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Article

Predicting Deep Body Temperature (Tb) from Forehead Skin Temperature: Tb or Not Tb?

1
Department of Automation, Biocybernetics and Robotics, Jozef Stefan Institute, Jamova 39, SI-1000 Ljubljana, Slovenia
2
International Postgraduate School Jozef Stefan, Jamova 39, SI-1000 Ljubljana, Slovenia
3
School of Sport, Health and Exercise Science, University of Portsmouth, Portsmouth PO1 2EF, UK
*
Author to whom correspondence should be addressed.
Sensors 2022, 22(3), 826; https://doi.org/10.3390/s22030826
Submission received: 22 December 2021 / Revised: 17 January 2022 / Accepted: 18 January 2022 / Published: 22 January 2022
(This article belongs to the Section Biomedical Sensors)

Abstract

:
There is a need to rapidly screen individuals for heat strain and fever using skin temperature (Tsk) as an index of deep body temperature (Tb). This study’s aim was to assess whether Tsk could serve as an accurate and valid index of Tb during a simulated heatwave. Seven participants maintained a continuous schedule over 9-days, in 3-day parts; pre-/post-HW (25.4 °C), simulated-HW (35.4 °C). Contact thermistors measured Tsk (Tforehead, Tfinger); radio pills measured gastrointestinal temperature (Tgi). Proximal-distal temperature gradients (ΔTforehead–finger) were also measured. Measurements were grouped into ambient conditions: 22, 25, and 35 °C. Tgi and Tforehead only displayed a significant relationship in 22 °C (r: 0.591; p < 0.001) and 25 °C (r: 0.408; p < 0.001) conditions. A linear regression of all conditions identified Tforehead and ΔTforehead–finger as significant predictors of Tgi (r2: 0.588; F: 125.771; p < 0.001), producing a root mean square error of 0.26 °C. Additional residual analysis identified Tforehead to be responsible for a plateau in Tgi prediction above 37 °C. Contact Tforehead was shown to be a statistically suitable indicator of Tgi in non-HW conditions; however, an error of ~1 °C makes this physiologically redundant. The measurement of multiple sites may improve Tb prediction, though it is still physiologically unsuitable, especially at higher ambient temperatures.

1. Introduction

Two principal methods have been proposed to predict deep body temperature (Tb) from the measurement of heat loss from the skin surface. One method measures the conductive heat loss pathway [1] and requires sensor contact with the skin surface. The second is a non-contact method, monitoring radiative heat loss with infrared thermography. Common to both methods are their inaccuracy in estimating absolute Tb. Mekjavic and Tipton [2] concluded the prediction of Tb from one skin region, namely the forehead, is inaccurate, resulting in false positives and negatives. They suggest that other facial sites, such as the inner canthus of the eye, may prove superior to forehead skin temperature (Tsk). They also recommend that Tsk gradients between proximal and distal sites, such as the forehead (proximal site) and fingertip (distal site), may provide an improvement in the prediction of Tb. Namely, the proximal–distal skin temperature gradient (ΔTskP-D) reflects perfusion of distal sites and may indicate whether the elevated temperature is due to heat strain or fever, the former causing peripheral vasodilatation, and the latter vasoconstriction.
Recently, the need to rapidly screen individuals using Tb prediction in industry has become more important for a number of reasons. Disregard for the control of greenhouse gases has resulted in global warming, with potentially devastating consequences for future generations. Among these consequences are summer heatwaves (HWs), originally infrequent and occurring only during the peak summer months, they are now increasing in frequency, magnitude, and duration [3]. In an industrial environment, HWs may affect the health and well-being of workers [4] and result in reduced labor productivity [5,6,7] as a result of occupational heat strain. It has been suggested that HWs may have a cumulative effect on workers, resulting in a residual effect several days after the ambient temperature returns to normal [5]. To try and mitigate the debilitating effects of HWs in the working environment, many countermeasures are available to reduce metabolic heat production and enhance heat loss, if only in the short term. The countermeasures include the availability of cold drinking water, cool and ventilated rooms during rest breaks, and cooling vests [7]. However, the possibility of monitoring workers for impending signs of heat strain, such as monitoring Tb, has largely been ignored; a system of reactive rather than preventative monitoring is more common.
Additionally, the recent pandemic of the Severe Acute Respiratory Syndrome Coronavirus 2 (SARs-CoV-2), resulting in a global coronavirus disease starting in 2019 (COVID-19), caused a lockdown of industrial activity during peaks of the COVID-19 waves in 2020. The manufacturing industry maintained some operations and has consequently taken the recommended precautions (i.e., masks, distancing, etc.) to safeguard the workforce. Some companies have implemented the monitoring of workers’ surface temperatures using infrared thermography (IRT) to estimate Tb. Those identified by the scanners as having elevated body temperature, for whatever reason, are not allowed entry.
In view of increasing reliance on the prediction of Tb from Tsk, the present study evaluated whether contact measurements of Tsk can provide a suitable surrogate for direct measurement of Tb; for the purpose of screening workers for SARs-CoV-2 virus infection and impending heat strain during summer HW. It was hypothesized that Tsk would produce a significant association with Tb, but measurement of more sites to generate a ΔTskP-D will produce a stronger association, as hypothesized by Mekjavic and Tipton [2].

2. Materials and Methods

This study was part of a program of research conducted within the framework of the European Commission Heat Shield project, investigating the effect of HWs on the health, well-being, and labour productivity of workers in five key European industries (manufacturing, agriculture, construction, logistics, tourism). During four previous HWs, conditions within an industrial manufacturing plant employing 1500 workers (odelo d.o.o., Prebold, Slovenia) were monitored [5]. Due to the difficulty of continuous 24-h physiological monitoring of workers during a HW, a study was conducted simulating the industrial process in controlled laboratory conditions [8], using data from the HWs measured in central Slovenia. Consequently, measurements of Tsk and Tb were conducted hourly throughout a 9-day study, including both normothermic and simulated HW conditions, to assess the association with Tb using indirect measurements.

2.1. Participants

A sample size of seven participants was deemed to provide sufficient power to detect a statistical significance, assuming an α of 0.001 and β of 0.99 (G*Power Version 3.1.9.6, Bonn, Germany) using an effect size of effect size (d) of 1.8834 (f = 0.9417), based on the results of a previous study [8,9]. Seven young, healthy males (mean (SD); age: 21.1 (1.1) years; body stature: 180 (6.1) cm; body mass: 81.5 (15.6) kg; body mass index: 25.1 (4.4) kg·m2) participated in the study, which had received prior approval (Approval no. 0120-402/2020/4: 20 October 2020) by the Committee for Medical Ethics at the Ministry of Health (Republic of Slovenia). All were non-smokers, engaged in regular physical activity recreationally, and were free from known cardiovascular, respiratory, and autonomic disease. Prior to the commencement of the study, the participants were informed of the details of the experimental protocol and were familiarized with the procedures, before signing an informed consent agreement. The participants were aware that they could terminate participation in the study at any time during the 10-day duration.

2.2. Protocol

The study was conducted at the PlanHab facility (European Space Agency ground-based research facility) at the Olympic Sports Centre Planica (Rateče, Slovenia). Participants were confined to the facility for 9-days and had access to their rooms, a common area, laboratory, and dining area. They were provided with three meals and two snacks each day (breakfast, lunch, afternoon snack, dinner, evening snack) and could drink water ad libitum.
On arrival at the facility, the participants were acquainted with the entire facility and were familiarized with all the experimental procedures. They were instructed to refrain from venturing outside the designated areas of the facility, as the temperature and humidity were regulated only in the designated areas, using heaters controlled by temperature regulators. Ambient humidity within the laboratory remained constant at ~45%. The protocol was designed to mimic the routine daily activities in a manufacturing plant, as well as some of the activities at home. Participants were awakened each day at 0700 hrs. After breakfast, they entered the laboratory at 0840 hrs, which was arranged as a series of workstations equipped with personal computers. The work shift lasted until 1800 with breaks for snacks and lunch. Upon completion of the work shift, participants had dinner and then retired to their common area or individual rooms. Lights out was at 2300 hrs. This was the daily routine for nine consecutive days.
During the 9-day confinement, the temperatures within the living quarters and workplace (i.e., laboratory) were regulated, as displayed in Table 1. The first 3 days (pre-HW) represented normal conditions. The simulated HW was initiated at midnight at the end of day 3, with temperatures increasing in all areas. At midnight on day 6, the night-time/daytime temperature profile was re-adjusted to the same profile as in the first 3 days (post-HW). Experiments took place in ambient conditions of a 19.8 ± 1.8 Wet-Bulb Globe Temperature (from www.wunderground.com; accessed on 14 January 2022).

2.3. Measurements

Each morning the participants ingested a calibrated telemetric radio pill (Body Cap, Caen, France), a thermistor was secured to their forehead (Tforehead), and a distal phalanx pad was attached to the middle finger (Tfinger) (iButton, Type DS1921H, Maxim/Dallas Semiconductor Corp., Dallas, TX, USA). These devices provided continuous measurement of gastrointestinal temperature (Tgi) and Tsk, respectively, on each day. Validation of the calibrated telemetric radio pill against rectal thermistor during rest, water immersion, and steady-state exercise revealed no significant differences; furthermore, the system produces effective validity and test-retest reliability [10,11]. Additionally, the validation of iButton thermistors against calibrated thermocouples revealed no significant difference during steady-state, though response time to changes in temperature was slower than thermocouples [12].

2.4. Analyses

Tgi and Tsk were measured continuously, and an average of the last 10 min was taken in each hour for 23-h, every day. This averaging period was chosen to avoid potential artefacts by using a stable 10-min period. Each day, telemetric pills were ingested at 0700 hrs, immediately after waking up, and Tsk iButtons were attached to the skin in the evening at 2230 hrs. Temperature measurements were recorded during three distinct ambient conditions: 22 °C, 25 °C, and 35 °C. ΔTskP-D, an index of blood flow [13], was calculated between the forehead and fingertip (ΔTforehead–finger). When measured at the forearm–finger or calf–toe, a value ≥2 °C represents vasoconstriction and ≤0 °C represents vasodilation [14,15]. In the present study, in which the ΔTskP-D was assessed from Tsk at the forehead and fingertip, the thresholds for vasoconstriction and vasodilatation may likely be dissimilar to those reported by previous studies using the forearm–fingertip skin temperature gradient as an index of perfusion. Holm, et al. [16] have previously investigated the use of the forehead–fingertip skin temperature gradient as an index of mortality in hospital patients.
Means, standard deviations, and coefficient of variation (CoV) were calculated for Tgi, Tforehead, and Tfinger (Table 2).
The data, following calculation of normality by a Shapiro–Wilk test, were assessed using either a Pearson’s Correlation Coefficient or a Spearman’s Rank Correlation Coefficient. Additionally, a multiple linear regression using Tforehead, Tfinger and ΔTforehead-finger was conducted. All statistical tests were completed using an alpha value of p < 0.05 and conducted using IBM SPSS Statistics (Version 26, Armonk, NY, USA).
In addition to the multiple linear regression, root mean square error (RMSE) was also calculated between measured Tgi and predicted Tgi as produced from a regression equation, using the following equation [17]:
RMSE = [ i = 1 N ( Z f ( i ) Z O ( i ) ) 2 N ] 1 / 2
where,
Zf = forecast value
Zo = observed value
N = sample size

3. Results

All participants completed the 9-day confinement. There were no untoward effects of the 3-day HW. The physiological responses and labor productivity during the simulated normal weather and HW periods have been presented elsewhere [8].

3.1. Relationship between Tsk and Tgi

To assess the true relationship between Tforehead and Tgi, measurements from every day were compared simultaneously, encompassing all ambient conditions. The range of temperatures observed was greater for Tforehead (32.2–36 °C) than for Tgi (36.1–37.7 °C), whereas the average temperature of all measurements was higher for Tgi (Tgi: 36.9 ± 0.4 °C; Tforehead: 33.9 ± 1.4 °C), a significant difference (p < 0.001). A significant relationship was identified between the measurements of Tforehead and Tgi (r = 0.653; p < 0.001).

3.2. Tsk and Tgi at Different Ambient Temperatures (HW vs. Non-HW)

The above correlation analysis of the relationship between Tforehead and Tgi was repeated for the individual HW (35 °C) and non-HW (22 °C and 25 °C) ambient temperatures, as shown in Figure 1. A significant relationship was observed for the 22 °C (r = 0.591; p < 0.001) and 25 °C (r = 0.408; p < 0.001) ambient conditions, whereas there was no significant relationship at 35 °C (r = 0.263; p < 0.185). Table 2 displays mean (SD) Tsk and Tgi values measured in each ambient condition.

3.3. Proximal-Distal Temperature Gradient Prediction

Mekjavic and Tipton [2] suggest that an index derived from measurements made at multiple sites might provide a more accurate temperature screening, primarily using areas where the skin is exposed (i.e., face and hands). When creating a TskP-D between the forehead and fingertip (ΔTforehead–finger), the correlation between this variable and Tgi was significant (r = 0.637; p < 0.001). Additionally, a multiple linear regression for prediction of Tgi using Tforehead, Tfinger, and ΔTforehead–finger produced a significant linear model using Tforehead and ΔTforehead–finger only (r2 = 0.588; F: 125.771; p < 0.001):
Predicted   T gi = 29.349 + ( 0.225 × T forehead ) + ( 0.154 × T forehead finger )  
This linear regression model describes a suitable fit between the measured and predicted values of Tgi. RMSE analysis of this regression equation established an error of 0.26 °C between the actual and predicted Tgi. Figure 2 displays the correlation between the measured and predicted Tgi, which exhibits a plateau at higher measured Tgi. A second-order polynomial trendline was chosen (solid line in Figure 2) to best represent the associated fit of the correlation (r2 = 0.63).

4. Discussion

Screening workers for elevated Tb has become of particular importance with the prevalence of two major global maladies, global warming and the COVID-19 pandemic. Both of which cause dangerous elevations in Tb and have potentially serious, if not fatal, consequences. Presently, workers in the industry are being screened primarily for elevations in Tb arising from a viral infection. However, in the future, any such valid methodology has the potential to be used for monitoring workers for heat strain, particularly during episodes of summer HWs. The assessment of the currently used approach for screening for elevated Tb was the aim of the present study. The principal finding was that neither single skin sites (i.e., hand, forehead), nor the TskP-D in combination with Tforehead, were able to provide a physiologically accurate index of Tb (i.e., gastrointestinal temperature). The methodological approach of predicting Tb from Tforehead is therefore not valid.

4.1. Prediction of Tb Using Measurements of Tforehead and ∆Tforehead–fingertip

The statistical analysis in Section 3.1 revealed a significant correlation between the Tforehead and Tgi, but the association with absolute Tb on this basis may vary by as much as 2 °C. Therefore, based on statistical analysis, Tforehead appears to be a suitable index of Tb, however, this correlation is of limited physiological relevance as it may generate false positive/negative values. Of particular concern is the fact that the correlation becomes statistically non-significant during simulated HW conditions, conditions where an accurate prediction in an industrial setting would be required. The present study used contact thermometry to measure skin temperature, the method of choice in industry being Tforehead, obtained with infrared thermography (IRT). Using this technology, the measurement of surface Tsk may be adequate; however, as demonstrated by the results of the present study, the subsequent derivation of Tgi from the measurement of Tsk at one site, the preferred site being the forehead, is not physiologically valid.
The recent proposal of Mekjavic and Tipton [2], which suggests additional sites to that of the forehead alone might provide a better outcome in the prediction of Tgi, was also evaluated by conducting a linear regression to calculate Tgi with the proximal-distal skin temperature gradient (ΔTforehead–finger), and skin temperatures. This regression proved statistically significant, resulting in smaller errors in the predictions of Tb. Furthermore, a polynomial curve fit the relationship between measured and predicted Tgi identified a plateau at higher levels of predicted Tgi (Figure 2). This suggests that the association appears to be accurate at lower temperatures; however, it begins to underestimate Tb as Tgi increases. Residual analysis of independent variables in the regression equation identifies Tforehead as a contributor to this plateau due to increased variability and thus error at higher ambient temperatures. Additionally, whilst the average Tgi in the HW conditions was 37.3 °C, Tforehead only reached 35.5 °C, which means it was incapable of linearly matching rises in Tgi during higher ambient conditions. The combination of these two sources of error likely caused the plateau in the relationship between measured and predicted Tgi, making it unsuitable to use Tforehead as a prediction tool. It should also be emphasized that the industrial tasks simulated in the present study were that of checking the functioning of circuit boards; thus, a seated task. Any method for predicting heat strain in an industrial environment will need to be validated with tasks requiring elevated endogenous heat production, further increasing Tgi above Tforehead.
The ΔTskP-D between the forearm and fingertip has been demonstrated as an appropriate index of the perfusion of the fingers [13,14,15]. During exposure to a hot environment, as in the present study, a high distal (fingertip) Tsk would reflect vasodilatation, thus activation of the thermoregulatory heat loss mechanism. We hypothesized that if Tforehead was a valid surrogate of Tb, when combined with an index of peripheral perfusion, such as ΔTskP-D, this could provide an index of heat strain. However, unlike Tgi, Tforehead varied with ambient temperature, such that the observed variations in Tgi of ±1.5 °C, were accompanied by variations in Tforehead of ±3.8 °C, casting doubt on the validity of Tforehead as a valid surrogate measurement of Tb. Nevertheless, the ΔTforehead–finger alone displayed a significant relationship with Tgi. Furthermore, a multiple regression combining ΔTskP-D with Tforehead generated a regression equation, with an improved association with Tgi. The physiological validity of the derived regression model should be evaluated with a separate group of female and male subjects, of different ages, under conditions of elevated ambient temperatures, as would be experienced in the industry and during HWs.

4.2. Effect of Ambient Temperature on the Relation between Tsk and Tb

Mass screening of workers for elevated Tgi in an industrial setting may help to protect against heat stress or avoid the spread of viral disease. The ambient temperatures at which these measurements are taken may vary depending on the location of the measurement (indoor vs. outdoor), time of day (day shift vs. night shift), weather, and season. The large variation in Tsk, with little change in Tgi, is of concern with regard to the association of Tb with Tsk. In the present study, measurements taken in normal temperature (22 and 25 °C) ambient conditions provide a statistically significant relationship with Tgi, whereas measurements conducted during simulated HW (35 °C) conditions provided no statistically significant relationship. In the present study, increases in Tb were the result of high ambient temperatures. In contrast, a febrile temperature is the result of elevated endogenous heat production combined with decreased heat loss (vasoconstriction). Any method proclaiming to be able to predict Tb of active and/or febrile individuals regardless of the ambient temperature should be appropriately validated. Manufacturers of currently available scanners based on IRT technology do not provide the algorithms used to predict Tb based on Tforehead, nor do they provide any information regarding the validation of such algorithms. Due to the proven global importance of screening individuals for elevated Tb, it should only be a matter of time before this is regulated.

4.3. Accuracy of IRT to Contact Thermography

The aim of the present study was to assess the association of Tsk with Tb using contact thermography and not to validate IRT as a method for predicting Tb. However, IRT is the most commonly used method of measuring skin temperature in applied settings such as workplaces and hospitals, and its validity and accuracy should be considered in future Tsk predictions. The validity of IRT as a measurement of Tsk has been heavily debated, particularly with reference to its overestimation and comparison to a ‘gold standard’ of Tsk measurement. Maley et al. [18] propose that during hand rewarming, following cold water immersion, IRT overestimates Tsk measured by contact thermometry by 1.80 °C. However, this was countered by Havenith and Lloyd [19], who suggest that methodological issues such as camera accuracy and calibration commonly occur, and that contact thermometry cannot be considered a ‘gold standard’.
Any system for mass screening of workers based on the prediction of body temperature from forehead Tsk derived with IRT would need to utilize an infrared camera of high accuracy as differences occur commonly. Ng et al. [20] reported significant differences among the three infrared scanners used to measure Tforehead. The differences among these scanners were as high as ±2 °C. Such discrepancies among infrared cameras are also reflected in their ability to accurately measure Tsk when compared to contact thermography. Although a strong correlation between contact thermometry and non-contact IRT thermography has been reported [18,21], the authors reported that Tsk measured with IRT was 2.3 °C lower than that measured with a thermistor [21]. The above comparisons were made during a sleep study [21] and at rest [18]. During dynamic movement and exercise, as would be anticipated in an industrial setting, the agreement between contact and IRT measurements of Tsk is poor [22,23]. Irrespective of the validity achieved by IRT, the type of device specifications stipulated by the ‘Journal Temperature Toolbox’ [24], may be too stringent and impractical for many workplaces.

4.4. Prediction of Deep Body Temperature

Infrared scanners providing a predicted value of Tb based on a measurement of Tsk at a single site do so using proprietary algorithms, which are not available for scrutiny. This is unsatisfactory and unacceptable considering the impact elevated body temperature, whether due to viral infection or summer HW, has had not only on the industry but all aspects of our lives globally. The present study illustrates the errors in the association of Tb with Tsk that occur under controlled laboratory conditions, in which the measurements were conducted by trained individuals. It also emphasizes the need to discern between statistical and physiological significance. As an example, the correlation between Tforehead and Tgi (Figure 1) may be statistically significant, indicating that an increase in one variable is observed as an increase in the other; this relation does not, however, provide an accurate assessment of Tb. Alternatively, using a regression equation of multiple measurement sites provided a significant prediction of Tgi, the physiological significance of which is made clear using RMSE. This analysis of the regression equation proposes that the error between actual and predicted Tgi is as low as 0.3 °C, enabling more accurate extrapolation of Tgi from Tsk to occur. For measurements of Tb, the difference in values at one site could be the difference between a healthy temperature and heat strain or fever. It is most likely that future strategies of predicting Tb from exposed Tsk may need to incorporate several sites, and not just one, as suggested by Mekjavic and Tipton [2], as demonstrated in the present study for assessment of heat strain in workers during HW.

4.5. Limitations

As detailed above, differences lie in the mechanisms relating to changes in Tb, leading to differential heating and perfusion responses during either ambient heating or fever. The present study produced an equation for the prediction of Tb using several sites when participants were experiencing ambient heating at rest. Additional testing should consider the Tsk and Tb responses to the unique aspects of fever and exercise as methods of heating the human body. In addition, the participants in the present study, young, healthy males, did not appear to experience undue heat strain based on their Tgi. Though these participants were exposed to the conditions of a previously recorded HW [5], suggesting other non-thermal factors such as morphology, gender, acclimation, etc., should be considered in the prediction algorithm produced. Due to the relatively small and homogenous sample, the results of the present study should only be used as an example of the type of error associated with Tsk prediction. Finally, while the study design reflected certain applied conditions such as working schedules and tasks, the external validity should be cautioned and additional research with larger sample sizes in applied conditions advised.

5. Conclusions

Measurement of contact Tsk at the forehead appears to be a suitable site from which Tgi can be extrapolated at lower ambient temperatures. However, while statistically significant, this relationship cannot be considered physiologically appropriate due to an error of ~1 °C. The measurement of multiple sites, including a proximal-distal temperature gradient, may provide a more suitable prediction of Tb with a lower error (0.3 °C), however again this is not appropriate due to a plateauing of the prediction efficacy at higher temperatures, likely due to lower and more variable Tsk measurements. The methodological approach of predicting Tb from Tsk is therefore not physiologically valid in young males, particularly in higher ambient temperatures. In the future, indirect Tsk measurements should consider the effect of ambient temperature, the use of multiple sites, inclusion of a perfusion index, and the source of raised Tb, in their algorithms.

Author Contributions

Conceptualization, I.B.M. and M.J.T.; methodology, J.T.F., L.G.I. and I.B.M.; formal analysis, J.T.F.; investigation, J.T.F., U.C. and L.G.I.; resources, L.G.I. and I.B.M.; data curation, J.T.F., U.C. and L.G.I.; writing—original draft preparation, J.T.F.; writing—review and editing, J.T.F., U.C., M.J.T., L.G.I. and I.B.M.; visualization, J.T.F.; supervision, I.B.M.; project administration, L.G.I., I.B.M.; funding acquisition, U.C., I.B.M. All authors have read and agreed to the published version of the manuscript.

Funding

The study has received funding from the European Union’s Horizon 2020 Research and Innovation program (Contract number 668786). Jason Fisher is recipient of a Slovene Research Agency Young Investigator Scholarship (PR-10488).

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki and approved by the Ethics Committee of the Committee for Medical Ethics at the Ministry of Health (Republic of Slovenia) (Approval no. 0120-402/2020/4: 20 October 2020).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

Data available on request.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Gunga, H.-C.; Sandsund, M.; Reinertsen, R.E.; Sattler, F.; Koch, J. A non-invasive device to continuously determine heat strain in humans. J. Therm. Biol. 2008, 33, 297–307. [Google Scholar] [CrossRef]
  2. Mekjavic, I.B.; Tipton, M.J. Myths and methodologies: Degrees of freedom—Limitations of infrared thermographic screening for Covid-19 and other infections. Exp. Physiol. 2021. [Google Scholar] [CrossRef] [PubMed]
  3. Pogačar, T.; Casanueva, A.; Kozjek, K.; Ciuha, U.; Mekjavić, I.B.; Bogataj, L.K.; Črepinšek, Z. The effect of hot days on occupational heat stress in the manufacturing industry: Implications for workers’ well-being and productivity. Int. J. Biometeorol. 2018, 62, 1251–1264. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Kjellstrom, T.; Kovats, R.S.; Lloyd, S.J.; Holt, T.; Tol, R.S. The direct impact of climate change on regional labor productivity. Arch. Environ. Occup. Health 2009, 64, 217–227. [Google Scholar] [CrossRef]
  5. Ciuha, U.; Pogačar, T.; Bogataj, L.K.; Gliha, M.; Nybo, L.; Flouris, A.D.; Mekjavic, I.B. Interaction between indoor occupational heat stress and environmental temperature elevations during heat waves. Weather. Clim. Soc. 2019, 11, 755–762. [Google Scholar] [CrossRef] [Green Version]
  6. Flouris, A.D.; Dinas, P.C.; Ioannou, L.G.; Nybo, L.; Havenith, G.; Kenny, G.P.; Kjellstrom, T. Workers’ health and productivity under occupational heat strain: A systematic review and meta-analysis. Lancet Planet. Health 2018, 2, e521–e531. [Google Scholar] [CrossRef] [Green Version]
  7. Ioannou, L.G.; Mantzios, K.; Tsoutsoubi, L.; Nintou, E.; Vliora, M.; Gkiata, P.; Dallas, C.N.; Gkikas, G.; Agaliotis, G.; Sfakianakis, K. Occupational heat stress: Multi-country observations and interventions. Int. J. Environ. Res. Public Health 2021, 18, 6303. [Google Scholar] [CrossRef]
  8. Ioannou, L.G.; Mantzios, K.; Tsoutsoubi, L.; Panagiotaki, Z.; Kapnia, A.K.; Ciuha, U.; Nybo, L.; Flouris, A.D.; Mekjavic, I.B. Effect of a simulated heat wave on physiological strain and labour productivity. Int. J. Environ. Res. Public Health 2021, 18, 3011. [Google Scholar] [CrossRef]
  9. Ioannou, L.G.; Tsoutsoubi, L.; Samoutis, G.; Bogataj, L.K.; Kenny, G.P.; Nybo, L.; Kjellstrom, T.; Flouris, A.D. Time-motion analysis as a novel approach for evaluating the impact of environmental heat exposure on labor loss in agriculture workers. Temperature 2017, 4, 330–340. [Google Scholar] [CrossRef]
  10. Bongers, C.C.; Daanen, H.A.; Bogerd, C.P.; Hopman, M.T.; Eijsvogels, T.M. Validity, Reliability, and Inertia of Four Different Temperature Capsule Systems. Med. Sci. Sports Exerc. 2017, 50, 169–175. [Google Scholar] [CrossRef]
  11. Travers, G.J.; Nichols, D.S.; Farooq, A.; Racinais, S.; Périard, J.D. Validation of an ingestible temperature data logging and telemetry system during exercise in the heat. Temperature 2016, 3, 208–219. [Google Scholar] [CrossRef] [PubMed]
  12. van Marken Lichtenbelt, W.D.; Daanen, H.A.; Wouters, L.; Fronczek, R.; Raymann, R.J.; Severens, N.M.; Van Someren, E.J. Evaluation of wireless determination of skin temperature using iButtons. Physiol. Behav. 2006, 88, 489–497. [Google Scholar] [CrossRef]
  13. Rubinstein, E.H.; Sessler, D.I. Skin-surface temperature gradients correlate with fingertip blood flow in humans. Anesthesiology 1990, 73, 541–545. [Google Scholar] [CrossRef] [PubMed]
  14. House, J.R.; Tipton, M.J. Using skin temperature gradients or skin heat flux measurements to determine thresholds of vasoconstriction and vasodilatation. Eur. J. Appl. Physiol. 2002, 88, 141–145. [Google Scholar] [CrossRef]
  15. Keramidas, M.E.; Geladas, N.D.; Mekjavic, I.B.; Kounalakis, S.N. Forearm–finger skin temperature gradient as an index of cutaneous perfusion during steady-state exercise. Clin. Physiol. Funct. Imaging 2013, 33, 400–404. [Google Scholar] [CrossRef]
  16. Holm, J.K.; Kellett, J.G.; Jensen, N.H.; Hansen, S.N.; Jensen, K.; Brabrand, M. Prognostic value of infrared thermography in an emergency department. Eur. J. Emerg. Med. 2018, 25, 204–208. [Google Scholar] [CrossRef]
  17. Barnston, A.G. Correspondence among the correlation, RMSE, and Heidke forecast verification measures; refinement of the Heidke score. Weather. Forecast. 1992, 7, 699–709. [Google Scholar] [CrossRef] [Green Version]
  18. Maley, M.J.; Hunt, A.P.; Bach, A.J.; Eglin, C.M.; Costello, J.T. Infrared cameras overestimate skin temperature during rewarming from cold exposure. J. Therm. Biol. 2020, 91, 102614. [Google Scholar] [CrossRef] [PubMed]
  19. Havenith, G.; Lloyd, A.B. Counterpoint to “Infrared cameras overestimate skin temperature during rewarming from cold exposure”. J. Therm. Biol. 2020, 92, 102663. [Google Scholar] [CrossRef]
  20. Ng, D.K.-k.; Chan, C.-h.; Chan, E.Y.-t.; Kwok, K.-l.; Chow, P.-y.; Lau, W.-F.; Ho, J.C.-S. A brief report on the normal range of forehead temperature as determined by noncontact, handheld, infrared thermometer. Am. J. Infect. Control 2005, 33, 227–229. [Google Scholar] [CrossRef]
  21. van den Heuvel, C.J.; Ferguson, S.A.; Dawson, D.; Gilbert, S.S. Comparison of digital infrared thermal imaging (DITI) with contact thermometry: Pilot data from a sleep research laboratory. Physiol. Meas. 2003, 24, 717. [Google Scholar] [CrossRef] [PubMed]
  22. de Andrade Fernandes, A.; dos Santos Amorim, P.R.; Brito, C.J.; de Moura, A.G.; Moreira, D.G.; Costa, C.M.A.; Sillero-Quintana, M.; Marins, J.C.B. Measuring skin temperature before, during and after exercise: A comparison of thermocouples and infrared thermography. Physiol. Meas. 2014, 35, 189. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. James, C.; Richardson, A.; Watt, P.; Maxwell, N. Reliability and validity of skin temperature measurement by telemetry thermistors and a thermal camera during exercise in the heat. J. Therm. Biol. 2014, 45, 141–149. [Google Scholar] [CrossRef] [Green Version]
  24. Foster, J.; Lloyd, A.B.; Havenith, G. Non-contact infrared assessment of human body temperature: The journal Temperature toolbox. Temperature 2021, 8, 306–319. [Google Scholar] [CrossRef] [PubMed]
Figure 1. The relation between the temperature of the gastrointestinal tract measured with a radio pill (Tgi) and the temperature of the forehead using a contact thermistor (Tforehead). Measurements were obtained while participants were exposed to three ambient temperatures: 22 °C (upper panel), 25 °C (middle panel), and 35 °C (lower panel). Regression lines with associated 95% confidence bands for each temperature are also shown.
Figure 1. The relation between the temperature of the gastrointestinal tract measured with a radio pill (Tgi) and the temperature of the forehead using a contact thermistor (Tforehead). Measurements were obtained while participants were exposed to three ambient temperatures: 22 °C (upper panel), 25 °C (middle panel), and 35 °C (lower panel). Regression lines with associated 95% confidence bands for each temperature are also shown.
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Figure 2. Relationship between measured temperature of the gastrointestinal tract (Tgi) and predicted Tgi using Equation (1). Measurements and predictions based on skin temperatures were obtained while participants were exposed to three ambient temperatures: 22 °C (white dots), 25 °C (grey dots), and 35 °C (black dots). A second-order polynomial trendline (y = −0.4464x2 + 33.512x − 591.75) represents the best fit (r2 = 0.63).
Figure 2. Relationship between measured temperature of the gastrointestinal tract (Tgi) and predicted Tgi using Equation (1). Measurements and predictions based on skin temperatures were obtained while participants were exposed to three ambient temperatures: 22 °C (white dots), 25 °C (grey dots), and 35 °C (black dots). A second-order polynomial trendline (y = −0.4464x2 + 33.512x − 591.75) represents the best fit (r2 = 0.63).
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Table 1. Temperature during daily work and rest periods. Temperature is presented as a mean (SD) of each 3-day testing condition.
Table 1. Temperature during daily work and rest periods. Temperature is presented as a mean (SD) of each 3-day testing condition.
Work (0840–1800 hrs)Rest/Sleep (1800–0840 hrs)
Temperature (°C)Temperature (°C)
Pre-HW25.4 (0.3)22.3 (0.5)
HW35.5 (0.3)26.3 (0.8)
Post-HW25.5 (0.7)23.1 (0.7)
HW: Heatwave. Pre-HW: Testing days 1–3. HW: Testing days 4–6. Post-HW: Testing days 7–9.
Table 2. Mean (±SD), and coefficient of variation (CoV) of Tsk and Tgi measurements at each ambient condition.
Table 2. Mean (±SD), and coefficient of variation (CoV) of Tsk and Tgi measurements at each ambient condition.
Ambient ConditionMeasurementMean (SD)CoV (%)
22 °CTgi36.7 (0.4)1.2
Tforehead34.2 (1.4)4.1
Tfinger33.2 (0.5)1.5
25 °CTgi37.0 (0.4)1.0
Tforehead33.9 (1.3)3.7
Tfinger33.8 (0.5)1.4
35 °CTgi37.3 ± 0.20.6
Tforehead35.9 ± 0.71.9
Tfinger35.5 ± 0.61.7
Tgi: gastrointestinal temperature. Tforehead: forehead temperature. Tfingertip: fingertip temperature.
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Fisher, J.T.; Ciuha, U.; Tipton, M.J.; Ioannou, L.G.; Mekjavic, I.B. Predicting Deep Body Temperature (Tb) from Forehead Skin Temperature: Tb or Not Tb? Sensors 2022, 22, 826. https://doi.org/10.3390/s22030826

AMA Style

Fisher JT, Ciuha U, Tipton MJ, Ioannou LG, Mekjavic IB. Predicting Deep Body Temperature (Tb) from Forehead Skin Temperature: Tb or Not Tb? Sensors. 2022; 22(3):826. https://doi.org/10.3390/s22030826

Chicago/Turabian Style

Fisher, Jason T., Urša Ciuha, Michael J. Tipton, Leonidas G. Ioannou, and Igor B. Mekjavic. 2022. "Predicting Deep Body Temperature (Tb) from Forehead Skin Temperature: Tb or Not Tb?" Sensors 22, no. 3: 826. https://doi.org/10.3390/s22030826

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