1. Introduction
In small animal practice, magnetic resonance imaging (MRI) examination requires general anesthesia or sedation in order to ensure that dogs remain motionless during examination, thereby facilitating capture of high-quality images for appropriate diagnosis [
1]. However, general anesthesia or sedation causes hypothermia as one of the undesirable effects [
2], which can be more serious in MRI examinations than in common surgical operations, the reasons of which are described later.
Inhalant or injection anesthetics used for MRI examinations cause a physiological decrease in body temperature by suppressing the hypothalamus, which is the center of peripheral vasodilation and thermoregulation [
2,
3]. Furthermore, physical heat losses due to radiation, conduction, convection, and evaporation enhance the decrease in body temperature under general anesthesia or sedation [
4]. As hypothermia can cause a variety of adverse events, including decreased drug metabolism, organ dysfunction, and abnormalities in the immune system, it is necessary to prevent hypothermia or to reduce the decrease in body temperature during MRI examination under general anesthesia or sedation [
3].
There are two major reasons for the increased severity of hypothermia or decrease in body temperature during MRI examinations. First, in recent veterinary practice, various methods have been adopted to prevent hypothermia during anesthetic treatment, such as use of a forced-air warming system, a heat-retaining mat, and intravenous infusion warming devices, in addition to classical methods such as hot water bottles or blankets [
5,
6]. These devices are effective and safe to use in a place without restrictions, such as a surgical theater. However, these devices cannot be used in an MRI examination room due to the inclusion of magnetic materials. Therefore, methods to prevent hypothermia during MRI examinations are limited. The second reason is that the room temperature of the MRI examination room is kept low to maintain the equipment [
7]. Low-temperature environments enhance hypothermia due to convention; cold air surrounds the body surface causing heat loss [
3,
4,
8]. Thus, during MRI examinations, a lower room temperature worsens hypothermia induced by general anesthesia.
Therefore, prevention or attenuation of hypothermia in anesthetized dogs during MRI examination is recognized as a challenging issue. In veterinary medicine, only Onozawa et al. have reported the effect of an insulation device in preventing hypothermia during MRI examinations in dogs and cats under general anesthesia [
9]. In human pediatric medicine, similar to veterinary medicine, hypothermia during MRI examination is regarded as a serious problem because children who have difficulty remaining still during an MRI scan may require sedation or general anesthesia to minimize movement. Previous reports have shown that hypothermia is common in anesthetized children undergoing MRI: methods to prevent hypothermia have not been addressed [
10,
11]. We were unable to obtain useful information from human medicine. Based on scientific evidence, there are no standard or recommended methods to prevent or attenuate hypothermia in anesthetized dogs during MRI examinations, although hot water bottles, blankets, or other insulations are customarily used.
The use of hot water bottles is a possible way to prevent or attenuate anesthesia-induced hypothermia in an MRI examination room. Recently, although it is a method not often used in the operating room, a hot water bottle was used to mitigate hypothermia during anesthesia and to promote recovery from hypothermia [
12,
13]. A hot water bottle that does not contain magnetic material, such as a resin bottle or rubber glove filled with hot water, can be safely brought into an MRI room. In Onozawa’s study, hot water bottles were used to prevent hypothermia in dogs and cats during MRI examinations. This study reported the insulative effect of bubble wrap and down blankets covering hot water bottles in dogs and cats during MRI examinations, although the effect of hot water bottles themselves on body temperature was not investigated [
9]. However, there have been no reports on the effect of hot water bottles during MRI examinations on body temperature of animals or their role in prevention or alleviation of hypothermia.
Therefore, in the present study, we aimed to retrospectively investigate the effect of hot water bottles on body temperature during MRI examinations in dogs under general anesthesia.
2. Materials and Methods
This was a retrospective, observational study. The subjects of this study were included from the anesthesia records of dogs that underwent MRI examinations at the Veterinary Medical Teaching Hospital, Okayama University of Science (OUS-VMTH), from November 2018 to May 2021.
In this study, dogs meeting the following inclusion criteria were included: (1) those that underwent MRI examinations under general anesthesia; (2) those with a pre-anesthetic rectal temperature (Pre-RT) between 37 and 40 °C; (3) those with the American Society of Anesthesiologists Physical Status (ASA-PS) classification of 1 to 3; (4) those that underwent MRI examinations for more than 60 min; and (5) those for which hot water bottles and a shredded paper comforter, or only a shredded paper comforter was applied for body temperature management. The anesthetic records of dogs that met these inclusion criteria were used as data for retrospective observations. Dogs were excluded from the study even if one of the inclusion criteria was not met.
The hot water bottle in this study was an infusion solution bag containing 500 mL of water, which was heated in a 600 W microwave oven for 90 s before use. The cases in which hot water bottles were applied met two conditions: (1) the two hot water bottles were wrapped in separate face towels—to avoid the risk of burn injuries—and placed on the left and right sides of the dog’s abdomen; and (2) the hot water bottle was not replaced throughout the MRI examination duration. The paper comforter used in the study was paper shredded by a shredder packed in a plastic bag. Cases in which the paper comforter was applied met the following condition: a paper comforter was placed over the dog, covering from the neck to the tip of the tail.
The following information was extracted from the target data: breed, ASA-PS, sex, age, body weight (BW), Body Condition Score (BCS), rectal temperature (RT) at each time point, sedatives or anesthetics administered, and dose.
To analyze the effect of the hot water bottles on body temperature, cases were divided into the following two groups: the hot water bottle (HWB) group, including dogs treated with both, a hot water bottle and a paper comforter for body temperature management, and the shredded paper comforter (SPC) group, including dogs treated with a SPC alone. For further analysis, dogs from the HWB and SPC groups were assigned to subgroups based on their BW and RT before induction of anesthesia (Pre-RT). Dogs with Pre-RT < 38.5 °C or >38.5 °C were designated as HWB-L or SPC-L and HWB-H or SPC-H groups, respectively. Dogs with BW < 5 or >5 kg were designated as HWB < 5 or SPC < 5 and HWB ≥ 5 or SPC ≥ 5 groups, respectively.
The variables sex, age, BCS, ASA-PS, and RT were considered for statistical analyses, performed using GraphPad Prism (9.0, GraphPad Software, Inc., San Diego, CA, USA). Sex was compared between the groups or subgroups using Fisher’s exact test. The continuous variables, RT at each measurement point, age, and weight, and categorical variables, BCS and ASA-PS, were compared between the HWB and SPC groups using the Mann–Whitney test. RT at each measurement point, age, weight, BCS, and ASA-PS were compared between subgroups using Kruskal–Wallis analysis of variance on ranks and Dunn’s multiple comparison test. The Friedman and Dunn’s multiple comparisons test were used to compare RT at each measurement point and Pre-RT within each group or subgroup. Statistical significance was set at p < 0.05.
3. Results
3.1. Demographics
The total number of animals used in this study was 100. The cases included 57 males and 43 females, aged 115 (3–201) months [median (range)], weighing 5.6 (0.7–40) kg, with an evaluated BCS of 5 (2–8), and ASA of 2 (1–3). The dogs belonged to the following 23 breeds (number of dogs): Mongrel dog (16), Miniature Dachshund (16), Chihuahua (14), Toy Poodle (13), French Bulldog (7), Beagle dog (4), Shih Tzu (3), Pembroke Welsh Corgi (3), Pug (3), Miniature Schnauzer (3), Golden Retriever (2), Shiba Inu (2), Boston Terrier (2), Pomeranian (2), Yorkshire Terrier (2), Tea Cup Poodle (1), English Cocker Spaniel (1), Kaninchhen Dachshund (1), Jack Russell Terrier (1), Chinese Crested Dog (1), Papillon (1), Border Collie (1), and Miniature Pinscher (1).
Before anesthesia induction, each dog was premedicated with butorphanol (butorphanol 5 mg, Meiji Seika Pharma Co., Ltd., Tokyo, Japan), midazolam (Dorumicum Injection 10 mg, Maruishi Co., Ltd., Osaka, Japan), both, or none. General anesthesia was induced with propofol (1% 20 mL intravenous propofol injection “Pfizer,” Maruishi Co., Ltd., Osaka, Japan) or Alfaxalone (Alfaxan, Meiji Seika Pharma Co., Ltd., Tokyo, Japan), and the dog’s trachea was intubated (
Table 1). After intubation, general anesthesia was maintained with sevoflurane delivered in oxygen via a rebreathing system.
As per the above-mentioned criteria, 50 dogs were assigned to each HWB and SPC group and divided into subgroups (
Table 2). There were no statistically significant differences in sex, age, BCS, or ASA-PS between the HWB and SPC groups; however, BW showed a significant difference. No statistical differences in sex, age, BCS, ASA-PS, or weight were found between the HWB-L, HWB-H, SPC-L, and SPC-H subgroups and the HWB < 5, HWB ≥ 5, SPC < 5, and SPC ≥ 5 subgroups. There were significant differences in body weight between the HWB < 5 and HWB ≥ 5, HWB < 5 and SPC ≥ 5, SPC < 5 and HWB ≥ 5, and SPC < 5 and SPC ≥ 5 subgroups.
All MRI examinations were performed with a 1.5 T superconducting machine (Vantage Elan, Canon Medical Systems, Otawara, Japan), and the MRI room temperature was maintained at 23 ± 1 °C throughout the investigation period. Image artifacts caused by the hot water bottles were not reported.
3.2. Rectal Temperature
There were significant differences in Pre-RT between the HWB-L and HWB-H groups, the SPC-L and SPC-H groups, the HWB-L and SPC-H groups, and the HWB-H and SPC-L groups (
Table 3). In contrast, no statistical differences in Pre-RT were found between the HWB and SPC groups, HWB-L, SPC-L, HWB-H, and SPC-H subgroups, and HWB < 5, SPC < 5, HWB ≥ 5, and SPC ≥ 5 subgroups.
RT decreased significantly from T15 to T60 in the HWB and SPC groups compared to Pre-RT. There were no statistically significant differences in RT between the HWB and SPC groups at any time point. However, when the difference between Pre-RT and RT calculated at each time point (ΔT15-, 30-, 45-, and 60-Pre), ΔT15-Pre in the HWB group (−0.4 ± 0.3 °C) was significantly smaller than that in the SPC group (−0.6 ± 0.5 °C).
In the HWB-H group, RT at T15 did not significantly decrease compared to Pre-RT. In the HWB-L, SPC-L, and SPC-H groups, RT decreased significantly from T15 to T60 compared with Pre-RT. In addition, in the HWB-H subgroup, RT significantly decreased from T30 to T60 compared with Pre-RT.
In the HWB-H and HWB-L subgroups at T15, RT was higher than that in the SPC-H and SPC-L subgroups, respectively. In addition, at T15, RTs were higher in the HWB-H group than in the HWB-L group and in the SPC-H subgroup than in the SPC-L subgroup. At T30, RT was higher in HWB-H than in HWB-L, in SPC-H than in SPC-L, in HWB-H than in SPC-L, and in SPC-H than in HWB-L. At T60, there were no statistically significant differences in RT among the HWB-L, HWB-H, SPC-L, and SPC-H subgroups.
In the HWB < 5, HWB ≥ 5, SPC < 5, and SPC ≥ 5 groups, RT decreased significantly from T15 to T60 compared to Pre-RT. There were no statistically significant differences in the RT between the HWB < 5, SPC < 5, HWB ≥ 5, and SPC ≥ 5 subgroups at any time point.
3.3. Safety
No adverse events associated with the hot water bottle placement—including burn injuries—occurred during the MRI examinations.
4. Discussion
In both the HWB and SPC groups, the RT decreased significantly within 30 min after anesthesia induction, regardless of body temperature or BW before induction. After anesthesia induction, the decrease in body temperature occurs in three phases: the redistributable (phase 1), linear (phase 2), and plateau (phase 3) phase [
14]. In phase 1, administration of anesthetics caused redistribution of heat due to peripheral vasodilation, resulting in a rapid decrease in core temperature within 1 h after the onset of general anesthesia. Thus, our results suggest that hot water bottles could not prevent a decrease in RT induced by redistribution of heat with anesthetic administration, such as propofol or alfaxalone, for MRI examinations [
15,
16].
However, the decline in RT at 15 min after anesthetic induction in the HWB group was significantly smaller than that in the SPC group. Furthermore, in the HWB-H subgroup, RT did not decrease significantly for 15 min after anesthetic induction, although the SPC-H subgroup showed a significant decrease at the same time point. The RT at 15 min after intubation was significantly higher in the HWB-H and HWB-L than in the SPC-H and SPC-L subgroups, respectively. There were no statistically significant differences in body temperature before anesthesia between the HWB-H and SPC-H groups and the HWB-L and SPC-L groups. These results suggest that hot water bottles attenuated the decrease in RT for 15 min after intubation. At the same time, it was also suggested that the effect of hot water bottles was sustained for about 15 min. Frequent renewal of hot water bottles may be required to sustain their effect on body temperature. However, in clinical practice, frequent bottle renewals are limited.
Between the SPC-L and SPC-H subgroups, a significant difference in RT was found 15 min after intubation. It has been suggested that RT before anesthesia also affects the maintenance of body temperature. In human medicine, pre-warming aimed at increasing the body temperature before anesthesia induction was reported to reduce the incidence of hypothermia during general anesthesia; even if hypothermia is not completely prevented, hypothermia may be mitigated [
17,
18,
19]. However, a study on dogs reported that pre-warming was not useful for maintaining body temperature during general anesthesia and remained controversial [
20,
21].
The RT and BCS did not significantly differ between the HWB/SPC < 5 and HWB/SPC ≥ 5 subgroups. These results suggest that BW did not affect the body temperature attenuation by hot water bottles in the absence of differences in BCS. In general, the smaller the animal, the larger the surface area-to-body mass ration, thereby promoting greater heat loss by convection [
22,
23]. Namely, dogs in the HWB/SPC < 5 subgroups lost their heat more easily than dogs in the HWB/SPC ≥ 5 subgroups. Thus, we expected the RT in the HWB/SPC < 5 subgroups to decrease more than that in the HWB/SPC ≥ 5 subgroups; however, such was not the case.
In the present study, administered drugs, including sedatives, anesthetics, and supportive drugs, were not considered in the analysis. Thus, the influence of different drugs on the effect of hot water bottles on body temperature in dogs was not discussed. This is a limitation of the present study.
5. Conclusions
Our retrospective investigation suggested that the use of hot water bottles might be effective for body temperature management in dogs during MRI examinations under general anesthesia, especially in the early period after anesthesia induction, although hypothermia could not be prevented. However, the attenuating effect of the hot water bottles on the decrease in body temperature was minimal and the risk of burn injuries could not be completely ruled out. The use of hot water bottles might be one of the methods to attenuate hypothermia in the early period but should not be expected for complete prevention of hypothermia, and it was not recommendable necessarily for body temperature management during MRI examinations in dogs under general anesthesia.
Author Contributions
Conceptualization, Y.S. and T.K.; methodology, Y.S., T.K. and K.I.; formal analysis, Y.S., T.K. and K.I.; investigation, Y.S., K.K., A.O., K.S. and M.M.; resources, T.K., T.A. and K.I.; data curation, Y.S.; writing—original draft preparation, Y.S.; writing—review and editing, T.K. and K.I.; visualization, Y.S. and T.K.; supervision, T.A.; project administration, T.K. All authors have read and agreed to the published version of the manuscript.
Funding
This research received no external funding.
Institutional Review Board Statement
The requirement of ethical review and approval were waived due to the retrospective nature of the study.
Informed Consent Statement
Informed consent was obtained from the guardians/owners of all the subjects involved in the study. Written informed consent was obtained from the dog owners for the publication of this paper.
Data Availability Statement
Not applicable.
Acknowledgments
We would like to thank Yuko Wada, Misaki Ishikawa, Miwa Masabayashi, Saki Yoshioka, Yoshie Fujii, and Asuka Iwano for their daily support and encouragement as veterinary nurses, as well as Kayo Furumoto, Noritaka Maeta, and Takamasa Itoi for their valuable advice in proceeding with this study.
Conflicts of Interest
The authors declare no conflict of interest.
References
- Tremoleda, J.L.; Macholl, S.; Sosabowski, J.K. Anesthesia and Monitoring of Animals During MRI Studies. Methods Mol. Biol. 2018, 1718, 423–439. [Google Scholar] [CrossRef] [PubMed]
- Bednarski, R.; Grimm, K.; Harvey, R.; Lukasik, V.M.; Penn, W.S.; Sargent, B.; Spelts, K. AAHA Anesthesia Guidelines for Dogs and Cats. J. Am. Anim. Hosp. Assoc. 2011, 47, 377–385. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- 17 Temperature Regulation During Anesthesia: Anesthetic-Associated Hypothermia and Hypothermia. In Handbook of Veterinary Anesthesia; Muir, W.W.; Hubbell, J.A.E.; Bednarski, R.M.; Lerche, P. (Eds.) Elsevier Mosby: St. Louis, MO, USA, 2013; pp. 330–347. ISBN 978-0-323-08069-9. [Google Scholar]
- Wang, L.; Yin, H.; Di, Y.; Liu, Y.; Liu, J. Human Local and Total Heat Losses in Different Temperature. Physiol. Behav. 2016, 157, 270–276. [Google Scholar] [CrossRef]
- Tan, C.; Govendir, M.; Zaki, S.; Miyake, Y.; Packiarajah, P.; Malik, R. Evaluation of Four Warming Procedures to Minimise Heat Loss Induced by Anaesthesia and Surgery in Dogs. Aust. Vet. J. 2004, 82, 65–68. [Google Scholar] [CrossRef] [PubMed]
- Brady, R.B.E.; Poppell, W.T. Effect of Intravenous Fluid Warming on Core Body Temperature during Elective Orthopedic Procedures. Can. Vet. J. 2020, 61, 5. [Google Scholar]
- Ruth, M.; Sridharan, N.; Rai, E.; Joselyn, A. A Prospective Observational Study to Evaluate the Magnitude of Temperature Changes in Children Undergoing Elective MRI under General Anesthesia. Saudi J. Anaesth. 2020, 14, 200. [Google Scholar] [CrossRef]
- Bindu, B.; Bindra, A.; Rath, G. Temperature Management under General Anesthesia: Compulsion or Option. J. Anaesthesiol. Clin. Pharmacol. 2017, 33, 306–316. [Google Scholar] [CrossRef]
- Onozawa, E.; Azakami, D.; Seki, S.; Hamamoto, Y.; Ishioka, K. Effect of an Insulation Device in Preventing Hypothermia during Magnetic Resonance Imaging Examinations for Dogs and Cats under General Anesthesia. Animals 2021, 11, 2378. [Google Scholar] [CrossRef]
- Cronin, J.A.; Shen, C.; Rana, S.; Fricke, S.T.; Matisoff, A. Association Between Magnetic Resonance Imaging in Anesthetized Children and Hypothermia. Pediatr. Qual. Saf. 2019, 4, e181. [Google Scholar] [CrossRef]
- Lo, C.; Ormond, G.; McDougall, R.; Sheppard, S.J.; Davidson, A.J. Effect of Magnetic Resonance Imaging on Core Body Temperature in Anaesthetised Children. Anaesth. Intensive Care 2014, 42, 333–339. [Google Scholar] [CrossRef] [Green Version]
- Haskins, S.C. Hypothermia and Its Prevention during General Anesthesia in Cats. Am. J. Vet. Res. 1981, 42, 856–861. [Google Scholar] [PubMed]
- Cabell, L.W.; Perkowski, S.Z.; Gregor, T.; Smith, G.K. The Effects of Active Peripheral Skin Warming on Perioperative Hypothermia in Dogs. Vet. Surg. 1997, 26, 79–85. [Google Scholar] [CrossRef]
- Sessler, D.I. Perioperative Heat Balance. Anesthesiology 2000, 92, 578–596. [Google Scholar] [CrossRef] [PubMed]
- Micieli, F.; Chiavaccini, L.; Paré, M.D.; Chagas, J.B.; Vesce, G.; Gianotti, G. Comparison of the Sedative Effects of Alfaxalone and Methadone with or without Midazolam in Dogs. Can. Vet. J. 2019, 60, 1060–1064. [Google Scholar] [PubMed]
- Bornkamp, J.L.; Robertson, S.; Isaza, N.M.; Harrison, K.; DiGangi, B.A.; Pablo, L. Effects of Anesthetic Induction with a Benzodiazepine plus Ketamine Hydrochloride or Propofol on Hypothermia in Dogs Undergoing Ovariohysterectomy. Am. J. Vet. Res. 2016, 77, 351–357. [Google Scholar] [CrossRef] [PubMed]
- De Brito Poveda, V.; Clark, A.M.; Galvão, C.M. A Systematic Review on the Effectiveness of Prewarming to Prevent Perioperative Hypothermia. J. Clin. Nurs. 2013, 22, 906–918. [Google Scholar] [CrossRef] [PubMed]
- Jun, J.-H.; Chung, M.H.; Kim, E.M.; Jun, I.-J.; Kim, J.H.; Hyeon, J.-S.; Lee, M.H.; Lee, H.S.; Choi, E.M. Effect of Pre-Warming on Perioperative Hypothermia during Holmium Laser Enucleation of the Prostate under Spinal Anesthesia: A Prospective Randomized Controlled Trial. BMC Anesthesiol. 2018, 18, 201. [Google Scholar] [CrossRef] [Green Version]
- Becerra, Á.; Valencia, L.; Saavedra, P.; Rodríguez-Pérez, A.; Villar, J. Effect of Prewarming on Body Temperature in Short-Term Bladder or Prostatic Transurethral Resection under General Anesthesia: A Randomized, Double-Blind, Controlled Trial. Sci. Rep. 2021, 11, 20762. [Google Scholar] [CrossRef]
- Aarnes, T.K.; Bednarski, R.M.; Lerche, P.; Hubbell, J.A.E. Effect of Pre-Warming on Perioperative Hypothermia and Anesthetic Recovery in Small Breed Dogs Undergoing Ovariohysterectomy. Can. Vet. J. 2017, 58, 175–179. [Google Scholar] [PubMed]
- Rigotti, C.F.; Jolliffe, C.T.; Leece, E.A. Effect of Prewarming on the Body Temperature of Small Dogs Undergoing Inhalation Anesthesia. J. Am. Vet. Med. Assoc. 2015, 247, 765–770. [Google Scholar] [CrossRef] [PubMed]
- Sharma, D.; Sharma, P.; Shastri, S. Golden 60 Minutes of Newborn’s Life: Part 2: Term Neonate. J. Matern.-Fetal Neonatal Med. 2017, 30, 2728–2733. [Google Scholar] [CrossRef] [PubMed]
- Pinheiro, J.M.B. Preventing Hypothermia in Preterm Newborns—Simple Principles for a Complicated Task. J. Pediatr. 2018, 94, 337–339. [Google Scholar] [CrossRef] [PubMed]
Table 1.
Anesthetic and sedative drugs administered for anesthetic management.
Table 1.
Anesthetic and sedative drugs administered for anesthetic management.
Drugs | Number of Dogs | Dose (mg/kg) |
---|
Premedication | | |
midazolam | 7 | 0.2 (0.2–1.9) |
butorphanol | 41 | 0.2 (0.1–1.4) |
midazolam + butorphanol | 6 | 0.2 (0.2–1.7) + 0.2 (0.2–1.4) |
none | 46 | - |
Induction | | |
Alfaxalone | 73 | 2.2 (0.4–6.1) |
propofol | 27 | 4.0 (0.9–7.3) |
Table 2.
Demographic data of each analyzed group and subgroup.
Table 2.
Demographic data of each analyzed group and subgroup.
| HWB | SPC |
---|
HWB-L | HWB-H | HWB < 5 | HWB ≥ 5 | SPC-L | SPC-H | SPC < 5 | SPC ≥ 5 |
---|
Number of dogs | 50 | | | | 50 | | | |
33 | 17 | 26 | 24 | 21 | 29 | 18 | 32 |
Age (months) | 104 ± 51 | | | | 113 ± 44 | | | |
105 ± 51 | 101 ± 52 | 95 ± 53 | 116 ± 49 | 121 ± 40 | 108 ± 46 | 113 ± 48 | 114 ± 42 |
Sex (male/female) | 31/19 | | | | 26/24 | | | |
19/14 | 10/7 | 14/12 | 15/9 | 13/8 | 13/16 | 10/8 | 16/16 |
BW (kg) | 5.7 ± 3.7 b | | | | 8.1 ± 6.5 a | | | |
5.7 ± 3.8 | 5.4 ± 3.2 | 3.2 ± 1.2 i,j | 8.5 ± 3.4 g,h | 7.3 ± 3.6 | 8.7 ± 8.0 | 3.5 ± 1.0 i,j | 10.6 ± 7.0 g,h |
BCS | 4 (2–7) | | | | 4 (2–8) | | | |
4 (3–7) | 4 (2–7) | 4 (2–7) | 5 (4–7) | 4 (2–6) | 5 (3–8) | 4 (2–6) | 5 (3–8) |
ASA–PS | 2 (1–3) | | | | 2 (1–3) | | | |
2 (1–3) | 2 (1–3) | 2 (1–3) | 2 (1–3) | 2 (1–3) | 2 (1–3) | 2 (1–3) | 2 (1–3) |
Pre-RT (°C) | 38.3 ± 0.4 | | | | 38.4 ± 0.4 | | | |
38.0 ± 0.2 e,f | 38.8 ± 0.3 c,d | 38.3 ± 0.4 | 38.3 ± 0.4 | 38.0 ± 0.2 e,f | 38.7 ± 0.2 c,d | 38.4 ± 0.3 | 38.5 ± 0.4 |
Table 3.
Rectal temperature in each group and subgroup.
Table 3.
Rectal temperature in each group and subgroup.
| Time after Intubation |
---|
Treatments | Pre | T15 | T30 | T60 |
---|
HWB | 38.3 ± 0.4 | 37.9 ± 0.5 * | 37.2 ± 0.6 * | 37.0 ± 0.8 * |
HWB-L | 38.0 ± 0.2 e,f | 37.5 ± 0.3 *,d,e | 37.0 ± 0.6 *,e,f | 36.8 ± 0.8 * |
HWB-H | 38.8 ± 0.3 c,d | 38.3 ± 0.4 c,d,f | 37.6 ± 0.5 *,c,d | 37.4 ± 0.6 * |
HWB < 5 | 38.3 ± 0.4 | 37.8 ± 0.5 * | 37.2 ± 0.7 * | 37.0 ± 0.7 * |
HWB ≥ 5 | 38.3 ± 0.4 | 37.8 ± 0.6 * | 37.2 ± 0.6 * | 36.9 ± 0.8 * |
SPC | 38.4 ± 0.4 | 37.7 ± 0.6 * | 37.2 ± 0.6 * | 37.1 ± 0.7 * |
SPC-L | 38.0 ± 0.2 e,f | 37.4 ± 0.5 *,c,e,f | 36.9 ± 0.5 *,e,f | 36.8 ± 0.5 * |
SPC-H | 38.7 ± 0.2 c,d | 37.9 ± 0.6 *,d,f | 37.4 ± 0.6 *,c,d | 37.3 ± 0.7 * |
SPC < 5 | 38.4 ± 0.3 | 37.6 ± 0.6 * | 37.0 ± 0.6 * | 36.8 ± 0.7 * |
SPC ≥ 5 | 38.5 ± 0.4 | 37.7 ± 0.6 * | 37.4 ± 0.5 * | 37.2 ± 0.5 * |
| Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. |
© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).