Clinical pathology Flashcards

1
Q

Symmetric Dimethylarginine and Renal Function Analysis in Horses with Dehydration

A

-mod correlation with creatinine at admission in dehydrated horses, seems to be less affected by dehydration/extrarenal factors. (still positive correlation with rehydration= increase in GFR?)
- no association with prognosis
-no info on AKI in this study (1 case)
-serial monitoring likely more helpful
-Changes in SDMA concentrations within 12 h were positively correlated with changes in the concentrations of creatinine (r = .441, P = .001) and the GGT/creatinine ratio (r = .691, P = .02)- ischemia during rehydration?

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2
Q

Plasma Syndecan-1 as a Biomarker for Endothelial Glycocalyx Degradation in Septic adult horses

A

-Syndecan-1 levels were highest in septic horses (50.73 ± 84.24 μg/ml) compared to healthy (15.69 ± 11.28 μg/ml) and non-septic (16.88 ± 15.30 μg/ml) groups.
- Mild correlation with syndecan 1 and SIRS score (r2= 0.0307). No correlation with age.
-No difference between healthy and non-septic groups.
–> EG degredation occuring. Some evidence that normal is less than for humans- RR not established. Serial monitoring may be more useful.
- is also increased in non septic diseases, particularly ichemia reperfusion and intestinal injury.
-associated with prognosis not assessed

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3
Q

Concentrations of neutrophil gelatinase-associated lipocalin are increased in serum and peritoneal fluid from horses with inflammatory abdominal disease and non-strangulating intestinal infarctions

A

-Horses with NSII and inflammatory abdominal diseasehad higher serum and peritoneal fluid concentrations of NGAL than the other groups (p < 0.001).
- Peritoneal fluid NGAL concentrations in horses with NSII were higher than in horses with inflammatory abdominal disease (p = 0.03).
- Serum NGAL increased with duration of colic (peritoneal trended but no specific interval differences)
-seruma and peritoneal NGAL moderately correlated (r=.5). serum NGAL corrleated with inflammatory markers, and peritoneal NGAL correlated with peritoneal WCC (r=.6)
- differential expression in peritoneal fluid may differentiate NSII that may need Sx
-Rapid rise and fall pattern

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4
Q

Serum SDMA in Healthy Neonatal Thoroughbreds

A

-Cut off 168. All above adult normal (14) and limit for renal disease (32).
-Decreased with age- higher than adults at 6 months
- some evidence correlation with spuriouas hypercreatinaemia, but underpowered to investigate this.
- pos causes, increased arginine methylation, reduced liver clearance??
- TB only, small numbers and limited information on subclinical renal disease. Short follow up

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5
Q

Agreement of Stall-Side and Laboratory Crossmatch Tests with Reference Standard

A

KIT sensitivity: 91.4%, specificity: 73.5%. (100% Se for Aa, Ca). Substantial agreement 0.65
LAB sensitivity: 77.1%, specificity: 77.8%. (100% Se for Qab, Ca. Poor for Aa.). Mod agreement 0.55
Aim 2: KIT vs LAB in untyped, n-156
Fair agreement: 0.26 (0.52 for just TBs, 0.69 for just WBs)

KIT better for TBs where 85% Qa + (poor for SB), lab better for SB.
Se/Sp vary depending on prevalence in population so should repeat measurments on target population before use

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6
Q

Serum Amyloid A in Diagnosing Sepsis in Equine Neonates

A

Median SAA in septic foals: 114 µg/mL. Significantly greater than for other groups.
- For healthy vs septic: At diagnostic threshold of 100ug/ml, Sensitivity: 52.9%, specificity: 97.5%. High specificity but moderate sensitivity. PPV 75%, NPV 93.7%. AUC ROC curve 0.806
-could not distinguish healthy from SNS
-serial measurements may improve Se

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7
Q

Venous Blood Gas Parameters in Sick Neonatal Foals: Dirtect venepuncture vs push-pull

A

High agreement for most values,ICC >0.9 for most parameters at both time points.
except haematocrit (bias 3.24- -3.52, ICC 0.669)and PvO2 (bias -5.8 , ICC 0.733)
Not possible to withdraw blood in 3 foals (with otherwise normal IVC)
Did not assess IVC complications as a result (study stopped after 2nd pull at 24h)

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8
Q

Measurement of ANP, BNP, and Endothelin-1 in Jumping Horses with Valvular Regurgitation and their correlation with the dimensions of heart structures.

A

GENERALLY RUBBISH STUDY
Described an equine specific sandwich ELISA for measurement of ANP, BNP and endothelin-1
Association between BNP and valvular regurgitation, BNP and endothelin-1 and PR
ANP and endothelin-1 were correlated with ventricular width

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9
Q

Effect of Freeze-Thaw Cycles on ACTH Determination in Horses

A
  • Freeze thaw cycles had a significant reduction in ACTH. This was more profound (after 1 cycle vs 3) in horses with PPID
    -Resulted in missed diagnosis in 2 (1 93->10) and missing 3 equivocal cases. No FP
    -17% drop after 1 cycle, lots after 3.
  • also occurred after TRH stimulation
    -? more vulnerable in PPID- the ACTH forms are slighlty different- different origina and structure?
  • recommend not freezing, or if necessary then 2 cycles mac
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10
Q

Is Serum Amyloid A Elevated in Horses with Equine Gastric Ulcer Syndrome?

A

No signinficant increase of SAA with EGUS or type of ulceration. Medians all within rr.

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11
Q

Fibrinogen Heterogeneity in Horses

A
  • 2 types of fibrinogen exist- HMWT and LMWT (LMWT may be ex vivo degredation but regardless will be present in lab sample_
    -this may affect measurment, particularly with EDTA samples
    -Only 5 horses, and samples pooled
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12
Q

SDMA and Creatinine in Healthy Draft Horses

A

-cut off 14ug/dl >6mo
-higher in Clydesdales than other Draft horses- not clinically significant
-correlated with creatinine but not BUN
-assay performed well relative to MS. Stable for up to a week in storage.
-no associated with age, weight or sex
-Adult horses only.
-further associations with GFR need more work

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13
Q

SAA as a marker to detect sepsis and predict outcome in hospitalised foals

A

-SAA can rule out sepis (cut off 1050) Se 30% Sp 90%
-SAA can suggest non survival (cut off 1250). Se22% Sp 98%
- concentrations of SAA increased with increasing sepsis score and differed between septic and nonseptic foals, and survivors and nonsurvivors
-recommend repeated measures, lower cut offs or combining with other biomarkers
-is a more robust study than other one with 34 foals- more representative of a referral centre population

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14
Q

Paraoxonase-1 Activity as a diagnostic and prognostic marker in Horses and Foals with SIRS

A
  • Highly Sp (100%), poor Se (28%)
  • association between PON-1 category (high or low) and SIRS score.
  • any decreases in PON were generally transient.
  • decreased PON -> OR poor PX 2.4-3.9
    ?different metabolism of paraoxonase-1 in horses, lower magnitude of oxidation associated with SIRS in this species or the sensitivity of the assessment of SIRS status in identifying SIRS-positive horses.
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15
Q

Systemic Serum Amyloid A in Early Diagnosis of Synovial Structure Involvement

A

SAA is insufficient for the diagnosis of synovial sepsis-> synovial fluid analysis better
similar increases with penetrating injury vs sepsis. (around 200)

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16
Q

Evaluation of the Element Point-of-Care Blood Gas Analyzer

A

The Element POC blood analyser performs well for all analytes except Ca and PCO2. Would likely change with changing environmental conditions.

17
Q

Agreement of Two Electrolyte Analyzers for Identifying Acid-Base Disorders in sick horses

A

Poor agreement for the diagnosis of SID acidosis
WBGA often diagnosing more cases of SID4 acidosis, while PBMA identified more USI (unmeasured strong ion) acidosis.
These results only apply to these 2 analysers in this specific setting.

18
Q

Reference Intervals of Acute Phase Proteins in Healthy Andalusian Donkeys

A

SAA and haptoglobin (Hp) levels increased significantly as early as 2 hours post-lipopolysaccharide (LPS) injection, indicating their utility as early markers of systemic inflammatory response syndrome (SIRS).
SAA and Hp responses in donkeys were faster yet milder compared to those in horses.
Even moderate increases in SAA and Hp in donkeys could have clinical significance.

19
Q

Pre-Analytical Stability of Sorbitol Dehydrogenase in Equine Plasma

A

Is stable for up to 24h at 4oC in heparinised plasma- better than serum
At all temps for 4 hours. Thereafter degraded both at room temp and -20