| Literature DB >> 35201528 |
Heng Liu1,2, Li Zhao1, Junling Liu1, Fang Lan1, Li Cai1, Jingqin Fang3, Xue Li4.
Abstract
OBJECTIVES: To analyze the relationship between the dietary preparation status prior to contrast-enhanced CT (CECT) and adverse drug reactions (ADR) and emetic complications.Entities:
Keywords: Contrast media; Drug-related side effects and adverse reactions; Emetics; Fasting; Tomography (X-ray computed)
Year: 2022 PMID: 35201528 PMCID: PMC8873329 DOI: 10.1186/s13244-022-01173-z
Source DB: PubMed Journal: Insights Imaging ISSN: 1869-4101
Preparative dietary protocols at our institution
| Dietary preparation instructions | Solid food | Low residue/fiber food | Clear liquids | |
|---|---|---|---|---|
| Clinical scenarios | Rice, steamed buns, noodles, bread, meat, vegetables, fruits, eggs, etc. | Congee, yogurt, milk, soy milk, soup, etc. | Water, juice, non-carbonated beverages, tea, etc. | |
| Abdominal examination | The upper abdomen, the whole abdomen, or the combined examination involving the upper abdomen or the whole abdomen1 (the detection of the gastrointestinal cavity lesions is excluded) | Fast for 4 h | Fast for 3 h | Unrestricted ingestion |
| The lower abdomen (kidneys, adrenal glands, renal artery, urinary system, etc.), pelvic cavity (bladder, uterus, appendages, prostate, etc.) | Unrestricted ingestion (greasy and fried foods are excluded) | Unrestricted ingestion | Unrestricted ingestion | |
| Three-dimensional imaging of the lumen (such as gastrointestinal cavity enhanced CT) | Fast for 4–6 h | Fast for 3 h | Unrestricted ingestion | |
| Non-abdominal examination | Contrast-enhanced CT and angiography of head, neck, chest, limbs and other parts | Unrestricted ingestion (greasy and fried foods are excluded) | Unrestricted ingestion | Unrestricted ingestion |
| Special population | Severe esophageal diseases or gastric emptying disorders, patients at risk of aspiration2, patients require fasting for clinical treatment, examination under general anesthesia or sedation | Foods and water were restricted according to clinical treatment needs. Intravenous supplementation of sugar and salt water was performed when necessary | ||
1The dietary preparation regimen of patients undergoing multi-site combined examination was based on the site that required fasting
2The risk of aspiration included disturbance of consciousness, increased intracranial pressure, and impaired swallowing reflex, and so on
Summary of patient characteristics
| Fasting group (%) | Non-fasting group (%) | |
|---|---|---|
| Total number of patients | 49,676 (39.05) | 77,524 (60.95) |
| Gender | ||
| Male | 28,210 (56.79) | 42,287 (54.55) |
| Female | 21,466 (43.21) | 35,237 (45.45) |
| Age (years) | ||
| Mean ± standard deviation | 57 ± 13 | 60 ± 13 |
| < 70 | 40,302 (81.13) | 60,721 (78.33) |
| ≥ 70 | 9374 (18.87) | 16,803 (21.67) |
| Patient source | ||
| Inpatients | 21,106 (42.49) | 40,173 (51.82) |
| Outpatients | 28,570 (57.51) | 37,351 (48.18) |
| Examination sites | ||
| Abdominal | 30,462 (61.32) | 15,396 (19.86) |
| Non-abdominal | 19,214 (38.68) | 62,128 (80.14) |
| Risk factors and underlying diseases | ||
| ICM-ADR history | 97 (0.20) | 165 (0.21) |
| Other ADR histories | 3536 (7.12) | 6738 (8.69) |
| Asthma | 110 (0.22) | 194 (0.25) |
| Hypertension | 11,411 (22.97) | 22,718 (29.30) |
| Coronary heart disease | 1608 (3.24) | 4668 (6.02) |
| Heart failure | 173 (0.35) | 323 (0.42) |
| Renal insufficiency | 99 (0.20) | 151 (0.19) |
| Hyperthyroidism | 16 (0.03) | 45 (0.06) |
| Tumor radio-chemotherapy | 5391 (10.85) | 5324 (6.87) |
| β blockers | 1151 (2.32) | 12,965 (16.72) |
| Diabetes | 2079 (4.19) | 3945 (5.09) |
| ICM name | ||
| Iopromide 370 | 7833 (15.77) | 12,532 (16.17) |
| Iodixanol 270 | 3936 (7.92) | 5490 (7.08) |
| Ioversol 320 | 6693 (13.47) | 12,244 (15.79) |
| Iohexol 350 | 17,015 (34.25) | 26,764 (34.52) |
| Iopamidol 350 | 5603 (11.25) | 9625 (12.42) |
| Iobitridol 350 | 2993 (6.03) | 4392 (5.67) |
| Iodixanol 320 | 5603 (11.28) | 6477 (8.35) |
| Injection dose | ||
| < 100 mL | 46,817 (94.24) | 72,579 (93.62) |
| ≥ 100 mL | 2859 (5.76) | 4945 (6.38) |
| Injection rate | ||
| < 5 mL/s | 36,836 (74.15) | 49,524 (63.88) |
| ≥ 5 mL/s | 12,840 (25.85) | 28,000 (36.12) |
The same patient might have multiple risk factors and underlying diseases simultaneously
ICM iodinated contrast media, ADR adverse drug reactions
Fig. 1Flowchart illustrating population enrollment
Fig. 2a The ADR incidence. b The proportion of ADR with different severity degrees in patients who developed ADR. c The incidence of emetic complications. d The proportion of nausea and vomiting in patients who developed emetic complications. e The frequency of various symptoms in ADR patients
The ADR occurrence of patients in different patient subgroups
| Fasting group (%) | Non-fasting group (%) | ||
|---|---|---|---|
| Total number of patients | 105/49,676 (0.211) | 197/77,524 (0.254) | 0.126 |
| Examination sites | |||
| Abdominal | 94/30,462 (0.309) | 18/15,396 (0.117) | < 0.001 |
| Non-abdominal | 11/19,214 (0.057) | 179/62,128 (0.288) | < 0.001 |
| Patient source | |||
| Inpatients | 44/21,106 (0.208) | 93/40,173 (0.231) | 0.566 |
| Outpatients | 61/28,570 (0.214) | 104/37,351 (0.278) | 0.098 |
| Risk factors and underlying diseases | |||
| ICM-ADR history | 12/97 (12.371) | 4/165 (2.424) | 0.001 |
| Other ADR histories | 11/3536 (0.311) | 24/6738 (0.341) | 0.709 |
| Asthma | 0/110 | 2/194 (1.031) | N/A |
| Hypertension | 16/11,411 (0.140) | 57/22,718 (0.251) | 0.037 |
| Coronary heart disease | 1/1608 (0.062) | 12/4668 (0.257) | 0.244 |
| Heart failure | 0/173 | 2/323 (0.619) | N/A |
| Renal insufficiency | 1/99 (1.010) | 0/151 | N/A |
| Hyperthyroidism | 0/16 | 0/45 | N/A |
| Tumor radio-chemotherapy | 10/5391 (0.185) | 7/5324 (0.131) | 0.482 |
| β blockers | 1/1151 (0.087) | 41/12,965 (0.316) | 0.277 |
| Diabetes | 0/2079 | 13/3945 (0.330) | N/A |
| Age ≥ 70 years | 11/9374 (0.117) | 20/16,803 (0.119) | 0.970 |
| Injection dose ≥ 100 mL | 2/22,859 (0.070) | 25/4945 (0.506) | < 0.001 |
| Injection rate ≥ 5 mL/s | 2/12,840 (0.016) | 96/28,000 (0.343) | < 0.001 |
| ICM name | |||
| Iopromide 370 | 22/7833 (0.218) | 64/12,532 (0.511) | 0.014 |
| Iodixanol 270 | 12/3936 (0.305) | 25/5490 (0.455) | 0.249 |
| Ioversol 320 | 7/6693 (0.105) | 21/12,244 (0.172) | 0.252 |
| Iohexol 350 | 15/17,015 (0.088) | 27/26,764 (0.101) | 0.675 |
| Iopamidol 350 | 14/5603 (0.250) | 14/9625 (0.145) | 0.147 |
| Iobitridol 350 | 11/2993 (0.368) | 10/4392 (0.228) | 0.268 |
| Iodixanol 320 | 24/5603 (0.428) | 36/6477 (0.556) | 0.320 |
The same patient might have multiple risk factors and underlying diseases simultaneously. N/A, unapplicable for statistics due to the sample size
ICM iodinated contrast media, ADR adverse drug reactions
Fig. 3a Analysis of actual excessive fasting profile. b The ADR incidence in patients with different fasting durations. c The incidence of emetic complications in patients with different fasting durations
Fig. 4a Analysis of actual water ingestion within 1 h prior to the examination. b The ADR incidence in patients with different amounts of water ingestion. c The incidence of emetic complications in patients with different amounts of water ingestion