Skip Navigation LinksHome > August 2012 - Volume 117 - Issue 2 > What Factors Affect Intrapartum Maternal Temperature? A Pros...
Anesthesiology:
doi: 10.1097/ALN.0b013e31825a30ef
Perioperative Medicine

What Factors Affect Intrapartum Maternal Temperature? A Prospective Cohort Study: Maternal Intrapartum Temperature

Frölich, Michael A. M.D., M.S.*; Esame, Alice B.S.; Zhang, Kui Ph.D.; Wu, Jihua Ph.D.§; Owen, John M.D., M.S.P.H.

Free Access
Press Release
Article Outline
Collapse Box

Author Information

Collapse Box

Abstract

Background: In recent years, several reports have indicated that maternal temperature elevations during labor may also be observed in the absence of an infection. Presumed noninfectious causes of maternal temperature elevations include epidural analgesia, endogenous heat production generated by the contracting uterus, and delivery in an overheated room. To investigate the potential causes of noninfectious maternal temperature changes during labor, we conducted a prospective cohort study in women scheduled for labor induction.
Methods: We recorded hourly oral temperatures from admission to delivery. We calculated whether temperature changed during labor in 81 women. We then determined if body mass index, and duration of labor, or time from rupture of amniotic sac to delivery, or oxytocin dose, would affect maternal temperature. To evaluate the possible role of epidural analgesia, we compared the temperature slope before and after starting epidural analgesia.
Results: We observed an overall significant linear trend of temperature over time with an estimated temperature slope of +0.017°C/h (P = 0.0093). Patients with a positive temperature trend had also a significantly longer time from rupture of membranes to delivery (P = 0.0077) and a higher body mass index (P = 0.0067). Epidural analgesia had no effect on the temperature trend.
Conclusions: In our cohort of patients, there was an overall significant linear trend of temperature over time after correcting for heterogeneity among patients. Temperature increase was associated with higher body mass index values and longer time from rupture of membranes to delivery. Epidural analgesia had no effect on maternal temperature.
Back to Top | Article Outline

What We Already Know about This Topic

* Maternal temperature increases in some women during labor in the absence of evidence for infection and has been speculated to result in unnecessary fetal evaluation for sepsis.
* Whether epidural analgesia increases the risk of fever during pregnancy is unclear.
Back to Top | Article Outline

What This Article Tells Us That Is New

* Maternal temperatures were recorded in 81 women with induced labor. Slightly more than half of the women showed a small positive temperature trend.
* Increasing body weight and the duration of rupture of membranes were associated with increasing temperature, but epidural analgesia had no effect on maternal temperature.
ALTHOUGH maternal infections are recognized as the foremost cause for fever during childbirth, other causes have been investigated. In more recent years, an association of temperature increase during childbirth and epidural analgesia has been described.13 More importantly, it has also been postulated that maternal intrapartum fever may be associated with poor neonatal outcome.47 Whereas some investigators implied that epidural analgesia might be the cause for maternal fever,810 others asserted that the observed associations are noncausal, noting that women who request epidural analgesia tend to have longer labors, and thus a higher chance of developing chorioamnionitis.8,11 The discussion about the potential role of epidural analgesia in maternal fever has stimulated a broader conversation about whether maternal temperature elevation during labor is a real phenomenon and whether it could have a noninfectious etiology.12
In general, fever occurs when the hypothalamic thermoregulatory center is reset at a higher temperature by “endogenous pyrogens” produced by specific host cells in response to infection, inflammation, injury, or an antigenic challenge.1315 Some noninfectious reasons for maternal fever are anticholinergic drugs such as atropine, which raise core temperature by inhibiting sweating or vasodilatation without changing the normal hypothalamic set point. Other noninfectious causes may include endogenous heat production generated by the contracting uterus and maternal expulsive efforts with delivery in an overheated room. Theories to explain the association of maternal intrapartum fever and epidural analgesia are based on the concept that epidural analgesia may suppress heat-dissipating mechanisms such as pain-associated hyperventilation, or that epidural analgesia may facilitate a placental inflammatory process that in turn triggers maternal intrapartum fever.10,13,1620
These theories on the causation of maternal intrapartum fever by epidural analgesia are not very convincing. From a physiologic perspective, the sympathetic blockade caused by epidural analgesia should result in hypothermia from the redistribution of heat from the core to the periphery, and thus a net heat loss to the environment.21 Most of the existing publications focus on large temperature changes and compare the relative proportion of febrile patients based on type of labor analgesia rather than evaluating small changes in temperature. We designed our study to evaluate subtle changes in maternal temperature and to determine the possible effect of several intrapartum factors, including epidural analgesia, on maternal temperature. Because oxytocin induces uterine contractions and associated endogenous heat production, we studied patients scheduled for labor induction.
Our primary research aim was to study the time-course of maternal temperature individually and as a group. Our secondary research aims were to investigate whether duration of labor, epidural analgesia, oxytocin dose, or length of time from rupture of membranes to delivery would be associated with a maternal temperature increase.
Back to Top | Article Outline

Materials and Methods

Design
The Institutional Review Board of the University of Alabama at Birmingham (Birmingham, Alabama) approved this study. After obtaining written informed consent, 90 women were recruited at University of Alabama at Birmingham's Women and Infants Center from November 2008 to September 2010 scheduled for induction of labor. Upon admission to the labor and delivery unit, patients were screened to determine study eligibility. We excluded patients with medical conditions that would affect temperature regulation or the normal course of labor, particularly chorioamnionitis. Patients who received medications known to affect body temperature (acetaminophen, prostaglandin, or ibuprofen), and patients with active cardiac, pulmonary, or neurologic disease were also ineligible. The diagnosis of chorioamnionitis was based on a combination of fever (temperature more than 38.0°C) or a combination of at least two of the following findings: significant maternal tachycardia (more than 120 beats per minute [bpm]), fetal tachycardia (more than 160 bpm), purulent or foul-smelling amniotic fluid or vaginal discharge, uterine tenderness, or maternal leukocytosis (total blood leukocyte count more than 18,000 cells/μl). Obstetrical indications for labor inductions included multiparity and a gestational age of at least 39 weeks, postterm for women with gestational age of more than 40 weeks, and fetal conditions such as suspected fetal growth retardation.
Once enrolled, we recorded a set of baseline study parameters about the patient. This consisted of date and time of admission to the labor and delivery unit, date of birth, admissions weight, height, ethnicity (white, African-American, Hispanic, Asian-American, or other), parity (number of full-term deliveries, preterm deliveries, abortions, and living children), group B streprococcal (GBS) status (positive, negative, or unknown), and leukocyte count on admission. After delivery, the following supplemental information was documented: time and date of initiation of epidural analgesia, rupture of membranes (ROM) and delivery, diagnosis of chorioamnionitis (yes/no), acetaminophen administration intrapartum (yes/no), and prostaglandin administration (yes/no). Epidural analgesia, consisting of bupivacaine 0.1% with 2 μg/ml fentanyl, was delivered as patient-controlled analgesia using a basal rate of 8 ml/h and a demand bolus of 4 ml every 20 min. During the course of labor, nurses recorded the following information each hour: cervical dilation of the last vaginal examination, contraction intensity, oxytocin dose, and maternal temperature.
Participating delivery nurses were educated on the purpose of the study and the particular requirements and received the same information as checklist as part of the study data entry forms used. We particularly emphasized the importance of obtaining accurate hourly temperature readings. Labor and delivery nursing protocols at the University of Alabama at Birmingham specify that body temperatures should not be obtained immediately after the patient had received ice chips. Oral temperature, given the latter restriction, most accurately reflects core body temperature when compared with skin, tympanic, or axillary temperature.22 After ROM, an intrauterine pressure catheter was inserted to measure labor intensity in Montevideo units. These units were calculated as uterine pressure above baseline tone multiplied by the number of contractions in a 10-min period. Oxytocin dose was then adjusted by the nurse, according to protocol, to induce and maintain adequate labor, defined as at least 200 Montevideo units using the peak contraction pressure values obtained from the intrauterine pressure catheter.
Back to Top | Article Outline
Statistical Analysis
Analysis 1: Does Temperature Change Over Time?
We used a mixed linear model with a random intercept and slope. This model is ideally suited for this type of repeated measures data because it estimates a common intercept and slope and also accounts for individual baseline temperatures and individual temperature slopes. The statistical model can be expressed as
Equation (Uncited)
Equation (Uncited)
Image Tools
where the Greek letters β0 and β1 denote estimates for the common intercept and slope and the Latin letters b0i and b1i denote estimates for the ith subject intercepts and slope.
We also tested higher-order polynomial models for temperature.
Back to Top | Article Outline
Analysis 2: Do Covariates Have an Effect on Temperature Trend?
Fig. 1
Fig. 1
Image Tools
We tested the effects of covariates on temperature with a regression analysis where individual temperature slopes from Analysis 1 were used as outcome variables and duration of labor, total oxytocin dose, time from ROM to delivery, and body mass index (BMI), and the interaction of duration of labor and BMI as explanatory variables. To illustrate the effect of individual covariates, we also arranged participants into patients with a positive temperature slope more than 0 (N = 44) and patients with a negative temperature slope less than 0 (N = 37) and compared groups with a Student t test (fig. 1).
Back to Top | Article Outline
Analysis 3: Effect of Epidural Analgesia on Temperature Slope?
To test whether epidural analgesia had an effect on temperature, we calculated temperature slopes before and after initiation of epidural analgesia and then tested whether the change of slope was different from zero. We used a paired Student t test assuming unequal variances for this analysis. We required that each subject used for this analysis be observed for at least 4 h prior and after the initiation of epidural analgesia. The resulting sample size for this paired Student t test was n = 39.
Back to Top | Article Outline
Statistical Power
We calculated a minimum sample size of n = 23 to detect a slope change of 0.025°C/h assuming a SD of temperature slopes of 0.035°C/h, an α level of 0.05, and 90% power. We expected that we could only use a proportion of the total sample for the comparison of slopes before and after initiation of epidural anesthesia (Analysis 3) because many patients might not have enough data points to obtain stable estimates for the comparison of slopes before and after initiation of epidural anesthesia (Analysis 3). Therefore, we estimated that we would need 3 or 4 times the sample size required for Analysis 1 to carry out all analyses with adequate power.
We used the statistical software SAS (SAS Institute, Cary, NC) version 9.2 (modules PROC MIXED, PROC TTEST, and PROC UNIVATIATE) for our statistical analysis.
Back to Top | Article Outline

Results

Subject Characteristics
Table 1-a. Parity, L...
Table 1-a. Parity, L...
Image Tools
Out of 90 patients enrolled in the study, four were excluded because they received acetaminophen for intrapartum pain, whereas one patient was excluded based on the clinical diagnosis of chorioamnionitis. From the 85 eligible participants, we excluded another four from analysis who were not observed for at least 4 h. Their inclusion does eliminate patients with faster labor but would possibly result in unreliable estimates of temperature slopes. Therefore, 81 patients were included in Analyses 1 and 2. Summary data on the patient baseline characteristics leukocyte count, parity, and cervical dilation are provided in table 1.
Table 1-b. Parity, L...
Table 1-b. Parity, L...
Image Tools
Table 2
Table 2
Image Tools
Summary statistics of the 81 patients included in the analysis are provided in table 2. The average duration of labor was 11 h and 41 min. Our patient population included similar proportions of white (48%) and African-American (45%) women with an average BMI of 34.4 kg/m2 and a leukocyte count of 9.4 ± 2.7/l on admission.
Back to Top | Article Outline
Results for Analysis 1
Fig. 2
Fig. 2
Image Tools
The population slope in the linear mixed model was estimated to be 0.017°C/h with 95% CI = [0.0044, 0.0302], significantly different from zero (P = 0.0093), indicating that there was a significant linear trend of temperature. Higher-order polynomial models did not improve the fit. The root mean square error remained at 0.433. The overall temperature course over time is illustrated in figure 2; N = 37 participants had a slope less than 0 and n = 44 participants had a slope more than 0.
Back to Top | Article Outline
Results for Analysis 2
The interaction term of the time of ROM to delivery and BMI was significant (P = 0.0475). Therefore, as weight increased the effect of the duration of ROM on maternal temperature (positive temperature slope) was more pronounced. The results of our supplemental analysis of covariates by slope category are depicted in figure 1. As we observed in our regression model, in this categorical analysis, patients with a positive temperature trend had a significantly longer time from rupture of membranes to delivery (P = 0.0077) and a higher body mass index (P = 0.0067). To adjust for multiple comparisons in the latter analysis, a P value of 0.05/4 = 0.0125 was considered statistically significant (Bonferroni correction).
Back to Top | Article Outline
Results for Analysis 3
All but three patients included in the study received epidural analgesia. The median duration and interquartile range of epidural analgesia was 7.9 (4.3, 12.1) hrs. To study whether epidural analgesia had an effect on temperature, we compared temperature slopes before initiating epidural analgesia (admission to epidural) with temperature slopes after initiating epidural analgesia (epidural to delivery). The parameter estimate and 95% CI for the mean difference of the slope before versus after initiation of epidural analgesia was −0.0068, 0.00338. This indicates that in our study group epidural analgesia had no effect on the temperatures slope.
Back to Top | Article Outline

Discussion

Several investigators have reported maternal temperature elevations in women whom received epidural analgesia.9,10,13,14,1719,2226 This observation received widespread attention by anesthesiologists, obstetricians, and the media when Liebermann et al. suggested that neonatal sepsis evaluations were attributable to the use of epidural analgesia.10 The study on which this opinion was based, as well as other retrospective studies, have several important limitations9,17,19,22, because the investigators had no control of the quality of temperature recordings and frequency at which these measures were obtained and investigators could not reliably rule out that some patients may have received medications that either increase temperature such as prostaglandins or lower an increased temperature (antipyretics).
There are few prospective randomized controlled trials that also describe an association of maternal temperature increases and epidural analgesia in the context of placental inflammation,1315 neonatal sepsis work-up,18 pregnancy-induced hypertension,23 or labor progress and mode of delivery.24,25,27 Philip et al.28 investigated the incidence of maternal fever, defined as temperature more than 38.0°C, as primary outcome. They also found a higher proportion of patients with longer labor in the epidural group. Because we were interested in the noninfectious etiology of maternal intrapartum fever, we purposefully excluded patients with maternal fever at the beginning of our study and excluded women with clinical evidence for infection. We evaluated the temperature trend of all patients, regardless of whether they met a predefined temperature cutoff or not.
It is not surprising that the average temperature trend is very small, a temperature increase of approximately 0.2 of a degree over 10 h of labor. It is well established that mild fluctuations in temperature (0.25°C) are observed as physiologic variations of the female menstrual cycle and studies in animals have shown that estrogen and progesterone can act directly on specific sex steroid-binding neurons in the preoptic/anterior hypothalamus.29,30 However, because the mechanisms of temperature variation during labor are different than those associated with diurnal or menstrual changes, even a subtle change that would otherwise be considered inconsequential may be important because it may be indicative of an inflammatory process that is potentially harmful to the neonate. Segal12 pointed out that the observed maternal temperature change, summarized across treatment groups in the randomized clinical trials, could be an “averaging artifact,” a suspicion that we can confirm. Using the mixed model analysis, we learned that only 54% of individuals had a temperature slope greater than or equal to zero and the remaining 46% had a temperature slope less than zero.
A very important question from the anesthesiologist's perspective is whether epidural analgesia is indeed associated with maternal temperature changes during labor as suggested by some authors.16,31 Most researchers would argue that the best way to address this question is to randomly assign patients to either receive intravenous or epidural analgesia. However, withholding epidural analgesia would probably be considered unethical in current practice. Moreover, even past studies where investigators attempted such a design were flawed with a relatively low recruitment rate and high crossover from intravenous to epidural analgesia. We therefore took a different approach. One of the important early studies on the topic by Camann et al.3 compared patients receiving epidural analgesia with patients who received parenteral opioids for labor pain relief. With this design it is possible that patient groups, apart from the obvious treatment allocation, were dissimilar. For example, the parenteral opioid group might have received acetaminophen. It is also possible that parenteral opioids by themselves may have a mitigating effect on temperature elevation during labor as opposed to epidural analgesia having a thermogenic effect. To avoid this ambiguity, we designed our study such that patients acted as their own control. We used a mixed model to estimate individual temperature slopes (random effects) and then compared individual temperature slopes before and after epidural anesthesia with a paired Student t test. With each individual patient serving as her own control, we compared the temperature slope before initiation of epidural analgesia with the slope after starting epidural analgesia. Using a paired Student t test, we found no difference. This observation indicates that epidural analgesia had no discernable impact on maternal temperature.
Noteworthy is also the absence of a temperature drop following the first 4 h after initiation of epidural anesthesia because of blood flow redistribution as described by Holdcroft et al.21 Given the low local anesthetic concentration of 0.1% used in our study when compared with 0.5% for surgical anesthesia in Holcroft's study, the absence of a temperature reduction is not surprising. One might expect that more advanced labor might produce a greater amount of metabolic heat and thus a greater degree of temperature elevation. The absence of such an effect is best explained by our practice of maintaining labor at an adequate pattern with oxytocin based on calculated Montevideo units (uterine activity).
A variety of potential theories on noninfectious factors affecting maternal temperature have been proposed. Fusi et al.2 proposed the theory of high ambient temperatures in the delivery room. An alternative theory is based on an imbalance of metabolic heat production and heat-dissipation during labor. Compensatory mechanisms such as sweating and pain-related hyperventilation may be attenuated by epidural analgesia.3234 Others argue that intravenous μ-receptor agonist narcotics such as fentanyl may have a modest effect in preventing maternal temperature elevations.35,36 Probably the best-supported and most plausible theory is based on the systemic effect of thermogenic inflammatory mediators, such as interleukin-6, released from the placental-myometrial interface into the maternal circulation.13,16,20,37 In our study, we recorded oxytocin dose and contraction strength to evaluate the possible fever-producing effect of the contracting uterus, the duration of labor, time from ROM to delivery, and BMI information possibly related to inflammatory processes.
Among those variables, the time from rupture of membrane (ROM) to delivery and BMI showed a significant positive association with temperature, and duration of labor and total oxytocin dose showed a notable positive trend. Long labor, prolonged uterine activity, or a long time from ROM to delivery may sustain an inflammatory process that may result in the temperature elevation in those patients. The same mechanism may be responsible for the observed association of obesity and a positive temperature slope since the link of obesity to inflammation has been well established.38
Summarizing the key findings of our study, we conclude that induced labor is associated with a small temperature increase. We found an overall significant linear trend of temperature over time after correcting for heterogeneity among patients. Patients with higher BMI and longer duration from ROM to delivery are more likely to increase their body temperature during labor. In our study of women scheduled for induction of labor, epidural analgesia had no effect on maternal temperature.
Back to Top | Article Outline

References

1. Kapusta L, Confino E, Ismajovich B, Rosenblum Y, David MP: The effect of epidural analgesia on maternal thermoregulation in labor. Int J Gynaecol Obstet 1985; 23:185–9

2. Fusi L, Steer PJ, Maresh MJ, Beard RW: Maternal pyrexia associated with the use of epidural analgesia in labour. Lancet 1989; 1:1250–2

3. Camann WR, Hortvet LA, Hughes N, Bader AM, Datta S: Maternal temperature regulation during extradural analgesia for labour. Br J Anaesth 1991; 67:565–58

4. Impey LW, Greenwood CE, Black RS, Yeh PS, Sheil O, Doyle P: The relationship between intrapartum maternal fever and neonatal acidosis as risk factors for neonatal encephalopathy. Am J Obstet Gynecol. 2008; 198:49.e1–6

5. Impey L, Greenwood C, MacQuillan K, Reynolds M, Sheil O: Fever in labour and neonatal encephalopathy: A prospective cohort study. BJOG 2001; 108:594–7

6. Goetzl L, Korte JE: Interaction between intrapartum maternal fever and fetal acidosis increases risk for neonatal encephalopathy. Am J Obstet Gynecol. 2008; 199:e9

7. Lieberman E, Lang J, Richardson DK, Frigoletto FD, Heffner LJ, Cohen A: Intrapartum maternal fever and neonatal outcome. Pediatrics 2000; 105:8–13

8. Churgay CA, Smith MA, Blok B: Maternal fever during labor–what does it mean? J Am Board Fam Pract 1994; 7:14–24

9. Ploeckinger B, Ulm MR, Chalubinski K, Gruber W: Epidural anaesthesia in labour: Influence on surgical delivery rates, intrapartum fever and blood loss. Gynecol Obstet Invest 1995; 39:24–7

10. Lieberman E, Lang JM, Frigoletto F Jr., Richardson DK, Ringer SA, Cohen A: Epidural analgesia, intrapartum fever, and neonatal sepsis evaluation. Pediatrics 1997; 99:415–9

11. Vallejo MC, Kaul B, Adler LJ, Phelps AL, Craven CM, Macpherson TA, Sweet RL, Ramanathan S: Chorioamnionitis, not epidural analgesia, is associated with maternal fever during labour. Can J Anaesth 2001; 48:1122–6

12. Segal S: Labor epidural analgesia and maternal fever. Anesth Analg 2010; 111:1467–75

13. Dashe JS, Rogers BB, McIntire DD, Leveno KJ: Epidural analgesia and intrapartum fever: Placental findings. Obstet Gynecol 1999; 93:341–4

14. Smulian JC, Bhandari V, Vintzileos AM, Shen-Schwarz S, Quashie C, Lai-Lin YL, Ananth CV: Intrapartum fever at term: Serum and histologic markers of inflammation. Am J Obstet Gynecol 2003; 188:269–74

15. Saper CB, Breder CD: The neurologic basis of fever. N Engl J Med 1994; 330:1880–6

16. Goetzl L, Evans T, Rivers J, Suresh MS, Lieberman E: Elevated maternal and fetal serum interleukin-6 levels are associated with epidural fever. Am J Obstet Gynecol 2002; 187:834–8

17. Mayer DC, Chescheir NC, Spielman FJ: Increased intrapartum antibiotic administration associated with epidural analgesia in labor. Am J Perinatol 1997; 14:83–6

18. Kaul B, Vallejo M, Ramanathan S, Mandell G: Epidural labor analgesia and neonatal sepsis evaluation rate: A quality improvement study. Anesth Analg 2001; 93:986–90

19. Vinson DC, Thomas R, Kiser T: Association between epidural analgesia during labor and fever. J Fam Pract 1993; 36:617–22

20. Riley LE, Celi AC, Onderdonk AB, Roberts DJ, Johnson LC, Tsen LC, Leffert L, Pian-Smith MC, Heffner LJ, Haas ST, Lieberman ES: Association of epidural-related fever and noninfectious inflammation in term labor. Obstet Gynecol 2011; 117:588–95

21. Holdcroft A, Hall GM, Cooper GM: Redistribution of body heat during anaesthesia. A comparison of halothane, fentanyl and epidural anaesthesia. Anaesthesia 1979; 34:758–64

22. Herbst A, Wølner-Hanssen P, Ingemarsson I: Risk factors for fever in labor. Obstet Gynecol 1995; 86:790–4

23. Lucas MJ, Sharma SK, McIntire DD, Wiley J, Sidawi JE, Ramin SM, Leveno KJ, Cunningham FG: A randomized trial of labor analgesia in women with pregnancy-induced hypertension. Am J Obstet Gynecol 2001; 185:970–5

24. Ramin SM, Gambling DR, Lucas MJ, Sharma SK, Sidawi JE, Leveno KJ: Randomized trial of epidural versus intravenous analgesia during labor. Obstet Gynecol 1995; 86:783–9

25. Sharma SK, Sidawi JE, Ramin SM, Lucas MJ, Leveno KJ, Cunningham FG: Cesarean delivery: A randomized trial of epidural versus patient-controlled meperidine analgesia during labor. ANESTHESIOLOGY 1997; 87:487–94

26. Yancey MK, Zhang J, Schwarz J, Dietrich CS 3rd, Klebanoff M: Labor epidural analgesia and intrapartum maternal hyperthermia. Obstet Gynecol 2001; 98:763–70

27. Sharma SK, Alexander JM, Messick G, Bloom SL, McIntire DD, Wiley J, Leveno KJ: Cesarean delivery: A randomized trial of epidural analgesia versus intravenous meperidine analgesia during labor in nulliparous women. ANESTHESIOLOGY 2002; 96:546–51

28. Philip J, Alexander JM, Sharma SK, Leveno KJ, McIntire DD, Wiley J: Epidural analgesia during labor and maternal fever. ANESTHESIOLOGY 1999; 90:1271–5

29. Silva NL, Boulant JA: Effects of testosterone, estradiol, and temperature on neurons in preoptic tissue slices. Am J Physiol 1986; 250:R625–32

30. McEwen BS: Neural gonadal steroid actions. Science 1981; 211:1303–11

31. Lieberman E, O'donoghue C: Unintended effects of epidural analgesia during labor: A systematic review. Am J Obstet Gynecol 2002; 186:S31–8

32. Goodlin RC, Chapin JW: Determinants of maternal temperature during labor. Am J Obstet Gynecol 1982; 143:97–103

33. Hägerdal M, Morgan CW, Sumner AE, Gutsche BB: Minute ventilation and oxygen consumption during labor with epidural analgesia. ANESTHESIOLOGY 1983; 59:425–7

34. Marx GF, Loew DA: Tympanic temperature during labour and parturition. Br J Anaesth 1975; 47:600–2

35. Evron S, Ezri T, Protianov M, Muzikant G, Sadan O, Herman A, Szmuk P: The effects of remifentanil or acetaminophen with epidural ropivacaine on body temperature during labor. J Anesth 2008; 22:105–11

36. Negishi C, Lenhardt R, Ozaki M, Ettinger K, Bastanmehr H, Bjorksten AR, Sessler DI: Opioids inhibit febrile responses in humans, whereas epidural analgesia does not: An explanation for hyperthermia during epidural analgesia. ANESTHESIOLOGY 2001; 94:218–22

37. Goetzl L, Zighelboim I, Badell M, Rivers J, Mastrangèlo MA, Tweardy D, Suresh MS: Maternal corticosteroids to prevent intrauterine exposure to hyperthermia and inflammation: A randomized, double-blind, placebo-controlled trial. Am J Obstet Gynecol 2006; 195:1031–7

38. McGuire TR, Brusnahan SK, Bilek LD, Jackson JD, Kessinger MA, Berger AM, Garvin KL, O'Kane BJ, Tuljapurkar SR, Sharp JG: Inflammation associated with obesity: Relationship with blood and bone marrow endothelial cells. Obesity (Silver Spring) 2011; 19:2130–6

Cited By:

This article has been cited 1 time(s).

Clinics in Perinatology
The Association Between Epidural Labor Analgesia and Maternal Fever
Arendt, KW; Segal, BS
Clinics in Perinatology, 40(3): 385-+.
10.1016/j.clp.2013.06.002
CrossRef
Back to Top | Article Outline

© 2012 American Society of Anesthesiologists, Inc.

Publication of an advertisement in Anesthesiology Online does not constitute endorsement by the American Society of Anesthesiologists, Inc. or Lippincott Williams & Wilkins, Inc. of the product or service being advertised.
Login

Article Tools

Images

Share