Table 2.

Antibiotic use and treatment-associated adverse events among children with and without ARLA.

Treatment CharacteristicsResolved < 3 Mos, n = 188ARLA, n = 49p1
Antibiotics
  Oral antibiotics185 (98)49 (100)0.992
  Amoxicillin109 (58)24 (49)0.26
  Doxycycline91 (48)43 (88)< 0.001
  Cefuroxime8 (4)6 (12)0.052
  Other2 (1)00.992
  Days of oral antibiotics, median (IQR)28 (28–30)57 (56–72)< 0.0013
  IV antibiotics13 (7)28 (57)< 0.001
  Ceftriaxone13 (7)28 (57)< 0.001
  Days of IV antibiotics, median (IQR)428 (21–28)28 (21–28)0.303
  Total days of antibiotics, median (IQR)30 (28–35)76 (58–88)< 0.0013
Prescribed NSAID57 (30)39 (80)< 0.001
Adverse events during antibiotic treatment period
  Any recorded treatment-associated adverse event529 (15)18 (37)0.001
  Fever3 (2)2 (4)0.282
  Rash8 (4)9 (18)0.0022
  Non-rash allergic reactions02 (4)0.042
  Heartburn1 (1)2 (4)0.112
  Abdominal pain7 (4)3 (6)0.442
  Vomiting8 (4)3 (6)0.702
  Diarrhea5 (3)00.592
  Headache2 (1)4 (8)0.022
  Dizziness1 (1)00.992
  Altered mental status01 (2)0.212
  Clostridium difficile or other infection00
  Thrombosis00
  Mechanical IV problem02 (4)0.042
Hospitalization for any treatment-associated adverse event61 (1)3 (6)0.032
  • Values are expressed as n (%) unless otherwise indicated.

  • 1 Calculated from chi-square test except where indicated.

  • 2 Calculated from Fisher’s exact test.

  • 3 Calculated from Wilcoxon rank-sum test.

  • 4 Calculated among subjects who received ceftriaxone.

  • 5 Some subjects had > 1 adverse event.

  • 6 Excluding hospitalization for worsening disease (e.g., leg swelling from popliteal cyst rupture). ARLA: antibiotic-refractory Lyme arthritis; IQR: interquartile range; IV: intravenous; NSAID: nonsteroidal antiinflammatory drugs.