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. 2018 Mar 22;32(3):1060–1069. doi: 10.1111/jvim.15084

Table 1.

Descriptive baseline data of dogs in pulse dose cohort, daily dose cohort, and all dogs combined

Variable Pulse cohort Daily cohort All dogs
Number of dogs 17 21 38
Median age (years) 9 (range 5–16) 9 (range 4–12) 9 (range 4–16)
Sex
Male intact 1 3 4
Male neutered 8 12 20
Female intact 0 0 0
Female spayed 8 6 14
Female: Male 0.9:1 0.4:1 0.6:1
Presenting clinical signs
Lethargy/weakness 5 15 20/38 (53%)
Polyuria/polydipsia 8 6 14/38 (37%)
Inappetence 3 12 15/38 (39%)
Weight loss 5 7 12/38 (32%)
Ocular abnormalities 4 3 7/38 (18%)
Lameness/pain 3 3 6/38 (16%)
Nausea/vomiting 2 4 6/38 (16%)
Bleeding diathesis 2 3 5/38 (13%)
Diarrhea 3 0 3/38 (8%)
Paraparesis 1 2 3/38 (8%)
Fever 2 1 3/38 (8%)
Vision loss 2 1 3/38 (8%)
Peripheral lymphadenopathy 1 1 2/38 (5%)
Cutaneous lesions 1 1 2/38 (5%)
CNS abnormalities a 1 0 1/38 (3%)
Presenting clinicopathologic abnormalities
Bone marrow plasmacytosis b 12 13 25/27 (93%)
Hyperglobulinemia 14 20 34/38 (90%)
Proteinuria 10 12 22/38 (58%)
Hypercalcemia c 9 10 19/38 (50%)
Hypoalbuminemia 10 9 19/38 (50%)
Osteolytic lesions d 7 9 16/38 (42%)
Abdominal organ involvement e 9 7 16/28 (57%)
Spleen 8 6 14/16 (88%)
Liver 3 2 5/16 (31%)
Jejunal lymph node 0 1 1/16 (6%)
Hyperviscosity syndrome f 6 6 12/38 (32%)
Renal disease g 5 4 9/38 (24%)
IRIS AKI grade I h 1 2 3/8 (38%)
IRIS AKI grade II h 1 2 3/8 (38%)
IRIS AKI grade III h 2 0 2/8 (25%)
Circulating plasma cells 1 0 1/38 (3%)
Cytopenias i 10 16 26/38 (68%)
Anemia 8 10 18/38 (47%)
1 6 8 14/18 (78%)
2 2 2 4/18 (22%)
3 0 0 0/18 (0%)
4 0 0 0/18 (0%)
Neutropenia 3 1 4/38 (11%)
1 0 1 1/4 (25%)
2 1 0 1/4 (25%)
3 2 0 2/4 (50%)
4 0 0 0/4 (0%)
Thrombocytopenia 7 10 17/38 (45%)
1 0 5 5/14 (36%)
2 6 0 6/14 (43%)
3 0 3 3/14 (21%)
4 1 2 3/14 (21%)
Pathologic fracture 0 2 2/38 (5%)
Hypertension 6 6 12/38 (32%)
Increased M component 14 17 31/31 (100%)
Monoclonal 12 13 25/31 (81%)
Biclonal 2 4 6/31 (19%)
IgA 2 9 11/14 (79%)
IgG 1 2 3/14 (21%)

aDogs with abnormal mentation, cranial nerve deficits or seizure activity were categorized as having CNS abnormalities.

bBone marrow plasmacytosis was defined as plasma cells representing >10% of the marrow population.

cHypercalcemia was based on ionized calcium values above the normal reference range.

dOsteolytic lesions were based on radiographic findings of discrete radiolucent lytic lesions, diffuse osteopenia, or a combination of both.

eAbdominal organ involvement was based on cytologically or histologically confirmed neoplastic plasma cells.

fDogs were considered to have hyperviscosity syndrome if they had one or more of the following clinical abnormalities: bleeding diathesis (including epistaxis, petechiae, ecchymosis, or gingival bleeding), neurologic signs (including dementia, lethargicness, seizure activity, or coma) and ocular abnormalities (including dilated and tortuous retinal vessels, retinal hemorrhage, or retinal detachment).

gRenal disease was defined as blood urea nitrogen and creatinine above the upper limit of the reference range with concurrent USG <1.030.

hDogs with renal disease were retrospectively graded according to the IRIS Grading of AKI (2016), based solely on creatinine level. Only 8 dogs were graded, as 1 of the 9 dogs with renal disease had only increased BUN (and not creatinine) reported.

iHighest grade reported for each dog.