Professional Documents
Culture Documents
*
G.R. No. 168512. March 20, 2007.
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* THIRD DIVISION.
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570
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571
YNARES-SANTIAGO, J.:
2
This is a petition for review under Rule 45 of the 3Rules of
Court assailing the February 27, 2004 Decision of the
Court of Appeals in CA-G.R. CV No. 58668 finding
petitioner Orlando D. Garcia liable4 for gross negligence;
and its June 16, 2005 Resolution denying petitioner’s
motion for reconsideration.
On October 1, 1993, respondent Ranida D. Salvador
started working as a trainee in the Accounting Department
of Limay Bulk Handling Terminal, Inc. (the Company). As
a prerequisite for regular employment, she underwent a
medical examination at the Community Diagnostic Center
(CDC). Garcia who is a medical technologist, conducted the
HBs Ag (Hepatitis B Surface Antigen) test5
and on October
22, 1993, CDC issued the test result indicating that
Ranida was “HBs Ag: Reactive.” The result bore the name
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572
Ranida underwent8
another HBs Ag test at the said hospital
and the result indicated that she is non-reactive. She
informed Sto. Domingo of this development but was told
that the test conducted by CDC was more reliable because
it used the Micro-Elisa Method.
Thus, Ranida went back to CDC for confirmatory
testing, and this time, the Anti-HBs
9
test conducted on her
indicated a “Negative” result.
Ranida also underwent another HBs Ag test at the
Bataan Doctors Hospital using the Micro-Elisa 10
Method.
The result indicated that she was non-reactive.
Ranida submitted the test results from Bataan Doctors
Hospital and CDC to the Executive Officer of the Company
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8 Id., at p. 188.
9 Id., at p. 189.
10 Id., at p. 190.
11 Id., at p. 192.
12 Id., at p. 209.
13 Id., at pp. 1-7.
573
On September
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26, 1994, respondents amended their
complaint by naming Castro as the “unknown
pathologist.”
Garcia denied the allegations of gross negligence and
incompetence and reiterated the scientific explanation for
the “false positive” result of the first HBs15 Ag test in his
December 7, 1993 letter to the respondents.
For his part, Castro claimed that as pathologist, he
rarely went to CDC and only when a case was referred to
him; that he did not examine Ranida; and that the test
results bore only his rubber-stamp signature.
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On September 1, 1997, the trial court dismissed the
complaint for failure of the respondents to present
sufficient evidence to prove the liability of Garcia and
Castro. It held that respondents should have presented Sto.
Domingo because he was the one who interpreted the test
result issued by CDC. Likewise, respondents should have
presented a medical expert to refute the testimonies of
Garcia and Castro regarding the medical 17
explanation
behind the conflicting test results on Ranida.
Respondents appealed to the Court of Appeals which
reversed the trial court’s findings, the dispositive portion of
which states:
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19 Estacion v. Bernardo, G.R. No. 144723, February 27, 2006, 483 SCRA
222, 231.
20 Child Learning Center, Inc. v. Tagorio, G.R. No. 150920, November
25, 2005, 476 SCRA 236, 242.
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21 Garcia-Rueda v. Pascasio, 344 Phil. 323, 331; 278 SCRA 769, 778
(1997).
22 Department of Health (DOH) Administrative Order 49-B (1988), Sec.
3.
23 Cipriano v. Court of Appeals, 331 Phil. 1019, 1025; 263 SCRA 711,
717 (1996).
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9.1 Head of the Clinical Laboratory: The head is that person who
assumes technical and administrative supervision and control of the
activities in the laboratory.
For all categories of clinical laboratories, the head shall be a licensed
physician certified by the Philippine Board of Pathology in either
Anatomic or Clinical Pathology or both provided that:
(1) This shall be mandatory for all categories of freestanding clinical
laboratories; all tertiary category hospital laboratories and for all
secondary category hospital laboratories located in areas with sufficient
available pathologist.
xxxx
Sec. 11. Reporting: All laboratory requests shall be considered
as consultations between the requesting physician and
pathologist of the laboratory. As such all laboratory reports on
various examinations of human specimens shall be construed as
consultation report and shall bear the name of the pathologist or
his associate. No person in clinical laboratory shall issue a report,
orally or in writing, whole portions thereof without a directive
from the pathologist or his authorized associate and only to the
requesting physician or his
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24 Records, p. 193.
25 Id., at pp. 456-457.
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for purposes of complying with the rules and regulations and orders
issued by the Department of Health through the Bureau of Research and
Laboratories. Defendant pathologist does not stay that long period of
time at the Community Diagnostic Center but only periodically or
whenever a case is referred to him by the laboratory. Defendant
pathologist does not appoint or select the employees of the laboratory nor
26
“[He] does not know, and has never known or met, the plaintiff-
patient even up to this time nor has he personally examined any
specimen, blood, urine or any other tissue, from the plaintiff-
patient otherwise his own handwritten signature would have
appeared in the result and not merely 28
stamped as shown in
Annex “B” of the Amended Complaint.”
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Judgment affirmed.
——o0o——
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