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. Author manuscript; available in PMC: 2013 Oct 28.
Published in final edited form as: N Engl J Med. 2008 Dec 3;359(25):10.1056/NEJMoa0806450. doi: 10.1056/NEJMoa0806450

Table 2.

Clinical Characteristics of the 152 Adverse Reactions after Administration of Heparin.*

Characteristic All Reactions
(N = 152)
Probable
Reactions
(N = 116)
Definite
Reactions
(N = 36)
Time from administration of heparin to reaction
    — min
 During hemodialysis 5.1±9.1 5.3±10.0 4.5±6.2
 During treatment for cardiac conditions 14±17.2 15.9±17.7 1±0
 During photopheresis 30±13.1 30±13.1
Manifestation — no. (%)
 Facial edema
  Any 36 (23.7) 0 36 (100)
  Lips 23 (15.1) 0 23 (63.9)
  Eyelids 17 (11.2) 0 17 (47.2)
  Throat 12 (7.9) 0 12 (33.3)
  Tongue 11 (7.2) 0 11 (30.6)
  Mouth 10 (6.6) 0 10 (27.8)
 Urticaria 5 (3.3) 0 5 (13.9)
 Low blood pressure 76 (50.0) 69 (59.5) 7 (19.4)
  Systolic pressure <80 mm Hg 17 (11.2) 14 (12.1) 3 (8.3)
 Nausea 74 (48.7) 56 (48.3) 18 (50.0)
 Shortness of breath 57 (37.5) 38 (32.8) 19 (52.8)
 Vomiting 37 (24.3) 27 (23.3) 10 (27.8)
 Tingling 36 (23.7) 28 (24.1) 8 (22.2)
 Flushing 35 (23.0) 31 (26.7) 4 (11.1)
 Tachycardia 33 (21.7) 29 (25.0) 4 (11.1)
 Diaphoresis 23 (15.1) 23 (19.8) 0
 Abdominal pain 17 (11.2) 12 (10.3) 5 (13.9)
 Diarrhea 8 (5.3) 7 (6.0) 1 (2.8)
 Loss of consciousness 6 (3.9) 6 (5.2) 0
 Chills 2 (1.3) 2 (1.7) 0
 Fever 1 (0.7) 1 (0.9) 0
 Difficulty swallowing 0 0 0
 Wheezing 0 0 0
Follow-up care — no./total no. (%)
 Blood cultures obtained 32/144 (22.2) 26/109 (23.9) 6/35 (17.1)
 Evaluation in an emergency department§ 22/144 (15.3) 9/109 (8.3) 13/35 (37.1)
 Hospitalization§ 13/144 (9.0) 5/109 (4.6) 8/35 (22.9)
Use of intravenous heparin — no. (%) 149 (98.0) 115 (99.1) 34 (94.4)
Brand of heparin — no. (%)
 Baxter Healthcare 141 (92.8) 110 (94.8) 31 (86.1)
 APP Pharmaceuticals 6 (3.9) 4 (3.4) 2 (5.6)
 Baxter or APP 2 (1.3) 1 (0.9) 1 (2.8)
 Not reported 3 (2.0) 1 (0.9) 2 (5.6)
*

Plus–minus values are means ±SD.

Although heparin is administered at the beginning of photophoresis, the patient is not exposed to it until later in the process.

The total numbers exclude eight reactions (one definite and seven probable) owing to missing data.

§

The total numbers exclude the eight reactions (one definite and seven probable) that occurred in patients undergoing treatment for cardiac conditions because these patients were hospitalized at the time of the adverse reactions.