
  • 21.
    Clinical Pearls 21 1.I learntabout Haemovigilance in India National Institute of Biologicals https://nib.gov.inHaemovigilance Programme of India (HvPI) 2.I also learned about Ring and messmer scale which is used for severity of Allergic reactions.
  • 22.
    Refference 1.https://jmsh.ac.in/articles/a-study-of-transfusion-related-adverse- events-at-a-tertiary-care-center-in-central-india-a-retrospective- evaluation? 2.Pai S. Surveillanceof Transfusion Related Adverse Reactions in a Tertiary Care Centre in Bangalore: A 4-Year Hemovigilance Initiative. Indian J Hematol Blood Transfus. 2020;36(4):733-739. doi:10.1007/s12288-020-01312-w 3.https://www.researchgate.net/figure/Ring-and-Messmer-grading- scale-for-allergic-reactions-25_tbl1_371121943 4.https://www.mayoclinic.org/drugs-supplements/prednisolone-oral- route/description/drg-20075189 5.https://nib.gov.in/haemovigilance.aspx 22