IoT-Based Neonatal Incubator Monitoring System
IoT-Based Neonatal Incubator Monitoring System
Abstract—Neonatal incubators are essential in neonatology ranges defined by both the manufacturer and the institution
rooms and, as they are life support equipment, they require a that owns the equipment [7].
maintenance frequency of at least every six months to guarantee
their performance and safety. To analyze them, several devices There are neonatal incubator analyzers from different man-
exist designed to measure parameters such as temperature, ufacturers and different models. However, one of the most
humidity, and noise level inside the baby´s chamber. A complete widely used analyzers worldwide is the Fluke INCU II. It is
analysis consists of 9 tests with a duration of 5 hours and 56 easy to use and gives reliable results ensuring the safety of
minutes overall. During this time, the workflow of the incubator babies [7].
is interrupted. The objective of this research is to develop an
IoT-based prototype capable of monitoring the parameters inside The UNE-EN 60601-2-19 standard describes the essential
the chamber; without stopping the operation of the equipment safety requirements for the proper operation of neonatal incu-
and that provides the security of not affecting the health of bators, ensuring the health of the newborn and the operator.
the premature baby. The IoT architecture was designed and the This standard contains the mechanical and electrical safety
safety criteria for each component used to build the prototype
were determined. Experimentation was used to perform tests in guidelines, as well as regulations related to protection against
simulated environments and in a real environment. The results excessive temperatures and alarm systems [8].
measured by the prototype were compared with those obtained The Fluke analyzer allows you to verify all international
by the certified measurement instrument Fluke INCU II. The standards: IEC 60601-2-19, IEC 60601-2-20 and IEC 60601-2-
values were compared using non-parametric statistic analysis to
determine points for improvement. 21. This device allows to check incubators and radiant heaters.
Index Terms—biomedical engineering, IoT, monitoring system, It performs 9 different tests [7].
neonatal incubators, prototype It is important to mention that each test has a different
duration time. The analyzer needs 5 hours and 56 minutes to
I. I NTRODUCTION run all tests. It is not possible to analyze an incubator without
stopping it’s use and altering the workflow within a hospital.
Neonatal incubators are the medical devices that create an This research project proposes the development of an initial
ideal environment for premature babies where temperature, prototype capable of performing certain tests of a neonatal
humidity, noise, and oxygen flow are regulated [1]. This incubator analyzer that does not interrupt workflow and is safe
devices provide a protected environment for low birth weight for the baby. This device allows real-time monitoring of certain
infants [2]. These are used to increase the chances of survival environmental parameters created by the incubator.
of premature babies in the extrauterine environment [3]. It This paper is divided in chapters. Chapter II shows the
allows the baby’s body reduce the heat loss [4]. state of the art. Chapter III the methodology used for the
A neonatal incubator has a chamber to place the baby development of the prototype, IV shows the results and finally
covered by a transparent canopy. Several access ports allow chapter V the conclusions.
the medical team access to the baby for feeding, examination
and treatment. The baby is laid on a mattress inside located
on top of a fan and heater. These are responsible for providing II. S TATE OF THE A RT
a forced circulation of hot air within the compartment [5].
The malfunction of neonatal incubators can cause serious Multiple medical devices, sensors, diagnostic and imaging
injuries and even death of premature babies. The most frequent devices can be seen as smart objects. IoT-based healthcare
factors that cause these events are: the lack of inspection, the services are expected to reduce costs, increase quality of life
lack of an analysis protocol, errors in the production of said and enrich the user experience [9]. The IoT healthcare network
equipment and environmental noise [4] [6]. facilitates the transmission and reception of medical data, and
An incubator analyzer measures parameters such as temper- allowing the use of communications [15]. IoT in healthcare
ature, humidity, sound, and air circulation inside the incubator. has multiple applications like remote monitoring; this includes
It´s main objective is to verify that it is operating within the patients and clinical settings [11] [16].
A. Temperature And Relative Humidity Verification Device standard was used to determine the safety requirements inside
Inside Infant Incubator Through IoT in Thailand neonatal incubators. The criteria taken into consideration for
The authors of reference [6] developed a device that mea- the development of the prototype are:
sures the temperature and humidity inside the chamber of • The device casing must be able to withstand temperatures
the neonatal incubator remotely through IoT. 5 sensors are of at least 38°C.
positioned on the baby’s mattress that transmit the data to • The temperature sensor must have an accuracy of ± 0.8
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B. Prototype´s Case
The size of the device were designed so that does not
interfere with the access to the chamber. The casing has four
suction cups on its front face to firmly hold the device in place
and prevent it from falling.
Fig. 3 shows an isometric view of the prototype casing
in SolidWorks with it´s size in cm. A laser cutter was used
to make the acrylic cuts precisely. The size of the casing is
enough to keep all components safely inside and small to be Fig. 5. Prototype´s IoT architecture
placed inside the incubator, as seen in Fig. 4.
The prototype design provides the facility to open its
casing for maintenance in case any component fails. It also D. Prototype testing in controlled environment
provides the opportunity of cleaning the device to prevent Pilot tests of the prototype were carried out in a controlled
cross-contamination. environment, for which the control booths of the Industrial
Engineering laboratory of UNITEC, Tegucigalpa were used.
These cabins have sound, high temperature, low temperature,
and humidity simulators.
The prototype’s data was compared to a hygrometer and
decibel meter. The prototype was fixed to the wall of the
controlled cabin to see if the suction cups can keep it in place.
It was observed that data was transferred simultaneously to
UBIDOTS.
E. Prototype testing in real environment
Fig. 3. Isometric view of casing
Functional tests of the prototype were carried out in a
neonatal incubator at Hospital María in Tegucigalpa. A Fluke
INCU II was used simultaneously to compare the data. Fig. 6
shows both devices measuring the 3 parameters.
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2023 IEEE Latin American Electron Devices Conference (LAEDC) Puebla, México, July 3-5, 2023
hour and every hour until completing 6 hours. The results for Temperature measurements are significantly similar between
the temperature sensor are shown in Table I with the difference the prototype and the Fluke analyzer, which indicates this
between both devices. The same was done for the humidity parameter shows the real temperature inside the incubator and
and noise levels. can be used as an analyzer.
For the humidity and noise level was not the case; mea-
TABLE I surements are significantly different, which indicates those
T EMPERATURE READINGS IN 6 HOURS
parameters are not correctly displayed by the prototype. This
Time(min) Prototype(ºC) Fluke(ºC) Difference(ºC)
error could be solved using a correction factor on the code o
selecting more accurate sensors.
0 29.7 32.1 -2.4
5 30 32 -2 The next step for this research is improve the code to be able
10 31.2 32.1 -0.9 to emulate more tests performed by a certified analyzer.This
15 31.4 32.2 -0.8 prototype is the first step to develop an incubator analyzer that
20 31.6 32.2 -0.6
25 31.8 32.28 -0.48 can perform each test indicated by the standards.
30 31.9 32.3 -0.4
35 31.9 32.2 -0.3 ACKNOWLEDGMENT
40 32 32.3 -0.3
45 32.2 32.37 -0.17 Thanks to Hospital María de Especialidades Pediatricas, for
50 32.2 32.35 -0.15
60 33.6 33 0.6 its openness and willingness to perform the last tests for the
70 33.6 33 0.6 prototype. Specially, to Engineer Gracia Girón, for her time
80 33.4 32.71 0.69 and willingness to collaborate.
90 33.3 32.57 0.73
100 33.1 32.7 0.4 This work was supported by the Research Fund of Univer-
110 32.7 32.7 0 sidad Tecnológica Centroamericana (UNITEC), Honduras.
120 32.7 32.8 -0.1
180 33.3 32.81 0.49
240 33 32.75 0.25 R EFERENCES
300 33 32.86 0.14
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