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CASE PRESENTATION
ON
MALARIA
PRESENTED BY,
IMRAN SUFAIR.M
Reg.no:15Q3407 3RD
pharm.D(2017-18)
Department Of Pharmacy Practice
Mallige College Of Pharmacy, B’lore-90
MALARIA
 an intermittent and remittent fever caused by a protozoan parasite (Ex:- P.
falciparum, P. vivax, P. ovale, P. Malaria) which invades the red blood cells and is
transmitted by the bite of female anopheles mosquito in many tropical and
subtropical regions.
 Each year approximately 2.5 million cases and 4,000 deaths are reported in south east
asia.
 India reported the highest number of malaria cases in the Region and the second highest
number of deaths due to malaria.
PATHOPHYSIOLOGY
SUBJECTIVE EVIDENCE
 Age: 40 yrs. Sex: MALE
 DOA: 07-11-2017 DOD: 12-07-2017
 Complaints on admission:
 C/O Fever since 10 days with chills.
 C/O dry cough since 2 days.
 C/O generalized weakness since 5 days.
 C/O body ache since 1 week.
PERSONAL HISTORY
 PAST MEDICAL HISTORY:- Nothing significant
 MEDICATION HISTORY :- Nothing significant
 SOCIAL HISTORY:-
 Appetite:- DECREASED
 DIET:- Mixed
 Bowel and bladder:- Normal
 Sleep :- decreased
 FAMILY HISTORY :- Nothing significant
OBJECTIVE EVIDENCE
 PHYSICAL EXAMINATION:
 P I C C L E : NEGATIVE
 PR- 100 bpm
 BP-130/90 mmHg
 temp – 102.6*F
 SYSTEMIC EXAMINATION:
 CVS: S1, S2 normal
 RS : NVBS B/L (+)
 CNS: Conscious and oriented
 PELVIC ABDOMEN(PA): Soft
 PROVISIONAL DIAGNOSIS : ????MALARIA
LAB INVESTIGATION
Biochemical investigation
Test Observed value Reference value
HAEMATOLOGY
Red Blood Corpuscles 4.0 miilion cells/ul (4.2-5.4 million cells/ul.)
platelets 0.32 lakhs /mm3 (1.5-4 lakhs /mm3 )
PCV(packed cell volume) 37.8% (40-54%)
Neutrophills 74% (45-73%)
ESR 17 mm/hr (1-15mm/hr)
RAPID DIAGNOSTIC TEST(RDT) FOR MALARIAL PARASITE
Blood smear:- Positive for all stages.ie; ring forms, schizonts and gametocytes of malarial
parasite plasmodium vivax.
FINAL DIAGNOSIS
 From the subjective and objective evidence, The patient was diagnosed as:
MALARIAE (PLASMODIUM.VIVAX)
GOAL OF THERAPY
 Patient specific:
To relieve from the symptoms such as fever, dry cough, weakness, body ache.
 Disease specific:
 To prevent further progression of disease.
 To eradicate the malarial parasite.
ASSESMENT OF CURRENT THERAPY
Brand name Generic name DOSE ROA FRE Indication TOA
(BF/AF/WF/WW)
Start
date
End
date
IV. fluid fluids 2*NS
2*RL
2*DNS
27-11-17 01-12-17
Inj.pantodac Inj. Pantoprazole 40mg IV 1-0-0 It decrease amount of acid
produced in stomach to
protect from erosive stomach
BF 27-11-17 02-11-17
inj.ALZONE Inj. ceftriaxone 1gm IV 1-0-1 cephalosporin antibiotic
which used to suppress or to
kill harmful bacterial growth
AF 27-11-17 02-11-17
T. PCT paracetamol 650 mg PO 1-0-1 Antipyretics which used to
decrease the body
temperature.
AF 27-11-17 02-11-17
Inj. falcigo artesunate 120 mg IV 1-0-1 Anti malarials medication
used to treat malaria . Often
it is used as part of
combination therapy
AF 27-11-17 29-11-17
T. malirid primaquine 15 mg PO 1-0-0 Anti malarial medication used
to treat and
prevent malaria. Specifically
it is used for malaria due
to P
.vivax and P.ovale
AF 01-12-17 02-11-17
T. emeset ondesteron 4mg PO 1-0-0 Prevention of nausea and
vomiting
AF 01-12-17 01-12-17
Syp.tuspel Turbutaline-1.25 mg
Bromehexine- 4 mg
2 tspn PO 1-1-1 used for Coughing, Cough,
Bronchitis, Asthma, Breathing
problems, Chest tightness and
AF 01-12-17 02-11-17
PROGRESS CHART
DAY1 DAY2 DAY3 DAY 4 DAY 5
B.P
(Mm of Hg)
110/70 110/70 110/70 120/70 110/80
Pulse
(beats/min )
110 80 80 86 82
Platelets
count
0.33
lakhs/cumm
0.28
lakhs/cumm
0.49
lakhs/cumm
0.87
lakhs/cumm
1.60
lakhs/cumm
PLANNING
DAY 1 DAY 2 DAY 3 DAY 4 DAY 5
PROBLEMS • Bacterial
infection
Rx:
ceftriaxone
• FEVER
Rx: paracetamol
For cough
Rx:
turbutaline and
bromhexine syrup
Gastric irritation
Rx :
inj. Pantodac
For M.parasite
Rx: artesunate and
Repeated all Repeated all Repeated all Repeated all
DISCHARGE MEDICATION
GENERIC
NAME
DOSE
( mg)
FREQUENCY DAYS INDICATION ROUTE TIME
T. dolo acetaminop
hen
650 mg SOS Antipyretics PO After food
T.emeset ondensteron 4 mg 1-1-1 7 days Anti emetic PO After Food
Pantodac pantaprazol
e
40mg 1-0-1 2 weeks PPI PO before food
Tab. malirid primaquine 15 mg 1-0-0 9 days antimalarials PO afterfood
Syp.tuspel Turbutaline
and
bromhexine
2 tspn SOS For cough PO afterfood
PHARMACIST INTERVENTION
 All the drugs prescribed were screened for adverse drug
reactions and found no adverse drug reactions.
TOXICITY PARAMETER
 Pantoprazole- GI tract infection, head ache, myalgia, hyperlipidemia, anxiety,
nausea, abdominal pain.
 Ondensetron- Headache, malaise/fatigue, constipation, drowsiness, fever, dizziness,
anxiety, cold sensation, rash, diarrhea, urinary retention, local injection site reaction
(pain, redness, burning), hypoxia
 Ceftriaxone:- Nausea, vomiting, dysuria, hematuria, toxic nephropathy.
 Tuspel plus:- Tremor, palpitations, increased heart rate, dizziness, headache.
 Aresunate:-Transient and reversible reticulocytopenia, drug fever, rash,
bradycardia.
 Primaquine:- Mild anaemia, leukocytosis, leukopenia, headache, pruritis
PATIENT COUNSELLING
 DRUG SPECIFIC:
ONDANSERTON:-
 Instruct patient to report signs or symptoms of serious cardiac arrhythmias.
 Advise patient to report hypersensitivity reactions, including anaphylaxis and
bronchospasm .
PANTOPRAZOLE:-
 Take each dose at the same time each day.
 Swallow the tablet whole.
 Avoid alcohol.
 Report any persistent side effects to your doctor.
 Administer 30 minutes before food in order to avoid gastric irritation.
Ceftriaxone:-
 Instruct the patient to report any sign or symptoms like serum sickness
like reactions(rash,urticaria,arthralgia,fever,malaise)
Primaquine:-
 It should be taken with food to avoid GI upset.
 Inform the patient that the drug may turn urine colour to brown.
 DISEASE SPECIFIC:
 Personal protection to avoid mosquito bites includes use of clothes
extending upto the wrists and ankles.
 Use insect-repellant creams.
 Use biological methods to decrease the vector density.
 Prophylaxis should be started 1-2 weeks before exposure and
continued for 4 weeks after returning from the endemic area.
THANK YOU
IMRAN SUFAIR.M

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malaria.pptx

  • 1. CASE PRESENTATION ON MALARIA PRESENTED BY, IMRAN SUFAIR.M Reg.no:15Q3407 3RD pharm.D(2017-18) Department Of Pharmacy Practice Mallige College Of Pharmacy, B’lore-90
  • 2. MALARIA  an intermittent and remittent fever caused by a protozoan parasite (Ex:- P. falciparum, P. vivax, P. ovale, P. Malaria) which invades the red blood cells and is transmitted by the bite of female anopheles mosquito in many tropical and subtropical regions.  Each year approximately 2.5 million cases and 4,000 deaths are reported in south east asia.  India reported the highest number of malaria cases in the Region and the second highest number of deaths due to malaria. PATHOPHYSIOLOGY
  • 3. SUBJECTIVE EVIDENCE  Age: 40 yrs. Sex: MALE  DOA: 07-11-2017 DOD: 12-07-2017  Complaints on admission:  C/O Fever since 10 days with chills.  C/O dry cough since 2 days.  C/O generalized weakness since 5 days.  C/O body ache since 1 week.
  • 4. PERSONAL HISTORY  PAST MEDICAL HISTORY:- Nothing significant  MEDICATION HISTORY :- Nothing significant  SOCIAL HISTORY:-  Appetite:- DECREASED  DIET:- Mixed  Bowel and bladder:- Normal  Sleep :- decreased  FAMILY HISTORY :- Nothing significant
  • 5. OBJECTIVE EVIDENCE  PHYSICAL EXAMINATION:  P I C C L E : NEGATIVE  PR- 100 bpm  BP-130/90 mmHg  temp – 102.6*F  SYSTEMIC EXAMINATION:  CVS: S1, S2 normal  RS : NVBS B/L (+)  CNS: Conscious and oriented  PELVIC ABDOMEN(PA): Soft  PROVISIONAL DIAGNOSIS : ????MALARIA
  • 6. LAB INVESTIGATION Biochemical investigation Test Observed value Reference value HAEMATOLOGY Red Blood Corpuscles 4.0 miilion cells/ul (4.2-5.4 million cells/ul.) platelets 0.32 lakhs /mm3 (1.5-4 lakhs /mm3 ) PCV(packed cell volume) 37.8% (40-54%) Neutrophills 74% (45-73%) ESR 17 mm/hr (1-15mm/hr) RAPID DIAGNOSTIC TEST(RDT) FOR MALARIAL PARASITE Blood smear:- Positive for all stages.ie; ring forms, schizonts and gametocytes of malarial parasite plasmodium vivax.
  • 7. FINAL DIAGNOSIS  From the subjective and objective evidence, The patient was diagnosed as: MALARIAE (PLASMODIUM.VIVAX)
  • 8. GOAL OF THERAPY  Patient specific: To relieve from the symptoms such as fever, dry cough, weakness, body ache.  Disease specific:  To prevent further progression of disease.  To eradicate the malarial parasite.
  • 9. ASSESMENT OF CURRENT THERAPY Brand name Generic name DOSE ROA FRE Indication TOA (BF/AF/WF/WW) Start date End date IV. fluid fluids 2*NS 2*RL 2*DNS 27-11-17 01-12-17 Inj.pantodac Inj. Pantoprazole 40mg IV 1-0-0 It decrease amount of acid produced in stomach to protect from erosive stomach BF 27-11-17 02-11-17 inj.ALZONE Inj. ceftriaxone 1gm IV 1-0-1 cephalosporin antibiotic which used to suppress or to kill harmful bacterial growth AF 27-11-17 02-11-17 T. PCT paracetamol 650 mg PO 1-0-1 Antipyretics which used to decrease the body temperature. AF 27-11-17 02-11-17 Inj. falcigo artesunate 120 mg IV 1-0-1 Anti malarials medication used to treat malaria . Often it is used as part of combination therapy AF 27-11-17 29-11-17 T. malirid primaquine 15 mg PO 1-0-0 Anti malarial medication used to treat and prevent malaria. Specifically it is used for malaria due to P .vivax and P.ovale AF 01-12-17 02-11-17 T. emeset ondesteron 4mg PO 1-0-0 Prevention of nausea and vomiting AF 01-12-17 01-12-17 Syp.tuspel Turbutaline-1.25 mg Bromehexine- 4 mg 2 tspn PO 1-1-1 used for Coughing, Cough, Bronchitis, Asthma, Breathing problems, Chest tightness and AF 01-12-17 02-11-17
  • 10. PROGRESS CHART DAY1 DAY2 DAY3 DAY 4 DAY 5 B.P (Mm of Hg) 110/70 110/70 110/70 120/70 110/80 Pulse (beats/min ) 110 80 80 86 82 Platelets count 0.33 lakhs/cumm 0.28 lakhs/cumm 0.49 lakhs/cumm 0.87 lakhs/cumm 1.60 lakhs/cumm
  • 11. PLANNING DAY 1 DAY 2 DAY 3 DAY 4 DAY 5 PROBLEMS • Bacterial infection Rx: ceftriaxone • FEVER Rx: paracetamol For cough Rx: turbutaline and bromhexine syrup Gastric irritation Rx : inj. Pantodac For M.parasite Rx: artesunate and Repeated all Repeated all Repeated all Repeated all
  • 12. DISCHARGE MEDICATION GENERIC NAME DOSE ( mg) FREQUENCY DAYS INDICATION ROUTE TIME T. dolo acetaminop hen 650 mg SOS Antipyretics PO After food T.emeset ondensteron 4 mg 1-1-1 7 days Anti emetic PO After Food Pantodac pantaprazol e 40mg 1-0-1 2 weeks PPI PO before food Tab. malirid primaquine 15 mg 1-0-0 9 days antimalarials PO afterfood Syp.tuspel Turbutaline and bromhexine 2 tspn SOS For cough PO afterfood
  • 13. PHARMACIST INTERVENTION  All the drugs prescribed were screened for adverse drug reactions and found no adverse drug reactions.
  • 14. TOXICITY PARAMETER  Pantoprazole- GI tract infection, head ache, myalgia, hyperlipidemia, anxiety, nausea, abdominal pain.  Ondensetron- Headache, malaise/fatigue, constipation, drowsiness, fever, dizziness, anxiety, cold sensation, rash, diarrhea, urinary retention, local injection site reaction (pain, redness, burning), hypoxia  Ceftriaxone:- Nausea, vomiting, dysuria, hematuria, toxic nephropathy.  Tuspel plus:- Tremor, palpitations, increased heart rate, dizziness, headache.  Aresunate:-Transient and reversible reticulocytopenia, drug fever, rash, bradycardia.  Primaquine:- Mild anaemia, leukocytosis, leukopenia, headache, pruritis
  • 15. PATIENT COUNSELLING  DRUG SPECIFIC: ONDANSERTON:-  Instruct patient to report signs or symptoms of serious cardiac arrhythmias.  Advise patient to report hypersensitivity reactions, including anaphylaxis and bronchospasm . PANTOPRAZOLE:-  Take each dose at the same time each day.  Swallow the tablet whole.  Avoid alcohol.  Report any persistent side effects to your doctor.  Administer 30 minutes before food in order to avoid gastric irritation. Ceftriaxone:-  Instruct the patient to report any sign or symptoms like serum sickness like reactions(rash,urticaria,arthralgia,fever,malaise) Primaquine:-  It should be taken with food to avoid GI upset.  Inform the patient that the drug may turn urine colour to brown.
  • 16.  DISEASE SPECIFIC:  Personal protection to avoid mosquito bites includes use of clothes extending upto the wrists and ankles.  Use insect-repellant creams.  Use biological methods to decrease the vector density.  Prophylaxis should be started 1-2 weeks before exposure and continued for 4 weeks after returning from the endemic area.