| Literature DB >> 35935629 |
Liviu-Nicolae Ghilencea1, Maria-Roxana Chiru2, Miroslava Stolcova3, Gabriel Spiridon4, Laura-Maria Manea1, Ana-Maria Alexandra Stănescu5, Awais Bokhari6, Ismail Dogu Kilic7, Gioel Gabriel Secco8, Nicolas Foin9, Carlo Di Mario3,10,11.
Abstract
The recent pandemic with SARS-CoV-2 raises questions worldwide regarding telemedicine for housebound patients, including those with cardiovascular conditions. The need for further investigation, monitoring and therapeutic management are advancing practical issues which had not been identified for consideration prior to the pandemic. Using the marketing assessment, we identified the needs of the patients and evaluated the future steps necessary in the short term to meet them. The research found progress made via telemedicine in monitoring and conducting minor decisions (like up-titrating the doses of different medication regimens) in patients with several cardiovascular diseases (heart failure, atrial fibrillation, high blood pressure), as there is a worldwide trend to develop new telemonitoring biosensors and devices based on implantable delivered transcatheter. The worldwide telemedicine trend encourages a switch from small and hesitating steps to a more consistent assessment of the patients, based on high technology and Interventional Cardiology. Cardiovascular telemedicine, although made a sustainable effort in managing patients' health, has many obstacles to overcome before meeting all their needs. Data security, confidentiality and reimbursement are the top priorities in developing remote Cardiology. The regulatory institutions need to play an integrative role in leading the way for defining the framework of future telemedicine activities. The SARS-CoV-2 outbreak with all its tragedy served to reinforce the message that telemedicine services can be life-saving for cardiovascular patients. Once the Covid-19 era will fade away, telemedicine is likely to remain a complementary service of standard care. There is still room to improve the remote identification and investigation of heart disease, provide an accurate diagnosis and therapeutic regimen, and update regulations and guidelines to the new realities of technological progress in the field.Entities:
Keywords: COVID-19; SWOT analysis; cardiovascular disease; heart failure; implantable devices; systemic hypertension and arrhythmia; telemedicine; telemonitoring
Year: 2022 PMID: 35935629 PMCID: PMC9347362 DOI: 10.3389/fcvm.2022.868635
Source DB: PubMed Journal: Front Cardiovasc Med ISSN: 2297-055X
Telemedicine groups and description.
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| Real-time online assessment | Virtual video visits of patients (Teleconsultation) | Virtual outpatient's clinic | Patient at home directly connected via online video link with the cardiologist in the hospital |
| Second opinion offered by cardiologists to other health professionals (Teleexpertise) | Ambulance crew for patients with chest pain and dynamic ECG changes | Cardiologist on-call confirming the presumption of STEMI and indication to emergency catheterization | |
| GPs in medical unit/ surgery requesting medical advice for acute patients | In-hospital on-call cardiologists providing skilled support for undiagnosed and inconclusive cases | ||
| General medicine physicians in small hospitals seeking medical expertise | Performing clinical examination via video link and echocardiographic assessment to inpatients | ||
| Online video conference MDT meetings with clinical and interventional cardiologists, cardiothoracic surgeons, radiologists. | Experts of different specialities assessing difficult cases and taking management decisions | ||
| Remote monitoring | Wearable devices and implantable biosensors (Telemonitoring) | Heart failure monitoring | Weight, HR, LAP |
| Palpitations /syncope monitoring | ECG recording/ events record/ ILR | ||
| Systemic hypertension | BP curve |
ECG, electrocardiogram; MDT, multidisciplinary team; HR, heart rate; LAP, left atrial pressure; BP, blood pressure; GP, general practitioner; ILR, implantable loop recorder.
Figure 1The strengths, weaknesses, opportunities and threats (SWOT analysis) of telemedicine (1–11, 13–17).
Summary of different heart failure telemedicine studies.
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| HFHC | Randomized, controlled trial Multicentre | Alere Day Link HF Monitoring System (non-invasive device) | 315 | Treatment failure (rehospitalizations + cardiovascular deaths at 6 months) | No significant statistical differences |
| Kulshreshtha et al. ( | Randomized, controlled trial | Remote monitoring equipment | 150 | Primary: All-cause rehospitalizations | No significant statistical differences |
| TELE-HF | Randomized, controlled trial | Telemonitoring of symptoms | 1,653 | Readmission + Death of any cause | No significant statistical differences |
| WISH | Randomized, controlled trial | Weight monitoring: automatically transmitted vs telephone messaging | 344 | Primary: Cardiac rehospitalization | No significant statistical differences |
| CHAMPION | Prospective, single blind trial, NYHA class III HF | Wireless monitoring of pulmonary artery pressures with CardioMEMS heart sensor | 550 | Rate of hospital admissions | Positive |
| TIM-HF | Randomized, controlled trial | Telemonitoring of weight, ECG, blood pressure | 710 | Death of any cause | No significant statistical differences |
| INH | Randomized, controlled trial | Telephone based monitoring of blood pressure, heart rate, symptoms | 715 | Time to death or rehospitalizations | No significant statistical differences |
| CHAT | Randomized, controlled trial | Telewatch system (symptoms assessment through questionnaires) + follow-up by nurses | 405 | Primary: Packer clinical composite score | No significant statistical differences |
| IN-TIME | Randomized, controlled trial | Daily, multiparameter telemonitoring based on the ICD/CRT-D | 664 | Composite clinical score (including all-cause deaths and overnight hospital admission) | Positive |
| Blum et al. ( | Randomized, controlled trial | Remote monitoring of symptoms, blood pressure, heart rate | 204 | Primary: Readmissions in the first month | Positive only for the primary end-point |
| EFFECT De Simone et al. ( | Prospective, non-randomized | ICD telemonitoring | 987 | Mortality and rehospitalizations | Positive |
| OPTI-LINK HF | Randomized, controlled trial | ICD telemonitoring; Fluid status alert | 1,002 | Composite of deaths of any cause and cardiovascular rehospitalizations | No significant statistical differences |
| COMMIT-HF | Observational prospective cohort study | Daily ICD/CRT-D telemonitoring | 822 | Long term all-cause mortality | Positive |
| TIM-HF 2 | Randomized, controlled trial | Telemonitoring of symptoms, weight, blood pressure, heart rate | 1,571 | All-cause deaths or percentage of days lost due to unplanned cardiac readmissions | Positive |
| BeAT-HF | Randomized, prospective, multicentre, controlled trial In patients with HFrEF | Baroreflex activation therapy with BAROSTIM NEO system (electrode placed on the carotid sinus connected to a subcutaneous pulse generator) | 408 | Changes from baseline in 6 months for quality of life score, 6-min walk test, NT-proBNP levels | Positive |
| Bowers et al. ( | Randomized, prospective, controlled trial in patients with HFrEF | Active telemonitoring (symptoms, weight) | 209 | Primary: mortality rate | No significant statistical differences |
| Ploux et al. ( | Observational retrospective cohort study (one month before vs after the first French lockdown) | Multiparametric remote monitoring system (weight, blood pressure, heart rate, symptoms) | 53 | Medical contact index (cardiological/overall) | Decreased medical contact index after lockdown |
Summary of different atrial fibrillation telemedicine studies.
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| CRYSTAL AF | Randomized, controlled trial−2 arms in patients with cryptogenic strokes (insertable cardiac monitor | ECG monitoring with an insertable cardiac monitor | 441 | Primary: Time to first detection of AF in the first 6 months | 8.9 |
| Stegmann et al. ( | Randomized, controlled trial in patients with heart failure−2 arms (daily ECG | Daily ECG transmitted to a telemedical center | 879 | Newly documented AF | Positive (AF three times more frequently detected) |
| Lambert et al. ( | Unblinded, randomized, controlled trial in patients with recent AF ablation−2 arms (smartphone ECG | ECG recordings once per week or during symptoms (Kardia Mobile devices) | 100 | AF detection during the 6-month follow-up period | No significant statistical differences |
| Fitbit Heart study | Prospective single arm study | Fitbit trackers/ Smartwatches One week ECG patch monitor for patients with irregular heart rhythm detected by the device | 1,057 eligible individuals | Positive predictive value (PPV) of the first irregular heart rhythm detection in atrial fibrillation detection | PPV 98.2% (95% CI: 95.5–99.5%) |
| Bernstein et al. ( | Randomized, controlled trial−2 arms in patients with stroke due to large or small vessel disease (insertable cardiac monitor | ECG monitoring with an insertable cardiac monitor | (455; 699 initially enrolled) | Incident AF (>30 s) in 12 months | 12.1% |
| LOOP | Randomized, controlled trial, open label 1:3 (implantable loop recorder | ECG monitoring via implantable loop recorder | 493 | Primary outcome: stroke or arterial embolism | Negative for the primary outcome 31.8% |
Figure 2Vectorious Medical Technologies V-LAP™ wireless sensor, a second-generation heart failure (HF) monitoring system, used for remote LAP-guided Therapy Optimization during COVID-19 era at a patient with HF. (A) The unexpanded biosensor before implantation; (B) The biosensor after ex vivo expansion; (C) The catheter with the biosensor during deployment; (D) The 3D echocardiographic check of the biosensor positioning, as part of the interatrial septum (detail image) between the right atrium and left atrium (above); (E) The external unit (the belt for the patient) continuously captures and records the left atrial pressure; (F) The continuous diagram recording of the mean left arterial pressure monitored with V-LAP™. Alerts of the mean arterial pressure overpassing the normal values are transmitted via mobile to the cardiologist, allowing her/him to take action by optimizing the therapy. Reproduced from Di Mario et al. (58), with the courtesy of the authors.
Summary of different hypertension telemedicine studies.
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| Wakefield et al. ( | Randomized, controlled trial−3 treatment groups (high intensity vs. low intensity | Home telehealth device (daily BP monitoring and differentiated questionnaire low vs. high intensity group) and nurse management | 302 | Primary outcome: SBP change | Positive for the high intensity group |
| Hebert et al. ( | Randomized, controlled trial−3 arms (nurse management vs. home monitoring | Nurse counseling; Informing on strategies for controlling BP | 416 | Changes in SBP and DBP at 9 and 18 months | Positive for SBP in the nurse counseling group |
| Pan et al. ( | Randomized, controlled trial−2 arms | Home telemonitoring for blood pressure (delivered by a GP, a hypertension specialist, a nurse) | 198 | Change in SBP at 1, 3, and 6 months | Positive |
| Margolis et al. ( | Randomized, controlled trial−2 arms | Home BP monitoring and pharmacist management | 450 | Changes in SBP and DBP | Positive (for up to 24 months) |
| McManus et al. ( | Randomized, controlled trial−3 arms (self-monitoring | Self-monitoring with electronic sphygmomanometer | 1,003 | Change in SBP at 12 months | Positive in both intervention groups |
| Mohsen et al. ( | Randomized, controlled trial – 2 arms | Nurse counseling by follow-up phone calls | 100 | Changes in mean arterial pressure and body-mass index | Positive |