Skip to main content
. Author manuscript; available in PMC: 2019 Aug 1.
Published in final edited form as: Am J Ophthalmol. 2018 Mar 17;192:229–238. doi: 10.1016/j.ajo.2018.03.013

Table 2.

Comparison of prevalence of systemic diseases and surgical procedures in sickle cell patients and controls (ANOVA)*

CATEGORY Controls
N (%)
Hgb subtypes SC vs Control
SS
N (%)
SC
N (%)
SThal
N (%)
Number of patients 39 161 68 31 260 vs 39
Systemic disease ANOVA P value
Acute chest syndrome 0 81 (50) 19 (28) 10 (31) <.001
Avascular necrosis of any joint 0 42 (26) 19 (28) 13 (41) .001
Pulmonary hypertension 0 37 (23) 5 (7) 1 (3) <.001
Stroke 0 36 (22) 4 (6) 1 (3) <.001
Kidney disease 0 35 (22) 4 (6) 1 (3) <.001
Hypertension 12 (31) 27 (16) 22 (32) 5 (16) .025
Liver disease 2 (5) 17 (11) 1 (1) 0 .026
Pulmonary embolism 0 15 (9) 5 (7) 3 (9) .262
Deep venous thrombosis 0 15 (9) 3 (4) 1 (3) .11
Seizure disorder 1 (3) 15 (9) 2 (3) 0 .068
Gallstones 0 13 (8) 2 (3) 3 (9) .139
Diabetes 3 (8) 4 (2) 5 (7) 2 (6) .283
Surgical procedure
Cholecystectomy 2 (5) 76 (47) 16 (24) 6 (19) <.001
Hip replacement 0 19 (12) 5 (7) 8 (25) .006
Tonsillectomy 0 16 (10) 2 (3) 2 (6) .069

ANOVA, analysis of variance; Hgb, hemoglobin; SC, sickle cell Hgb SC subtype; SS, sickle cell Hgb SS subtype; SThal, sickle cell Hgb SThal subtype.

*

P values <.003 (ie, 0.05/16) are considered significant based on Bonferroni correction and are in bold type.