JOURNAL HOME CME HOME THIS MONTH PAST ISSUES ETOC COLLECTIONS
AUTHORS REVIEWERS EDITORIAL BOARD FEEDBACK RSS HELP
A&A International Anesthesia Research Society
QUICK SEARCH:   [advanced]


     

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a colleague
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (2)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Crandall, C. G.
Right arrow Articles by Dellaria, S. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Crandall, C. G.
Right arrow Articles by Dellaria, S. M.
Related Collections
Right arrow Surgery
Right arrow Pharmacology

Anesth Analg 2005;100:277-283
© 2005 International Anesthesia Research Society
doi: 10.1213/01.ANE.0000139359.46635.2D

GENERAL ARTICLES

Palmar Skin Blood Flow and Temperature Responses Throughout Endoscopic Sympathectomy

Craig G. Crandall, PhD*,{dagger}, Dan M. Meyer, MD{ddagger}, Scott L. Davis, PhD*,{dagger}, and Suzanne M. Dellaria, MD§

*Institute for Exercise and Environmental Medicine, Presbyterian Hospital of Dallas, Texas; and Departments of {dagger}Internal Medicine, {ddagger}Cardiothoracic Surgery, and §Anesthesiology and Pain Management, University of Texas Southwestern Medical Center at Dallas, Texas

Address correspondence and reprint requests to Craig G. Crandall, PhD, Institute for Exercise and Environmental Medicine, Presbyterian Hospital of Dallas, 7232 Greenville Ave., Dallas, TX 75231. Address e-mail to craigcrandall{at}texashealth.org


   Abstract
Top
 Abstract
Introduction
 Methods
 Results
 Discussion
 References
 
Thoracic surgical sympathectomy is often performed to treat primary palmar and axillary hyperhidrosis. An increase in palmar skin temperature is frequently used to identify the success of the procedure. Because changes in palmar skin temperature occur secondary to changes in skin blood flow, the objective of this study was to test the hypothesis that monitoring palmar skin blood flow would provide greater temporal resolution relative to monitoring palmar skin temperature. In 11 patients with palmar and/or axillary hyperhidrosis, we measured palmar skin temperature and blood flow (via laser Doppler flowmetry) throughout the sympathectomy procedure. Five minutes after the initial cautery, skin blood flow increased from 48 ± 7 perfusion units to 121 ± 17 perfusion units (P < 0.001), whereas no significant change in temperature was observed (31.0°C ± 0.5°C to 31.3°C ± 0.5°C; P > 0.05). The time required to reach peak skin blood flow (22 ± 3 min) was significantly less than the time required to reach peak skin temperature (34 ± 0.3 min; P < 0.001). Finally at 5, 10, and 15 min after the initial cautery, skin blood flow increased to a larger percentage of the total increase in skin blood flow relative skin temperature (all P < 0.006). These data suggest that monitoring skin blood flow provides greater temporal resolution when compared with monitoring skin temperature during thoracic sympathectomy. However, the initial cautery of the parietal pleura over the ganglion may result in increases in skin blood flow before physical disruption of the ganglion. This occurrence may limit the utility of skin blood-flow measurements in identifying the success of the procedure.

IMPLICATIONS: Thoracic surgical sympathectomy is a common procedure to treat hyperhidrosis. This study revealed that palmar skin blood flow increased during cautery of the parietal pleura before the disruption of the ganglion. This observation may limit the utility skin blood-flow responses for confirming a successful sympathectomy.


   Introduction
Top
 Abstract
 Introduction
Methods
 Results
 Discussion
 References
 
Primary palmar hyperhidrosis is a common disorder characterized by profuse sweating of the palms. This condition has been reported to affect 0.6% to 1% of the Israeli population (1), and a recent report suggests a similar prevalence in the United States (2). Depending on the severity of the condition, palmar hyperhidrosis can be physically and emotionally debilitating in professional and social settings. A number of noninvasive or minimally invasive treatments are available for this condition, such as topical administration of aluminum chloride creams, water iontophoresis and, more recently, botulinum toxin injections (3). However, each of these treatments requires repeated application throughout the individual’s life, often with limited effectiveness. For this reason, many individuals seek a permanent surgical solution of upper thoracic sympathectomy or sympathotomy to eliminate the effects of this condition and axillary hyperhidrosis (4–9). For treatment of these conditions, surgical disruption (i.e., resection, clipping, or disconnection via electrocautery) of the second and/or third thoracic ganglia is the most common procedure performed.

A number of intraoperative techniques for identification of a successful sympathectomy have been used. The most common technique is monitoring palmar temperature (6,10–14). The literature reports a wide range of increases in palmar skin temperature (0.4°C to 10°C) that are observed with a successful sympathectomy (4,6,11,14). The width of this range may be related to relatively slow changes in palmar temperature upon disruption of the ganglion, the time at which the investigator obtained the final reading, or an influence of the surgical suite temperature on palmar temperature. It is interesting that in a few cases successful sympathectomies were performed with inconsistent changes in palmar skin temperature (10).

Increases in palmar skin temperature during the surgical procedure occur secondary to increases in skin blood flow. In humans, neural modulation of blood flow to the glabrous skin of the palm is controlled solely by a sympathetic vasoconstrictor system, whereas neural control of nonglabrous skin is governed by a sympathetic vasoconstrictor system and a separate active vasodilator system (15–18). Upon neural disruption of glabrous skin during thoracic sympathectomy, large increases in skin blood flow have been reported (5,6,10,19). However, those studies limited their assessment of skin blood-flow responses to pre- and postsurgical periods. Therefore, little is known about the dynamic characteristics of skin blood flow, and how it relates to skin temperature, during the surgical procedure. Thus, the purpose of this study was to assess the utility of measuring intraoperative skin blood flow and to test the hypothesis that increases in palmar skin blood flow will precede increases in palmar skin temperature upon successful disruption of the ganglion. Such an outcome may demonstrate the usefulness, and perhaps the superiority, of intraoperative monitoring of skin blood flow over skin temperature during surgical sympathectomy for hyperhidrosis.


   Methods
Top
 Abstract
 Introduction
 Methods
Results
 Discussion
 References
 
This study received approval from the IRB committees at both Presbyterian Hospital of Dallas and the University of Texas Southwestern Medical Center. The study design and associated risks of participation were explained to each subject, and each subject signed an approved consent form.

Eleven healthy subjects (four men and seven women; ASA class I) participated in this study. The average age of the subjects was 27 ± 3 yr, and they were of normal weight (77 ± 5 kg) and height (169 ± 4 cm). Ten subjects exhibited clinical manifestations of palmar and/or axillary hyperhidrosis, and one subject sought treatment for pronounced facial blushing and hyperhidrosis.

A peripheral IV catheter was placed, and 1–2 mg of midazolam was administered for sedation. The patient was transported to the operating room, where standard monitors were used, including a five-lead electrocardiogram, pulse oximetry, and automated oscillometry. The induction of general anesthesia was accomplished with 1 µg/kg fentanyl and 1.5 mg/kg propofol followed by 0.6 mg/kg rocuronium or 0.1 mg/kg cisatracurium to facilitate endotracheal intubation. A left-sided double-lumen endotracheal tube was placed, and its correct position was confirmed by fiberoptic bronchoscopy. Anesthesia was maintained with 1%–3% sevoflurane or 6%–7% desflurane at a fresh flow rate of 2 L/min. Up to 150 µg of supplementary fentanyl was administered if necessary.

Each subject was positioned with his or her arms supported anterior to the forehead. Uninsulated thermocouple temperature probes (Sable Systems, Las Vegas, NV) were placed on the thenar eminence of both palms. Integrated laser Doppler flowprobes (Perimed, Sweden) were positioned adjacent to the temperature probes. Care was taken to avoid placing the probes over superficial veins. Laser Doppler flowmetry is a widely used and accepted method of quantifying skin blood flow (5,6,10,19–24).

Each subject underwent bilateral endoscopic thoracic sympathectomy by the same surgeon (DMM). Three 3-mm incisions were made along the inframammary fold, through which thoracoscopic ports were inserted. Ganglia at the level of T2 (n = 2), T3 (n = 7), or T4 (n = 2) were identified and removed by using monopolar cautery. Periosteum over the adjacent ribs was cauterized to ablate any accessory nervous pathways. There were no differences in responses due to the level of ganglion removed, and thus data from all three levels were combined. In all cases, sympathectomy was first performed on the left side, followed by sympathectomy on the right side.

Each sympathectomy was treated as a unique observation. Experimental complications pertaining to either equipment or human error resulted in 19 sympathectomy procedures being analyzed. Skin blood-flow and temperature values were continuously sampled at 50 Hz via a commercial data-acquisition system (Biopac, Santa Barbara, CA). Baseline skin blood-flow and temperature values were obtained after the induction of general anesthesia and the insertion of endoscopic ports, but before any cautery was performed. In addition to baseline values, palmar skin blood flow and temperature were obtained at 5, 10, and 15 min after the initial cautery. Peak skin blood-flow and temperature responses were also obtained upon identification of a plateau of these responses. Four statistical analyses were performed on these data. 1) At each time point, responses for each variable (i.e., skin blood flow and temperature) were statistically analyzed via a one-way repeated-measures analysis of variance followed by a Student-Newman-Keuls post hoc test when a significant main effect was identified. 2) Differences in the duration from initial cautery to peak response between skin blood flow and temperature were statistically analyzed via a paired Student’s t-test. 3) The percentage increase in the response of each variable at the aforementioned times was calculated relative to the total increase of that variable (i.e., the range) by using the following equation:


{50MM1}

where X is the value at 5, 10, or 15 min after the initial cautery.

This calculation resulted in a value that represented a percentage of the total response at each of the listed times. At each time point, differences between these values for skin blood flow and temperature were statistically compared via a paired Student’s t-test. 4) To assess the effect of sympathectomy on the variability of the oscillations in skin blood flow, the coefficients of variation (SD x mean–1 x 100) between baseline and peak skin blood-flow responses were obtained and statistically analyzed via a paired Student’s t-test. The P value for statistical significance was set at 0.05. All data are presented as mean ± SEM.


   Results
Top
 Abstract
 Introduction
 Methods
 Results
Discussion
 References
 
All subjects considered the surgery successful and reported a pronounced reduction in sweating in the affected areas after recovery. In each case, histological analysis of the removed tissue confirmed the tissue as ganglia. A typical response for the first 15 min after cautery is illustrated in Figure 1. Before cauterizing of any tissue, skin blood flow averaged 48 ± 7 perfusion units (PU), and temperature averaged 31.0°C ± 0.5°C. Five minutes after the initial cautery, skin blood flow increased to 121 ± 17 PU (P < 0.001), whereas no significant difference in skin temperature was identified (31.3°C ± 0.5°C; P > 0.05). Both skin blood flow and temperature were significantly increased from baseline 10 and 15 min after the initial cautery (Fig. 2). Peak skin blood flow and peak temperature after sympathectomy were 182 ± 17 PU and 33.8°C ± 0.3°C, respectively. However, the time required to reach peak skin blood flow (22 ± 3 min) after the initial cautery was significantly less than the time required to reach peak skin temperature (34 ± 0.3 min; P < 0.001).



View larger version (28K):
[in this window]
[in a new window]
  		Figure 1. Typical palmar skin blood-flow and temperature responses during the sympathectomy procedure. The label indicated as "cautery" represents the initial cautery of the parietal pleura over the ganglion. The subsequent time points depict the time after this initial cautery. Notice the large increase in skin blood flow associated with the initial cautery. For this subject, the ganglion was sectioned ~5 min after the initial cautery. The increase in skin temperature lagged behind the increase in skin blood flow. PU = perfusion units.

 


View larger version (36K):
[in this window]
[in a new window]
  		Figure 2. Average increases in palmar skin blood flow and temperature. Skin blood flow was significantly increased at 5 min postcautery and remained increased relative to baseline throughout data collection. In contrast, skin temperature at 5 min was not significantly different from that at baseline. Skin temperature was significantly more than baseline at 10 and 15 min after the initial cautery. Lines above the columns indicate statistical differences between adjacent periods (P < 0.05). Times depict the duration after initial cautery.

 
To identify the delay between the increase in skin blood flow relative to the increase in skin temperature, the percentage increase in the respective value relative to the total range of that value was calculated at each time point and is depicted in Table 1. At 5 min postcautery, 45% ± 9% of the increase in skin blood flow had occurred, whereas only 11% ± 5% of the increase in skin temperature had occurred (P = 0.002). At 10 min postcautery, 68% ± 7% of the increase in skin blood flow had occurred, whereas 43% ± 7% of the increase in skin temperature had occurred (P = 0.006). Finally, at 15 min postcautery, 82% ± 4% of the increase in skin blood flow had occurred, whereas 59% ± 6% of the increase in skin temperature had occurred (P < 0.001).


View this table:
[in this window]
[in a new window]
  		Table 1. Percentage Increase in the Measured Variable Relative to the Range of Increase as a Result of the Sympathectomy Procedure
 
At baseline and at peak blood flows, the coefficient of variation was calculated to identify the variability of blood-flow oscillations. At baseline, this value for palmar skin blood flow was significantly greater (28% ± 2%) relative to peak blood flow after sympathectomy (7% ± 1%; P < 0.001). It is interesting that at baseline oscillations in palmar skin, blood flow occurred at frequencies associated with Mayer waves (i.e., approximately 0.05 to 0.15 Hz) or appeared to be random. In contrast, after sympathectomy, these low-frequency oscillations were substantially minimized, whereas oscillations associated with the cardiac cycle were larger than at baseline (Fig. 3).



View larger version (35K):
[in this window]
[in a new window]
  		Figure 3. Palmar skin blood flow at baseline before cautery (A) and at peak response after sympathectomy (B) from a representative subject. Notice the large magnitude of low-frequency fluctuations before sympathectomy that was absent after sympathectomy. However, after sympathectomy, variation in skin blood flow associated with the cardiac cycle was greatly enhanced. PU = perfusion units.

 

   Discussion
Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
References
 
The primary objective of this study was to assess the usefulness of intraoperative skin blood flow monitoring during surgical sympathectomy and to identify whether increases in palmar skin blood flow precede increases in palmar skin temperature. Although others have reported that palmar skin blood flow is increased after sympathectomy (6,11,14), this study and the companion study (25) are the first to simultaneously record and compare palmar skin blood flow and temperature responses during the surgical procedure. Three primary, and related, findings confirm the hypothesis that skin blood-flow responses precede skin temperature responses during this operation. The first evidence is illustrated in Figures 1 and 2. In Figure 1, skin blood flow rapidly increased after the initial cautery, whereas skin temperature did not begin to increase until approximately five minutes later for this subject. In Figure 2, average data demonstrate that five minutes after the initial cautery, skin blood flow was more than twice the baseline value, whereas there was no significant change in skin temperature at this time. Second, the time after initial cautery to achieve a plateau of skin temperature was approximately 12 minutes after the plateau in skin blood flow. Third, the percentage increase in skin blood flow relative to the total increase in skin blood flow during surgery (i.e., peak – baseline) was significantly greater for each time point when compared with skin temperature (Table 1). Stated another way, at the observed time points, skin blood flow increased to a larger fraction of the total increase of this variable relative to skin temperature. Together, these data confirm that skin blood-flow responses preceded skin temperature responses throughout the procedure.

Palmar skin blood flow is primarily governed by a sympathetic vasoconstrictor system (15,18). When tonic sympathetic activity to the palm is disrupted, large increases in skin blood flow occur (26). Monitoring of palm or fingertip temperature has become the standard in identification of successful sympathectomy (6,10–14). Assuming that environmental temperature is constant, changes in palm or fingertip temperature during surgery will occur secondary to changes in skin blood flow. Thus, it is not surprising that these data support the hypothesis that changes in skin blood flow precede changes in skin temperature during this surgery. Nevertheless, by monitoring skin blood flow, the surgeon will be able to more rapidly identify whether the region being disrupted innervates the palmar area.

Despite the reported findings, enthusiasm for the use of laser Doppler flowmetry to assess the success of surgical sympathectomy must be tempered. For most subjects, increases in skin blood flow occurred in association with the initial cautery of the parietal pleura overlying the sympathetic chain. The point labeled as "cautery" in Figure 1 depicts the initial cauterization of pleural tissue. At this time, the sympathetic chain remained intact and was not physically disrupted by the cautery probe. However, it is likely that current associated with cautery over the ganglion disrupted neural transmission at this location and that this disruption persisted through the period when the ganglion was sectioned. Once the sympathetic chain was cut, at approximately five minutes for the subject illustrated in Figure 1, a large fraction of the increase in skin blood flow had already occurred. If the initial cautery temporarily disrupts neural transmission in this area, a surgeon may incorrectly conclude that the initial increase in skin blood flow indicates a successful sympathectomy. Thus, a critical finding from this study is that an abrupt increase in palmar skin blood flow is insufficient to conclude that the sympathetic chain is permanently disrupted.

Another method to identify the success of the sympathectomy procedure may be to assess oscillatory characteristics of skin blood flow during the surgery. Before cautery, palmar skin blood flow showed typical fluctuations characteristic of glabrous skin (27–29). These fluctuations are primarily due to sympathetic modulation of arterial venous anastomoses, which are numerous in glabrous skin (30). At baseline, the average coefficient of variation was quite large (28% ± 2%). Although insufficient baseline data were obtained to appropriately perform a spectral analysis of this response, the frequency of these oscillations was within the range previously reported from glabrous skin (29). After removal of the ganglion, these low-frequency fluctuations were abolished. However, it is interesting that blood-flow oscillations associated with the cardiac cycle became quite prevalent (Fig. 3). An increase in oscillations associated with the cardiac cycle may be related to an increase in the compliance of the vasculature upon removal of tonic sympathetic activity.

Although conclusions regarding the delay in skin temperature relative to skin blood flow during the surgical procedure are similar between this article and its companion (25), a few key differences are worth noting. The present surgical procedure, in which the desired ganglion is removed, is the more common technique. This is in contrast to the procedure of the companion study (25), in which the connection between the stellate ganglion and the T2 ganglion is permanently disrupted (sympathotomy). A detailed description of the differences of these surgical methods (i.e., sympathectomy and sympathotomy) to treat hyperhidrosis has recently been reported (4). A key limitation of the interpretation of our data is the possible confounding effects of the initial cautery leading to increases in palmar skin blood flow before physical disruption of the ganglion. Such a limitation may not exist or may be minimized with the sympathotomy procedure. It is likely that because the ganglion is not removed with the sympathotomy procedure, less cauterization occurs before disconnection of the T2 ganglion from the stellate ganglion. Thus, the abrupt increases in skin blood flow observed in the companion study (25) may be more an effect of interruption of the neural connection than an effect of application of current in this area when compared with the present study.

Both studies report the time from cautery until the peak skin blood-flow and temperature responses. However, the values between these studies are quite different: this study reports an average duration of 22 minutes for skin blood flow and 34 minutes for skin temperature, whereas the companion study (25) reports an average duration for skin blood flow and temperature of approximately 1 and 5 minutes, respectively. Although in both studies skin blood-flow responses preceded skin temperature responses, differences in the duration to peak responses between these studies can only be speculated at this time and may be related to the aforementioned differences between the sympathectomy and sympathotomy procedures. For the sympathectomy procedure, the time from the initial cautery until physical disruption of the ganglion has the potential to be substantially longer than the sympathotomy procedure. The initial increase in skin blood flow and the associated increase in skin temperature during the sympathectomy procedure is likely due to the application of current. This would be followed by the physical disruption of the ganglion and subsequent further increases in skin blood flow and temperature. Moreover, given the possibility that the sympathotomy procedure may be performed quicker than the sympathectomy procedure, differences in the time to peak response between these studies may also be related to the duration that the responses are observed after the initial disruption of the ganglion.

In this study, the average increase in skin temperature associated with the procedure was ~2.8°C, whereas the companion study (25) showed an increase in skin temperature of ~1.2°C. These differences may be a factor of the duration after the initial cautery that the responses were observed. As previously discussed, it is likely that the time necessary to remove the ganglion (sympathectomy) was longer than the time required to disconnect the ganglion (sympathotomy), thus allowing for a larger increase in skin temperature to be observed with the sympathectomy procedure. Another distinction between these studies is the location of the temperature probe. In this study, the temperature probe was placed as close as possible to the laser Doppler flowmetry probe, and both were located near or on the thenar eminence. This is in contrast to the companion study, in which the temperature probe was placed on the finger.

In conclusion, data from this study support the hypothesis that skin blood-flow responses, as measured via laser Doppler flowmetry, precede skin temperature responses during surgical sympathectomy. These findings suggest that monitoring skin blood flow may provide greater temporal resolution when compared with skin temperature during the surgical procedure. However, the surgeon needs to be aware that cautery of the parietal pleura over the ganglion may result in increases in skin blood flow without physical disruption of the ganglion, and this may limit the utility of skin blood-flow measurements in identifying the success of the procedure.


   Acknowledgments
 
Supported in part by National Institutes of Health Grants HL61388 and HL67422.

We would like to express appreciation to Kimberly Williams, RN, for her assistance with this project, as well as to the surgical support staff at St. Paul University Hospital at Southwestern Medical Center.


   References
Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 References
 

  1. Adar R, Kurchin A, Zweig A, Mozes M. Palmar hyperhidrosis and its surgical treatment: a report of 100 cases. Ann Surg 1977; 186: 34–41.[Web of Science][Medline]
  2. Strutton D, Kowalski J, Glaser D, Stang P. US prevalence of hyperhidrosis: results from a national consumer panel. American Academy of Dermatology 61st Annual Meeting, 2003.
  3. Connolly M, de Berker D. Management of primary hyperhidrosis: a summary of the different treatment modalities. Am J Clin Dermatol 2003; 4: 681–97.[Web of Science][Medline]
  4. Atkinson JL, Fealey RD. Sympathotomy instead of sympathectomy for palmar hyperhidrosis: minimizing postoperative compensatory hyperhidrosis. Mayo Clin Proc 2003; 78: 167–72.[Abstract/Free Full Text]
  5. Kao MC. Video endoscopic sympathectomy using a fiberoptic CO2 laser to treat palmar hyperhidrosis. Neurosurgery 1992; 30: 131–5.[Web of Science][Medline]
  6. Kao MC, Tsai JC, Lai DM, et al. Autonomic activities in hyperhidrosis patients before, during, and after endoscopic laser sympathectomy. Neurosurgery 1994; 34: 262–8;discussion 8.[Web of Science][Medline]
  7. Claes G. Indications for endoscopic thoracic sympathectomy. Clin Auton Res 2003; 13 (Suppl 1): I16–9.
  8. Drott C. Results of endoscopic thoracic sympathectomy (ETS) on hyperhidrosis, facial blushing, angina pectoris, vascular disorders and pain syndromes of the hand and arm. Clin Auton Res 2003; 13 (Suppl 1): I26–30.
  9. Doolabh N, Horswell S, Williams M, et al. Thoracoscopic sympathectomy for hyperhidrosis: indications and results. Ann Thorac Surg 2004; 77: 410–4;discussion 4.
  10. Ng I, Yeo TT. Palmar hyperhidrosis: intraoperative monitoring with laser Doppler blood flow as a guide for success after endoscopic thoracic sympathectomy. Neurosurgery 2003; 52: 127–30;discussion 30–1.
  11. Chuang TY, Yen YS, Chiu JW, et al. Intraoperative monitoring of skin temperature changes of hands before, during, and after endoscopic thoracic sympathectomy: using infrared thermograph and thermometer for measurement. Arch Phys Med Rehabil 1997; 78: 85–8.[Web of Science][Medline]
  12. Wu JJ, Hsu CC, Liao SY, et al. Contralateral temperature changes of the finger surface during video endoscopic sympathectomy for palmar hyperhidrosis. J Auton Nerv Syst 1996; 59: 98–102.[Web of Science][Medline]
  13. Lu K, Liang CL, Lee TC, et al. Changes of bilateral palmar skin temperature in transthoracic endoscopic T-2 sympathectomy. J Neurosurg 2000; 92: 44–9.
  14. Chen HJ, Liang CL, Lu K. Associated change in plantar temperature and sweating after transthoracic endoscopic T2–3 sympathectomy for palmar hyperhidrosis. J Neurosurg 2001; 95: 58–63.
  15. Roddie IC. Circulation to skin and adipose tissue. In: Shepherd JT, Abboud FM, eds. Handbook of physiology: the cardiovascular system. Section 2. The cardiovascular system. Bethesda, MD: American Physiological Society, 1983: 285–317.
  16. Lewis T, Pickering GW. Vasodilation in the limbs in response to warming the body: with evidence for sympathetic vasodilator nerves in man. Heart 1931; 16: 33–51.
  17. Grant RT, Holling HE. Further observations on the vascular responses of the human limb to body warming: evidence for sympathetic vasodilator nerves in the normal subject. Clin Sci (Lond) 1938; 3: 273–85.
  18. Johnson JM, Proppe DW. Cardiovascular adjustments to heat stress. In: Blatteis C, Fregly M, eds. Handbook of physiology: adaptations to the environment. Bethesda, MD: American Physiological Society, 1996: 215–43.
  19. Sano T, Fukushige T, Miyagawa Y, et al. [Intraoperative assessment by laser-Doppler skin blood flowmetry of the efficacy of endoscopic thoracic sympathectomy]. Masui 1999; 48: 481–6.[Medline]
  20. Eun HC. Evaluation of skin blood flow by laser Doppler flowmetry. Clin Dermatol 1995; 13: 337–47.[Web of Science][Medline]
  21. Saumet JL, Kellogg DL Jr, Taylor WF, Johnson JM. Cutaneous laser-Doppler flowmetry: influence of underlying muscle blood flow. J Appl Physiol 1988; 65: 478–81.[Abstract/Free Full Text]
  22. Braverman IM. The cutaneous microcirculation. J Investig Dermatol Symp Proc 2000; 5: 3–9.[Web of Science][Medline]
  23. Oberg PA. Laser-Doppler flowmetry. Crit Rev Biomed Eng 1990; 18: 125–63.[Web of Science][Medline]
  24. Johnson JM. The cutaneous circulation. In: Shepherd AP, Öberge PÅ, eds. Laser Doppler blood flowmetry. Boston: Kluwer Academic, 1990: 121–40.
  25. Eisenach JH, Pike T, Wick DE, et al. Comparison of peripheral skin blood flow and temperature during endoscopic thoracic sympathotomy. Anesth Analg 2004; 99: XXXX–XXX.
  26. Roddie IC. Sympathetic vasodilatation in human skin. J Physiol 2003; 548: 336–7.[Abstract/Free Full Text]
  27. Lossius K, Eriksen M, Walloe L. Fluctuations in blood flow to acral skin in humans: connection with heart rate and blood pressure variability. J Physiol 1993; 460: 641–55.[Abstract/Free Full Text]
  28. Eriksen M, Lossius K. A causal relationship between fluctuations in thermoregulatory skin perfusion and respiratory movements in man. J Auton Nerv Syst 1995; 53: 223–9.[Web of Science][Medline]
  29. Bernardi L, Hayoz D, Wenzel R, et al. Synchronous and baroceptor-sensitive oscillations in skin microcirculation: evidence for central autonomic control. Am J Physiol 1997; 273: H1867–78.
  30. Hurley HJ Jr, Mescon H, Moretti G. The anatomy and histochemistry of the arteriovenous anastomosis in human digital skin. J Invest Dermatol 1956; 27: 133–45.[Web of Science][Medline]
Accepted for publication June 24, 2004.




This article has been cited by other articles:


Home page
 Ann. Thorac. Surg.Home page
X. Li, Y.-R. Tu, M. Lin, F.-C. Lai, J.-F. Chen, and H.-W. Miao
Minimizing endoscopic thoracic sympathectomy for primary palmar hyperhidrosis: guided by palmar skin temperature and laser Doppler blood flow.
Ann. Thorac. Surg., February 1, 2009; 87(2): 427 - 431.
[Abstract] [Full Text] [PDF]

Home page
 J. Thorac. Cardiovasc. Surg.Home page
P. Maga, J. Kuzdzal, R. Nizankowski, A. Szczeklik, and K. Sladek
Long-term effects of thoracic sympathectomy on microcirculation in the hands of patients with primary Raynaud disease
J. Thorac. Cardiovasc. Surg., June 1, 2007; 133(6): 1428 - 1433.
[Abstract] [Full Text] [PDF]

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a colleague
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (2)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Crandall, C. G.
Right arrow Articles by Dellaria, S. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Crandall, C. G.
Right arrow Articles by Dellaria, S. M.
Related Collections
Right arrow Surgery
Right arrow Pharmacology

Lippincott, Williams & Wilkins Anesthesia & Analgesia® is published for the International Anesthesia Research Society® by Lippincott Williams & Wilkins with the assistance of Stanford University Libraries' HighWire Press®. Copyright 2006 by the International Anesthesia Research Society. Online ISSN: 1526-7598   Print ISSN: 0003-2999 HighWire Press