This document outlines a dissertation protocol that aims to evaluate the role of reticulocyte indices in assessing the cause of pancytopenia. The study will analyze reticulocyte percentage, immature reticulocyte fraction, and mean reticulocyte volume in 100 pancytopenia patients over 18 months. These indices will be correlated with clinical and laboratory findings to categorize the etiology and formulate a diagnostic algorithm. Obtaining informed consent and maintaining confidentiality addresses ethical aspects of the study.
It is also called as complete blood picture/complete blood count(CBP/CBC)
The FBC assesses several different parameters and can provide a great deal of information.
The red cell variables will determine whether or not the patient is anaemic. If anaemia is present the MCV is likely to provide clues as to the cause of the anaemia.
The white cells are often raised in infection neutrophilia in bacterial infections and lymphocytosis in viral (but not always so).
Platelets (size or number) may be abnormal either as a direct effect of underlying blood disease.
It is also called as complete blood picture/complete blood count(CBP/CBC)
The FBC assesses several different parameters and can provide a great deal of information.
The red cell variables will determine whether or not the patient is anaemic. If anaemia is present the MCV is likely to provide clues as to the cause of the anaemia.
The white cells are often raised in infection neutrophilia in bacterial infections and lymphocytosis in viral (but not always so).
Platelets (size or number) may be abnormal either as a direct effect of underlying blood disease.
Sickle Cell Disease (SCD) is major health problem in
Tanzania. Every year, approximately 11000 babies are born
with SCD1, and this number is expected to double by the year
2050. Tanzania has the fourth greatest number of annual
SCD births in all of Africa, and the fifth greatest in the world.
In addition, almost 20% of the Tanzanian population carries a
copy of the sickle gene in a form of sickle cell trait (AS).
Despite these staggering statistics, Tanzania has made
progress in the fight against SCD over the past decade. In
2008, the Ministry of Health and Social Welfare by then,
recognized SCD as a priority disease in the National strategy
for Non-communicable disease 2009- 2015, calling for all
sector to cooperate in combating the disease. A chapter on
SCD was also included in the national Non-communicable
Disease Treatment Manual.
Hydroxyurea is useful in the management of individuals with SCD. It reduces the complications
of SCD in infants, children and adults based on its ability to:
o Increase haemoglobin F levels
o Increase steady state hemoglobin counts
o Lower WBC and PLTs hence moderate the chronic inflammation state in SCD
Indications for starting hydroxyurea:
All children 9 months and above with proven SCD
Adolescents and adults with the following:
o Recurrent VOC ( 3 or more severe episodes requiring admission in the last 12
months)
o Severe and/or recurrent ACS (2 or more episodes in a lifetime)
o History of stroke or abnormal TCD (≥199cm/sec)
o Severe symptomatic chronic anemia that interferes with daily activities or quality of
life
o To reduce the risk of new or recurrent stroke where chronic transfusion therapy is not
feasible.
o Recurrent priapism
o Patient with chronic kidney disease on erythropoietin to improve anemia
#SickleCell disease#Indications for Hydroxyurea#Hamisi Mkindi#CKD#Investigations:
FBP - absolute neutrophil count (ANC) > 1,500/µl, platelet > 100,000/ul, Hb> 6g/dl.
If Hb is less than 6gm/dl do Reticulocyte Count[Do not start hydroxyurea in patients with
Hgb< 6 g/dl AND absolute reticulocyte count (ARC)<100,000/µL]
Serum Creatinine - should be within normal range,
Serum ALT – should not be greater than twice the upper limit of normal,
Bilirubin Total and direct
Urine Pregnancy Test in women
HPLC - Quantification of HbF (if this test cannot be done, Hydroxyurea should be prescribed
nevertheless and an elevated baseline HbF should not affect the decision to initiate
hydroxyurea)
Why there is a need of film review in iso compliant hema labs in this days of...honorinamagnonuguid
Blood Slide Morphology is very much needed to affirm the Flags of Each Cell Histograms, nothing beats the human eyes to assess the unstromatolyzed morphology, nucleolar structures, NC ratio /etc inherent to particular cell in question... EDTA platelet sattelitism, even on those days of early 80's , we usually read the blood films of the presence of even filarial worms, malarial gametocytes/ring forms...cytoplasmic granules even, once I had seen that lysosomal granules in the leukocytes, it was a very challenging job before the advent of the latest VCS / Cytoflowmetry...I think a very well trained morphologist have an edge in handling bothwise, wont you agree? So lets not forget the efficacy of our H and E polychromatophiles...God Bless our hematology labs, bring out the best in our skills to detect and identify for the betterment of the health consumers.
Sickle Cell Disease (SCD) is major health problem in
Tanzania. Every year, approximately 11000 babies are born
with SCD1, and this number is expected to double by the year
2050. Tanzania has the fourth greatest number of annual
SCD births in all of Africa, and the fifth greatest in the world.
In addition, almost 20% of the Tanzanian population carries a
copy of the sickle gene in a form of sickle cell trait (AS).
Despite these staggering statistics, Tanzania has made
progress in the fight against SCD over the past decade. In
2008, the Ministry of Health and Social Welfare by then,
recognized SCD as a priority disease in the National strategy
for Non-communicable disease 2009- 2015, calling for all
sector to cooperate in combating the disease. A chapter on
SCD was also included in the national Non-communicable
Disease Treatment Manual.
Hydroxyurea is useful in the management of individuals with SCD. It reduces the complications
of SCD in infants, children and adults based on its ability to:
o Increase haemoglobin F levels
o Increase steady state hemoglobin counts
o Lower WBC and PLTs hence moderate the chronic inflammation state in SCD
Indications for starting hydroxyurea:
All children 9 months and above with proven SCD
Adolescents and adults with the following:
o Recurrent VOC ( 3 or more severe episodes requiring admission in the last 12
months)
o Severe and/or recurrent ACS (2 or more episodes in a lifetime)
o History of stroke or abnormal TCD (≥199cm/sec)
o Severe symptomatic chronic anemia that interferes with daily activities or quality of
life
o To reduce the risk of new or recurrent stroke where chronic transfusion therapy is not
feasible.
o Recurrent priapism
o Patient with chronic kidney disease on erythropoietin to improve anemia
#SickleCell disease#Indications for Hydroxyurea#Hamisi Mkindi#CKD#Investigations:
FBP - absolute neutrophil count (ANC) > 1,500/µl, platelet > 100,000/ul, Hb> 6g/dl.
If Hb is less than 6gm/dl do Reticulocyte Count[Do not start hydroxyurea in patients with
Hgb< 6 g/dl AND absolute reticulocyte count (ARC)<100,000/µL]
Serum Creatinine - should be within normal range,
Serum ALT – should not be greater than twice the upper limit of normal,
Bilirubin Total and direct
Urine Pregnancy Test in women
HPLC - Quantification of HbF (if this test cannot be done, Hydroxyurea should be prescribed
nevertheless and an elevated baseline HbF should not affect the decision to initiate
hydroxyurea)
Why there is a need of film review in iso compliant hema labs in this days of...honorinamagnonuguid
Blood Slide Morphology is very much needed to affirm the Flags of Each Cell Histograms, nothing beats the human eyes to assess the unstromatolyzed morphology, nucleolar structures, NC ratio /etc inherent to particular cell in question... EDTA platelet sattelitism, even on those days of early 80's , we usually read the blood films of the presence of even filarial worms, malarial gametocytes/ring forms...cytoplasmic granules even, once I had seen that lysosomal granules in the leukocytes, it was a very challenging job before the advent of the latest VCS / Cytoflowmetry...I think a very well trained morphologist have an edge in handling bothwise, wont you agree? So lets not forget the efficacy of our H and E polychromatophiles...God Bless our hematology labs, bring out the best in our skills to detect and identify for the betterment of the health consumers.
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
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Slides from:
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Track: Artificial Intelligence
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2. ROLE OF RETICULOCYTE INDICES
IN EVALUATION OF
PANCYTOPENIA
DR.MIDHAT AEJAZ
DISSERTATION FOR THE COURSE OF MD PATHOLOGY
GUIDE: DR. S R NIVEDITHA
PROFESSOR,DEPARTMENT OF PATHOLOGY
KEMPEGOWDA INSTITUTE OF MEDICAL SCIENCES,BANGALORE
3. INTRODUCTION
• Pancytopenia is a term used for the reduction in the count of red
blood cells,white blood cells and platelets.
• Identifying the underlying cause is challenging as there are wide
range of etiologies ( infections, drugs ,autoimmune,
hemophagocytosis and inherited conditions).
• The reticulocyte indices given by the automated cell counters are
found to help in assessing the bone marrow activity, thereby
categorising the various causes.
4. NEED FOR STUDY
• Pancytopenia - involves a wide number of causes primarily or
secondarily involving the bone marrow.
• Cornerstone for evaluation of pancytopenia is Bone marrow study
(BMA & BMBx)
• However, Reticulocyte indices generated by advance coulters can aid
in identifying the cause of pancytopenia in least invasive fashion.
• Also an algorithmic approach of various clinical,routine
hematologiical and reticulocyte indices can help in early diagnosis
and management of pancytopenia.
5. AIM AND OBJECTIVES
• Recording reticulocyte indices( Reticulocyte percentage, Immature
reticulocyte fraction,Mean reticulocyte volume) in pancytopenia.
• Correlation of the reticulocyte indices with the etiological factors of
pancytopenia.
• Formulate a diagnostic algorithm to categorise pancytopenia effectively.
6. SUBJECT OR MATERIAL
• STUDY DURATION- 18 months
• STUDY DESIGN- Cross sectional study
• SAMPLE SIZE-100
• SAMPLING METHOD-Purposive
• INCLUSION CRITERIA-
Samples with Hb<13.5g/dl in males ans<11.5g/dl in females,
Total leucocyte count<4000/cumm
Platelet count<1.5lakh/cumm
• EXCLUSION CRITERIA-
Hemolysed samples
Detailed clinical history not available
Patient who have received recent blood transfusion(<3 weeks)
7. METHODS AND PROCEDURES
• The study will be conducted in central laboratory ,Department of
pathology.
• Hundred cases of pancytopenia (irrespective of age and gender) will
be the study group after obtaining consent.
• The reticulocyte indices generated by SYSMEX XN-1000 auto
analyser will be noted .
• Relevant clinical details , biochemical investigations will be
documented and correlated with the reticulocyte indices.