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Annals of medicine · 2022

When to investigate for secondary hyperhidrosis: data from a retrospective cohort of all causes of recurrent sweating.

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Collercandy N, Thorey C, Diot E, Grammatico-Guillon L, Thillard EM, Bernard L, Maillot F, Lemaignen A

Аннотация

Background: Identification of underlying diseases is crucial for secondary hyperhidrosis management, but data are lacking to guide appropriate investigation.Objective: To describe aetiologies of recurrent sweating in a hospital setting and the diagnostic performance parameters of their respective clinical/biological features.Patients and Methods: We performed a monocentric evaluative study in a tertiary care centre. Patients with recurrent generalised sweating were selected via the Clinical Data Warehouse (CDW) by screening all electronic hospital documents from the year 2018 using a keyword-based algorithm. All in and out-patients aged ≥ 18 years having reported recurrent sweating for at least 2 weeks in 2018 were included, with a minimum one-year follow-up after symptoms' onset.Results: A total of 420 patients were included. Over 130 different aetiologies were identified; 70 patients (16.7%) remained without diagnosis. Solid organ cancers (14.3% with 13 lung cancers), haematologic malignancies (14.0% with 35 non-Hodgkin's lymphomas) and Infectious Diseases (10.5% including 13 tuberculosis) were the most frequent diagnoses. Other aetiologies were gathered into inflammatory (16.9%) and non-inflammatory (27.6%) conditions. To distinguish non-inflammatory and undiagnosed hyperhidrosis from other causes, fever had a specificity of 94%, impaired general condition a sensitivity of 78%, and C-reactive protein (CRP) > 5.6 mg/l a positive predictive value of 0.86. Symptoms' duration over 1 year was in favour of non-infectious and non-malignant causes (94% specificity).Conclusions: We identified fever, impaired general condition, duration, and CRP as helpful orientation parameters to assess the need for complementary explorations for hyperhidrosis. The study provides a diagnostic algorithm for the investigation of recurrent sweating.KEY MESSAGESIn a hospital setting, malignancies and infections are the most frequently associated diseases, but 1/5 remain without diagnosis.Fever is a specific but not sensitive sign to distinguish inflammatory conditions.Over 1 year duration of symptoms significantly reduce the probability of malignancy or infection as the underlying diagnosis.

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https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/ ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Introduction

Thermoregulatory sweating is a physiological mechanism to maintain thermoregulation homoeostasis in humans. Sweating is triggered by a body temperature increase, which is sensed by peripheral and central thermoreceptors under the central control of the hypothalamus [ 1 , 2 ]. The hypothalamus, in turn, activates the autonomic nervous system through the efferent sympathetic pathway. Sweat is primarily produced by eccrine glands, which are widespread throughout the skin in significant numbers (1.6–4 million on the whole body) with variable density. These glands have muscarinic receptors that can be bound to acetylcholine, a neurotransmitter released from sudomotor nerves. Upon stimulation, human sweat glands can produce an average sweat rate of 1.4 l/h. This rate is regulated by body fluid volume and mechanically by skin hydration status [ 2 ].

In certain conditions, sweating rate can increase apart from exercise or elevated environmental temperature. Isolated, sweating out of those settings could be defined as primary hyperhidrosis, with a poorly understood pathophysiology, which may involve an autonomic pathway overstimulation exceeding thermoregulatory needs [ 3 , 4 ]. Hyperhidrosis is defined as excessive sweating causing negative impact on patients’ quality of life, and is thus a subjective symptom [ 5 ]. Secondary hyperhidrosis relies on an underlying condition. Excessive sweating has been reported in association with numerous diseases, including tuberculosis, lymphoma, and endocarditis, typically occurring at night, wetting clothes and bedsheets [ 6 , 7 ]. Sweating is often associated with fever as an appropriate response to body temperature increase, although there is not always body temperature elevation in secondary hyperhidrosis. In contrast to the more frequent focal presentation of primary hyperhidrosis, secondary hyperhidrosis is usually generalized to the whole body [ 5 ]. The proper diagnosis of secondary hyperhidrosis is crucial as life-threatening diseases can potentially be involved. Besides the consequences due to the underlying disorder, hyperhidrosis impacts quality of life by itself, notably involving psychosocial impairment [ 8 , 9 ].

To date, very limited data are available regarding the potential aetiologies and epidemiology of hyperhidrosis, although this symptom is quite common in primary care [ 10 , 11 ]. Studies in this field are mostly represented by literature reviews of case reports and are not able to provide the frequency of each diagnosis [ 6 , 7 , 12 ]. Only one retrospective study in an outpatient dermatology department has provided valuable clinical information about the differentiation of secondary hyperhidrosis from primary hyperhidrosis [ 13 ]. However, based on only one department, primary hyperhidrosis was predominantly represented along with few underlying diseases, and no data in hospitalised patients were available. Clinicians are thus lacking guidelines to support appropriate extensive investigation when they are confronted with generalised sweating in adults.

The aim of this study was to assess the possible aetiologies of recurrent sweating in a hospital setting and the diagnostic performance parameters of respective clinical and biological features, using one teaching hospital data warehouse.

Patients and methods

A retrospective cohort of patients with recurrent generalised sweating was built to collect clinical and biological features from all in- and out-patients of one university hospital using the electronic medical records from a Clinical Data Warehouse for the year 2018.

Because of the absence of diagnostic criteria for recurrent sweating, we empirically based our hypothetical definition of recurrent sweating to tend towards the standard definition of prolonged fever of unknown origin, considering symptoms occurring a minimum of 2 weeks from the onset of symptoms [ 14 ].

Data source

Data were collected using eHOP®, the Clinical Data Warehouse software of the tertiary care hospital of Tours; it integrates all electronic medical documents produced in the hospital information system [ 15 , 16 ]. We developed a research algorithm to detect the keywords “sweat” and its synonyms in French, including plural spelling, which were subsequently followed, within fewer than four words, by the French words for “prolonged”, “chronic”, “recurrent”, “night”, “day(s)”, “week(s)”, “month(s)”, or “year(s)”. The algorithm excluded documents where keywords were preceded by a negation within fewer than seven words.

Studied population and data collection

Our research algorithm was performed based on the data warehouse screening among all hospital documents produced between 1 January 2018 and 31 December 2018. All adults ≥ 18 years old admitted as in-patients and out-patients in 2018 were selected. As the datamining was carried out up to December 2020, all patients had at least a one-year follow-up after the onset of symptoms. We thoroughly analysed each patient’s medical record to include all patients who reported generalized sweating episodes for at least two weeks. Initial diagnosis was defined as the imputed diagnosis for the recurrent sweating symptomatology at hospital discharge. Final diagnosis for each secondary hyperhidrosis case was the most recent imputed diagnosis provided by the referring hospital physician at the time of data collection. Other data collected from the data warehouse included: age, sex, department of hospitalisation/consultation, duration of symptoms, associated symptoms, medical history, treatments, and laboratory results.

Pharmacovigilance database

We searched in PubMed and Google Scholar electronic databases by using combinations of the following keywords: “hyperhidrosis”, “sweating” and “drug-induced”, “drugs”, “medications”. For drugs of interest that were suspected by the attending physician, we identified all cases of “hyperhidrosis” (using preferred term according to MedDRA classification) reported to French pharmacovigilance database (FPVD) and to the WHO pharmacovigilance database (Vigilyze®) until January 2022. Cases with multiple suspected drugs were excluded. Only drugs with more than five cases in FPVD and 100 cases in Vigilyze® were labelled as reported in the respective database.

Statistical analysis

Variations between two groups were compared using Student’s t -test. Diagnostic performances for the dependent variable for a binary criterion, including sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV), were estimated using the associated contingency table [ 17 ]. Accuracy was defined as: (True positive + True negative)/total number of patients. Continuous biological variables were assessed using an ROC curve in order to establish an optimal cut-point for diagnosis. Sensitivity and specificity were assessed for different cut-points and the optimal cut-point was defined as the maximisation of Youden’s index. ROC curve confidence intervals were estimated using bootstrap simulations on the performance measures. For all calculations, statistical significance was defined as a p -value of < .05. Statistical analyses were performed using both R software version 3.1 through the GMRC Shiny Stat interface from Strasbourg University Hospital (2017) and GraphPad Prism version 9.1.1.

Ethical approval

Ethical approval (no. 2020_057) was provided by the Ethics Committee in Human Research ERERC Centre Val de Loire, Tours, France (Chairperson Dr B. Birmele) on 10 July 2020. No patient consent was needed as this retrospective study was non-interventional. All patients admitted to Tours University Hospital are informed about and able to refuse the use of their anonymized data for research purposes.

Results

Flow chart

Our algorithm found 808 patients matching our primary research criteria. A total of 421 patients matched inclusion criteria following our manual analysis of medical records, out of 161,423 patients from our DataMart (0.3%). One patient was excluded due to an early death before any diagnosis was made. Eventually, 420 initial and final diagnoses were collected and enabled including 420 patients ( Figure 1 ).

Figure 1. Flow chart.
Figure 1. Flow chart.

Referring departments

Recurrent sweating was reported in patients from 27 different medical departments among the same tertiary care centre during the year 2018, including both out-patients and in-patients ( Appendix 1 ). Half of those reports were spread across only four departments: Internal Medicine, Haematology, Pneumology, and Infectious Diseases ( N = 223/50.2%; single-patient multiple admissions being counted individually).

Aetiological findings

Recurrent sweating occurred among 420 patients and over 130 aetiologies or groups of pathologies were identified after at least one year of follow-up ( Table 1 and Appendix 2 ). No secondary cause was found for 70 patients (16.7%). Malignancy was the most frequent diagnosis group, including 119 patients (28.3%), half of them presenting with haematologic malignancies. Non-Hodgkin’s lymphoma ( N = 35) was the most frequent haematologic malignancy and lung cancer ( N = 13) was the most frequent solid organ cancer. Infectious diseases were identified for 44 patients (10.5%) and medications were involved in 33 patients (7.9%). Tuberculosis was the most frequently involved infection ( N = 13). Drug-induced recurrent sweating included 19 different pharmacological classes ( Table 2 ). All the patients’ medication data at the time the symptoms occurred were collected and each pharmacological class frequency was compared between patients, with no aetiological findings for their symptomatology and patients with established diagnoses as a comparison group. No statistical difference could be found between the two groups (data not shown). Systemic autoimmune and autoinflammatory diseases were identified in 24 patients (5.7%) and endocrine diseases in 22 (5.2%). Other following organs/systems involvement represented less than 5% of the diagnoses each: rheumatologic, psychiatric, neurologic, respiratory, non-oncologic haematologic, digestive and cardiovascular diseases. Non-pathologic conditions including menopause and pregnancy were also associated with recurrent sweating in 6 patients (1.4%). Surgical complications, obesity, allergies, dermatologic, ear nose throat (ENT), gynaecologic, and environmental diseases were among the rarest diagnoses and involved less than 1% of patients each. Extensive follow-up provided a diagnosis for 14 additional patients who did not have one at the end of their initial exploration. It also corrected the initial diagnosis in 13 cases.

Table 1.
Main aetiologies of recurrent sweating.
N = 420 patients (aetiologies with a frequency of 1 in 420 are not shown and are presented in Appendix 2 ). *Including allergies, dermatologic, and gynaecologic diseases, ENT-related diseases, environmental and nutritional diseases, and surgical complications.

AetiologiesNN (%)
Cancer (non-haematologic)Lung carcinoma1360 (14.3)
Renal carcinoma6
Breast carcinoma5
Cholangiocarcinoma5
Pancreatic adenocarcinoma5
Colorectal adenocarcinoma4
Prostate adenocarcinoma3
Hepatocellular carcinoma2
Kaposi’s sarcoma2
Leiomyosarcoma2
Melanoma2
Non-seminomatous mediastinal germ cell tumour2
Metastasis (undetermined)2
CardiovascularHigh blood pressure49 (2.1)
Vasovagal syncope2
DigestiveCrohn’s disease510 (2.4)
Ulcerative colitis2
Chronic inflammatory bowel disease (unspecified)2
EndocrineDysthyroidism822 (5.2)
Pituitary adenoma5
Adrenal insufficiency2
Diabetes2
Ovarian insufficiency2
Haematologic
OncologicLymphoma4759 (14)
Non-Hodgkin’s lymphoma35
Hodgkin’s lymphoma11
Chronic lymphocytic leukaemia8
Multiple myeloma3
Non-OncologicMyelofibrosis312 (2.9)
Histiocytosis2
Infectious diseasesMycobacterium tuberculosis1344 (10.5)
Non-tuberculous mycobacteria2
HIV3
Cytomegalovirus3
Helicobacter pylori gastritis2
Chronic osteoarticular infection3
Male urinary tract infection2
Malaria2
Pneumonia2
Post-viral syndrome2
Medications(see Table 2 )33 (7.9)
NeurologicPeripheral neuropathy413 (3.1)
Neuropathic pain3
Dysautonomia2
PhysiologicMenopause/perimenopause56 (1.4)
PsychiatricDepressive and/or anxiety disorder1217 (4)
Withdrawal syndrome3
RespiratoryObstructive sleep apnoea512 (2.9)
RheumatologicPeripheral spondyloarthropathy319 (4.5)
Fibromyalgia2
Rheumatoid arthritis2
RS3PE2
Arthritis (unspecified)2
SystemicVasculitis624 (5.7)
(General,Lupus3
Autoimmune orSarcoidosis3
Autoinflammatory)Autoinflammatory disease (unspecified)3
Still’s disease2
Primary hyperhidrosis / No aetiology70(16.7)
Others*10(2.3)

Table 2.
Drug-induced recurrent sweating.
Ab: antibodies; SNRI: Serotonin-Noradrenaline Reuptake Inhibitors; SSRI: Selective Serotonin Reuptake Inhibitors. For precise database results, see Appendix 3 . a Medications with a mention of sweat-inducing potential in their summary of product characteristics. b Medications with no mention of sweat-inducing potential in their summary of product characteristics but with a previously reported association with sweating in scientific literature [ 12 , 13 , 20–24 ] . c Medications with no mention of sweat-inducing potential in their summary of product characteristics nor in scientific literature but with reported cases in pharmacovigilance databases.

Pharmacological classNMain reported drugsPathophysiology
Corticosteroids3bIncreased sympathetic activity through glucocorticoid receptors
Immunosuppressive therapy3Tacrolimus a , Mycophenolate mofetil b , Leflunomide c
Anti-PD-1 Ab2Pembrolizumab
TNFα inhibitors2Adalimumab a , Infliximab aImbalance in cytokines network
Anti-IL-17 Ab1Ixekizumab
Tyrosine kinase inhibitors1Sunitinib
Chemotherapy (unspecified)1b
Anti-androgen/GnRH agonists3Cyproterone acetate, Leuprorelinea + Abiraterone, Triptorelin aAnti-estrogenic action
Aromatase inhibitor2Letrozole a , Exemestane cAnti-estrogenic action
Estrogen receptor modulators1Tamoxifen bAnti-estrogenic action
Hormonal contraception1Ethinylestradiol + Levonorgestrel c
Antiretroviral1Emtricitabine + Rilpivirine + Tenofovir alafenamide
Morphine2Fentanyl aHistamine release
Cholinesterase inhibitors1Pyridostigmine aCholinesterase inhibition
SNRI3Venlafaxine aSerotonergic effect on hypothalamus or spinal cord
SSRI3Paroxetine a , Fluoxetine aSerotonergic effect on hypothalamus or spinal cord
GABA-R modulators1Etifoxine
Antipsychotic1Paliperidone
Antiepileptic1Lamotrigine c , Lacosamide

Clinical and biological characteristics

We divided the patients into five groups: malignancies, infection, other inflammatory diseases, other non-inflammatory diseases, and the absence of aetiological findings, based on the pathophysiological mechanisms of each disease ( Table 3 ). We provided each group with clinical and biological characteristics. If overall sex ratio was close to 1, men did more frequently present with malignancies (60%) and infections (70%) than women. Patients with malignancies were significantly older than other groups (64 [IQR 51.5–73] vs 50 [IQR 36–63] years; p < .01). BMI did not differ between groups. Immunodeficiency was more frequent in patients with other inflammatory diseases, notably due to immunosuppressive treatments ( N = 17; 23.9%). Four of 15 patients with solid organ transplants remained without diagnosis. Among patients without diagnosis, six (8.6%) had a history of sleep apnoea and 25 (35.7%) were smokers. Patients with non-inflammatory diseases and those without diagnosis were less frequently hospitalised (39.7% and 34.3% vs 67.2% for malignancies, 70.5% for infections, and 63.4% for other inflammatory diseases) and were largely treated in out-patient clinics.

Table 3.
Patients’ characteristics by group of pathologies.
Data are N (%) or median (± IQR). a Among the female population. b Immunodeficiency. c Solid organ transplant. d White blood cells.

TotalMalignancyInfectionOther inflammatoryOther non- inflammatoryNo diagnosis
N420 (100)119 (28.3)44 (10.5)71 (16.9)116 (27.6)70 (16.7)
Sex (F/M) (N)213/20748/7113/3140/3169/4743/27
Age (median)53 (39–67)64 (51.5–73)43 (28.5–53)49 (33.5–66)53 (39–64)47 (39.5–61)
BMI (median)24 (21–27.4)24.3 (21.4–27.1)22.9 (19.2–25)23.6 (21.3–28)25 (22.5–30.8)23.6 (20.5–27.3)
Menopause a ( N )111 (52.4)36 (75)3 (23.1)17 (42.5)41 (59.4)14 (33.3)
Medical history ( N )
ID b76 (18.1)17 (14.3)8 (18.2)17 (23.9)20 (17.2)14 (20)
HIV17 (4)5 (4.2)4 (9.1)1 (1.4)4 (3.4)3 (4.3)
SOT c15 (3.6)4 (3.4)2 (4.5)1 (1.4)4 (3.4)4 (5.7)
Sleep apnoea23 (5.5)4 (3.4)1 (2.3)1 (1.4)11 (9.5)6 (8.6)
Smokers119 (28.3)28 (23.5)13 (29.5)17 (23.9)36 (31)25 (35.7)
Hospitalized226 (53.8)80 (67.2)31 (70.5)45 (63.4)46 (39.7)24 (34.3)
Duration (N)
15 to 21 days19 (4.5)2 (1.7)10 (22.7)3 (4.2)3 (2.6)1 (1.4)
≥ 21 days to 3 months192 (45.7)69 (58)21 (47.7)30 (42.3)47 (40.5)25 (35.7)
≥ 3 months to 12 months124 (29.5)39 (32.8)12 (27.3)21 (29.6)32 (27.6)20 (28.6)
≥ 1 year85 (20.2)9 (7.6)1 (2.3)17 (23.9)34 (29.3)24 (34.3)
Fever (N)87 (20.9)26 (24.8)22 (51.2)28 (39.4)7 (6)4 (5.7)
General state impairment (N)248 (59)98 (82.4)33 (75)51 (71.8)39 (33.6)27 (38.6)
Symptoms’ occurrence (N)
Night only375 (89.3)106 (89.1)40 (90.1)70 (98.6)97 (83.6)62 (88.6)
Night and day42 (10)12 (10.1)4 (9.1)19 (26.8)1 (0.9)6 (8.6)
Day only3 (0.7)1 (0.8)0002 (2.9)
Laboratory characteristics
CRP (mg/l)8.2 (1.3–55.6)26 (4.9–85.2)44.1 (6.1–86.3)14.9 (1.3–72.4)2.2 (0.7–8.2)1.2 (0.7–2.2)
LDH (UI/l)235 (187–313)261 (206–354)235 (170–247)235 (191–266)223 (180–260)183 (159–240)
WBC d (10 9 cells/l)8 (6–10.8)9.1 (7–13.6)7.9 (5.8–10.5)8.2 (5.9–11.1)7.4 (6–8.8)6.6 (4.8–8.4)
Lymphocytes (10 9 cells/l)1.7 (1.2–2.3)1.5 (0.9–2.2)1.6 (1.1–2.2)1.8 (1.2–2.3)2 (1.5–2.4)1.9 (1.4–2.6)
Neutrophils (10 9 cells/l)5 (3.3–7.2)5.7 (3.7–8.2)5.3 (3.3–7.1)5.2 (3.1–8)4.5 (3.3–6)3.9 (2.8–5.2)
Haemoglobin (g/dl)12.9 (11.4–13.9)11.8 (10.7–13.2)12.8 (11.8–13.5)12.4 (11.3–13.9)13.6 (12.6–14.4)13.7 (12.3–15.1)

Symptoms occurred mostly during the night ( N = 375; 89.3%), less frequently during both night and day ( N = 42; 10%), and exceptionally exclusively during daytime ( N = 3; 0.7%). Symptoms occurring during both night and day were more frequently caused by other inflammatory diseases (19 of 42). Regarding duration of symptoms, for patients who reported recurrent sweating for more than 2 weeks and less than 3 weeks, 10 of 19 had an infection. Recurrent sweating with an onset between 3 weeks and 3 months before admission was more frequently reported ( N = 192; 45.7%). When considering patients with recurrent sweating between 3 weeks and 3 months and those between 3 months and 1 year, we found similar proportions between the 5 groups of pathologies. Patients with recurrent sweating for at least one year had a lower proportion of malignancy and infection, and a higher proportion of other inflammatory and non-inflammatory diseases, as well as absence of diagnosis.

Fever and impaired general condition were more frequent as well as higher CRP, LDH, and neutrophil counts in patients with malignancy, infection, and other inflammatory diseases compared to groups of other non-inflammatory diseases and the group without diagnosis.

Diagnostic tests

We evaluated the diagnostic performance of fever, impaired general condition (defined by asthenia, anorexia, and/or weight loss), elevation of CRP, LDH or neutrophils for the distinction between inflammatory aetiologies and others, as well as a one-year symptom duration to distinguish non-infectious and non-malignant causes from the others ( Table 4 ). Fever had a high specificity (94%) but a low sensitivity (33%), with a positive predictive value (PPV) of 0.87 in favour of malignancies, infection, and other inflammatory diseases as compared to non-inflammatory aetiologies. Impaired general condition had a sensitivity of 78% and a specificity of 65% in favour of the same 3 groups. To distinguish malignancies, infection, and inflammation from other causes, for a threshold of 5.6 mg/l, CRP had a high PPV of 0.86. For a threshold of 226.5 UI/l, LDH had a PPV of 0.8. And for a threshold of 5.3 × 10 9 cells/l, neutrophils had a PPV of 0.77. A duration of symptoms greater than one year had a high specificity (94%) and a PPV of 0.88 in favour of non-infectious and non-malignant diseases.

Table 4.
Diagnostic performance of clinical and biological parameters.
For continuous variables, optimal cut-points were established using a ROC curve. Sensitivity and specificity were assessed for different cut-points and the optimal cut-point was defined as the maximisation of Youden’s index. Accuracy is defined as: (True positive + True negative)/total of patients. PPV: Positive predictive value; NPV: Negative predictive value; AUC: Area under the curve; Imp. Gen. condition: Impaired general condition.

ParameterCut-pointPPVNPVSensitivity (95% CI)Specificity (95% CI)AUC (95% CI)Accuracy
In favour of malignancy, infection, and other inflammatory aetiologies (vs others)
Fever0.870.533394–0.6
Imp. Gen. condition0.730.77865–0.72
CRP5.6 mg/l0.860.5771.1 (65–77.2)76.5 (68.4–85)79.2 (74.1–84.4)0.73
LDH226.5 UI/l0.80.3959.8 (51.2–68.5)63.5 (50–75.1)65.2 (56.5–73.8)0.61
Neutrophils5.3 × 10 9 /l0.770.4351.2 (44.5–57.9)70.4 (62–78.7)61.1 (54.9–67.3)0.58
In favour of other aetiologies and primary hyperhidrosis (vs malignancy and infection)
≥ 1 year duration0.880.462994–0.54

Discussion

When confronted to the symptomatology of recurrent sweating, the recognition of underlying diseases is a key challenge for clinicians. It may sometimes be difficult to distinguish between secondary and primary hyperhidrosis. To our knowledge, no available data on the aetiologies of recurrent sweating in hospitalised patients have been published to date. Our retrospective cohort of 420 patients is the largest set of diagnoses to date associated with recurrent sweating and the largest cohort of secondary hyperhidrosis. Walling et al. suggested that primary hyperhidrosis onset was classically between 14 and 25 years old, with excessive sweating of more than 6 months’ duration, involving eccrine-dense sites, bilateral and symmetric, associated with a family history, and occurring only during the day [ 13 ]. We suggest that those criteria, which were developed in an outpatient dermatology department, are not applicable in certain settings, especially in hospitalised patients. Our patients were mainly over 25 years old, and other studies have reported idiopathic night sweats among elderly patients [ 10 ]. Almost all of the patients had nocturnal sweating episodes, including those identified as having undiagnosed hyperhidrosis, which may exclude day-time occurrence as a clear-cut criterion. After proper follow-up, our undiagnosed patients may be considered to actually have primary hyperhidrosis, and the current criteria might be expanded. We also showed that a duration cut-point of one year instead of 6 months might be more appropriate to consider primary hyperhidrosis in older patients, as it better decreased the risk of missing life-threatening diseases such as malignancies and infection.

Taking into account our main findings, we suggest a diagnostic approach by the mean of an algorithm for the investigation of recurrent sweating ( Figure 2 ). Duration of less than 3 weeks is mainly associated with infectious diseases. Proper investigation of recurrent sweating should be considered after at least 3 weeks’ duration. We suggest key clinical examination points and simple tests that could help orientate the investigation according to the aetiologies we report. Duration of one year or more is poorly associated with infections and malignancies, and other diagnoses should thus be considered in the absence of other signs in favour. Fever, impaired general condition, and CRP > 5.6 mg/l could be useful signs to consider inflammatory diseases. Second-line diagnostic procedures should be directed by examination. In the event of strong suspicion of malignancy or infection, FDG-PET/CT may help the investigation [ 18 ].

Figure 2. Diagnostic approach for recurrent sweating. CBC: Blood cell count; ANCA: antineutrophil cytoplasmic antibodies; TSH: thyroid-stimulating hormone: GH: growth hormone; IGF…
Figure 2. Diagnostic approach for recurrent sweating. CBC: Blood cell count; ANCA: antineutrophil cytoplasmic antibodies; TSH: thyroid-stimulating hormone: GH: growth hormone; IGF-1: Insulin-like growth factor 1; LH: Luteinizing hormone; FSH: follicle-stimulating hormone.

Several reviews detailed available therapeutic options for hyperhidrosis [ 19–21 ]. Treatment of secondary hyperhidrosis relies on the treatment of the underlying diseases. In some cases, if treatment is ineffective, unavailable, or if the symptoms are poorly tolerated, generalized hyperhidrosis could be treated using oral or transcutaneous anticholinergic drugs. Their use is however limited by their numerous adverse effects and contra-indications, especially in the elderly. Other oral alternatives include beta-blockers, clonidine, indomethacin, and calcium channel blockers, but with limited data. None have been formally approved in this indication by drug agencies. Options for the treatment of focal hyperhidrosis consist of topical antiperspirants, iontophoresis, botulinum toxin injections, and local surgical procedures including sympathectomy.

Our study’s design strength is that retrospective research using a Clinical Data Warehouse enabled us to largely include patients from multiple departments and prevented a selection bias. We aimed to provide an as complete as possible list of diagnoses associated with recurrent sweating to be considered for differential diagnosis in order not to miss the rarest aetiologies. Our study also had some limitations. Being monocentric, data came from only a single centre in France. Our results should be confirmed in other centres and might not be comparable to the aetiologies of secondary hyperhidrosis worldwide, such as tropical countries with a wider range of infectious diseases. Its retrospective design, including documents from departments which were not specialized in the management of hyperhidrosis, did not allow for detailed description of the symptomatology. Some departments may also have searched more systematically than others for the occurrence of sweating. Our centre is a tertiary university hospital and patients with rare diseases may be over-represented. Thus, although primary hyperhidrosis is usually described as more frequent than secondary hyperhidrosis, our cohort lacked younger subjects who typically present with primary hyperhidrosis. We included patients from both in and out-patient clinics in similar proportions. However, if those two groups enabled a comprehensive overview of diseases that can be faced within a hospital, they differed as hospitalised patients present with worsened conditions and should be explored accordingly. Adequate warning signs are more frequent in the event of hospitalization.

Conclusion

We identified the main aetiologies of recurrent sweating in a university hospital setting and identified warning signs including fever, impaired general condition, alteration to or elevated CRP to help clinicians identify situations requiring extensive investigation. On the contrary, the absence of those warning signs, or a prolonged duration greater than a year, associated with a negative examination-based exploration, should not systematically be investigated by invasive or irradiating tests. Primary hyperhidrosis may have late onset and more studies are needed to confirm those findings.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Data availability statement

The data that support the findings of this study are available from Nived Collercandy, upon reasonable request. All authors had access to the data and a role in writing the manuscript.

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Departments of consultation or hospitalization of patients presenting with recurrent sweating

Patients referred to multiple departments were counted in each one separately. Percentage of total is the proportion in our study population ( N = 420).

*1%: Intensive Care, Cardiology, Neurosurgery, Orthopaedic surgery, Geriatrics, Nutrition; < 1%: ENT, Palliative care, Thoracic surgery, Nuclear Medicine, Physiatry.

DepartmentTotal N (%)Hospitalization NConsultation N
Internal Medicine82 (20)4834
Haematology60 (14)3129
Pneumology47 (11)3116
Infectious Diseases46 (11)3214
Emergency29 (7)1415
Rheumatology25 (6)214
Hepato-Gastro-Enterology21 (5)174
Nephrology & Transplantation20 (5)911
Endocrinology19 (4)712
Oncology17 (4)710
Neurology16 (4)88
Dermatology16 (4)88
Psychiatry11 (2)38
Gynaecology & Obstetrics8 (2)35
Digestive Surgery7 (2)43
Others*36 (9)––

Aetiologies of recurrent sweating

N = 420 patients.

AetiologiesNN total (%)
AllergyGrass pollen allergy1(0.2)
Cancer (non-haematologic)Lung carcinoma1360 (14.3)
Metastatic7
Renal carcinoma6
Metastatic4
Breast carcinoma5
Metastatic3
Cholangiocarcinoma5
Metastatic5
Pancreatic adenocarcinoma5
Metastatic3
Colorectal adenocarcinoma4
Metastatic3
Prostate adenocarcinoma3
Metastatic1
Hepatocellular carcinoma2
Kaposi’s sarcoma2
Leiomyosarcoma2
Melanoma2
Metastatic2
Non-seminomatous mediastinal germ cell tumour2
Adrenocortical carcinoma1
Cutaneous squamous-cell carcinoma1
Endometrial adenocarcinoma1
Larynx carcinoma1
Metastatic1
Oropharyngeal carcinoma1
Osteosarcoma1
Pheochromocytoma1
Metastasis (undetermined)2
CardiovascularHigh blood pressure49 (2.1)
Vasovagal syncope2
Heart failure1
Leriche syndrome1
Orthostatic hypotension1
DermatologicBullous pemphigoid12 (0.5)
Chronic wound1
DigestiveCrohn’s disease510 (2.4)
Ulcerative colitis2
Chronic inflammatory bowel disease (unspecified)2
Auto-immune hepatitis1
EndocrineDysthyroidism822 (5.2)
Graves’ orbitopathy1
Pituitary adenoma5
Growth hormone3
IGF-1 + prolactin1
Prolactin1
Adrenal insufficiency2
Diabetes2
Ovarian insufficiency2
Adrenal adenoma1
Hypercalcemia1
Thymoma1
ENTMeniere’s disease1(0.2)
EnvironmentalSynthetic duvet1(0.2)
GynaecologicEndometriosis12 (0.5)
Uterine fibroid necrosis1
Haematologic
OncologicLymphoma4759 (14)
Non-Hodgkin’s lymphoma35
Diffuse large B-cell lymphoma16
T-cell lymphoma5
Follicular lymphoma4
Mantle cell lymphoma4
Waldenström’s macroglobulinemia3
Marginal zone lymphoma1
Hodgkin’s lymphoma11
Chronic lymphocytic leukaemia8
Multiple myeloma3
Acute lymphoblastic leukaemia1
Non-OncologicMyelofibrosis312 (2.9)
Histiocytosis2
AL Amyloidosis1
Essential thrombocythemia1
Hemophagocytic lymphohistiocytosis (no primary aetiological finding)1
Lymphoid hyperplasia1
Lymphangiomatosis1
Mastocytosis1
Myelodysplastic syndrome1
Infectious diseasesMycobacterium tuberculosis1344 (10.5)
Pulmonary10
Lymphadenitis5
Pericarditis1
Spinal/bone1
Erythema nodosum1
Non-tuberculous mycobacteria2
HIV3
Pneumocystis jirovecii1
Mycobacterium intermediae1
Cytomegalovirus colitis1
Non-compliance with treatment1
Cytomegalovirus (acute infection)2
Cytomegalovirus (reactivation)1
Parvovirus B19 (acute infection)1
Helicobacter pylori gastritis2
Chronic osteoarticular infection3
Cutibacterium acnes1
Staphylococcus epidermidis1
Streptococcus mitis1
Male urinary tract infection2
Endocarditis1
Staphylococcus aureus1
Bartonella henselae (meningitis and hepatitis)1
Coxiella urnetiid / Q fever (acute infection)1
Plasmodium ovale1
Plasmodium vivax1
Post-streptococcal erythema nodosum1
Pneumonia2
Pulmonary abscess1
Cutaneous abscess1
Ovarian abscess (with peritonitis)1
Viral infection (undetermined)1
Post-viral syndrome2
Non documented infection1
MedicationsCorticosteroids333 (7.9)
Tacrolimus1
Mycophenolate mofetil1
Leflunomide1
Pembrolizumab2
Infliximab1
Adalimumab1
Ixekizumab1
Sunitinib1
Chemotherapy (unspecified)1
Cyproterone acetate1
Ethinylestradiol + Levonorgestrel1
Enantone + Abiraterone1
Exemestane1
Tamoxifen1
Letrozole1
Triptorelin1
Emtricitabine + Rilpivirine + Tenofovir alafenamide1
Morphine2
Pyridostigmine1
Venlafaxine3
Paroxetine2
Fluoxetine1
Etifoxine1
Paliperidone1
Lamotrigine + Lacosamide1
NutritionObesity1(0.2)
NeurologicPeripheral neuropathy413 (3.1)
Neuropathic pain3
Dysautonomia2
Chronic polyradiculoneuritis1
Occipital neuralgia1
Small fibre neuropathy1
Tolosa-Hunt syndrome1
PhysiologicMenopause/perimenopause56 (1.4)
Pregnancy1
PsychiatricDepressive and/or anxiety disorder1217 (4)
Depressive disorder4
Anxiety disorder10
Withdrawal syndrome3
Burn-out1
Psychogenic non-epileptic seizure1
RespiratoryObstructive sleep apnoea512 (2.9)
Asthma1
Chronic obstructive pulmonary disease1
Cystic fibrosis1
Lymphocytic interstitial pneumonia1
Post-infectious bronchiolitis1
Post-radiotherapy pneumonia1
Pulmonary arterial hypertension1
RheumatologicPeripheral spondyloarthropathy319 (4.5)
Fibromyalgia2
Rheumatoid arthritis2
RS3PE2
Arthritis (unspecified)2
Ankylosing spondylitis1
Avascular necrosis of the talus1
Chondrocalcinosis1
Complex regional pain syndrome1
Polymyalgia rheumatica1
Sciatica1
Seronegative arthritis1
Inflammatory arthromyalgia (unspecified)1
Surgical complicationPost-operative pain12 (0.5)
Inflammatory periprosthetic lymphocele (breast)1
SystemicVasculitis624 (5.7)
(General,Giant cell arteritis1
Autoimmune orGranulomatosis with polyangiitis2
Autoinflammatory)Microscopic polyangiitis1
Polyarteritis nodosa1
Not specified1
Lupus3
Sarcoidosis3
Autoinflammatory disease (unspecified)3
Still’s disease2
Familial Mediterranean fever1
Erythema nodosum1
IgA deficiency1
Non-allergic histaminic angioedema1
Polyserositis (unspecified)1
Polyadenitis (unspecified)1
Relapsing polychondritis1
Primary hyperhidrosis / No aetiology70(16.7)

Sweat-inducing potential of drugs in medical databases

Very common (≥ 1/10); common (≥ 1/100 to < 1/10); uncommon (≥ 1/1,000 to < 1/100); rare ( ≥ 1/10,000 to < 1/1,000); very rare (< 1/10,000), not known (cannot be estimated from the available data).

Values in bold represent drugs that were considered sufficiently reported in their respective database (N ≥ 5 for FPVD and N ≥ 100 for Vigilyze).

Pharmacological classMain reported drugsSummary of product characteristicsFrench National PV databaseWorldwide PV database (= Vigilyze)
CorticosteroidsNo
Immunosuppressive therapyTacrolimus Mycophenolate mofetil LeflunomideYes (hyperhidrosis, common) No No1 1 580 77 105
Anti-PD-1 AbPembrolizumabNo085
TNFα inhibitorsAdalimumab InfliximabYes (night sweats, uncommon) Yes (hyperhidrosis, common)21 644012 1483
Anti-IL-17 AbIxekizumabNo1113
Tyrosine kinase inhibitorsSunitinibNo0181
Chemotherapy (unspecified)
Anti-androgen / GnRH agonistsCyproterone acetate Leuproreline TriptorelinNo Yes (sweats, very common) Yes (hyperhidrosis, very common)3 3 024 1283 105
Aromatase inhibitorLetrozole ExemestaneYes (very common) No5 6267 133
Estrogen receptor modulatorsTamoxifenNo4249
Hormonal contraceptionEthinylestradiol + LevonorgestrelNo7128
AntiretroviralEmtricitabine + Rilpivirine + Ténofovir alafenamideNo224
MorphineFentanylYes (hyperhidrosis, common)223166
Cholinesterase inhibitorsPyridostigmineYes (not known)641
SNRIVenlafaxineYes (hyperhidrosis, including night sweats, very common)782549
SSRIParoxetine FluoxetineYes (hyperhidrosis, very rare) Yes (hyperhidrosis, common)91 272958 1073
GABA-R modulatorsEtifoxineNo12
AntipsychoticPaliperidoneNo4126
AntiepilepticLamotrigine LacosamideNo No12 1295 39

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты