Back to Authors

Klaas, Kelsey

https://orcid.org/0000-0002-8524-4068

Mayo Clinic

Mayo Clinic

Citations 9

Answers to Common Questions About Postural Orthostatic Tachycardia Syndrome and Chronic Orthostatic Intolerance
Mauriello, Daniel, Mitchell, Brooke, Klaas, Kelsey

Pediatric Annals | March 5, 2026 | Volume: 55 | Issue: 3 | Pages: No page available

10.3928/19382359-20260112-04 Get It

How is postural orthostatic tachycardia syndrome (POTS) diagnosed? What about adolescents who seem to have POTS but do not meet the diagnostic criteria? How can we treat POTS and related conditions? How can we best respond to common questions of frustrated patients and parents and guardians? This article provides evidence- and expert-based answers to questions that frequently arise when caring for patients with POTS and related conditions.
Postural Orthostatic Tachycardia Syndrome and Chronic Orthostatic Intolerance: Common, Challenging, and Manageable
Klaas, Kelsey , Fischer, Philip R.

Pediatric Annals | March 5, 2026 | Volume: 55 | Issue: 3 | Pages: No page available

10.3928/19382359-20260112-02 Get It

Outcomes of Pediatric Patients with Excessive Postural Tachycardia After Attending an Intensive Interdisciplinary Pain Program: A Pilot Study
Harbeck‐Weber, Cynthia , Klaas, Kelsey , Sim, Leslie , Weiss, Karen , Shappell, April, Harrison, Tracy E. , Harrison, Tracy, Harbeck‐Weber, Cynthia

Children | February 5, 2025 | Volume: 12 | Issue: 2 | Pages: 186

10.3390/children12020186 Get It

Background/Objectives: Adolescents with autonomic disorders who attend Intensive Interdisciplinary Pain Treatment (IIPT) programs report improvements in functioning. However, it is unclear whether they experience corresponding improvements in physiological measures. As such, the aim of this pilot study was to examine changes in physiological measures in youth attending an IIPT program who demonstrated excessive postural tachycardia on an active stand test. The secondary goal was to examine associations between physiological measurements and self-reported measures of chronic orthostatic intolerance (cOI) and functioning. Methods: At admission and discharge, eighteen adolescents and young adults (AYAs) attending IIPT (M age = 17.39 years; SD = 2.15 years) completed an active stand test, measures of breathing rate and muscle tension, as well as self-reported measures of cOI symptoms and functioning. Results: AYAs showed significant reduction in active stand test heart rate increase (p < 0.001; d = 1.07) and maximum heart rate (p = 0.002, d = 0.76) from admission to discharge. Improvements were also observed in resting respiration rate (p = 0.001, d = 89) and resting trapezoid tension (p = 0.03, d = 0.49). Although patients showed significant improvements on self-report measures of functioning (p < 0.001, d = 1.78), changes on subjective report of cOI symptoms did not reach significance. Exploratory analyses that only included patients with a POTS diagnosis were consistent with the overall results. Conclusions: Youth who demonstrated excessive postural tachycardia on active stand test at admission to an IIPT showed significant improvements from admission to discharge in their active stand maximum heart rate and heart rate increase, as well as respiration rate, muscle tension, and reports of their functioning. Future research is necessary to examine the mechanisms of change that contribute to symptom improvement.
Reply to “BASCULE syndrome: Additional evidence for the association with autonomic dysfunction”
Reinhart, Jacob P. , Kumar, Anagha , Rooke, Thom W. , Sartori‐Valinotti, Julio C. , Tollefson, Megha M. , Klaas, Kelsey , Davis, Dawn Marie R. , Kumar, Anagha Bangalore , Sartori-Valinotti, Julio C., Davis, Dawn M R , Reinhart, Jacob , Casanegra, Ana I.

Pediatric Dermatology | May 14, 2024 | Volume: 41 | Issue: 3 | Pages: 566-566

10.1111/pde.15549 Get It

Da Costa’s Syndrome and Postural Tachycardia Syndrome: A rose by any other name? (P2.031)
Klaas, Kelsey , Burkholder, David B.

Neurology | December 7, 2023 | Volume: 88 | Issue: 16_supplement | Pages: No page available

10.1212/wnl.88.16_supplement.p2.031 Get It

Bridging the gap in BASCULE syndrome: A retrospective case series of a recently described clinical entity
Reinhart, Jacob P. , Kumar, Anagha , Casanegra, Ana I. , Rooke, Thom W. , Sartori‐Valinotti, Julio C. , Tollefson, Megha M. , Klaas, Kelsey , Davis, Dawn Marie R. , Kumar, Anagha Bangalore , Davis, Dawn M R , Casanegra, Ana I , Reinhart, Jacob

Pediatric Dermatology | November 28, 2023 | Volume: 41 | Issue: 1 | Pages: 46-50

10.1111/pde.15470 Get It

AbstractBackgroundBier anemic spots, cyanosis with urticaria‐like eruption (BASCULE) syndrome is a recently described entity with episodic urticarial lesions and white anemic halos on a background of erythrocyanosis, commonly affecting the lower extremities. Possible association with autonomic dysfunction remains poorly understood. Existing publications are limited, but the condition is suggested as highly underrecognized.ObjectiveTo further characterize clinical and epidemiologic data for BASCULE syndrome.MethodsWe performed an IRB‐approved retrospective chart review on patients with BASCULE syndrome evaluated at Mayo Clinic from April 2021 to November 2022.ResultsA total of 17 patients were identified (13 female, 4 male). Median age of onset was 12 years (range 9–17). Lower extremities were involved in all patients (17). Most patients were symptomatic with pruritus (8) or burning pain (8); three were asymptomatic. Triggers were standing (11), hot showers or hot environments (7), or no clear trigger (4). Autonomic dysfunction was present in 10 patients. Treatment responses were observed from propranolol (3) and high‐dose cetirizine (1).ConclusionNovel epidemiologic data from 17 pediatric and young adult patients with BASCULE syndrome further supports an association with autonomic dysfunction and suggests a higher prevalence than previously acknowledged.
Stretchy Skin and Hyperextensibility: A Case of Vascular Abnormalities
Warring, Simrit K. , Castillo, Richmond , Klaas, Kelsey , Taggart, Nathaniel W. , Fischer, Philip R.

Pediatrics | March 1, 2023 | Volume: 141 | Issue: 1_MeetingAbstract | Pages: 703-703

10.1542/peds.141.1ma8.703 Get It

Excessive Postural Tachycardia and Postural Orthostatic Tachycardia Syndrome in Youth: Associations With Distress, Impairment, Health Behaviors, and Medication Recommendations
Klaas, Kelsey , Segner, Sara, Owens, Michele Tsai , Fahrenkamp, Amy J., Geske, Jennifer R. , Hofschulte, Deanna R., Farrell, Michael , Harbeck‐Weber, Cynthia , Biggs, Bridget K. , Klaas, Kelsey M , Fischer, Philip R. , Geske, Jennifer, Hofschulte, Deanna, HARBECK-WEBER, CYNTHIA, Biggs, Bridget K , Geske, Jennifer , Harbeck‐Weber, Cynthia

Journal of Child Neurology | May 19, 2022 | Volume: 37 | Issue: 7 | Pages: 599-608

10.1177/08830738221078410 Get It

Among adolescents with fatigue and postural dizziness, it is unclear how health behaviors and emotional distress relate to the presence of excessive postural tachycardia. We prospectively evaluated adolescents aged 13-22 years presenting with symptoms suggestive of autonomic dysfunction between September 2017 and December 2018. Patients underwent standard 10-minute, 70-degree head-up tilt testing. Clinician diagnoses and recommendations were recorded from the medical record. Patients completed validated self-report measures of lifestyle factors, autonomic symptoms, depression, anxiety, and functional disability. Of 179 patients, 58 were diagnosed with postural orthostatic tachycardia syndrome and 59 had excessive postural tachycardia, with 90.5% concordance between the 2 groups. Presence of excessive postural tachycardia was associated with greater baseline fluid intake and likelihood of medication prescription in their treatment plan. Medication findings were replicated for postural orthostatic tachycardia syndrome diagnosis. Presence of excessive postural tachycardia or postural orthostatic tachycardia syndrome did not differentiate patients on perceived symptom severity, emotional distress, disability, or health behaviors but did appear to determine treatment recommendations.
Treatment of Postural Orthostatic Tachycardia Syndrome With Medication: A Systematic Review
Hasan, Bashar , Almasri, Jehad , Marwa, Bilal , Klaas, Kelsey , Klaas, Kelsey M, Fischer, Philip R. , Hasan, Bashar

Journal of Child Neurology | August 25, 2020 | Volume: 35 | Issue: 14 | Pages: 1004-1016

10.1177/0883073820948679 Get It

Purpose: Postural orthostatic tachycardia syndrome has been recognized for decades, but treatment is largely based on anecdotal experience and expert opinion. Pharmacologic treatment is inconsistent and unstandardized. We did a systematic review to identify controlled studies from which informed treatment decisions can be made. Method: Through a standard systematic review following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines, we identified all English-language studies of a medication treatment for postural orthostatic tachycardia syndrome that included a comparison or control group and followed outcomes for at least 1 week of treatment. Results: A total of 626 studies were identified by the search criteria, and 8, involving a total of 499 patients, met the criteria. No studies were adequately similar to allow for meta-analysis. Of the identified 8 studies, 2 were randomized controlled trials and 4 had been subjected to peer review. In individual studies, there was some favorable effect with fludrocortisone, beta blockers, midodrine, and selective serotonin reuptake inhibitors. Conclusion: There is a paucity of high-quality data about effectiveness of medication in the treatment of postural orthostatic tachycardia syndrome. Nonetheless, 2 randomized trials and 6 other reports show some favorable effects of medication.